ω-agatoxin IVA blocks nicotinic receptor channels in bovine chromaffin cells

Ricardo Granja, JoséM Fernández-Fernández, Victor Izaguirre, Carmen González-García, Valentin Ceña

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

We have studied the contribution of P-type voltage-dependent Ca2+ channels to both catacholamine (CA) and ATP secretion from bovine chromaffin cells induced by high K+ or nicotine using ω-agatoxin IVA, a selective blocker of P-type voltage-dependent Ca2+ channels. We found that high K+ (75 mM) induced the release of about 13% of norepinephrine, 5% epinephrine and 11% ATP, and that ω-agatoxin (100 nM) did not affect this secretion. However, both nicotine-induced CA and ATP secretion were significantly blocked (about 50%) by ω-agatoxin IVA (100 nM). In addition, this toxin also reversibly blocked (about 70%) the inward current induced by nicotine in bovine chromaffin cells. The results suggest that, besides its known action of blocking P-type voltage-dependent channels, ω-agatoxin is a potent and reversible blocker of the nicotinic receptor channel in chromaffin cells, and that this action would explain the blockade of nicotine-induced secretion.

Original languageEnglish
Pages (from-to)15-18
Number of pages4
JournalFEBS Letters
Volume362
Issue number1
DOIs
StatePublished - 27 Mar 1995

Bibliographical note

Funding Information:
Acknowledgements: This work was supported, in part, by grants from Fundaci6n Salud 2000, Direcci6n General de Investigaci6n Cientifica y T6cnica, Grant PM92-0112, and the European Economic Community, Grant SC1"-CT91-0709. R.G. was supported by a University of Alicante fellowship, J.M.F. by a CAM fellowship, and V.I. by a Gener-alitat Valenciana fellowship.

Keywords

  • Calcium channel
  • Chromaffin cell
  • Nicotinic receptor
  • P-type
  • Secretion
  • ω-Agatoxin IVA

Fingerprint

Dive into the research topics of 'ω-agatoxin IVA blocks nicotinic receptor channels in bovine chromaffin cells'. Together they form a unique fingerprint.

Cite this