Literature DB >> 217974

Central and peripheral control of siphon-withdrawal reflex in Aplysia californica.

A J Perlman.   

Abstract

1. The defensive withdrawal reflex of the siphon of Aplysia is a local response (exhibited by the organ that is stimulated) mediated by the conjoint action of both the central and peripheral nervous systems. 2. Three independent methods were used to determine the contribution of the central and peripheral nervous systems to the siphon-withdrawal reflex: 1) acute reversible deganglionation, 2) chronic deganglionation, and 3) a selective reversible hyperpolarization. With each of these techniques, the central nervous system was found to contribute about 55% of the total reflex. 3. Seven motor neurons were identified and characterized with respect to their electrophysiological properties and the motor actions. Three of the central motor cells belong to the LD clusters of cells (LDS1, LDS2, LDS3) and one is an RD cell (RDS). These four cells all receive excitatory synaptic input from siphon stimulation, excitatory synaptic input from the activity of the respiratory command cells network (interneuron II). large spontaneous IPSPs, and exhibit hyperpolarizing responses (H response) to iontophoretically applied acetylcholine (ACh). These cells all participate in the siphon-withdrawal component of a centrally commanded fixed-action pattern: spontaneous pumping movements of the mantle organs driven by the respiratory command cells. They receive an EPSP burst during the activity of the respiratory command cells and are competent to mediate the siphon motion. Three central siphon motor cells belong to the LB cluster (LBS1, LBS2, LBS3). These cells also receive excitatory input following stimulation of the siphon, a spontaneously occurring IPSP, and have H response to iontophoretically applied ACh. These cells, however, receive an IPSP burst during spontaneous pumping movement and thus do not participate in the active contraction phase of this behavior. LBS1 and LDS1 were examined with respect to their transmitter biochemistry and were found to be noncholinergic. 4. The siphon-withdrawal reflex habituates with comparable kinetics to repeated tactile stimulation when it is under central and peripheral control and when it is under peripheral control only. Thus, not only do both systems act conjointly to produce the defensive withdrawal reflex, but also they have similar response properties and are well matched to mediate the two parts of this siphon behavior.

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Year:  1979        PMID: 217974     DOI: 10.1152/jn.1979.42.2.510

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


  11 in total

1.  The contribution of facilitation of monosynaptic PSPs to dishabituation and sensitization of the Aplysia siphon withdrawal reflex.

Authors:  I Antonov; E R Kandel; R D Hawkins
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  The contribution of activity-dependent synaptic plasticity to classical conditioning in Aplysia.

Authors:  I Antonov; I Antonova; E R Kandel; R D Hawkins
Journal:  J Neurosci       Date:  2001-08-15       Impact factor: 6.167

Review 3.  Control of the cardiovascular system of Aplysia by identified neurons.

Authors:  M Skelton; A Alevizos; J Koester
Journal:  Experientia       Date:  1992-09-15

Review 4.  The bag cell neurons of Aplysia. A model for the study of the molecular mechanisms involved in the control of prolonged animal behaviors.

Authors:  P J Conn; L K Kaczmarek
Journal:  Mol Neurobiol       Date:  1989       Impact factor: 5.590

5.  Classical conditioning of the Aplysia siphon-withdrawal reflex exhibits response specificity.

Authors:  R D Hawkins; N Lalevic; G A Clark; E R Kandel
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

Review 6.  Neural control of the circulatory system of Aplysia.

Authors:  J Koester; U T Koch
Journal:  Experientia       Date:  1987-09-15

Review 7.  Separate effects of a classical conditioning procedure on respiratory pumping, swimming, and inking in Aplysia fasciata.

Authors:  M Levy; A J Susswein
Journal:  Learn Mem       Date:  1999 Jan-Feb       Impact factor: 2.460

8.  Localized neuronal outgrowth induced by long-term sensitization training in aplysia.

Authors:  Marcy L Wainwright; Han Zhang; John H Byrne; Leonard J Cleary
Journal:  J Neurosci       Date:  2002-05-15       Impact factor: 6.167

Review 9.  Activity-dependent presynaptic facilitation: an associative mechanism in Aplysia.

Authors:  T W Abrams
Journal:  Cell Mol Neurobiol       Date:  1985-06       Impact factor: 5.046

10.  Directional control and the functional organization of defensive responses in Aplysia.

Authors:  E T Walters; M T Erickson
Journal:  J Comp Physiol A       Date:  1986-09       Impact factor: 1.836

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