-
Notifications
You must be signed in to change notification settings - Fork 0
/
shc.bib
1556 lines (1460 loc) · 163 KB
/
shc.bib
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
276
277
278
279
280
281
282
283
284
285
286
287
288
289
290
291
292
293
294
295
296
297
298
299
300
301
302
303
304
305
306
307
308
309
310
311
312
313
314
315
316
317
318
319
320
321
322
323
324
325
326
327
328
329
330
331
332
333
334
335
336
337
338
339
340
341
342
343
344
345
346
347
348
349
350
351
352
353
354
355
356
357
358
359
360
361
362
363
364
365
366
367
368
369
370
371
372
373
374
375
376
377
378
379
380
381
382
383
384
385
386
387
388
389
390
391
392
393
394
395
396
397
398
399
400
401
402
403
404
405
406
407
408
409
410
411
412
413
414
415
416
417
418
419
420
421
422
423
424
425
426
427
428
429
430
431
432
433
434
435
436
437
438
439
440
441
442
443
444
445
446
447
448
449
450
451
452
453
454
455
456
457
458
459
460
461
462
463
464
465
466
467
468
469
470
471
472
473
474
475
476
477
478
479
480
481
482
483
484
485
486
487
488
489
490
491
492
493
494
495
496
497
498
499
500
501
502
503
504
505
506
507
508
509
510
511
512
513
514
515
516
517
518
519
520
521
522
523
524
525
526
527
528
529
530
531
532
533
534
535
536
537
538
539
540
541
542
543
544
545
546
547
548
549
550
551
552
553
554
555
556
557
558
559
560
561
562
563
564
565
566
567
568
569
570
571
572
573
574
575
576
577
578
579
580
581
582
583
584
585
586
587
588
589
590
591
592
593
594
595
596
597
598
599
600
601
602
603
604
605
606
607
608
609
610
611
612
613
614
615
616
617
618
619
620
621
622
623
624
625
626
627
628
629
630
631
632
633
634
635
636
637
638
639
640
641
642
643
644
645
646
647
648
649
650
651
652
653
654
655
656
657
658
659
660
661
662
663
664
665
666
667
668
669
670
671
672
673
674
675
676
677
678
679
680
681
682
683
684
685
686
687
688
689
690
691
692
693
694
695
696
697
698
699
700
701
702
703
704
705
706
707
708
709
710
711
712
713
714
715
716
717
718
719
720
721
722
723
724
725
726
727
728
729
730
731
732
733
734
735
736
737
738
739
740
741
742
743
744
745
746
747
748
749
750
751
752
753
754
755
756
757
758
759
760
761
762
763
764
765
766
767
768
769
770
771
772
773
774
775
776
777
778
779
780
781
782
783
784
785
786
787
788
789
790
791
792
793
794
795
796
797
798
799
800
801
802
803
804
805
806
807
808
809
810
811
812
813
814
815
816
817
818
819
820
821
822
823
824
825
826
827
828
829
830
831
832
833
834
835
836
837
838
839
840
841
842
843
844
845
846
847
848
849
850
851
852
853
854
855
856
857
858
859
860
861
862
863
864
865
866
867
868
869
870
871
872
873
874
875
876
877
878
879
880
881
882
883
884
885
886
887
888
889
890
891
892
893
894
895
896
897
898
899
900
901
902
903
904
905
906
907
908
909
910
911
912
913
914
915
916
917
918
919
920
921
922
923
924
925
926
927
928
929
930
931
932
933
934
935
936
937
938
939
940
941
942
943
944
945
946
947
948
949
950
951
952
953
954
955
956
957
958
959
960
961
962
963
964
965
966
967
968
969
970
971
972
973
974
975
976
977
978
979
980
981
982
983
984
985
986
987
988
989
990
991
992
993
994
995
996
997
998
999
1000
@article{jimenez_large_2013,
title = {Large fibre size in skeletal muscle is metabolically advantageous},
volume = {4},
copyright = {© 2013 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.},
url = {http:/\linebreak[0]/\linebreak[0]www.nature.com/\linebreak[0]ncomms/\linebreak[0]2013/\linebreak[0]130712/\linebreak[0]ncomms3150/\linebreak[0]full/\linebreak[0]ncomms3150.html},
doi = {10.1038/ncomms3150},
abstract = {Skeletal muscle fibre size is highly variable, and while diffusion appears to limit maximal fibre size, there is no paradigm for the control of minimal size. The optimal fibre size hypothesis posits that the reduced surface area to volume in larger fibres reduces the metabolic cost of maintaining the membrane potential, and so fibres attain an optimal size that minimizes metabolic cost while avoiding diffusion limitation. Here we examine changes during hypertrophic fibre growth in metabolic cost and activity of the Na+-K+-{ATPase} in white skeletal muscle from crustaceans and fishes. We provide evidence for a major tenet of the optimal fibre size hypothesis by demonstrating that larger fibres are metabolically cheaper to maintain, and the cost of maintaining the membrane potential is proportional to fibre surface area to volume. The influence of surface area to volume on metabolic cost is apparent during growth in 16 species spanning a 20-fold range in fibre size, suggesting that this principle may apply widely.},
language = {en},
urldate = {2013-09-12},
journal = {Nature Communications},
author = {Jimenez, Ana Gabriela and Dillaman, Richard M. and Kinsey, Stephen T.},
month = jul,
year = {2013},
keywords = {Biological sciences, Cell biology, evolution},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/Q774F33I/Jimenez et al. - 2013 - Large fibre size in skeletal muscle is metabolical.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/FW6SCZEA/ncomms3150.html:text/html}
},
@article{novakovic_mechanical_2006,
title = {Mechanical reconfiguration mediates swallowing and rejection in \textit{{A}plysia} \textit{californica}},
volume = {192},
url = {http:/\linebreak[0]/\linebreak[0]dx.doi.org/\linebreak[0]10.1007/\linebreak[0]s00359-\linebreak[0]006-\linebreak[0]0124-\linebreak[0]7},
doi = {10.1007/s00359-006-0124-7},
abstract = {Abstract Muscular hydrostats, such as tongues, trunks or tentacles, have fewer constraints on their degrees of freedom than musculoskeletal systems, so changes in a structure’s shape may alter the positions and lengths of other components (i.e., induce mechanical reconfiguration). We studied mechanical reconfiguration during rejection and swallowing in the marine mollusk Aplysia californica. During rejection, inedible material is pushed out of an animal’s buccal cavity. The grasper (radula/odontophore) closes on inedible material, and then a posterior muscle, I2, pushes the grasper toward the jaws (protracts it). After the material is released, an anterior muscle complex (the {I1/I3/jaw} complex) pushes the grasper toward the esophagus (retracts it). During swallowing, the grasper is protracted open, and then retracts closed, pulling in food. Grasper closure changes its shape. Magnetic resonance images show that grasper closure lengthens I2. A kinetic model quantified the changes in the ability of I2 and {I1/I3} to exert force as grasper shape changed. Grasper closure increases I2’s ability to protract during rejection, and increases {I1/I3’s} ability to retract during swallowing. Motor neurons controlling radular closure may therefore affect the behavioral outputs of I2’s and {I1/I3’s} motor neurons. Thus, motor neurons may modulate the outputs of other motor neurons through mechanical reconfiguration.},
number = {8},
urldate = {2007-12-26},
journal = {Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology},
author = {Novakovic, Valerie A. and Sutton, Gregory P. and Neustadter, David M. and Beer, Randall D. and Chiel, Hillel J.},
year = {2006},
pages = {857--870},
file = {PubMed Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/9QSCMVS8/entrez.html:text/html;SpringerLink Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/BVEJCHDJ/Novakovic et al2006Mechanical reconfiguration mediates swallowing and.pdf:application/pdf;SpringerLink Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/6RT2ZBAZ/54t3762132r83803.html:text/html}
},
@article{levi_dual_2004,
title = {Dual Sensory-Motor Function for a Molluskan Statocyst Network},
volume = {91},
url = {http:/\linebreak[0]/\linebreak[0]jn.physiology.org/\linebreak[0]cgi/\linebreak[0]content/\linebreak[0]abstract/\linebreak[0]91/\linebreak[0]1/\linebreak[0]336},
doi = {10.1152/jn.00753.2003},
abstract = {In mollusks, statocyst receptor cells ({SRCs)} interact with each other forming a neural network; their activity is determined by both the animal's orientation in the gravitational field and multimodal inputs. These two facts suggest that the function of the statocysts is not limited to sensing the animal's orientation. We studied the role of the statocysts in the organization of search motion during hunting behavior in the marine mollusk, Clione limacina. When hunting, Clione swims along a complex trajectory including numerous twists and turns confined within a definite space. Search-like behavior could be evoked pharmacologically by physostigmine; application of physostigmine to the isolated {CNS} produced "fictive search behavior" monitored by recordings from wing and tail nerves. Both in behavioral and in vitro experiments, we found that the statocysts are necessary for search behavior. The motor program typical of searching could not be produced after removing the statocysts. Simultaneous recordings from single {SRCs} and motor nerves showed that there was a correlation between the {SRCs} activity and search episodes. This correlation occurred even though the preparation was fixed and, therefore the sensory stimulus was constant. The excitation of individual {SRCs} could in some cases precede the beginning of search episodes. A biologically based model showed that, theoretically, the hunting search motor program could be generated by the statocyst receptor network due to its intrinsic dynamics. The results presented support for the idea that the statocysts are actively involved in the production of the motor program underlying search movements during hunting behavior.},
number = {1},
urldate = {2009-06-16},
journal = {J Neurophysiol},
author = {Levi, R. and Varona, P. and Arshavsky, Y. I. and Rabinovich, M. I. and Selverston, A. I.},
month = jan,
year = {2004},
pages = {336--345},
file = {HighWire Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/BQC3BBUF/Levi et al. - 2004 - Dual Sensory-Motor Function for a Molluskan Statoc.pdf:application/pdf;HighWire Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/7V7364IA/336.html:text/html}
},
@article{yu_biomechanical_1999,
title = {Biomechanical properties and a kinetic simulation model of the smooth muscle {I}2 in the buccal mass of \textit{{A}plysia}},
volume = {81},
issn = {03401200},
abstract = {The muscle I2 is a smooth muscle from the buccal mass of the marine mollusc Aplysia californica whose neural control, in vivo kinematics, and behavioral role have been extensively analyzed. In this study, we measured the activation and contractile dynamics of the muscle in order to construct a Hill-type kinetic model of the muscle. This is the first study to our knowledge, of Aplysia muscle contractile dynamics. The isometric force-frequency relationship of I2 had a frequency threshold of about 6-8 Hz, and its force output saturated at 20-25 Hz, properties that match the high frequency (20 Hz) bursts generated by the {B31/B32} neurons that innervate it. Peak isometric force was generated at about 118\% of the in situ relaxed length. These results and I2's estimated in vivo kinematics suggest that it generates maximum force at the onset of protraction. The muscle tension during iso-velocity lengthening and shortening was an asymmetric function of velocity. Short range stiffness and yielding responses were observed in lengthening, whereas muscle tension decreased smoothly in shortening. These visco-elastic properties suggest that the I2 muscle can serve to brake forceful retraction movements. A Hill-type model, parameterized from the measurements, captured many of the mechanical properties of I2. Our results provide a quantitative understanding of the biomechanical significance of the muscle's neural control and provide a basis for simulation studies of the control of feeding behavior.},
number = {5-6},
journal = {Biological Cybernetics},
author = {Yu, S N and Crago, P E and Chiel, H J},
month = nov,
year = {1999},
keywords = {Animals, Aplysia, Behavior, Animal, Biomechanics, Cheek, Cybernetics, Elasticity, Electric Stimulation, Isometric Contraction, Kinetics, Models, Biological, Muscle, Smooth, Viscosity},
pages = {505--13},
file = {PubMed Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/VBMMNWSC/entrez.html:text/html;Yu et al1999Biomechanical properties and a kinetic simulation .pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/IQ94HZ4H/Yu et al1999Biomechanical properties and a kinetic simulation .pdf:application/pdf}
},
@article{church_activity_1994,
title = {Activity of multiple identified motor neurons recorded intracellularly during evoked feedinglike motor programs in \textit{{A}plysia}},
volume = {72},
url = {http:/\linebreak[0]/\linebreak[0]jn.physiology.org/\linebreak[0]cgi/\linebreak[0]content/\linebreak[0]abstract/\linebreak[0]72/\linebreak[0]4/\linebreak[0]1794},
number = {4},
urldate = {2010-09-09},
journal = {J Neurophysiol},
author = {Church, P. J. and Lloyd, P. E.},
month = oct,
year = {1994},
pages = {1794--1809},
file = {HighWire Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/47V3FX4C/Church and Lloyd - 1994 - Activity of multiple identified motor neurons reco.pdf:application/pdf;HighWire Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/TT59F9A4/1794.html:text/html}
},
@article{morton_timing_1993,
title = {The timing of activity in motor neurons that produce radula movements distinguishes ingestion from rejection in \textit{{A}plysia}},
volume = {173},
url = {http:/\linebreak[0]/\linebreak[0]dx.doi.org/\linebreak[0]10.1007/\linebreak[0]BF00197761},
doi = {10.1007/BF00197761},
