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Non-competitive antagonism by hirsuteine of nicotinic receptor-mediated dopamine release from rat pheochromocytoma cells.

Abstract
Effects of hirsuteine, an indole alkaloid extracted from Uncaria genus, on nicotine- and high K-induced responses were investigated in rat pheochromocytoma PC12 cells. Hirsuteine (300 nM-10 microM) inhibited dopamine release evoked by 100 microM nicotine in a concentration-dependent manner. Hirsuteine did not produce a parallel shift of the concentration-response relationship curve for nicotine, but reduced maximal dopamine release. Dopamine release evoked by 60 and 155 mM KCl was also inhibited by hirsuteine, but the concentration necessary for significant inhibition was higher (more than 10 microM). Under whole cell voltage-clamp, hirsuteine reversibly inhibited inward currents activated by 100 microM nicotine. The current inhibition was slightly accelerated by hyperpolarization. The results suggest that hirsuteine non-competitively antagonizes nicotine-evoked dopamine release by blocking ion permeation through nicotinic receptor channel complexes. The blockade of Ca channels, which are activated during nicotine-evoked depolarization, may not play a major role in the antagonism.
AuthorsT Watano, K Nakazawa, T Obama, M Mori, K Inoue, K Fujimori, A Takanaka
JournalJapanese journal of pharmacology (Jpn J Pharmacol) Vol. 61 Issue 4 Pg. 351-6 (Apr 1993) ISSN: 0021-5198 [Print] Japan
PMID8320880 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Alkaloids
  • Calcium Channel Blockers
  • Drugs, Chinese Herbal
  • Nicotinic Antagonists
  • hirsuteine
  • Nicotine
  • Adenosine Triphosphate
  • Potassium
  • Dopamine
Topics
  • Adenosine Triphosphate (pharmacology)
  • Alkaloids (pharmacology)
  • Animals
  • Calcium Channel Blockers (pharmacology)
  • Dopamine (metabolism)
  • Drugs, Chinese Herbal
  • Ion Channel Gating (drug effects)
  • Membrane Potentials (drug effects)
  • Nicotine (pharmacology)
  • Nicotinic Antagonists
  • PC12 Cells
  • Potassium (pharmacology)
  • Rats

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