6-Hydroxydopamine treatment increases beta-adrenoceptors and Ca2+ channels in rat heart

Eur J Pharmacol. 1986 Aug 15;127(3):287-9. doi: 10.1016/0014-2999(86)90378-x.

Abstract

Rats received 6-hydroxydopamine (50 mg/kg i.v.) on two successive days. After 14 days cardiac beta-adrenoceptors and Ca2+ channels were measured by radioligand binding. Ca2+ channel binding [( 3H]nitrendipine) was increased 31% with no change in affinity, and beta-adrenoceptor binding [( 3H]dihydroalprenolol) was increased 28% with no change in affinity. Innervation may be important in the regulation of Ca2+ channel expression.

Publication types

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

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Heart / drug effects*
  • Heart / innervation
  • Hydroxydopamines / pharmacology*
  • Ion Channels / analysis*
  • Male
  • Myocardium / analysis
  • Oxidopamine
  • Rats
  • Receptors, Adrenergic, beta / analysis*

Substances

  • Hydroxydopamines
  • Ion Channels
  • Receptors, Adrenergic, beta
  • Oxidopamine
  • Calcium