[Effects of genistein on contractility of isolated right ventricular muscles in guinea pig]

Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2008 Nov;24(4):406-9.
[Article in Chinese]

Abstract

Aim: To study the effect of genistein (GEN) on contractility of isolated right ventricular muscles in guinea pig and its mechanisms.

Methods: Isolated guinea pig ventricular muscles were suspended in organ baths containing K-H solution.After an equilibration period, the effect of GEN on contraction of myocardium was observed.

Results: GEN and isoprenaline hydrochloride had the positive inotropic effects on contractity of myocardium. Meanwhile, the effect of GEN (1-100 micromol x L(-1)) was in dose-dependent manner. Propranolol (1 micromol x L(-1)) and verapamil hydrochloride (0.5 micromol x L(-1)) attenuated the positive inotropic effect of isoprenaline hydrochloride (1 micromol x L(-1)), but did not change the effect of GEN (50 micromol x L(-1)). Further more, the enhancement of the contraction induced by elevation of extracellular Ca2+ concentration in ventricular muscles had no change after pretreatment with GEN (1.10 micromol x L(-1)). In addition,the positive inotropic effect of GEN was inhibited partially by tamoxifen (1 micromol x L(-1)) and SQ22536 (1 micromol x L(-1)), also, could be attenuated by bpV (1 micromol x L(-1)).

Conclusion: GEN has the positive inotropic effect on guinea pig ventricular muscles, which is not related to the activation of beta adrenoceptor, Ca2+ channel on cell membrane,but may involve in cAMP of intracellular signal transduction and tyrosine kinase pathway.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiotonic Agents / pharmacology*
  • Cyclic AMP / metabolism
  • Genistein / pharmacology*
  • Guinea Pigs
  • Heart Ventricles / drug effects*
  • In Vitro Techniques
  • Male
  • Myocardial Contraction / drug effects*
  • Protein-Tyrosine Kinases / metabolism

Substances

  • Cardiotonic Agents
  • Genistein
  • Cyclic AMP
  • Protein-Tyrosine Kinases