abstract = {{1.We} have studied the neural circuitry mediating ingestion and rejection in Aplysia using a reduced preparation that produces ingestion-like and rejection-like motor patterns in response to physiological {stimuli.2.We} have characterized 3 buccal ganglion motor neurons that produce specific movements of the radula and buccal mass. B8a and B8b act to close the radula. B10 acts to close the jaws and retract the {radula.3.The} patterns of activity in these neurons can be used to distinguish the ingestion-like and rejection-like motor patterns. B8a, B8b and B10 are active together during the ingestion-like pattern. Activity in B8a and B8b ends prior to the onset of activity in B10 during the rejection-like {pattern.4.Our} data suggest that these neurons undergo similar patterns of activity in vivo. During both feeding-like patterns, the activity and peripheral actions of B8a, B8b, and B10 are consistent with radula movements observed during ingestion and rejection. In addition, the extracellular activity produced by these neurons is consistent with neural activity observed in vivo during ingestion and {rejection.5.Our} data suggest that the different activity patterns observed in these motor neurons contribute to the different radula movements that distinguish ingestion from rejection.},
number = {5},
urldate = {2009-06-22},
journal = {Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology},
author = {Morton, D. W. and Chiel, H. J.},
month = nov,
year = {1993},
pages = {519--536},
file = {PubMed Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/PDV2548A/entrez.html:text/html;SpringerLink Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/DBF7G4HW/Morton and Chiel - 1993 - The timing of activity in motor neurons that produ.pdf:application/pdf;SpringerLink Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/UBPI2CPJ/m1x43m56766w77g3.html:text/html}
},
@article{varona_competing_2004,
title = {Competing sensory neurons and motor rhythm coordination},
volume = {58-60},
issn = {0925-2312},
url = {http:/\linebreak[0]/\linebreak[0]www.sciencedirect.com/\linebreak[0]science/\linebreak[0]article/\linebreak[0]B6V10-\linebreak[0]4BVP69M-\linebreak[0]M/\linebreak[0]2/\linebreak[0]c7aa0434cb0551bbe9ac6b1707b52ba7},
doi = {10.1016/j.neucom.2004.01.093},
abstract = {The marine mollusk Clione limacina has a peculiar hunting behavior characterized by a complex sequence of loops and turns. We have developed a model of the receptor network of Clione's gravimetric organ to explain this behavior. In this paper we discuss the possible role of an activation phase lock among the statocyst receptor neurons to coordinate the motion during hunting. As a result of a winnerless competition among receptor cells, an apparent intricate but coordinated sequence of signals emerges. This sequence can drive complex but, at the same time, organized movements.},
urldate = {2009-05-05},
journal = {Neurocomputing},
author = {Varona, Pablo and Levi, Rafael and Arshavsky, Yuri I. and Rabinovich, Mikhail I. and Selverston, Allen I.},
month = jun,
year = {2004},
keywords = {Motor coordination, Statocyst receptor network, Winnerless competition},
pages = {549--554},
file = {ScienceDirect Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/NJVE6ZIZ/Varona et al - 2004 - Competing sensory neurons and motor rhythm coordin.pdf:application/pdf;ScienceDirect Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/9SH5QGIA/science.html:text/html}
},
@article{guckenheimer_structurally_1988,
title = {Structurally Stable Heteroclinic Cycles},
volume = {103},
doi = {10.1017/S0305004100064732},
abstract = {This paper describes a previously undocumented phenomenon in dynamical systems theory; namely, the occurrence of heteroclinic cycles that are structurally stable within the space of Cr vector fields equivariant with respect to a symmetry group. In the space X(M) of Cr vector fields on a manifold M, there is a residual set of vector fields having no trajectories joining saddle points with stable manifolds of the same dimension. Such heteroclinic connections are a structurally unstable phenomenon [4]. However, in the space {XG(M)} ⊂ X(M) of vector fields equivariant with respect to a symmetry group G, the situation can be quite different. We give an example of an open set U of topologically equivalent vector fields in the space of vector fields on 3 equivariant with respect to a particular finite subgroup G ⊂ O(3) such that each X U has a heteroclinic cycle that is an attractor. The heteroclinic cycles consist of three equilibrium points and three trajectories joining them.},
number = {01},
urldate = {2010-03-13},
journal = {Mathematical Proceedings of the Cambridge Philosophical Society},
author = {Guckenheimer, John and Holmes, Philip},
year = {1988},
pages = {189--192},
file = {Cambridge Journals Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/TVFB3HJU/displayAbstract.html:text/html;gh_sshc_1988.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/ZJAGIBDT/gh_sshc_1988.pdf:application/pdf}
},
@article{ijspeert_central_2008,
title = {Central pattern generators for locomotion control in animals and robots: A review},
volume = {21},
issn = {0893-6080},
shorttitle = {Central pattern generators for locomotion control in animals and robots},
url = {http:/\linebreak[0]/\linebreak[0]www.sciencedirect.com/\linebreak[0]science/\linebreak[0]article/\linebreak[0]B6T08-\linebreak[0]4SH6B9F-\linebreak[0]2/\linebreak[0]2/\linebreak[0]2e0a2fdad02d315becc218a6602f054d},
doi = {10.1016/j.neunet.2008.03.014},
abstract = {The problem of controlling locomotion is an area in which neuroscience and robotics can fruitfully interact. In this article, I will review research carried out on locomotor central pattern generators ({CPGs)}, i.e. neural circuits capable of producing coordinated patterns of high-dimensional rhythmic output signals while receiving only simple, low-dimensional, input signals. The review will first cover neurobiological observations concerning locomotor {CPGs} and their numerical modelling, with a special focus on vertebrates. It will then cover how {CPG} models implemented as neural networks or systems of coupled oscillators can be used in robotics for controlling the locomotion of articulated robots. The review also presents how robots can be used as scientific tools to obtain a better understanding of the functioning of biological {CPGs.} Finally, various methods for designing {CPGs} to control specific modes of locomotion will be briefly reviewed. In this process, I will discuss different types of {CPG} models, the pros and cons of using {CPGs} with robots, and the pros and cons of using robots as scientific tools. Open research topics both in biology and in robotics will also be discussed.},
number = {4},
urldate = {2010-11-11},
journal = {Neural Networks},
author = {Ijspeert, Auke Jan},
month = may,
year = {2008},
keywords = {Central pattern generators, Computational models, Dynamical systems, Locomotion, neural networks, Robots, Systems of coupled oscillators},
pages = {642--653},
file = {ScienceDirect Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/8WGMW9PD/Ijspeert - 2008 - Central pattern generators for locomotion control .pdf:application/pdf;ScienceDirect Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/WTP3ITEP/science.html:text/html}
},
@article{rabinovich_transient_2008,
title = {Transient Cognitive Dynamics, Metastability, and Decision Making},
volume = {4},
url = {http:/\linebreak[0]/\linebreak[0]dx.plos.org/\linebreak[0]10.1371/\linebreak[0]journal.pcbi.1000072},
doi = {10.1371/journal.pcbi.1000072},
abstract = {The modeling of the temporal structure of cognitive processes is a key step for understanding cognition. Cognitive functions such as sequential learning, short-term memory, and decision making in a changing environment cannot be understood using only the traditional view based on classical concepts of nonlinear dynamics, which describe static or rhythmic brain activity. The execution of many cognitive functions is a transient dynamical process. Any dynamical mechanism underlying cognitive processes has to be reproducible from experiment to experiment in similar environmental conditions and, at the same time, it has to be sensitive to changing internal and external information. We propose here a new dynamical object that can represent robust and reproducible transient brain dynamics. We also propose a new class of models for the analysis of transient dynamics that can be applied for sequential decision making.},
number = {5},
urldate = {2009-04-07},
journal = {{PLoS} Comput Biol},
author = {Rabinovich, Mikhail I. and Huerta, Ramón and Varona, Pablo and Afraimovich, Valentin S.},
month = may,
year = {2008},
pages = {e1000072},
file = {PLoS Computational Biology: Transient Cognitive Dynamics, Metastability, and Decision Making:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/AU7K7QPU/info3Adoi2F10.13712Fjournal.pcbi.html:text/html;PLoS One Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/B3VFA49F/Rabinovich et al - 2008 - Transient Cognitive Dynamics, Metastability, and D.pdf:application/pdf}
},
@article{neustadter_kinematics_2002,
title = {Kinematics of the buccal mass during swallowing based on magnetic resonance imaging in intact, behaving \textit{{A}plysia} \textit{californica}},
volume = {205},
url = {http:/\linebreak[0]/\linebreak[0]jeb.biologists.org/\linebreak[0]cgi/\linebreak[0]content/\linebreak[0]abstract/\linebreak[0]205/\linebreak[0]7/\linebreak[0]939},
abstract = {A novel magnetic resonance imaging interface has been developed that makes it possible to image movements in intact, freely moving subjects. We have used this interface to image the internal structures of the feeding apparatus (i.e. the buccal mass) of the marine mollusc Aplysia californica. The temporal and spatial resolution of the resulting images is sufficient to describe the kinematics of specific muscles of the buccal mass and the internal movements of the main structures responsible for grasping food, the radula and the odontophore. These observations suggest that a previously undescribed feature on the anterior margin of the odontophore, a fluid-filled structure that we term the prow, may aid in opening the jaw lumen early in protraction. Radular closing during swallowing occurs near the peak of protraction as the radular stalk is pushed rapidly out of the odontophore. Retraction of the odontophore is enhanced by the closure of the lumen of the jaws on the elongated odontophore, causing the odontophore to rotate rapidly towards the esophagus. Radular opening occurs after the peak of retraction and without the active contraction of the protractor muscle 12 and is due, in part, to the movement of the radular stalk into the odontophore. The large variability between responses also suggests that the great flexibility of swallowing responses may be due to variability in neural control and in the biomechanics of the ingested food and to the inherent flexibility of the buccal mass.},
number = {7},
urldate = {2007-11-27},
journal = {Journal of Experimental Biology},
author = {Neustadter, David M. and Drushel, Richard F. and Chiel, Hillel J.},
month = apr,
year = {2002},
pages = {939--958},
file = {HighWire Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/57WSE6TK/939.html:text/html;Neustadter et al2002Kinematics of the buccal mass during swallowing ba.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/8BAJD867/Neustadter et al2002Kinematics of the buccal mass during swallowing ba.pdf:application/pdf}
},
@article{evans_proprioceptive_1998,
title = {Proprioceptive Input to Feeding Motor Programs in \textit{{A}plysia}},
volume = {18},
url = {http:/\linebreak[0]/\linebreak[0]www.jneurosci.org/\linebreak[0]cgi/\linebreak[0]content/\linebreak[0]abstract/\linebreak[0]18/\linebreak[0]19/\linebreak[0]8016},
abstract = {Although central pattern generators ({CPGs)} can produce rhythmic activity in isolation, it is now generally accepted that under physiological conditions information from the external and internal environment is incorporated into {CPG-induced} motor programs. Experimentally advantageous invertebrate preparations may be particularly useful for studies that seek to characterize the cellular mechanisms that make this possible. In these experiments, we study sensorimotor integration in the feeding circuitry of the mollusc Aplysia. We show that a premotor neuron with plateau properties, B51, is important for generating the radula closing/retraction phase of ingestive motor programs. When B51 is depolarized in semi-intact preparations, radula closing/retractions are enhanced. When B51 is hyperpolarized, radula closing/retractions are reduced in size. In addition to being important as a premotor interneuron, B51 is also a sensory neuron that is activated when the feeding apparatus, the radula, rotates backward. The number of centripetal spikes in B51 is increased if the resistance to backward rotation is increased. Thus, B51 is a proprioceptor that is likely to be part of a feedback loop that insures that food will be moved into the buccal cavity when difficulty is encountered. Our data suggest, therefore, that Aplysia are able to adjust feeding motor programs to accommodate the specific qualities of the food ingested because at least one of the neurons that generates the basic ingestive motor program also serves as an on-line monitor of the success of radula movements.},
number = {19},
urldate = {2009-11-06},
journal = {J. Neurosci.},
author = {Evans, Colin G. and Cropper, Elizabeth C.},
month = oct,
year = {1998},
pages = {8016--8031},
file = {HighWire Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/GXRT7PHU/Evans and Cropper - 1998 - Proprioceptive Input to Feeding Motor Programs in .pdf:application/pdf;HighWire Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/52ST6ESW/8016.html:text/html}
},
@article{afraimovich_origin_2004,
title = {On the origin of reproducible sequential activity in neural circuits},
volume = {14},
issn = {10541500},
