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FMRFamide modulates the action of phase shifting agents on the ocular circadian pacemakers of Aplysia and Bulla.

Abstract
The eye of the marine mollusk Aplysia californica contains a photo-entrainable circadian pacemaker that drives an overt circadian rhythm of spontaneous compound action potentials in the optic nerve. Both light and serotonin are known to influence the phase of this ocular rhythm. The current study evaluated the effect of FMRFamide on both light and serotonin induced phase shifts of this rhythm. The application of FMRFamide was found to block serotonin induced phase shifts but, by itself, FMRFamide did not cause significant phase shifts. Furthermore, the effects of FMRFamide on light-induced phase shifts appeared to be phase dependent (i.e., the application of FMRFamide inhibited light-induced phase delays but actually enhanced the magnitude of phase advances). As in Aplysia, the eye of Bulla gouldiana also contains a circadian pacemaker. In Bulla, FMRFamide prevented light-induced phase advances and delays. Although FMRFamide alone generated phase dependent phase shifts, it did not cause phase shifts at the phases where it blocked the effects of light. These data demonstrate that FMRFamide can have pronounced modulatory effects on phase shifting inputs to the ocular pacemakers of both Aplysia and Bulla.
AuthorsC S Colwell, S B Khalsa, G D Block
JournalJournal of comparative physiology. A, Sensory, neural, and behavioral physiology (J Comp Physiol A) Vol. 170 Issue 2 Pg. 211-5 (Feb 1992) Germany
PMID1583606 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Neuropeptides
  • Serotonin Antagonists
  • FMRFamide
Topics
  • Animals
  • Aplysia (physiology)
  • Circadian Rhythm (drug effects, physiology)
  • Eye (drug effects)
  • FMRFamide
  • Mollusca (physiology)
  • Neurons, Efferent (drug effects, physiology)
  • Neuropeptides (physiology)
  • Ocular Physiological Phenomena
  • Photic Stimulation
  • Retina (drug effects, physiology)
  • Serotonin Antagonists (pharmacology)

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