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Effects of reduced external sodium concentration and multivalent cations on caffeine contractures in young ferret atrial trabeculae.

Abstract
The characteristics of caffeine (1.25-80 mM) transient contractures have been examined in small atrial trabeculae (diameters 50-250 microns) isolated from young (1-1.5 months) ferret hearts. In the control medium, the half-saturation constant and the maximum contracture strength (at infinite caffeine concentration) were 37.8 +/- 10.2 mM and 0.9 +/- 0.2 kN.kg-1 (n = 11), respectively. The contractile response to caffeine was markedly enhanced following reduction of external sodium (70-0 mM). The perfusion of young ferret trabeculae with the sodium-free medium (up to 3 min) decreased the half-saturation constant by a factor of three (12.4 +/- 1.6 mM, n = 8) with an increase in maximum contracture strength (1.09 +/- 0.3 kN.kg-1, n = 8). The effects of various divalent and trivalent cations have been tested on the 10 mM caffeine contracture in trabeculae perfused with Na-containing (140 mM) solution. The order of cation effectiveness is Gd3+ (half effect 0.04-0.07 mM) greater than Cd2+ (0.15-0.25 mM) greater than Ni2+ (2-2.5 mM) greater than Co2+ (7-7.5 mM) much greater than Mn2+. In conclusion, the present work has shown that in atrial trabeculae isolated from young ferret hearts, the strength of the caffeine contracture was markedly affected by the activity of the sarcolemmal Na-Ca exchange.
AuthorsJ Noireaud, S Baudet, C Huchet, C Leoty
JournalCanadian journal of physiology and pharmacology (Can J Physiol Pharmacol) Vol. 70 Issue 1 Pg. 60-7 (Jan 1992) ISSN: 0008-4212 [Print] Canada
PMID1581856 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Cations
  • Caffeine
  • Sodium
  • Calcium
Topics
  • Animals
  • Atrial Function
  • Caffeine (pharmacology)
  • Calcium (metabolism)
  • Cations (pharmacology)
  • Ferrets
  • Heart Atria (drug effects)
  • In Vitro Techniques
  • Ion Exchange
  • Myocardial Contraction (drug effects, physiology)
  • Sodium (metabolism, pharmacology)

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