url = {http:/\linebreak[0]/\linebreak[0]link.aip.org/\linebreak[0]link/\linebreak[0]CHAOEH/\linebreak[0]v14/\linebreak[0]i4/\linebreak[0]p1123/\linebreak[0]s1\&\linebreak[0]Agg=doi},
doi = {10.1063/1.1819625},
number = {4},
urldate = {2010-11-30},
journal = {Chaos: An Interdisciplinary Journal of Nonlinear Science},
author = {Afraimovich, V. S. and Zhigulin, V. P. and Rabinovich, M. I.},
year = {2004},
pages = {1123},
file = {Afraimovich_origin_2004.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/MU4GR5TD/Afraimovich_origin_2004.pdf:application/pdf}
},
@article{hurwitz_activity_1996,
title = {Activity patterns of the {B31/B32} pattern initiators innervating the {I}2 muscle of the buccal mass during normal feeding movements in \textit{{A}plysia} \textit{californica}},
volume = {75},
issn = {00223077},
abstract = {1. B31 and B32 are pattern-initiator neurons in the buccal ganglia of Aplysia. Along with the {B61/B62} neurons, {B31/B32} are also motor neurons that innervate the 12 buccal muscle via the I2 nerve. This research was aimed at determining the physiological functions of the {B31/B32} and {B61/B62} neurons, and of the I2 muscle. 2. Stimulating the I2 muscle in the radula rest position produces radula protraction. In addition, in behaving animals lesioning either the muscle or the I2 nerve greatly reduces radula protraction. 3. During buccal motor programs in reduced preparations, {B31/B32} and B61/62 fire preceding activity in neuron B4, whose firing indicates the onset of radula retraction. In addition, during both ingestion-like and rejection-like patterns the activity in the I2 nerve is correlated with protraction. 4. {B31/B32} fire at frequencies of 15-25 Hz. Neither {B31/B32} nor {B61/B62} elicit facilitating end-junction potentials ({EJPs)} and electromyograms ({EMGs)} in the I2 muscle. {EMGs} from {B31/B32} are smaller than those from {B61/B62.} {B31/B32} and {B61/B62} innervate all areas of the muscle approximately uniformly. 5. In behaving animals, {EMGs} consistent with {B31/B32} activity are seen in the I2 muscle during the protraction phase of biting, swallowing, and rejection movements. In addition, the I2 muscle receives inputs that cannot be attributed to either the {B31/B32} or {B61/B62} neurons, either because the potentials are too large, firing frequencies are too low, or a prominent facilitation is seen. Such potentials are associated with lip movements, and also with radula retraction. 6. {EMGs} were recorded from the I2 muscle during feeding behavior after a lesion of the I2 nerve. Animals that had severe deficits in protraction showed no activity consistent with {B31/B32} or {B61/B62}, but did show activity during retraction. 7. Our data indicate that the I2 muscle and the {B31/B32} motor neurons are essential constituents contributing to protraction movements. Activity in these neurons is associated with radula protraction, which occurs as a component of a number of different feeding movements. The I2 muscle may also contribute to retraction, via activation by other motor neurons.},
number = {4},
journal = {Journal of Neurophysiology},
author = {Hurwitz, I and Neustadter, D and Morton, D W and Chiel, H J and Susswein, A J},
month = apr,
year = {1996},
keywords = {Action Potentials, Animals, Aplysia, Cheek, electromyography, Feeding Behavior, Ganglia, Invertebrate, Membrane Potentials, Motor Neurons, Movement, Muscle, Skeletal, Neuromuscular Junction, Neurons},
pages = {1309--26},
file = {Hurwitz et al1996Activity patterns of the B31B32 pattern initiator.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/XXMUJ3CC/Hurwitz et al1996Activity patterns of the B31B32 pattern initiator.pdf:application/pdf;PubMed Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/KHDBM4NK/entrez.html:text/html}
},
@article{hurwitz_different_1997,
title = {Different Roles of Neurons {B}63 and {B}34 That Are Active During the Protraction Phase of Buccal Motor Programs in \textit{{A}plysia} \textit{californica}},
volume = {78},
url = {http:/\linebreak[0]/\linebreak[0]jn.physiology.org/\linebreak[0]content/\linebreak[0]78/\linebreak[0]3/\linebreak[0]1305.abstract},
abstract = {Hurwitz, Itay, Irving Kupfermann, and Abraham J. Susswein. Different roles of neurons B63 and B34 that are active during the protraction phase of buccal motor programs in Aplysia californica. J. Neurophysiol. 78: 1305–1319, 1997. The buccal ganglion of Aplysia contains a central pattern generator ({CPG)} that organizes sequences of radula protraction and retraction during food ingestion and egestion. Neurons B63 and B34 have access to, or are elements of, the {CPG.} Both neurons are depolarized along with {B31/B32} during the protraction phase of buccal motor programs. Both cells excite the contralateral {B31/B32} neurons and inhibit B64 and other neurons active during the retraction phase. B63 and B34 also both have an axon exiting the buccal ganglia via the contralateral cerebrobuccal connective. Despite their similarities, B63 and B34 differ in a number of properties, which reflects their different functions. B63 fires during both ingestion and egestion-like buccal motor programs, whereas B34 fires only during egestion-like programs. The bilateral B63 neurons, along with the bilateral B31 and B32 neurons, act as a single functional unit. Sufficient depolarization of any of these neurons activates them all and initiates a buccal motor program. B63 is electrically coupled to both the ipsilateral and the contralateral {B31/B32} neurons but monosynaptically excites the contralateral neurons with a mixed electrical and chemical excitatory postsynaptic potential ({EPSP).} Positive feedback caused by electrical and chemical {EPSPs} between B63 and {B31/B32} contributes to the sustained depolarization in {B31/B32} and the firing of B63 during the protraction phase of a buccal motor program. B34 is excited during the protraction phase of all buccal motor programs, but, unlike B63, it does not always reach firing threshold. The neuron fires in response to current injection only after it is depolarized for 1–2 s or after preceding buccal motor programs in which it is depolarized. Firing of B34 produces facilitating {EPSPs} in the contralateral {B31/B32} and B63 neurons and can initiate a buccal motor program. Firing in B34 is strongly correlated with firing in the {B61/B62} motor neurons, which innervate the muscle (I2) responsible for much of protraction. B34 monosynaptically excites these motor neurons. B34 firing is also correlated with firing in motor neuron B8 during the protraction phase of a buccal motor program. B8 innervates the I4 radula closer muscle, which in egestion movements is active during protraction and in ingestion movements is active during retraction. B34 has a mixed, but predominantly excitatory, effect on B8 via a slow conductance-decrease {EPSP.} Thus firing in B34 leads to amplification of radula protraction that is coupled with radula closing, a pattern characteristic of egestion.},
number = {3},
urldate = {2011-01-26},
journal = {Journal of Neurophysiology},
author = {Hurwitz, Itay and Kupfermann, Irving and Susswein, Abraham J.},
year = {1997},
pages = {1305 --1319},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/BR7XTCXT/Hurwitz et al. - 1997 - Different Roles of Neurons B63 and B34 That Are Ac.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/2MPRKWWR/1305.html:text/html}
},
@article{neustadter_kinematics_2007,
title = {The kinematics of multifunctionality: comparisons of biting and swallowing in \textit{{A}plysia} \textit{californica}},
volume = {210},
shorttitle = {The kinematics of multifunctionality},
url = {http:/\linebreak[0]/\linebreak[0]jeb.biologists.org/\linebreak[0]cgi/\linebreak[0]content/\linebreak[0]abstract/\linebreak[0]210/\linebreak[0]2/\linebreak[0]238},
doi = {10.1242/jeb.02654},
abstract = {What are the mechanisms of multifunctionality, i.e. the use of the same peripheral structures for multiple behaviors? We studied this question using the multifunctional feeding apparatus of the marine mollusk Aplysia californica, in which the same muscles mediate biting (an attempt to grasp food) and swallowing (ingestion of food). Biting and swallowing responses were compared using magnetic resonance imaging of intact, behaving animals and a three-dimensional kinematic model. Biting is associated with larger amplitude protractions of the grasper (radula/odontophore) than swallowing, and smaller retractions. Larger biting protractions than in swallowing appear to be due to a more anterior position of the grasper as the behavior begins, a larger amplitude contraction of protractor muscle I2, and contraction of the posterior portion of the {I1/I3/jaw} complex. The posterior {I1/I3/jaw} complex may be context-dependent, i.e. its mechanical context changes the direction of the force it exerts. Thus, the posterior of {I1/I3} may aid protraction near the peak of biting, whereas the entire {I1/I3/jaw} complex acts as a retractor during swallowing. In addition, larger amplitude closure of the grasper during swallowing allows an animal to exert more force as it ingests food. These results demonstrate that differential deployment of the periphery can mediate multifunctionality.},
number = {2},
urldate = {2007-12-26},
journal = {Journal of Experimental Biology},
author = {Neustadter, David M. and Herman, Robert L. and Drushel, Richard F. and Chestek, David W. and Chiel, Hillel J.},
month = jan,
year = {2007},
pages = {238--260},
file = {HighWire Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/EITJHWET/Neustadter et al2007The kinematics of multifunctionality comparisons .pdf:application/pdf;HighWire Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/3UUZCI8D/238.html:text/html;PubMed Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/VTN8ZRKQ/entrez.html:text/html}
},
@article{baxter_feeding_2006,
title = {Feeding behavior of \textit{{A}plysia}: A model system for comparing cellular mechanisms of classical and operant conditioning},
volume = {13},
shorttitle = {Feeding behavior of \textit{{A}plysia}},
url = {http:/\linebreak[0]/\linebreak[0]www.learnmem.org/\linebreak[0]cgi/\linebreak[0]content/\linebreak[0]abstract/\linebreak[0]13/\linebreak[0]6/\linebreak[0]669},
doi = {10.1101/lm.339206},
abstract = {Feeding behavior of Aplysia provides an excellent model system for analyzing and comparing mechanisms underlying appetitive classical conditioning and reward operant conditioning. Behavioral protocols have been developed for both forms of associative learning, both of which increase the occurrence of biting following training. Because the neural circuitry that mediates the behavior is well characterized and amenable to detailed cellular analyses, substantial progress has been made toward a comparative analysis of the cellular mechanisms underlying these two forms of associative learning. Both forms of associative learning use the same reinforcement pathway (the esophageal nerve, En) and the same reinforcement transmitter (dopamine, {DA).} In addition, at least one cellular locus of plasticity (cell B51) is modified by both forms of associative learning. However, the two forms of associative learning have opposite effects on B51. Classical conditioning decreases the excitability of B51, whereas operant conditioning increases the excitability of B51. Thus, the approach of using two forms of associative learning to modify a single behavior, which is mediated by an analytically tractable neural circuit, is revealing similarities and differences in the mechanisms that underlie classical and operant conditioning.},
number = {6},
urldate = {2008-07-22},
journal = {Learn. Mem.},
author = {Baxter, Douglas A. and Byrne, John H.},
month = nov,
year = {2006},
pages = {669--680},
file = {HighWire Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/M3VIRB5B/Baxter and Byrne - 2006 - Feeding behavior of Aplysia A model system for co.pdf:application/pdf;HighWire Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/IMZAXUMB/669.html:text/html}
},
@incollection{cataldo_computational_2006,
series = {Lecture Notes in Computer Science},
title = {Computational Model of a Central Pattern Generator},
volume = {4210},
url = {http:/\linebreak[0]/\linebreak[0]dx.doi.org/\linebreak[0]10.1007/\linebreak[0]11885191\_17},
booktitle = {Computational Methods in Systems Biology},
publisher = {Springer Berlin / Heidelberg},
author = {Cataldo, Enrico and Byrne, John and Baxter, Douglas},
year = {2006},
pages = {242--256},
file = {Cataldo_computational_2006.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/ERHTVTUX/Cataldo_computational_2006.pdf:application/pdf}
},
@article{stone_random_1990,
title = {Random Perturbations of Heteroclinic Attractors},
volume = {50},
issn = {00361399},
url = {http:/\linebreak[0]/\linebreak[0]www.jstor.org/\linebreak[0]stable/\linebreak[0]2101884},
doi = {10.2307/2101884},
abstract = {Estimates are derived for the mean recurrence time of orbits in the neighborhood of an attracting homoclinic orbit or heteroclinic cycle in an ordinary differential equation, subject to small additive random noise. The theory presented is illustrated with numerical simulations of several systems, including ones invariant under symmetry groups, for which such heteroclinic attractors are structurally stable. The physical implications of the work presented are briefly discussed.},
number = {3},
urldate = {2009-05-12},
journal = {{SIAM} Journal on Applied Mathematics},
author = {Stone, Emily and Holmes, Philip},
month = jun,
year = {1990},
pages = {726--743},
file = {JSTOR Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/WP52J44B/Stone and Holmes - 1990 - Random Perturbations of Heteroclinic Attractors.pdf:application/pdf;Random Perturbations of Heteroclinic Attractors:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/UFG3KBZT/2101884.html:text/html}
