Chronic ethanol treatment of rats and the myocardial beta-adrenoceptors

Alcohol. 1992 Jul-Aug;9(4):305-9. doi: 10.1016/0741-8329(92)90071-h.

Abstract

We examined the effect of chronic treatment with ethanol on the dynamics of beta-adrenoceptor binding in left ventricular myocardium of rats. After treatment with BAAM (20 mg/kg i.p.), an irreversible inhibitor of beta-adrenoceptors, the inhibition of beta-adrenoceptor binding was less, and the recovery of receptor binding was faster in chronically ethanol-treated rats compared to the control animals given equicaloric dextrin maltose treatment. When intracellular beta-adrenoceptor recycling was inhibited with colchicine, cytoplasmic left ventricular beta-adrenoceptor binding was greater in ethanol-treated compared to dextrin maltose-treated animals. We conclude that the previously reported decreased functional activity of the beta-adrenoceptor-mediated system probably reflects the contribution of ethanol-mediated effects not entirely restricted to the receptor-binding mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology
  • Alcoholism / metabolism*
  • Alprenolol / analogs & derivatives
  • Alprenolol / pharmacology
  • Animals
  • Colchicine / pharmacology
  • Ethanol / administration & dosage
  • Ethanol / pharmacology*
  • Male
  • Myocardium / metabolism*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Adrenergic, beta / drug effects
  • Receptors, Adrenergic, beta / metabolism*

Substances

  • Adrenergic beta-Antagonists
  • Receptors, Adrenergic, beta
  • Ethanol
  • bromoacetylalprenololmenthane
  • Alprenolol
  • Colchicine