Literature DB >> 1185181

Habituation and dishabituation mediated by the peripheral and central neural circuits of the siphon of Aplysia.

K Lukowiak, J Jacklet.   

Abstract

The siphon withdrawal response evoked by a weak tactile (water drop) or light stimulus is mediated primarily by neurons in the siphon. Central neurons (abdominal ganglion) contribute very little since the response amplitude and latency are not changed following removal of the abdominal ganglion. Similarly, habituation and dishabituation of this withdrawal response are not different after removal of the abdominal ganglion, indicating that the peripheral neural circuit in the isolated siphon can mediate habituation itself, and thus has many of the properties attributed to central neurons. Response evoked by electrical stimulation of the siphon nerve habituate, depending upon the stimulus intensity and interval. These habituated responses may be dishabituated by tactile or light stimulation of the siphon. These results show that each neural system, peripheral and central, has an excitatory modulatory influence on the other. Normally adaptive siphon responses must be shaped by the integrated activity of both of these neural systems.

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Year:  1975        PMID: 1185181     DOI: 10.1002/neu.480060206

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


  3 in total

1.  Facilitation at neuromuscular junctions: contribution to habituation and dishabituation of the Aplysia gill withdrawal reflex.

Authors:  J W Jacklet; J Rine
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

Review 2.  Interactions between depression and facilitation within neural networks: updating the dual-process theory of plasticity.

Authors:  S A Prescott
Journal:  Learn Mem       Date:  1998 Nov-Dec       Impact factor: 2.460

3.  Prolonged habituation of the gill-withdrawal reflex in Aplysia depends on protein synthesis, protein phosphatase activity, and postsynaptic glutamate receptors.

Authors:  Youssef Ezzeddine; David L Glanzman
Journal:  J Neurosci       Date:  2003-10-22       Impact factor: 6.167

  3 in total

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