Literature DB >> 10036255

Actions of a pair of identified cerebral-buccal interneurons (CBI-8/9) in Aplysia that contain the peptide myomodulin.

Y Xin1, I Hurwitz, R Perrins, C G Evans, V Alexeeva, K R Weiss, I Kupfermann.   

Abstract

A combination of biocytin back-fills of the cerebral-buccal connectives and immunocytochemistry of the cerebral ganglion demonstrated that of the 13 bilateral pairs of cerebral-buccal interneurons in the cerebral ganglion, a subpopulation of 3 are immunopositive for the peptide myomodulin. The present paper describes the properties of two of these cells, which we have termed CBI-8 and CBI-9. CBI-8 and CBI-9 were found to be dye coupled and electrically coupled. The cells have virtually identical properties, and consequently we consider them to be "twin" pairs and refer to them as CBI-8/9. CBI-8/9 were identified by electrophysiological criteria and then labeled with dye. Labeled cells were found to be immunopositive for myomodulin, and, using high pressure liquid chromatography, the cells were shown to contain authentic myomodulin. CBI-8/9 were found to receive synaptic input after mechanical stimulation of the tentacles. They also received excitatory input from C-PR, a neuron involved in neck lengthening, and received a slow inhibitory input from CC5, a cell involved in neck shortening, suggesting that CBI-8/9 may be active during forward movements of the head or buccal mass. Firing of CBI-8 or CBI-9 resulted in the activation of a relatively small number of buccal neurons as evidenced by extracellular recordings from buccal nerves. Firing also produced local movements of the buccal mass, in particular a strong contraction of the I7 muscle, which mediates radula opening. CBI-8/9 were found to produce a slow depolarization and rhythmic activity of B48, the motor neuron for the I7 muscle. The data provide continuing evidence that the small population of cerebral buccal interneurons is composed of neurons that are highly diverse in their functional roles. CBI-8/9 may function as a type of premotor neuron, or perhaps as a peptidergic modulatory neuron, the functions of which are dependent on the coactivity of other neurons.

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Year:  1999        PMID: 10036255     DOI: 10.1152/jn.1999.81.2.507

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


  8 in total

1.  Projection neurons with shared cotransmitters elicit different motor patterns from the same neural circuit.

Authors:  D E Wood; W Stein; M P Nusbaum
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

2.  Repetition priming of motor activity mediated by a central pattern generator: the importance of extrinsic vs. intrinsic program initiators.

Authors:  Michael J Siniscalchi; Elizabeth C Cropper; Jian Jing; Klaudiusz R Weiss
Journal:  J Neurophysiol       Date:  2016-07-27       Impact factor: 2.714

3.  A population of pedal-buccal projection neurons associated with appetitive components of Aplysia feeding behavior.

Authors:  Alice Robie; Manuel Díaz-Ríos; Mark W Miller
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2003-02-18       Impact factor: 1.836

4.  Feedforward compensation mediated by the central and peripheral actions of a single neuropeptide discovered using representational difference analysis.

Authors:  Jian Jing; Jonathan V Sweedler; Elizabeth C Cropper; Vera Alexeeva; Ji-Ho Park; Elena V Romanova; Fang Xie; Nikolai C Dembrow; Bjoern C Ludwar; Klaudiusz R Weiss; Ferdinand S Vilim
Journal:  J Neurosci       Date:  2010-12-08       Impact factor: 6.167

5.  Complementary interactions between command-like interneurons that function to activate and specify motor programs.

Authors:  Jin-Sheng Wu; Nan Wang; Michael J Siniscalchi; Matthew H Perkins; Yu-Tong Zheng; Wei Yu; Song-an Chen; Ruo-nan Jia; Jia-Wei Gu; Yi-Qing Qian; Yang Ye; Ferdinand S Vilim; Elizabeth C Cropper; Klaudiusz R Weiss; Jian Jing
Journal:  J Neurosci       Date:  2014-05-07       Impact factor: 6.167

6.  FMRF-NH2 -related neuropeptides in Biomphalaria spp., intermediate hosts for schistosomiasis: Precursor organization and immunohistochemical localization.

Authors:  Solymar Rolón-Martínez; Mohamed R Habib; Tamer A Mansour; Manuel Díaz-Ríos; Joshua J C Rosenthal; Xiao-Nong Zhou; Roger P Croll; Mark W Miller
Journal:  J Comp Neurol       Date:  2021-06-11       Impact factor: 3.028

7.  Identification and localization of a gonadotropin-releasing hormone-related neuropeptide in Biomphalaria, an intermediate host for schistosomiasis.

Authors:  Mariela Rosa-Casillas; Paola Méndez de Jesús; Laura C Vicente Rodríguez; Mohamed R Habib; Roger P Croll; Mark W Miller
Journal:  J Comp Neurol       Date:  2021-01-27       Impact factor: 3.028

8.  Synaptic mechanisms for motor variability in a feedforward network.

Authors:  Guo Zhang; Ke Yu; Tao Wang; Ting-Ting Chen; Wang-Ding Yuan; Fan Yang; Zi-Wei Le; Shi-Qi Guo; Ying-Yu Xue; Song-An Chen; Zhe Yang; Feng Liu; Elizabeth C Cropper; Klaudiusz R Weiss; Jian Jing
Journal:  Sci Adv       Date:  2020-06-19       Impact factor: 14.957

  8 in total

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