},
@article{nowotny_dynamical_2007,
title = {Dynamical Origin of Independent Spiking and Bursting Activity in Neural Microcircuits},
volume = {98},
url = {http:/\linebreak[0]/\linebreak[0]link.aps.org/\linebreak[0]abstract/\linebreak[0]PRL/\linebreak[0]v98/\linebreak[0]e128106},
doi = {10.1103/PhysRevLett.98.128106},
number = {12},
urldate = {2009-05-05},
journal = {Physical Review Letters},
author = {Nowotny, Thomas and Rabinovich, Mikhail I.},
month = mar,
year = {2007},
pages = {128106--4},
file = {Dynamical Origin of Independent Spiking and Bursting Activity in Neural Microcircuits:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/RQMVV9V8/GetabsServlet.html:text/html;Nowotny_dynamical_2007.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/V2IHWTD5/Nowotny_dynamical_2007.pdf:application/pdf}
},
@article{smith_atp_2013,
title = {{ATP} Consumption by Sarcoplasmic Reticulum Ca2+ Pumps Accounts for 40-50\% of Resting Metabolic Rate in Mouse Fast and Slow Twitch Skeletal Muscle},
volume = {8},
url = {http:/\linebreak[0]/\linebreak[0]dx.doi.org/\linebreak[0]10.1371/\linebreak[0]journal.pone.0068924},
doi = {10.1371/journal.pone.0068924},
abstract = {The main purpose of this study was to directly quantify the relative contribution of Ca2+ cycling to resting metabolic rate in mouse fast (extensor digitorum longus, {EDL)} and slow (soleus) twitch skeletal muscle. Resting oxygen consumption of isolated muscles ({VO2}, {µL/g} wet weight/s) measured polarographically at {30°C} was {\textasciitilde}20\% higher (P{\textless}0.05) in soleus (0.326 ± 0.022) than in {EDL} (0.261 ± 0.020). In order to quantify the specific contribution of Ca2+ cycling to resting metabolic rate, the concentration of {MgCl2} in the bath was increased to 10 {mM} to block Ca2+ release through the ryanodine receptor, thus eliminating a major source of Ca2+ leak from the sarcoplasmic reticulum ({SR)}, and thereby indirectly inhibiting the activity of the sarco(endo) plasmic reticulum Ca2+-{ATPases} ({SERCAs).} The relative (\%) reduction in muscle {VO2} in response to 10 {mM} {MgCl2} was similar between soleus (48.0±3.7) and {EDL} (42.4±3.2). Using a different approach, we attempted to directly inhibit {SERCA} {ATPase} activity in stretched {EDL} and soleus muscles (1.42x optimum length) using the specific {SERCA} inhibitor cyclopiazonic acid ({CPA}, up to 160 {µM)}, but were unsuccessful in removing the energetic cost of Ca2+ cycling in resting isolated muscles. The results of the {MgCl2} experiments indicate that {ATP} consumption by {SERCAs} is responsible for 40–50\% of resting metabolic rate in both mouse fast- and slow-twitch muscles at {30°C}, or 12–15\% of whole body resting {VO2.} Thus, {SERCA} pumps in skeletal muscle could represent an important control point for energy balance regulation and a potential target for metabolic alterations to oppose obesity.},
number = {7},
urldate = {2013-09-12},
journal = {{PLoS} {ONE}},
author = {Smith, Ian Curtis and Bombardier, Eric and Vigna, Chris and Tupling, A. Russell},
month = jul,
year = {2013},
pages = {e68924},
file = {PLoS Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/WEA5USNE/Smith et al. - 2013 - ATP Consumption by Sarcoplasmic Reticulum Ca2+ Pum.pdf:application/pdf;PLoS Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/99QSEJNI/infodoi10.1371journal.pone.html:text/html}
},
@article{spardy_dynamical_2011,
title = {A dynamical systems analysis of afferent control in a neuromechanical model of locomotion: {{II}.} Phase asymmetry},
volume = {8},
issn = {1741-2560, 1741-2552},
shorttitle = {A dynamical systems analysis of afferent control in a neuromechanical model of locomotion},
url = {http:/\linebreak[0]/\linebreak[0]iopscience.iop.org/\linebreak[0]1741-\linebreak[0]2560/\linebreak[0]8/\linebreak[0]6/\linebreak[0]065004},
doi = {10.1088/1741-2560/8/6/065004},
number = {6},
urldate = {2012-02-06},
journal = {Journal of Neural Engineering},
author = {Spardy, Lucy E and Markin, Sergey N and Shevtsova, Natalia A and Prilutsky, Boris I and Rybak, Ilya A and Rubin, Jonathan E},
month = oct,
year = {2011},
pages = {065004},
file = {A_dynamical_systems_analysis_of_afferent_control_in_a_neuromechanical_model_of_locomotion_II._Phase_.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/ETUNXJKC/A_dynamical_systems_analysis_of_afferent_control_in_a_neuromechanical_model_of_locomotion_II._Phase_.pdf:application/pdf}
},
@article{susswein_mechanisms_2002,
title = {Mechanisms Underlying Fictive Feeding in \textit{{A}plysia}: Coupling Between a Large Neuron With Plateau Potentials Activity and a Spiking Neuron},
volume = {87},
issn = {0022-3077, 1522-1598},
shorttitle = {Mechanisms Underlying Fictive Feeding in \textit{{A}plysia}},
url = {http:/\linebreak[0]/\linebreak[0]jn.physiology.org/\linebreak[0]content/\linebreak[0]87/\linebreak[0]5/\linebreak[0]2307.long},
abstract = {The buccal ganglia of Aplysia contain a central pattern generator ({CPG)} that organizes the rhythmic movements of the radula and buccal mass during feeding. Many of the cellular and synaptic elements of this {CPG} have been identified and characterized. However, the roles that specific cellular and synaptic properties play in generating patterns of activity are not well understood. To examine these issues, the present study developed computational models of a portion of this {CPG} and used simulations to investigate processes underlying the initiation of patterned activity. Simulations were done with the {SNNAP} software package. The simulated network contained two neurons, {B31/B32} and B63. The development of the model was guided and constrained by the available current-clamp data that describe the properties of these two protraction-phase interneurons {B31/B32} and B63, which are coupled via electrical and chemical synapses. Several configurations of the model were examined. In one configuration, a fast excitatory postsynaptic potential ({EPSP)} from B63 to {B31/B32} was implemented in combination with an endogenous plateau-like potential in {B31/B32.} In a second configuration, the excitatory synaptic connection from B63 to {B31/B32} produced both fast and slow {EPSPs} in {B31/B32} and the plateau-like potential was removed from {B31/B32.} Simulations indicated that the former configuration (i.e., electrical and fast chemical coupling in combination with a plateau-like potential) gave rise to a circuit that was robust to changes in parameter values and stochastic fluctuations, that closely mimicked empirical observations, and that was extremely sensitive to inputs controlling the onset of a burst. The coupling between the two simulated neurons served to amplify exogenous depolarizations via a positive feedback loop and the subthreshold activation of the plateau-like potential. Once a burst was initiated, the circuit produced the program in an all-or-none fashion. The slow kinetics of the simulated plateau-like potential played important roles in both initiating and maintaining the burst activity. Thus the present study identified cellular and network properties that contribute to the ability of the simulated network to integrate information over an extended period before a decision is made to initiate a burst of activity and suggests that similar mechanisms may operate in the buccal ganglia in initiating feeding movements.},
number = {5},
urldate = {2012-02-15},
journal = {Journal of Neurophysiology},
author = {Susswein, Abraham J and Hurwitz, Itay and Thorne, Richard and Byrne, John H and Baxter, Douglas A},
month = may,
year = {2002},
pages = {2307--2323},
file = {J Neurophysiol-2002-Susswein-2307-23.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/VW6B34TC/J Neurophysiol-2002-Susswein-2307-23.pdf:application/pdf;Mechanisms Underlying Fictive Feeding in Aplysia: Coupling Between a Large Neuron With Plateau Potentials Activity and a Spiking Neuron:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/AMGVKASA/2307.html:text/html;Mechanisms Underlying Fictive Feeding in Aplysia: Coupling Between a Large Neuron With Plateau Potentials Activity and a Spiking Neuron:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/B98AZNHC/2307.html:text/html}
},
@article{shaw_phase_2012,
title = {Phase Resetting in an Asymptotically Phaseless System: On the Phase Response of Limit Cycles Verging on a Heteroclinic Orbit},
volume = {11},
copyright = {© 2012 Society for Industrial and Applied Mathematics},
shorttitle = {Phase Resetting in an Asymptotically Phaseless System},
url = {http:/\linebreak[0]/\linebreak[0]link.aip.org/\linebreak[0]link/\linebreak[0]?SJA/\linebreak[0]11/\linebreak[0]350/\linebreak[0]1},
doi = {10.1137/110828976},
abstract = {Rhythmic behaviors in neural systems often combine features of limit-cycle dynamics (stability and periodicity) with features of near heteroclinic or near homoclinic cycle dynamics (extended dwell times in localized regions of phase space). Proximity of a limit cycle to one or more saddle equilibria can have a profound effect on the timing of trajectory components and response to both fast and slow perturbations, providing a possible mechanism for adaptive control of rhythmic motions. Reyn [{“Generation} of limit cycles from separatrix polygons in the phase plane” in Geometrical Approaches to Differential Equations, Lecture Notes in Math. 810, Springer, New York, 1980, pp. 264–289] showed that for a planar dynamical system with a stable heteroclinic cycle (or separatrix polygon), small perturbations satisfying a net inflow condition will generically give rise to a stable limit cycle (see also [J. Guckenheimer and P. Holmes, Nonlinear Oscillations, Dynamical Systems, and Bifurcations of Vector Fields, 3rd ed., Appl. Math. Sci. 42, Springer-Verlag, Berlin, 1990]). Here we consider the asymptotic behavior of the infinitesimal phase response curve ({iPRC)} for examples of two systems satisfying Reyn's inflow criterion, (i) a smooth system with a chain of four hyperbolic saddle points and (ii) a piecewise linear system corresponding to local linearization of the smooth system about its saddle points. For system (ii), we obtain exact expressions for the limit cycle and the {iPRC} as functions of a parameter \${\textbackslash}mu{\textgreater}0\$ representing the distance from a heteroclinic bifurcation point. In the \${\textbackslash}mu{\textbackslash}to 0\$ limit, we find that perturbations parallel to the unstable eigenvector direction in a piecewise linear region lead to divergent phase response, as previously observed [E. Brown, J. Moehlis, and P. Holmes, Neural Comput., 16 (2004), pp. 673–715]. In contrast to previous work, we find that perturbations parallel to the stable eigenvector direction can lead to either divergent or convergent phase response, depending on the phase at which the perturbation occurs. In the smooth system (i), we show numerical evidence of qualitatively similar phase specific sensitivity to perturbation. Having the exact expression for the {iPRC} for the piecewise linear system allows us to investigate its stability under diffusive coupling. In addition, we qualitatively compare {iPRCs} obtained for systems (i) and (ii) to {iPRCs} for the {Morris–Lecar} equations near a bifurcation from limit cycles to a saddle-homoclinic orbit.},
urldate = {2012-03-19},
journal = {{SIAM} Journal on Applied Dynamical Systems},
author = {Shaw, Kendrick M. and Park, Young-Min and Chiel, Hillel J. and Thomas, Peter J.},
year = {2012},
keywords = {bifurcation, central pattern generator, Computational neuroscience, heteroclinic orbit, homoclinic orbit, limit cycle, phase resetting curve, piecewise linear dynamical system, stable heteroclinic channel},
pages = {350--391},
file = {SJA000350.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/3QFHKDGJ/SJA000350.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/K7XRUUT3/p350_s1.html:text/html}
},
@article{glyn_dependence_1985,
title = {Dependence of adenosine triphosphatase activity of rabbit psoas muscle fibres and myofibrils on substrate concentration.},
volume = {365},
issn = {0022-3751, 1469-7793},
url = {http:/\linebreak[0]/\linebreak[0]jp.physoc.org/\linebreak[0]content/\linebreak[0]365/\linebreak[0]1/\linebreak[0]259},
abstract = {The rate of hydrolysis of adenosine triphosphate ({ATP)} by chemically skinned rabbit muscle fibres was measured as a function of Mg {ATP} concentration in the range 5 {microM} to 5 {mM.} Pyruvate kinase and lactate dehydrogenase were used to link adenosine diphosphate formation to oxidation of nicotinamide adenine dinucleotide which was followed by the change in absorption at 340 nm. The {ATPase} rate of a fully activated fibre ({pCa} = 4.5) increased monotonically with Mg {ATP} concentration in a manner that could be readily fitted by a hyperbola. At 15 degrees C, {pH} 7 and an ionic strength of 0.2 M the rate at saturating Mg {ATP} (Vm) was 1.78 +/- 0.2 s-1 per myosin head (mean +/- {S.D.;} n = 6) and the Mg {ATP} concentration needed for half the maximal rate (Km) was 16.6 +/- 2 {microM.} The {ATPase} of fibres that had been stabilized by cross-linking with 1-ethyl-3-(3-dimethyl-aminopropyl)carbodiimide ({EDC)} was also investigated. Cross-linking did not significantly affect the Vm or Km and these fibres proved useful for investigating the adequacy of the pyruvate kinase activity for regenerating hydrolysed {ATP.} Myofibrils were cross-linked with {EDC} or glutaraldehyde to prevent shortening. Their {ATPase} properties were investigated: the values of Vm were 0.85 +/- 0.18 (mean +/- {S.D.;} n = 14) and 0.82 +/- 0.05 s-1 (n = 6) and of Km were 18.0 +/- 2.8 and 12.4 +/- 2.4 {microM} respectively. The values of Vm and Km for {EDC} cross-linked myofibrils were fairly insensitive to ionic strength, the Km decreasing 40\% and the Vm increasing 50\% for a change from 0.2 to 0.3 M. This slight dependence on ionic strength is considered in relation to the ionic strength dependence of the elementary rate constants of the actomyosin subfragment-1 {ATPase} cycle.},
