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Apamin, a selective blocker of SK(Ca) channels, inhibits posthypoxic hyperexcitability but does not affect rapid hypoxic preconditioning in hippocampal CA1 pyramidal neurons in vitro.

Abstract
The aim of this study was to investigate the effects of apamin, a selective blocker of SK(Ca) channels, on the repeated brief hypoxia-induced posthypoxic hyperexcitability and rapid hypoxic preconditioning in hippocampal CA1 pyramidal neurons in vitro. The method of field potentials measurement in CA1 region of the rat hippocampal slices was used. Application of apamin (50nM) to the hippocampal slices during hypoxic episodes significantly abolished posthypoxic hyperexcitability induced by brief hypoxic episodes. However, in contrast to our previous results with iberiotoxin, a selective blocker of BK(Ca) channels, apamin significantly enhanced the depressive effect of brief hypoxia on the PS amplitude during hypoxic episode and did not abolish the rapid hypoxic preconditioning in CA1 pyramidal neurons. Present results indicate that SK(Ca) channels, along with previously implicated BK(Ca) channels, play an important role in the development of posthypoxic hyperexcitability induced by brief hypoxic episodes in CA1 pyramidal neurons. However, SK(Ca) channels, in contrast to the BK(Ca) channels, are not involved in the rapid hypoxic preconditioning in CA1 hippocampal region in vitro.
AuthorsSergei G Levin, Alina A Shamsutdinova, Oleg V Godukhin
JournalNeuroscience letters (Neurosci Lett) Vol. 484 Issue 1 Pg. 35-8 (Oct 22 2010) ISSN: 1872-7972 [Electronic] Ireland
PMID20708065 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2010 Elsevier Ireland Ltd. All rights reserved.
Chemical References
  • Small-Conductance Calcium-Activated Potassium Channels
  • Apamin
Topics
  • Animals
  • Apamin (pharmacology)
  • CA1 Region, Hippocampal (cytology, drug effects, physiopathology)
  • Hypoxia (physiopathology)
  • Male
  • Pyramidal Cells (drug effects, physiology)
  • Rats
  • Rats, Wistar
  • Small-Conductance Calcium-Activated Potassium Channels (antagonists & inhibitors)

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