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

Abstract
Despite representing perhaps the simplest form of memory, habituation is not yet well understood mechanistically. We used a reduced preparation to analyze the neurobiological mechanisms of persistent habituation of a simple behavior, the defensive withdrawal reflex of the marine snail Aplysia californica. This preparation permits direct infusion of drugs into the abdominal ganglion during training via a cannula in the abdominal artery. Using siphon-elicited gill withdrawal, we demonstrate habituation of withdrawal that persists for 1-6 hr after repeated, spaced blocks of habituating stimulation. This form of habituation exhibits site specificity and requires protein synthesis because it is blocked by the presence of anisomycin, a protein synthesis inhibitor. We also find that habituation of gill withdrawal requires protein phosphatase activity, because it is blocked by okadaic acid, an inhibitor of protein phosphatase. Finally, habituation of gill withdrawal requires activation of NMDA-type and AMPA-type postsynaptic receptors within the abdominal ganglion, because it is blocked by infusion of dl-2-amino-5-phosphonovaleric acid or 6,7-dinitroquinoxaline-2,3-dione. The requirement for activation of postsynaptic glutamatergic receptors indicates that homosynaptic depression, an exclusively presynaptic mechanism that has been implicated previously in habituation in Aplysia, does not play a significant role in persistent habituation of the withdrawal reflex. Our results indicate that postsynaptic mechanisms, possibly including modulation of glutamate receptor function, play a major, heretofore unsuspected, role in habituation in Aplysia.
AuthorsYoussef Ezzeddine, David L Glanzman
JournalThe Journal of neuroscience : the official journal of the Society for Neuroscience (J Neurosci) Vol. 23 Issue 29 Pg. 9585-94 (Oct 22 2003) ISSN: 1529-2401 [Electronic] United States
PMID14573538 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Enzyme Inhibitors
  • Excitatory Amino Acid Antagonists
  • Protein Synthesis Inhibitors
  • Receptors, AMPA
  • Receptors, Glutamate
  • Receptors, N-Methyl-D-Aspartate
  • Phosphoprotein Phosphatases
Topics
  • Animals
  • Aplysia (physiology)
  • Enzyme Inhibitors (pharmacology)
  • Excitatory Amino Acid Antagonists (pharmacology)
  • Gills (physiology)
  • Habituation, Psychophysiologic (physiology)
  • In Vitro Techniques
  • Phosphoprotein Phosphatases (antagonists & inhibitors, metabolism)
  • Protein Biosynthesis
  • Protein Synthesis Inhibitors (pharmacology)
  • Receptors, AMPA (antagonists & inhibitors, metabolism)
  • Receptors, Glutamate (metabolism)
  • Receptors, N-Methyl-D-Aspartate (antagonists & inhibitors, metabolism)
  • Reflex (physiology)
  • Synapses (metabolism)

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