language = {en},
number = {1},
urldate = {2013-09-12},
journal = {The Journal of Physiology},
author = {Glyn, H. and Sleep, J.},
month = aug,
year = {1985},
pages = {259--276},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/JJX58UZ5/Glyn and Sleep - 1985 - Dependence of adenosine triphosphatase activity of.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/TTABGU6R/259.html:text/html}
},
@article{butera_dissection_1996,
title = {Dissection and reduction of a modeled bursting neuron},
volume = {3},
issn = {0929-5313, 1573-6873},
url = {http:/\linebreak[0]/\linebreak[0]www.springerlink.com/\linebreak[0]content/\linebreak[0]n2733052qjgj5761/\linebreak[0]},
doi = {10.1007/BF00161132},
number = {3},
urldate = {2012-05-08},
journal = {Journal of Computational Neuroscience},
author = {Butera, R. J. and Clark, J. W. and Byrne, J. H. and Rinzel, John},
month = sep,
year = {1996},
pages = {199--223},
file = {Butera_et_al_Dissection and Reduction of a Modeled Bursting Neuron_JComputational Neuroscience_1996.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/3V4QQ8SU/Butera_et_al_Dissection and Reduction of a Modeled Bursting Neuron_JComputational Neuroscience_1996.pdf:application/pdf;Journal of Computational Neuroscience, Volume 3, Number 3 - SpringerLink:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/5BWU6Z5S/n2733052qjgj5761.html:text/html}
},
@article{rabinovich_robust_2011,
title = {Robust transient dynamics and brain functions},
volume = {5},
url = {http:/\linebreak[0]/\linebreak[0]www.frontiersin.org/\linebreak[0]Computational\_Neuroscience/\linebreak[0]10.3389/\linebreak[0]fncom.2011.00024/\linebreak[0]abstract},
doi = {10.3389/fncom.2011.00024},
abstract = {In the last few decades several concepts of dynamical systems theory ({DST)} have guided psychologists, cognitive scientists, and neuroscientists to rethink about sensory motor behavior and embodied cognition. A critical step in the progress of {DST} application to the brain (supported by modern methods of brain imaging and multi-electrode recording techniques) has been the transfer of its initial success in motor behavior to mental function, i.e., perception, emotion, and cognition. Open questions from research in genetics, ecology, brain sciences, etc., have changed {DST} itself and lead to the discovery of a new dynamical phenomenon, i.e., reproducible and robust transients that are at the same time sensitive to informational signals. The goal of this review is to describe a new mathematical framework – heteroclinic sequential dynamics – to understand self-organized activity in the brain that can explain certain aspects of robust itinerant behavior. Specifically, we discuss a hierarchy of coarse-grain models of mental dynamics in the form of kinetic equations of modes. These modes compete for resources at three levels: (i) within the same modality, (ii) among different modalities from the same family (like perception), and (iii) among modalities from different families (like emotion and cognition). The analysis of the conditions for robustness, i.e., the structural stability of transient (sequential) dynamics, give us the possibility to explain phenomena like the finite capacity of our sequential working memory – a vital cognitive function –, and to find specific dynamical signatures – different kinds of instabilities – of several brain functions and mental diseases.},
urldate = {2013-01-16},
journal = {Frontiers in Computational Neuroscience},
author = {Rabinovich, Mikhail I. and {Pablo Varona}},
year = {2011},
keywords = {binding, low frequency oscillations, mental disorders, mental modes, stable heteroclinic channel, transient neural dynamics, Winnerless competition, working memory},
pages = {24},
file = {fncom-05-00024.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/847KTT39/fncom-05-00024.pdf:application/pdf}
},
@incollection{nowotny_pacemaker_2011,
title = {Pacemaker and network mechanisms of neural rhythm generation},
booktitle = {Modern Pacemakers - Present and Future},
publisher = {{InTech}},
author = {Nowotny, T and Rabinovich, Mikhail I.},
editor = {Das, Mithilesh Kumar},
month = feb,
year = {2011},
pages = {405--426},
file = {InTech-Pacemaker_and_network_mechanisms_of_neural_rhythm_generation.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/N6BTCE2P/InTech-Pacemaker_and_network_mechanisms_of_neural_rhythm_generation.pdf:application/pdf}
},
@incollection{woodman_building_2011,
series = {Advances in Experimental Medicine and Biology},
title = {Building Neurocognitive Networks with a Distributed Functional Architecture},
copyright = {©2011 Springer {Science+Business} Media, {LLC}},
isbn = {978-1-4614-0163-6, 978-1-4614-0164-3},
url = {http:/\linebreak[0]/\linebreak[0]link.springer.com/\linebreak[0]chapter/\linebreak[0]10.1007/\linebreak[0]978-\linebreak[0]1-\linebreak[0]4614-\linebreak[0]0164-\linebreak[0]3\_9},
abstract = {In the past few decades, behavioral and cognitive science have demonstrated that many human behaviors can be captured by low-dimensional observations and models, even though the neuromuscular systems possess orders of magnitude more potential degrees of freedom than are found in a specific behavior. We suggest that this difference, due to a separation in the time scales of the dynamics guiding neural processes and the overall behavioral expression, is a key point in understanding the implementation of cognitive processes in general. In this paper we use Structured Flows on Manifolds ({SFM)} to understand the organization of behavioral dynamics possessing this property. Next, we discuss how this form of behavioral dynamics can be distributed across a network, such as those recruited in the brain for particular cognitive functions. Finally, we provide an example of an {SFM} style functional architecture of handwriting, motivated by studies in human movement sciences, that demonstrates hierarchical sequencing of behavioral processes.},
language = {en},
number = {718},
urldate = {2013-01-21},
booktitle = {From Brains to Systems},
publisher = {Springer New York},
author = {Woodman, Marmaduke and Perdikis, Dionysios and Pillai, Ajay S. and Dodel, Silke and Huys, Raoul and Bressler, Steven and Jirsa, Viktor},
editor = {Hernández, Carlos and Sanz, Ricardo and Gómez-Ramirez, Jaime and Smith, Leslie S. and Hussain, Amir and Chella, Antonio and Aleksander, Igor},
month = jan,
year = {2011},
keywords = {Artificial Intelligence (incl. Robotics), Computation by Abstract Devices, Information Systems Applications ({incl.Internet)}, Neurosciences, Signal, Image and Speech Processing},
pages = {101--109},
file = {68.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/MXZBDNNJ/68.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/57BAAKSG/10.html:text/html}
},
@article{friston_perception_2012,
title = {Perception and self-organized instability},
volume = {6},
issn = {1662-5188},
url = {http:/\linebreak[0]/\linebreak[0]www.ncbi.nlm.nih.gov/\linebreak[0]pmc/\linebreak[0]articles/\linebreak[0]PMC3390798/\linebreak[0]},
doi = {10.3389/fncom.2012.00044},
abstract = {This paper considers state-dependent dynamics that mediate perception in the brain. In particular, it considers the formal basis of self-organized instabilities that enable perceptual transitions during Bayes-optimal perception. The basic phenomena we consider are perceptual transitions that lead to conscious ignition (Dehaene and Changeux, ) and how they depend on dynamical instabilities that underlie chaotic itinerancy (Breakspear, ; Tsuda, ) and self-organized criticality (Beggs and Plenz, ; Plenz and Thiagarajan, ; Shew et al., ). Our approach is based on a dynamical formulation of perception as approximate Bayesian inference, in terms of variational free energy minimization. This formulation suggests that perception has an inherent tendency to induce dynamical instabilities (critical slowing) that enable the brain to respond sensitively to sensory perturbations. We briefly review the dynamics of perception, in terms of generalized Bayesian filtering and free energy minimization, present a formal conjecture about self-organized instability and then test this conjecture, using neuronal (numerical) simulations of perceptual categorization.},
urldate = {2013-01-21},
journal = {Frontiers in Computational Neuroscience},
author = {Friston, Karl and Breakspear, Michael and Deco, Gustavo},
month = jul,
year = {2012},
file = {PubMed Central Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/D27WNZI2/Friston et al. - 2012 - Perception and self-organized instability.pdf:application/pdf}
},
@article{ross_detecting_2010,
title = {Detecting dynamical boundaries from kinematic data in biomechanics},
volume = {20},
issn = {1054-1500},
url = {http:/\linebreak[0]/\linebreak[0]www.ncbi.nlm.nih.gov/\linebreak[0]pmc/\linebreak[0]articles/\linebreak[0]PMC2814835/\linebreak[0]},
doi = {10.1063/1.3267043},
abstract = {Ridges in the state space distribution of finite-time Lyapunov exponents can be used to locate dynamical boundaries. We describe a method for obtaining dynamical boundaries using only trajectories reconstructed from time series, expanding on the current approach which requires a vector field in the phase space. We analyze problems in musculoskeletal biomechanics, considered as exemplars of a class of experimental systems that contain separatrix features. Particular focus is given to postural control and balance, considering both models and experimental data. Our success in determining the boundary between recovery and failure in human balance activities suggests this approach will provide new robust stability measures, as well as measures of fall risk, that currently are not available and may have benefits for the analysis and prevention of low back pain and falls leading to injury, both of which affect a significant portion of the population.},
number = {1},
urldate = {2013-01-21},
journal = {Chaos},
author = {Ross, Shane D. and Tanaka, Martin L. and Senatore, Carmine},
month = mar,
year = {2010},
file = {PubMed Central Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/472QHPGD/Ross et al. - 2010 - Detecting dynamical boundaries from kinematic data.pdf:application/pdf}
},
@article{kirst_bifurcation_2007,
title = {Bifurcation From Networks of Unstable Attractors to Heteroclinic Switching},
url = {http:/\linebreak[0]/\linebreak[0]arxiv.org/\linebreak[0]abs/\linebreak[0]0709.3432},
doi = {10.1103/PhysRevE.78.065201},
abstract = {We present a dynamical system that naturally exhibits two unstable attractors that are completely enclosed by each others basin volume. This counter-intuitive phenomenon occurs in networks of pulse-coupled oscillators with delayed interactions. We analytically and numerically investigate this phenomenon and clarify the mechanism underlying it: Upon continuously removing the non-invertibility of the system, the set of two unstable attractors becomes a set of two non-attracting saddle states that are heteroclinically connected to each other. This transition from a network of unstable attractors to a heteroclinic cycle constitutes a new type of bifurcation in dynamical systems.},
urldate = {2013-01-21},
journal = {{arXiv:0709.3432}},
author = {Kirst, Christoph and Timme, Marc},
month = sep,
year = {2007},
keywords = {Condensed Matter - Disordered Systems and Neural Networks, Nonlinear Sciences - Adaptation and Self-Organizing Systems, Nonlinear Sciences - Chaotic Dynamics, Quantitative Biology - Neurons and Cognition},
file = {0709.3432 PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/AU686F8P/Kirst and Timme - 2007 - Bifurcation From Networks of Unstable Attractors t.pdf:application/pdf;arXiv.org Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/6W97UERG/0709.html:text/html}
},
@article{rabinovich_generation_2006,
title = {Generation and reshaping of sequences in neural systems},
volume = {95},
issn = {0340-1200, 1432-0770},
url = {http:/\linebreak[0]/\linebreak[0]link.springer.com/\linebreak[0]article/\linebreak[0]10.1007/\linebreak[0]s00422-\linebreak[0]006-\linebreak[0]0121-\linebreak[0]5},
doi = {10.1007/s00422-006-0121-5},
abstract = {The generation of informational sequences and their reorganization or reshaping is one of the most intriguing subjects for both neuroscience and the theory of autonomous intelligent systems. In spite of the diversity of sequential activities of sensory, motor, and cognitive neural systems, they have many similarities from the dynamical point of view. In this review we discus the ideas, models, and mathematical image of sequence generation and reshaping on different levels of the neural hierarchy, i.e., the role of a sensory network dynamics in the generation of a motor program (hunting swimming of marine mollusk Clione), olfactory dynamical coding, and sequential learning and decision making. Analysis of these phenomena is based on the winnerless competition principle. The considered models can be a basis for the design of biologically inspired autonomous intelligent systems.},
language = {en},
number = {6},
urldate = {2013-01-22},
journal = {Biological Cybernetics},
author = {Rabinovich, Mikhail I. and Huerta, Ramón and Varona, Pablo and Afraimovich, Valentin S.},
month = dec,
year = {2006},
keywords = {bioinformatics, Computer Appl. in Life Sciences, neurobiology, Neurosciences, Statistical Physics, Dynamical Systems and Complexity},
