Beta-adrenergic antagonists attenuate somatic and aversive signs of opiate withdrawal

Neuropsychopharmacology. 1993 Dec;9(4):303-11. doi: 10.1038/npp.1993.66.

Abstract

The current studies were designed to evaluate the effectiveness of beta-adrenergic antagonists on opiate withdrawal symptoms utilizing a variety of paradigms. Male Sprague-Dawley rats were made moderately dependent on morphine with daily incremental injections. Both the nonselective beta-antagonist propranolol and the selective beta 1-antagonist atenolol, in the dose range of 5 to 20 mg/kg, were found to significantly reduce many of the somatic responses to either naloxone-precipitated or abstinence-induced withdrawal from morphine. In addition, propranolol (10 mg/kg) significantly reduced a withdrawal-induced conditioned place aversion, while atenolol was effective only at the highest dose tested (20 mg/kg). These data indicate that beta-adrenergic antagonists might be effective in the treatment of opiate addictions.

Publication types

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

MeSH terms

  • Adrenergic beta-Antagonists / therapeutic use*
  • Animals
  • Atenolol / therapeutic use
  • Avoidance Learning / drug effects
  • Male
  • Naloxone / pharmacology
  • Narcotics*
  • Propranolol / therapeutic use
  • Rats
  • Rats, Sprague-Dawley
  • Substance Withdrawal Syndrome / drug therapy*
  • Substance Withdrawal Syndrome / psychology

Substances

  • Adrenergic beta-Antagonists
  • Narcotics
  • Naloxone
  • Atenolol
  • Propranolol