Literature DB >> 8727381

B64, a newly identified central pattern generator element producing a phase switch from protraction to retraction in buccal motor programs of Aplysia californica.

I Hurwitz1, A J Susswein.   

Abstract

1. Buccal motor programs in Aplysia are characterized by two phases of activity, which represent protraction and retraction of the radula in intact animals. The shift from protraction to retraction is caused by synaptic activity inhibiting neurons that are active during protraction and exciting neurons that are active during retraction. 2. B64, a newly identified neuron present bilaterally in the buccal ganglia, is partially responsible for the phase shift. Stimulating a single B64 causes bilateral inhibition of neurons B31/B32 and other neurons active during protraction and cause bilateral excitation of neurons B4/B5 and other neurons active during retraction. B64 is active throughout retraction. The amplitude and waveforms of the synaptic potentials caused by firing B64 are similar, but not identical, to those seen during retraction. 3. Some of the effects of B64 on B31/B32 and on B4/B5 are monosynaptic, as shown by their maintained presence in high divalent cation seawater, which blocks polysynaptic activity. 4. A brief depolarization of B64 leads to a long-lasting depolarization and firing. The ability of B64 to respond in this way is at least partially caused by an endogenous plateau potential, as this property is still seen after synaptic transmission is blocked. 5. Hyperpolarization of B64 bilaterally and preventing the somata from firing unmasks a large excitatory postsynaptic potential in B64. This procedure does not block the shift from protraction to retraction, indicating that spiking in the B64 somata is not necessary for the phase shift. 6. The firing pattern and synaptic connections of B64 are consistent with the hypothesis that the neuron is part of a central pattern generator underlying buccal motor programs. B64 is monosynaptically inhibited by neurons that are active along with B31/B32, which are responsible for producing the protraction phase of a buccal motor program. During the later portion of the protraction phase B64 is excited. In addition, firing B64 can phase advance and phase delay buccal motor programs. 7. Regulating the firing of B64 can regulate the expression of buccal motor programs. Stimulation of B64 at frequencies of 0.5-1.0 Hz leads to complete inhibition of buccal motor programs, whereas steady-state depolarization of B64 can lead to repetitive bursts of activity.

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Year:  1996        PMID: 8727381     DOI: 10.1152/jn.1996.75.4.1327

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


  46 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 types of control by identified interneurons in a sensory-activated rhythmic motor pattern.

Authors:  G Kemenes; K Staras; P R Benjamin
Journal:  J Neurosci       Date:  2001-04-15       Impact factor: 6.167

3.  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

4.  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

5.  In vitro analog of operant conditioning in aplysia. II. Modifications of the functional dynamics of an identified neuron contribute to motor pattern selection.

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

6.  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

7.  Regulation of spike initiation and propagation in an Aplysia sensory neuron: gating-in via central depolarization.

Authors:  Colin G Evans; Jian Jing; Steven C Rosen; Elizabeth C Cropper
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

8.  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

Review 9.  Neural mechanisms of operant conditioning and learning-induced behavioral plasticity in Aplysia.

Authors:  Romuald Nargeot; John Simmers
Journal:  Cell Mol Life Sci       Date:  2010-11-02       Impact factor: 9.261

10.  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

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