pages = {519--536},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/XCM55UKT/Rabinovich et al. - 2006 - Generation and reshaping of sequences in neural sy.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/HD4PA952/s00422-006-0121-5.html:text/html}
},
@article{harder_comparison_2006,
title = {Comparison of mechanical properties of four large, wave-exposed seaweeds},
volume = {93},
issn = {0002-9122, 1537-2197},
url = {http:/\linebreak[0]/\linebreak[0]www.amjbot.org/\linebreak[0]content/\linebreak[0]93/\linebreak[0]10/\linebreak[0]1426},
doi = {10.3732/ajb.93.10.1426},
abstract = {Seaweeds have a simple structural design compared to most terrestrial plants. Nonetheless, some species have adapted to the severe mechanical conditions of the surf zone. The material properties of either tissue sections or the whole stipe of four wave-exposed seaweeds, Durvillaea antarctica, D. willana, Laminaria digitata, and L. hyperborea, were tested in tension, bending, and torsion. Durvillaea has a very low modulus of elasticity in tension (Etension = 3–7 {MN·m−2)} and in bending (Ebending = 9–12 {MN} · m−2), torsion modulus (G = 0.3 {MN} · m−2) and strength (σbrk = 1–2 {MN} · m−2), combining a compliable and twistable stipe “material” with a comparatively high breaking strain (εbrk = 0.4–0.6). In comparison, the smaller stipes of Laminaria have a higher modulus of elasticity in tension (Etension = 6–28 {MN·m−2)} and in bending (Ebending = 84–109 {MN·m−2)}, similar strength (σbrk = 1–3 {MN·m−2)}, and a higher torsion modulus (G = 0.7–10 {MN·m−2)}, combined with a lower breaking strain (εbrk = 0.2–0.3) than Durvillaea. Time-dependent, viscoelastic reactions were investigated with cycling tests. The tested species dissipated 42–52\% of the loading energy in tension through plastic-viscoelastic processes, a finding that bears important ecological implications. Overall, there seems to be no correlation between single material properties and the size or habitat position of the tested seaweed species.},
language = {en},
number = {10},
urldate = {2013-04-23},
journal = {American Journal of Botany},
author = {Harder, Deane L. and Hurd, Catriona L. and Speck, Thomas},
month = oct,
year = {2006},
keywords = {Biomechanics, Durvillaea, Laminaria, modulus of elasticity, Phaeophyceae, tension tests, wave exposure},
pages = {1426--1432},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/227JUESF/Harder et al. - 2006 - Comparison of mechanical properties of four large,.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/UNV5Q8FP/1426.html:text/html}
},
@article{mullins_brain_2012,
title = {The brain matters: effects of descending signals on motor control},
volume = {107},
issn = {0022-3077, 1522-1598},
shorttitle = {The brain matters},
url = {http:/\linebreak[0]/\linebreak[0]www.frontiersin.org/\linebreak[0]10.3389/\linebreak[0]conf.fnbeh.2012.27.00417/\linebreak[0]event\_abstract},
doi = {10.1152/jn.00107.2012},
number = {10},
urldate = {2013-06-17},
journal = {Journal of Neurophysiology},
author = {Mullins, O. J. and Friesen, W. O.},
month = feb,
year = {2012},
pages = {2730--2741},
file = {Frontiers | The core of crawling: analysis of fictive motor patterns in the isolated Drosophila larval ventral nerve cord:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/VVWBK7KH/event_abstract.html:text/html}
},
@article{frigon_central_2012,
title = {Central Pattern Generators of the Mammalian Spinal Cord},
volume = {18},
issn = {1073-8584, 1089-4098},
url = {http:/\linebreak[0]/\linebreak[0]nro.sagepub.com/\linebreak[0]content/\linebreak[0]18/\linebreak[0]1/\linebreak[0]56},
doi = {10.1177/1073858410396101},
abstract = {Neuronal networks within the spinal cord of mammals are responsible for generating various rhythmic movements, such as walking, running, swimming, and scratching. The ability to generate multiple rhythmic movements highlights the complexity and flexibility of the mammalian spinal circuitry. The present review describes features of some rhythmic motor behaviors generated by the mammalian spinal cord and discusses how the spinal circuitry is able to produce different rhythmic movements with their own sets of goals and demands.},
language = {en},
number = {1},
urldate = {2013-06-17},
journal = {The Neuroscientist},
author = {Frigon, Alain},
month = feb,
year = {2012},
keywords = {central pattern generator, Locomotion, scratch, Spinal Cord, spinal cord injury},
pages = {56--69},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/2CCS8GBS/Frigon - 2012 - Central Pattern Generators of the Mammalian Spinal.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/Q4SEFMVU/56.html:text/html}
},
@article{anrep_double_1932,
title = {Double vagotomy in relation to respiration},
volume = {77},
issn = {0022-3751},
url = {http:/\linebreak[0]/\linebreak[0]www.ncbi.nlm.nih.gov/\linebreak[0]pmc/\linebreak[0]articles/\linebreak[0]PMC1394748/\linebreak[0]},
number = {1},
urldate = {2013-06-28},
journal = {The Journal of Physiology},
author = {Anrep, G. V. and Samaan, Adli},
month = dec,
year = {1932},
pages = {1--15},
file = {PubMed Central Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/RBUS4WZW/Anrep and Samaan - 1932 - Double vagotomy in relation to respiration.pdf:application/pdf}
},
@article{eugenin_chemosensory_1997,
title = {Chemosensory and cholinergic stimulation of fictive respiration in isolated {CNS} of neonatal opossum.},
volume = {501},
issn = {0022-3751},
url = {http:/\linebreak[0]/\linebreak[0]www.ncbi.nlm.nih.gov/\linebreak[0]pmc/\linebreak[0]articles/\linebreak[0]PMC1159489/\linebreak[0]},
abstract = {1. The aim of the present experiments was to characterize the central chemical drive of fictive respiration in the isolated {CNS} of the newborn opossum, Monodelphis domestica. This opossum preparation, in contrast to those of neonatal rats and mice, produces respiratory rhythm of high frequency in vitro. 2. Fictive respiration was recorded from C3-C5 ventral roots of the isolated {CNS} of 4- to 14-day-old opossums using suction electrodes. At room temperature (21-23 degrees C) the frequency of respiration was 43 +/- 5.3 min-1 (mean +/- {S.E.M.}, n = 50) in basal medium Eagle's medium ({BMEM)} equilibrated with 5\% {CO2-95\%} O2, {pH} 7.37-7.40. Respiratory discharges remained regular throughout 8 h experiments and continued for more than 20 h in culture. 3. Superfusion of the brainstem confirmed that solutions of {pH} 6.3-7.2 increased both the amplitude and frequency of respiration. High {pH} solutions (7.5-7.7) had the opposite effect and abolished the rhythm at {pH} 7.7. Addition of {ACh} (50-100 {microM)} or carbachol (0.01-10 {microM)} to the brainstem superfusion also increased the amplitude and frequency of respiratory activity, as did physostigmine (50-100 {microM)} or neostigmine (20-50 {microM).} Conversely, scopolamine (50-100 {microM)} reduced the amplitude and frequency of the basal respiratory rhythm by about 30\%. 4. H(+)- and cholinergic-sensitive areas on the surface of the isolated {CNS} were explored with a small micropipette (outer tip diameter, 100 microns) filled with {BMEM} ({pH} 6.5) or 1 {microM} carbachol. Carbachol applied to H(+)- and cholinergic-sensitive areas in the ventral medulla mimicked the changes of respiratory pattern produced by low {pH} application. Responses to altered {pH} and carbachol were abolished by scopolamine (50 {microM).} Histochemistry demonstrated several medullary groups of neurons stained for acetylcholinesterase. The superficial location of one of these groups coincided with a functional and anatomically well-defined {pH-} and carbachol-sensitive area placed medial to the hypoglossal roots. 5. Exploration of chemosensitive areas revealed that application of drugs or solutions of different {pH} to a single well-defined spot could have selective and distinctive effects upon amplitude and frequency of respiratory activity. 6. These results show that fictive respiration in the isolated {CNS} of the newborn opossum is tonically driven by chemical- and cholinergic-sensitive areas located on the ventral medulla, the activity of which regulates frequency and amplitude of respiration. They suggest that a cholinergic relay, although not essential for rhythm generation, is involved in the central {pH} chemosensory mechanism, or that cholinergic and chemical inputs converge upon the same input pathway to the respiratory pattern generator.},
number = {Pt 2},
urldate = {2013-06-28},
journal = {The Journal of Physiology},
author = {Eugenin, J and Nicholls, J G},
month = jun,
year = {1997},
pages = {425--437},
file = {PubMed Central Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/AKU24G7S/Eugenin and Nicholls - 1997 - Chemosensory and cholinergic stimulation of fictiv.pdf:application/pdf}
},
@article{dick_pontine_2008,
title = {Pontine respiratory-modulated activity before and after vagotomy in decerebrate cats},
volume = {586},
issn = {0022-3751, 1469-7793},
url = {http:/\linebreak[0]/\linebreak[0]jp.physoc.org/\linebreak[0]content/\linebreak[0]586/\linebreak[0]17/\linebreak[0]4265},
doi = {10.1113/jphysiol.2008.152108},
abstract = {The dorsolateral ({DL)} pons modulates the respiratory pattern. With the prevention of lung inflation during central inspiratory phase (no-inflation (no-I or delayed-I) tests), {DL} pontine neuronal activity increased the strength and consistency of its respiratory modulation, properties measured statistically by the η2 value. This increase could result from enhanced respiratory-modulated drive arising from the medulla normally gated by vagal activity. We hypothesized that {DL} pontine activity during delayed-I tests would be comparable to that following vagotomy. Ensemble recordings of neuronal activity were obtained before and after vagotomy and during delayed-I tests in decerebrate, paralysed and ventilated cats. In general, changes in activity pattern during the delayed-I tests were similar to those after vagotomy, with the exception of firing-rate differences at the inspiratory–expiratory phase transition. Even activity that was respiratory-modulated with the vagi intact became more modulated while withholding lung inflation and following vagotomy. Furthermore, we recorded activity that was excited by lung inflation as well as changes that persisted past the stimulus cycle. Computer simulations of a recurrent inhibitory neural network model account not only for enhanced respiratory modulation with vagotomy but also the varied activities observed with the vagi intact. We conclude that (a) {DL} pontine neurones receive both vagal-dependent excitatory inputs and central respiratory drive; (b) even though changes in pontine activity are transient, they can persist after no-I tests whether or not changes in the respiratory pattern occur in the subsequent cycles; and (c) models of respiratory control should depict a recurrent inhibitory circuitry, which can act to maintain the stability and provide plasticity to the respiratory pattern.},
language = {en},
number = {17},
urldate = {2013-07-01},
journal = {The Journal of Physiology},
author = {Dick, Thomas E. and Shannon, Roger and Lindsey, Bruce G. and Nuding, Sarah C. and Segers, Lauren S. and Baekey, David M. and Morris, Kendall F.},
month = sep,
year = {2008},
pages = {4265--4282},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/XBZ3W599/Dick et al. - 2008 - Pontine respiratory-modulated activity before and .pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/6TID8H3F/4265.html:text/html}
},
@article{eugenin_control_2000,
title = {Control of respiration in the isolated central nervous system of the neonatal opossum, Monodelphis domestica},
volume = {53},
issn = {0361-9230},
url = {http:/\linebreak[0]/\linebreak[0]www.sciencedirect.com/\linebreak[0]science/\linebreak[0]article/\linebreak[0]pii/\linebreak[0]S0361923000003944},
doi = {10.1016/S0361-9230(00)00394-4},
abstract = {7.1) or to topical application of 1.0 {μM} carbachol. Conversely, as expected, the rate and amplitude decrease in response to increased {pH} ({pH} 7.5–7.7), or 100 {μM} scopolamine. Two characteristic features of the control of respiration in the neonatal opossum are evident from such tests. First, changes in rate are achieved by changes in the duration of the expiratory phase of respiration. This result suggests that the timing of the respiratory cycle in the neonatal opossum is controlled by an expiratory instead of an inspiratory “off-switch”. Second, the rate and the amplitude of the respiratory excursions can be controlled independently, depending on the stimulus. For example, an increase in temperature increases the rate of fictive respiration without changing its amplitude, whereas noradrenaline decreases the rate while increasing the amplitude. Thus, changes of timing and amplitude need not go hand in hand. The opossum {CNS} offers a favorable preparation for the analysis of neural mechanisms that generate and modulate a motor rhythm, as the animal develops from embryonic to adult stages.},
number = {5},
urldate = {2013-07-01},
journal = {Brain Research Bulletin},
author = {Eugenı́n, Jaime and Nicholls, John G},
month = nov,
year = {2000},
keywords = {Central chemoreception, Control of breathing, development, Marsupials, Respiratory pattern generation},
pages = {605--613},
file = {ScienceDirect Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/TV3JHWG6/Eugenı́n and Nicholls - 2000 - Control of respiration in the isolated central ner.pdf:application/pdf;ScienceDirect Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/HW9BEGSZ/S0361923000003944.html:text/html}
},
@article{tomori_distinct_2010,
title = {Distinct generators for aspiration and expiration reflexes: localization, mechanisms and effects},
volume = {61},
issn = {1899-1505},
