Literature DB >> 3288711

Parallel processing of short-term memory for sensitization in Aplysia.

W N Frost1, G A Clark, E R Kandel.   

Abstract

How is the short-term memory for a single form of learning distributed among the various elements of a neuronal circuit? To answer this question, we examined the short-term memory for sensitization, using the siphon component of the defensive gill- and siphon-withdrawal reflex. We found that the memory for short-term sensitization is represented by at least four sites of circuit modification, each involving a different type of plasticity. These include (1) presynaptic facilitation of the sensory neuron connections onto both interneurons and motorneurons; (2) presynaptic inhibition at the connections of the L30 inhibitory neurons onto the excitatory interneuron L29; (3) posttetanic potentiation of the excitatory connections made by L29 onto a specific subclass of siphon motorneurons, the LFS cells; and (4) an increase in the tonic firing rate of the LFS siphon motor neurons, resulting in neuromuscular facilitation. Each of the heterosynaptic changes seems to involve a common modulatory transmitter and to utilize a common second messenger system. Moreover, each of these sites seems capable of encoding a different component of the short-term memory. Facilitation of the connections of sensory neurons should contribute to the increase in amplitude of the response; the disinhibition of the L29 interneurons and the posttetanic potentiation at L29 synapses should contribute to an increase in the duration of the response; and the increase in tonic firing of the LFS subclass of siphon motor neurons seems capable of contributing both to an increase in response amplitude and to changes in response topography.

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Year:  1988        PMID: 3288711     DOI: 10.1002/neu.480190402

Source DB:  PubMed          Journal:  J Neurobiol        ISSN: 0022-3034


  41 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.  Sites of plasticity in the neural circuit mediating tentacle withdrawal in the snail Helix aspersa: implications for behavioral change and learning kinetics.

Authors:  S A Prescott; R Chase
Journal:  Learn Mem       Date:  1999 Jul-Aug       Impact factor: 2.460

3.  Distributed and partially separate pools of neurons are correlated with two different components of the gill-withdrawal reflex in Aplysia.

Authors:  M Zochowski; L B Cohen; G Fuhrmann; D Kleinfeld
Journal:  J Neurosci       Date:  2000-11-15       Impact factor: 6.167

4.  Long-lasting reconfiguration of two interacting networks by a cooperation of presynaptic and postsynaptic plasticity.

Authors:  R Nargeot
Journal:  J Neurosci       Date:  2001-05-01       Impact factor: 6.167

5.  Synaptic augmentation contributes to environment-driven regulation of the aplysia siphon-withdrawal reflex.

Authors:  Robert J Calin-Jageman; Thomas M Fischer
Journal:  J Neurosci       Date:  2003-12-17       Impact factor: 6.167

Review 6.  Multiple serotonergic mechanisms contributing to sensitization in aplysia: evidence of diverse serotonin receptor subtypes.

Authors:  Demian Barbas; Luc DesGroseillers; Vincent F Castellucci; Thomas J Carew; Stéphane Marinesco
Journal:  Learn Mem       Date:  2003 Sep-Oct       Impact factor: 2.460

7.  The role of rapid, local, postsynaptic protein synthesis in learning-related synaptic facilitation in aplysia.

Authors:  Greg Villareal; Quan Li; Diancai Cai; David L Glanzman
Journal:  Curr Biol       Date:  2007-11-20       Impact factor: 10.834

8.  Reversal of synaptic depression by serotonin at Aplysia sensory neuron synapses involves activation of adenylyl cyclase.

Authors:  B A Goldsmith; T W Abrams
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-15       Impact factor: 11.205

9.  The potential role of postsynaptic phospholipase C activity in synaptic facilitation and behavioral sensitization in Aplysia.

Authors:  Daniel Fulton; Michael C Condro; Kaycey Pearce; David L Glanzman
Journal:  J Neurophysiol       Date:  2008-05-14       Impact factor: 2.714

10.  Postsynaptic regulation of long-term facilitation in Aplysia.

Authors:  Diancai Cai; Shanping Chen; David L Glanzman
Journal:  Curr Biol       Date:  2008-06-24       Impact factor: 10.834

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