Presynaptic mechanism of action induced by 5-HT in nerve terminals: Possible involvement of ryanodine and IP3 sensitive Ca2+ stores

Amanda J. Dropic, Eugen Brailoiu, Robin L. Cooper

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Although modulation of transmitter release by serotonin (5-HT) at crayfish neuromuscular junctions has been known since 1965, the mechanisms of action have not been established in this classical synaptic preparation. We show that injections of adenophostin-A (an IP3 analog) in the nerve terminals greatly enhances synaptic transmission. Exposure to ryanodine (Ry) produces a biphasic response: at low concentration it is excitatory and high concentration it is inhibitory. Likewise, a low concentration (1 μM) of caffeine enhances synaptic transmission, whereas a high concentration (10 mM) has little effect on transmission. The varied responses and sensitivity to Ry and caffeine suggest a Ca2+-induced Ca2+-release mechanism and/or the presence of an IP3-receptor within the terminal. Thus, it is likely 5-HT's response is due to activation of intracellular pathways, which subsequently release Ca2+ from internal stores.

Original languageEnglish
Pages (from-to)355-361
Number of pages7
JournalComparative Biochemistry and Physiology - A Molecular and Integrative Physiology
Volume142
Issue number3
DOIs
StatePublished - Nov 2005

Bibliographical note

Funding Information:
We thank Dr. M. Miyamoto at East TN State for critical editorial comments on the manuscript. Funding was provided by NSF grants IBN-9808631 and IBN-0131459 (RLC) and an undergraduate training fellowship by G. Ribble in the School of Biological Sciences at the University of Kentucky (AJF). Dropic's maiden name at time of research was Fox.

Keywords

  • Crayfish
  • Neuromodulation
  • Presynaptic
  • Serotonin
  • Synapse

ASJC Scopus subject areas

  • Biochemistry
  • Physiology
  • Molecular Biology

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