shorttitle = {Distinct generators for aspiration and expiration reflexes},
abstract = {Re-evaluation of our earlier c-Fos-like immuno-reactive studies and brainstem transection/lesion experiments in over 40 anaesthetized, non-paralyzed cats allowed comparison of two distinct airway defensive reflexes with the distinct generators for inspiration (I) and expiration (E), described recently in juvenile rats. The spiration reflex ({AspR)} is characterized by solitary rapid and strong inspiratory effort with a reciprocal inhibition, preventing a subsequent active expiration, while the expiration reflex ({ExpR)} manifests by rapid and strong expiratory effort, starting without a preceding, inspiration, or reciprocal inhibition of occasional spontaneous inspiration. The retro-trapezoid nucleus/parafacial respiratory group neurones described as the distinct generator for active E in rats, are activated also during the {ExpR} in adult cats. Brainstem transection 5 mm above the obex eliminates the E generator and the {ExpR}, but preserves the I generator located in the pre-Bötzinger Complex, and also the {AspR.} This suggests the existence of a distinct I generator in cats as well as rats, and its contribution to the generation of the {AspR.} Persistence of the {AspR} in adult cats during asphyxic gasping, their similar character and the strong activation of I neurones at many places in the medulla and pons, suggest a common brainstem neuronal circuit contributing to generation of both the gasping and the gasp-like {AspR.} That the {AspR} and {ExpR} have distinct multilevel brainstem control mechanisms supports the dual theory of control and provides unique models for testing respiratory rhythm and pattern generation. The {AspR} may be compared with the powerful "auto-resuscitation effects of asphyxic gasping"; the {ExpR} may underly the effectiveness of the laryngeal chemoreflexes in prevention of lung diseases.},
language = {eng},
number = {1},
journal = {Journal of physiology and pharmacology: an official journal of the Polish Physiological Society},
author = {Tomori, Z and Poliacek, I and Jakus, J and Widdicombe, J and Donic, V and Benacka, R and Gresova, S},
month = feb,
year = {2010},
keywords = {Animals, Brain Stem, Exhalation, Humans, Inhalation, Respiratory Mechanics, Startle Reaction},
pages = {5--12},
file = {5_02_10_article.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/W59BWQ9V/5_02_10_article.pdf:application/pdf}
},
@article{bassler_definition_1986,
title = {On the definition of central pattern generator and its sensory control},
volume = {54},
issn = {0340-1200, 1432-0770},
url = {http:/\linebreak[0]/\linebreak[0]link.springer.com/\linebreak[0]article/\linebreak[0]10.1007/\linebreak[0]BF00337116},
doi = {10.1007/BF00337116},
abstract = {A central pattern generator ({CPG)} is defined here as a neural network responsible for the production of the timing cues of a rhythmic motor output pattern in the isolated {CNS.} For the intact animal, model considerations show that this term is neither clearly delimited from the concept of a reflex chain nor from the concept of a pattern generator with functional principles different from those of the {CPG.} Therefore, it cannot be concluded from the existence of a {CPG} in the isolated nervous system that this {CPG} also provides the decisive timing cues in the intact animal. Consequences for the study of the neural basis of rhythmic movements are shown.},
language = {en},
number = {1},
urldate = {2013-07-03},
journal = {Biological Cybernetics},
author = {Bässler, Ulrich},
month = may,
year = {1986},
keywords = {Neurosciences, Zoology},
pages = {65--69},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/V7ZPFRVN/Bässler - 1986 - On the definition of central pattern generator and.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/7XPPFRNE/BF00337116.html:text/html}
},
@article{harri_effects_1977,
title = {The effects of temperature on a neuromuscular system of the crayfish, \textit{{A}stacus} \textit{leptodactylus}},
volume = {117},
issn = {0340-7594, 1432-1351},
url = {http:/\linebreak[0]/\linebreak[0]link.springer.com/\linebreak[0]article/\linebreak[0]10.1007/\linebreak[0]BF00605523},
doi = {10.1007/BF00605523},
abstract = {Slow and fast contractions, as well as the corresponding excitatory junction potentials (ejp's) were recorded from the closer muscle (adductor of the dactylopodite) of the third walking legs, subjected to temperatures ranging from +6 {°C} to +32 {°C.} In addition, the effect of temperature on resting potential and resting tension was studied, and in several preparations we investigated the effect of temperature on the efficacy of the inhibitory axon. The experimental animals had been acclimated at 12 {°C.} The membrane potential was found to increase with temperature. In the lower temperature range (e.g., between {6°C} and 14–18 {°C)} the slope was usually steeper; the maximal rate of change was 2 {mV/°C.} The amplitude of facilitated slow ejp's (10/s) changes only insignificantly over the temperature span from 6 {°C} to about 22 {°C} and declines at higher temperatures. Fast ejp's have maximal amplitudes at 20 {°C} and decline at lower and higher temperatures, the decline being insignificant, however, below 14 {°C.} Facilitation rate also changes little with temperature; a significant increase occurs near 30 {°C} in the case of fast ejp's, and between 15 {°C} and 20 {°C} in the case of slow ejp's. Above 28 {°C}, facilitation of slow ejp's declines. As the temperature is lowered, many muscles develop a contracture which may reach 10\% of maximal tension at 6 {°C.} These temperature-induced contractures can be abolished by stimulation of the inhibitory axon. The effectiveness of the inhibitory axon in reducing the contraction caused by the slow motor axon increases with decreasing temperature. The time course of the decay of both slow and fast ejp's increases with falling temperature, particularly in the temperature range below 12 {°C.} At a given frequency (1–30/s), both slow and fast contractions increased with falling temperature over the entire temperature range tested. This increased efficiency of the neuro-muscular system is attributed to the depolarization and the prolonged time course of the ejp's.},
language = {en},
number = {1},
urldate = {2013-07-08},
journal = {Journal of comparative physiology},
author = {Harri, Mikko and Florey, Ernst},
month = jan,
year = {1977},
keywords = {Animal Physiology, Neurosciences, Zoology},
pages = {47--61},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/TWJUMJNC/Harri and Florey - 1977 - The effects of temperature on a neuromuscular syst.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/5DDXKR88/BF00605523.html:text/html}
},
@article{pearson_phase-dependent_1983,
title = {Phase-dependent influences of wing stretch receptors on flight rhythm in the locust},
volume = {49},
url = {http:/\linebreak[0]/\linebreak[0]post.queensu.ca/\linebreak[0]~locust/\linebreak[0]Publications/\linebreak[0]pearson\%\linebreak[0]20reye\%\linebreak[0]20robertson\%\linebreak[0]201983\%\linebreak[0]20jnp.pdf},
number = {5},
urldate = {2013-07-08},
journal = {J Neurophysiol},
author = {Pearson, K. G. and Reye, D. N. and Robertson, R. M.},
year = {1983},
pages = {1168–1181},
file = {[PDF] from queensu.ca:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/EB5N2QVV/Pearson et al. - 1983 - Phase-dependent influences of wing stretch recepto.pdf:application/pdf}
},
@article{grillner_how_1975,
title = {How detailed is the central pattern generation for locomotion?},
volume = {88},
issn = {0006-8993},
url = {http:/\linebreak[0]/\linebreak[0]journals.ohiolink.edu/\linebreak[0]ejc/\linebreak[0]article.cgi?issn=00068993\&\linebreak[0]issue=v88i0002\&\linebreak[0]article=367\_hditcpgfl},
doi = {10.1016/0006-8993(75)90401-1},
number = {2},
journal = {Brain Research},
author = {Grillner, S. and Zangger, P.},
year = {1975},
pages = {367--371},
file = {Grillner_S.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/A9TEQ9JZ/Grillner_S.pdf:application/pdf}
},
@incollection{prochazka_neuromechanical_2007,
title = {The neuromechanical tuning hypothesis},
volume = {Volume 165},
isbn = {0079-6123},
shorttitle = {Computational Neuroscience: Theoretical Insights into Brain Function},
url = {http:/\linebreak[0]/\linebreak[0]www.sciencedirect.com/\linebreak[0]science/\linebreak[0]article/\linebreak[0]pii/\linebreak[0]S0079612306650164},
abstract = {Simulations performed with neuromechanical models are providing insight into the neural control of locomotion that would be hard if not impossible to obtain in any other way. We first discuss the known properties of the neural mechanisms controlling locomotion, with a focus on mammalian systems. The rhythm-generating properties of central pattern generators ({CPGs)} are discussed in light of results indicating that cycle characteristics may be preset by tonic drive to spinal interneuronal networks. We then describe neuromechanical simulations that have revealed some basic rules of interaction between {CPGs}, sensory-mediated switching mechanisms and the biomechanics of locomotor movements. We posit that the spinal {CPG} timer and the sensory-mediated switch operate in parallel, the former being driven primarily by descending inputs and the latter by the kinematics. The {CPG} timer produces extensor and flexor phase durations, which covary along specific lines in a plot of phase- versus cycle-duration. We coined the term “phase-duration characteristics” to describe such plots. Descending input from higher centers adjusts the operating points on the phase-duration characteristics according to anticipated biomechanical requirements. In well-predicted movements, {CPG-generated} phase durations closely match those required by the kinematics, minimizing the corrections in phase duration required of the sensory switching mechanism. We propose the term “neuromechanical tuning” to describe this process of matching the {CPG} to the kinematics.},
urldate = {2013-07-08},
booktitle = {Progress in Brain Research},
publisher = {Elsevier},
author = {Prochazka, Arthur and Yakovenko, Sergiy},
editor = {Paul Cisek, Trevor Drew and John F. Kalaska},
year = {2007},
keywords = {Central pattern generators, neural control of locomotion, sensory control of locomotion},
pages = {255--265},
file = {ScienceDirect Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/E2RPBXDE/Prochazka and Yakovenko - 2007 - The neuromechanical tuning hypothesis.pdf:application/pdf;ScienceDirect Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/DI7UFRDJ/S0079612306650164.html:text/html}
},
@article{forssberg_stumbling_1979,
title = {Stumbling corrective reaction: a phase-dependent compensatory reaction during locomotion},
volume = {42},
issn = {0022-3077, 1522-1598},
shorttitle = {Stumbling corrective reaction},
url = {http:/\linebreak[0]/\linebreak[0]jn.physiology.org/\linebreak[0]content/\linebreak[0]42/\linebreak[0]4/\linebreak[0]936},
language = {en},
number = {4},
urldate = {2013-07-09},
journal = {Journal of Neurophysiology},
author = {Forssberg, H.},
month = jul,
year = {1979},
pages = {936--953},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/DKRK4IID/Forssberg - 1979 - Stumbling corrective reaction a phase-dependent c.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/AZRX6MHQ/936.html:text/html}
},
@article{andersson_phasic_1978,
title = {Phasic gain control of the transmission in cutaneous reflex pathways to motoneurones during fictive locomotion},
volume = {149},
issn = {00068993},
url = {http:/\linebreak[0]/\linebreak[0]journals.ohiolink.edu/\linebreak[0]ejc/\linebreak[0]article.cgi?issn=00068993\&\linebreak[0]issue=v149i0002\&\linebreak[0]article=503\_pgcottrptmdl},
number = {2},
journal = {Brain Research},
author = {Andersson, O. and Forssberg, H. and Grillner, S. and Lindquist, M.},
year = {1978},
pages = {503--507},
file = {Andersson_O.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/8WKE8K48/Andersson_O.pdf:application/pdf;EJC - Phasic gain control of the transmission in cutaneous reflex pathways to motoneurones during ‘fictive’ locomotion:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/ZIC2UEJZ/article.html:text/html}
},
@article{forssberg_phase_1975,
title = {Phase dependent reflex reversal during walking in chronic spinal cats},
volume = {85},
issn = {00068993},
url = {http:/\linebreak[0]/\linebreak[0]journals.ohiolink.edu/\linebreak[0]ejc/\linebreak[0]article.cgi?issn=00068993\&\linebreak[0]issue=v85i0001\&\linebreak[0]article=103\_pdrrdwicsc},
number = {1},
journal = {Brain Research},
author = {Forssberg, H. and Grillner, S. and Rossignol, S.},
year = {1975},
pages = {103--107},
file = {EJC - Phase dependent reflex reversal during walking in chronic spinal cats:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/PXMVI2EH/article.html:text/html;Forssberg_H.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/4VP9NNKU/Forssberg_H.pdf:application/pdf}
},
@article{vandorpe_fmrfamide_1994,
title = {{FMRFamide} and membrane stretch as activators of the \textit{{A}plysia} {S}-channel.},
volume = {66},
issn = {0006-3495},
url = {http:/\linebreak[0]/\linebreak[0]www.ncbi.nlm.nih.gov/\linebreak[0]pmc/\linebreak[0]articles/\linebreak[0]PMC1275662/\linebreak[0]},
