Literature DB >> 8727380

Activity patterns of the B31/B32 pattern initiators innervating the I2 muscle of the buccal mass during normal feeding movements in Aplysia californica.

I Hurwitz1, D Neustadter, D W Morton, H J Chiel, A J Susswein.   

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.

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Year:  1996        PMID: 8727380     DOI: 10.1152/jn.1996.75.4.1309

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  57 in total

1.  Evolution and analysis of model CPGs for walking: II. General principles and individual variability.

Authors:  R D Beer; H J Chiel; J C Gallagher
Journal:  J Comput Neurosci       Date:  1999 Sep-Oct       Impact factor: 1.621

2.  Multiple memory processes following training that a food is inedible in Aplysia.

Authors:  D Botzer; S Markovich; A J Susswein
Journal:  Learn Mem       Date:  1998 Jul-Aug       Impact factor: 2.460

3.  A proprioceptive role for an exteroceptive mechanoafferent neuron in Aplysia.

Authors:  D Borovikov; C G Evans; J Jing; S C Rosen; E C Cropper
Journal:  J Neurosci       Date:  2000-03-01       Impact factor: 6.167

4.  In vitro analog of operant conditioning in aplysia. I. Contingent reinforcement modifies the functional dynamics of an identified neuron.

Authors:  R Nargeot; D A Baxter; J H Byrne
Journal:  J Neurosci       Date:  1999-03-15       Impact factor: 6.167

5.  Dynamical basis of intentions and expectations in a simple neuronal network.

Authors:  Alex Proekt; Vladimir Brezina; Klaudiusz R Weiss
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-14       Impact factor: 11.205

6.  Extending in vitro conditioning in Aplysia to analyze operant and classical processes in the same preparation.

Authors:  Björn Brembs; Douglas A Baxter; John H Byrne
Journal:  Learn Mem       Date:  2004-07-14       Impact factor: 2.460

7.  The construction of movement with behavior-specific and behavior-independent modules.

Authors:  Jian Jing; Elizabeth C Cropper; Itay Hurwitz; Klaudiusz R Weiss
Journal:  J Neurosci       Date:  2004-07-14       Impact factor: 6.167

8.  Passive hinge forces in the feeding apparatus of Aplysia aid retraction during biting but not during swallowing.

Authors:  G P Sutton; J B Macknin; S S Gartman; G P Sunny; R D Beer; P E Crago; D M Neustadter; H J Chiel
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2004-04-20       Impact factor: 1.836

9.  Newly Identified Aplysia SPTR-Gene Family-Derived Peptides: Localization and Function.

Authors:  Guo Zhang; Wang-Ding Yuan; Ferdinand S Vilim; Elena V Romanova; Ke Yu; Si-Yuan Yin; Zi-Wei Le; Ying-Yu Xue; Ting-Ting Chen; Guo-Kai Chen; Song-An Chen; Elizabeth C Cropper; Jonathan V Sweedler; Klaudiusz R Weiss; Jian Jing
Journal:  ACS Chem Neurosci       Date:  2018-03-27       Impact factor: 4.418

10.  Distinct inhibitory neurons exert temporally specific control over activity of a motoneuron receiving concurrent excitation and inhibition.

Authors:  Kosei Sasaki; Vladimir Brezina; Klaudiusz R Weiss; Jian Jing
Journal:  J Neurosci       Date:  2009-09-23       Impact factor: 6.167

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