Literature DB >> 2329360

Premotor neurons B51 and B52 in the buccal ganglia of Aplysia californica: synaptic connections, effects on ongoing motor rhythms, and peptide modulation.

M R Plummer1, M D Kirk.   

Abstract

1. Two buccal ganglia interneurons, labeled here as B51 and B52, have been identified on the basis of morphological and physiological criteria. 2. These neurons have multipolar cell bodies. B51 extends a major neurite, which arborizes in the neuropil ipsilateral to the soma; extends into the buccal commissure, where it branches profusely; and projects an axon out the radular nerve (n1); other processes emanating from the soma arborize in the adjacent cell body layer. B52 arborizes ipsilateral to its cell body and sends a major process out of the ipsilateral hemiganglion into the sheath that attaches the buccal ganglia to the buccal mass proper. Here the B52 axon projects through a previously undescribed structure, which forms an arch over the buccal commissure that we designate the commissural arch. The extraganglionic B52 axon sends several branches into the connective tissue and then returns to the contralateral hemiganglion, where it again branches. 3. Each neuron exhibits a unique set of physiological properties. B51 frequently produces plateau potentials, which persist and are even enhanced in solutions where Ca2+ is replaced with Co2+. On the other hand, B52 shows a powerful posthyperpolarization rebound that contributes to its burst formation during spontaneous and nerve-elicited cyclic motor output. 4. B51 and B52 display distinctive rhythmic bursting on stimulation of the radular nerve or esophageal nerve. Their burst-firing tended to occur at certain phase relationships with respect to firing in other buccal premotor and motor neurons. 5. When firing frequency is measured as a function of intracellularly injected current, B51 shows a steplike increase in firing with increasing current, whereas B52 firing frequency is continuously graded. 6. B51 and B52 were found to make extensive synaptic connections within the buccal ganglia. B51 exhibited primarily excitatory electrical connections with known premotor and motor neurons, including an electrotonic synapse with its contralateral homologue. 7. In contrast, B52 made bilateral inhibitory synapses with nearly all of the premotor and motor neurons of the ventral motor cluster. Most of these connections appeared to be monosynaptic, producing synaptic potentials with short and fixed latencies that persisted when the ganglia were bathed in solutions containing elevated concentrations of Ca2+ and Mg2+. 8. Other synaptic potentials produced by B52 were more variable in size and latency; these included slow inhibition of the B4 and B5 neurons and excitation of an identifiable neuron that projected out the radular nerve.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 2329360     DOI: 10.1152/jn.1990.63.3.539

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


  39 in total

1.  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

2.  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

3.  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

4.  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

5.  Rapid and persistent suppression of feeding behavior induced by sensitization training in Aplysia.

Authors:  Ama Acheampong; Kathleen Kelly; Maria Shields-Johnson; Julie Hajovsky; Marcy Wainwright; Riccardo Mozzachiodi
Journal:  Learn Mem       Date:  2012-03-14       Impact factor: 2.460

Review 6.  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

7.  Peptidergic motoneurons in the buccal ganglia of Aplysia californica: immunocytochemical, morphological, and physiological characterizations.

Authors:  P J Church; K P Cohen; M L Scott; M D Kirk
Journal:  J Comp Physiol A       Date:  1991-03       Impact factor: 1.836

8.  Training with inedible food in Aplysia causes expression of C/EBP in the buccal but not cerebral ganglion.

Authors:  David Levitan; Lisa C Lyons; Alexander Perelman; Charity L Green; Benny Motro; Arnold Eskin; Abraham J Susswein
Journal:  Learn Mem       Date:  2008-05-28       Impact factor: 2.460

9.  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

10.  In vitro analog of classical conditioning of feeding behavior in aplysia.

Authors:  Riccardo Mozzachiodi; Hilde A Lechner; Douglas A Baxter; John H Byrne
Journal:  Learn Mem       Date:  2003 Nov-Dec       Impact factor: 2.460

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