abstract = {The long-standing distinction between channels and transporters is becoming blurred, with one pump protein even able to convert reversibly to a channel in response to osmotic shock. In this light, it is plausible that stretch channels, membrane proteins whose physiological roles have been elusive, may be transporters exhibiting channel-like properties in response to mechanical stress. We recently described a case, however, where this seems an unlikely explanation. An Aplysia K channel whose physiological pedigree is well established (it is an excitability-modulating conductance mechanism) was found able to be activated by stretch. Here we establish more firmly the identity of this Aplysia conductance, the S-channel, as a stretch channel. We show that the permeation and fast kinetic properties of the stretch-activated channel and of the {FMRFamide-activated} S-channel are indistinguishable. We have also made progress in extending the kinetic analysis of the stretch channel to situations of multiple channel activity. This analysis implements a novel renewal theory approach and is therefore explained in some detail.},
number = {1},
urldate = {2013-07-30},
journal = {Biophysical Journal},
author = {Vandorpe, D H and Small, D L and Dabrowski, A R and Morris, C E},
month = jan,
year = {1994},
pages = {46--58},
file = {PubMed Central Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/3PQ7N7PW/Vandorpe et al. - 1994 - FMRFamide and membrane stretch as activators of th.pdf:application/pdf}
},
@article{zajac_muscle_1989,
title = {Muscle and tendon: properties, models, scaling, and application to biomechanics and motor control},
volume = {17},
issn = {0278-{940X}},
shorttitle = {Muscle and tendon},
abstract = {Skeletal muscles transform neural control signals into forces that act upon the body segments to effect a coordinated motor task. This transformation is complex, not only because the properties of muscles are complex, but because the tendon affects the transmission of muscle force to the skeleton. This review focuses on how to synthesize basic properties of muscle and tendon to construct models applicable to studies of coordination. After a review of the properties of muscle and tendon, their integrated ability to generate force statically and dynamically is studied by formulating a generic model of the "musculotendon actuator", which has only one parameter, the ratio of tendon length at rest to muscle fiber length at rest. To illustrate the utility of the model, it is analyzed to show how this one parameter specifies whether excitation-contraction or musculotendon contraction is the rate-limiting process of force generation, whether elastic energy is stored in tendon or muscle, and whether hip- and knee-extensor actuators function as springs or dashpots during walking.},
language = {eng},
number = {4},
journal = {Critical reviews in biomedical engineering},
author = {Zajac, F E},
year = {1989},
keywords = {Biomechanics, Central Nervous System, computer simulation, Humans, Models, Biological, Muscle Contraction, Muscles, Tendons},
pages = {359--411}
},
@article{dagostino_suggestion_1990,
title = {A Suggestion for Using Powerful and Informative Tests of Normality},
volume = {44},
copyright = {Copyright © 1990 American Statistical Association},
issn = {0003-1305},
url = {http:/\linebreak[0]/\linebreak[0]www.jstor.org/\linebreak[0]stable/\linebreak[0]2684359},
doi = {10.2307/2684359},
abstract = {For testing that an underlying population is normally distributed the skewness and kurtosis statistics, \${\textbackslash}sqrt\{b\_1\}\$ and b2, and the {D'Agostino-Pearson} K2 statistic that combines these two statistics have been shown to be powerful and informative tests. Their use, however, has not been as prevalent as their usefulness. We review these tests and show how readily available and popular statistical software can be used to implement them. Their relationship to deviations from linearity in normal probability plotting is also presented.},
number = {4},
urldate = {2013-08-02},
journal = {The American Statistician},
author = {{D'Agostino}, Ralph B. and Belanger, Albert and {D'Agostino}, Ralph B.},
month = nov,
year = {1990},
pages = {316--321},
file = {2684359.pdf:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/AWQNUDX8/2684359.pdf:application/pdf}
},
@book{loeb_einleitung_1899,
title = {Einleitung in die vergleichende Gehirnphysiologie und vergleichende psychologie, mit besonderer berücksichtigung der wirbellosen thiere},
lccn = {06468941},
url = {http:/\linebreak[0]/\linebreak[0]archive.org/\linebreak[0]details/\linebreak[0]einleitungindiev00loeb},
abstract = {Includes bibliographies},
language = {ger},
urldate = {2013-08-06},
publisher = {Leipzig, J. A. Barth},
author = {Loeb, Jacques},
collaborator = {{{MBLWHOI} Library}},
year = {1899},
keywords = {Brain}
},
@article{freusbcrg_reflexbewegungen_1874,
title = {Reflexbewegungen beim Hunde},
volume = {9},
issn = {0365-267x, 1432-2013},
url = {http:/\linebreak[0]/\linebreak[0]link.springer.com/\linebreak[0]article/\linebreak[0]10.1007/\linebreak[0]BF01612347},
doi = {10.1007/BF01612347},
language = {de},
number = {1},
urldate = {2013-08-06},
journal = {Archiv für die gesamte Physiologie des Menschen und der Tiere},
author = {Freusbcrg, Dr A.},
month = dec,
year = {1874},
keywords = {Human Physiology},
pages = {358--391},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/74S2CC6I/Freusbcrg - 1874 - Reflexbewegungen beim Hunde.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/8DJGQHMJ/10.html:text/html}
},
@article{sherrington_flexion-reflex_1910,
title = {Flexion-reflex of the limb, crossed extension-reflex, and reflex stepping and standing},
volume = {40},
issn = {0022-3751},
url = {http:/\linebreak[0]/\linebreak[0]www.ncbi.nlm.nih.gov/\linebreak[0]pmc/\linebreak[0]articles/\linebreak[0]PMC1533734/\linebreak[0]},
abstract = {Images
null},
number = {1-2},
urldate = {2013-08-06},
journal = {The Journal of Physiology},
author = {Sherrington, C. S.},
month = apr,
year = {1910},
pages = {28--121},
file = {PubMed Central Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/MCD5VNPU/Sherrington - 1910 - Flexion-reflex of the limb, crossed extension-refl.pdf:application/pdf}
},
@article{sherrington_further_1913,
title = {Further observations on the production of reflex stepping by combination of reflex excitation with reflex inhibition},
volume = {47},
issn = {0022-3751},
url = {http:/\linebreak[0]/\linebreak[0]www.ncbi.nlm.nih.gov/\linebreak[0]pmc/\linebreak[0]articles/\linebreak[0]PMC1420464/\linebreak[0]},
number = {3},
urldate = {2013-08-06},
journal = {The Journal of Physiology},
author = {Sherrington, C. S.},
month = nov,
year = {1913},
pages = {196--214},
file = {PubMed Central Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/PVZFKKXX/Sherrington - 1913 - Further observations on the production of reflex s.pdf:application/pdf}
},
@article{wilson_central_1961,
title = {The Central Nervous Control of Flight in a Locust},
volume = {38},
issn = {0022-0949, 1477-9145},
url = {http:/\linebreak[0]/\linebreak[0]jeb.biologists.org/\linebreak[0]content/\linebreak[0]38/\linebreak[0]2/\linebreak[0]471},
abstract = {1. The co-ordination of the flight movements of Schistocerca gregaria Forskål was examined in order to determine the extent of central patterning and reflex control.
2. Electrical recordings from wing sensory nerves showed many units which responded to wing movements of various kinds. During flight the sensory discharge was timed to certain phases of the wing-beat cycle.
3. Surgical removal of the sources of timed input did not abolish patterned output, which resembled that during flight, but the frequency of cycling was considerably reduced. Either electrical stimulation of the nerve cord or continuous wind on the head could elicit the pattern.
4. A multiplicity of oscillators in the flight control system was demonstrated.
5. It is suggested that the basic co-ordination of flight is an inherent function of the central nervous system but that peripheral feedback loops influence the frequency of Operation and details of pattern.},
language = {en},
number = {2},
urldate = {2013-08-06},
journal = {Journal of Experimental Biology},
author = {Wilson, Donald M.},
month = jun,
year = {1961},
pages = {471--490},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/NQXT5UBI/Wilson - 1961 - The Central Nervous Control of Flight in a Locust.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/UI867VHZ/471.html:text/html}
},
@book{selverston_model_1985,
address = {New York},
title = {Model neural networks and behavior},
isbn = {0306419491 9780306419492},
language = {English},
publisher = {Plenum Press},
author = {Selverston, Allen I},
year = {1985}
},
@incollection{kopell_coupled_1986,
series = {Lecture Notes in Biomathematics},
title = {Coupled Oscillators and Locomotion by Fish},
copyright = {©1986 Springer-Verlag Berlin Heidelberg},
isbn = {978-3-540-16481-4, 978-3-642-93318-9},
url = {http:/\linebreak[0]/\linebreak[0]link.springer.com/\linebreak[0]chapter/\linebreak[0]10.1007/\linebreak[0]978-\linebreak[0]3-\linebreak[0]642-\linebreak[0]93318-\linebreak[0]9\_10},
abstract = {Fish of many species propel themselves through water by rhythmic undulations; fins are used for stabilization and change of direction, but not for stereotypic straight line movements [1], The undulations are caused by contractions which pass down the muscles along the spinal cord (with muscles on the opposite sides of the fish 180° out of phase). These contractions are in turn directed by motoneurons which emerge from special positions in the spinal cord having a spatial periodicity that matches the segmentation of the backbone. Measurements from these positions (“ventral roots”) show rhythmic voltage changes (bursts of activity) at each such point, with a uniform frequency and a phase lag between any two points that are proportional to the distance between the points; i.e., the neural activity is a constant speed travelling wave. For technical reasons, much of this data has been gathered for dogfish and lamprey [1,2]; some of the observations have been corroborated for other species.},
language = {en},
number = {66},
urldate = {2013-08-06},
booktitle = {Nonlinear Oscillations in Biology and Chemistry},
publisher = {Springer Berlin Heidelberg},
author = {Kopell, N.},
editor = {Othmer, Hans G.},
month = jan,
year = {1986},
keywords = {Biophysics and Biological Physics, Mathematical and Computational Biology, Statistics for Life Sciences, Medicine, Health Sciences},
pages = {160--174},
file = {Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/JXXSZNBI/978-3-642-93318-9_10.html:text/html}
},
@article{sacco_effects_1994,
title = {Effects of length and stimulation frequency on fatigue of the human tibialis anterior muscle},
volume = {77},
issn = {8750-7587, 1522-1601},
url = {http:/\linebreak[0]/\linebreak[0]jap.physiology.org/\linebreak[0]content/\linebreak[0]77/\linebreak[0]3/\linebreak[0]1148},
abstract = {It has been suggested that the reduced fatigability of muscles exercised at short length may result from a decrease in the metabolic cost of contractions in the shortened position. We compared the fatigue properties and metabolic cost of stimulated isometric tetanic contractions in the tibialis anterior of 10 normal subjects at the optimum length (Lo) for force production and when the muscle was shortened (Ls). Six 15-s ischemic contractions at Ls caused force to decline to 53\% of the fresh value when tested at Lo, whereas muscles exercised and tested at Lo declined to 40\% of fresh force. However, the extent of fatigue was proportionately greater if the muscle was exercised and tested at Ls. The apparent fatigue resistance of short muscles was found to be a consequence of recovery occurring under ischemic conditions while the muscle was changed from Ls to Lo-. {31P-nuclear} magnetic resonance spectroscopy showed similar metabolic changes associated with 5-s stimulated contractions at Lo and Ls, indicating that any differences in fatigability at the two lengths were not caused by altered metabolic costs. The similarity between the force profiles of muscles fatigued at Ls and those fatigued by high-frequency stimulation supports the hypothesis that an enhanced activation failure occurs at Ls, possibly resulting from failure of sarcolemmal action potential propagation in the transverse tubules.},
language = {en},
number = {3},
urldate = {2013-09-12},
journal = {Journal of Applied Physiology},
author = {Sacco, P. and {McIntyre}, D. B. and Jones, D. A.},
month = sep,
year = {1994},
pages = {1148--1154},
file = {Full Text PDF:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/XAHCXNQM/Sacco et al. - 1994 - Effects of length and stimulation frequency on fat.pdf:application/pdf;Snapshot:/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/VMUXR3D9/1148.html:text/html}
},
@article{ermentrout_frequency_1984,
title = {Frequency Plateaus in a Chain of Weakly Coupled Oscillators, {I}.},
volume = {15},
issn = {0036-1410, 1095-7154},
url = {http:/\linebreak[0]/\linebreak[0]epubs.siam.org/\linebreak[0]doi/\linebreak[0]abs/\linebreak[0]10.1137/\linebreak[0]0515019},
doi = {10.1137/0515019},
number = {2},
urldate = {2013-08-06},
journal = {{SIAM} Journal on Mathematical Analysis},
author = {Ermentrout, George Bard and Kopell, Nancy},
month = mar,
year = {1984},
pages = {215--237},
file = {Frequency Plateaus in a Chain of Weakly Coupled Oscillators, I. : SIAM Journal on Mathematical Analysis: Vol. 15, No. 2 (Society for Industrial and Applied Mathematics):/home/kms15/.mozilla/firefox/h4enq183.default/zotero/storage/WN5MTVUQ/0515019.html:text/html}
},
@book{schiff_neural_2012,
address = {Cambridge, {MA}},
title = {Neural control engineering: the emerging intersection between control theory and neuroscience},
isbn = {9780262312080 0262312085 9781283834681 1283834685},
url = {http:/\linebreak[0]/\linebreak[0]search.ebscohost.com/\linebreak[0]login.aspx?direct=true\&\linebreak[0]scope=site\&\linebreak[0]db=nlebk\&\linebreak[0]db=nlabk\&\linebreak[0]AN=512645},
language = {English},
urldate = {2013-08-07},
publisher = {{MIT} Press},
author = {Schiff, Steven J},
year = {2012}
},