Role of serotonin (5-HT) in tolerance to ethanol and barbiturates

Adv Exp Med Biol. 1980:126:181-95. doi: 10.1007/978-1-4684-3632-7_17.

Abstract

Previously it has been shown that chronic administration of p-chlorophenylalanine (p-CPA), slowed the development of tolerance to ethanol, pentobarbital and cross-tolerance development to ethanol in rats chronically treated with pentobarbital. These findings have been extended by the following observations: (1) p-CPA slowed the development of tolerance to barbital as measured by motor impairment on the moving belt test, without altering the acute response. (2) p-CPA also reduced the tolerance to barbital as measured by sleeping time, in animals chronically treated with pentobarbital. (3) Administration of L-tryptophan increased the rate of tolerance development to ethanol as measured by motor impairment and hypothermia. These results further confirm and extend the generality of our observations that 5-HT may be involved in the development of tolerance and cross-tolerance to sedatives.

MeSH terms

  • Animals
  • Body Temperature / drug effects
  • Brain / drug effects
  • Brain / physiology
  • Drug Interactions
  • Drug Tolerance*
  • Ethanol / pharmacology*
  • Fenclonine / pharmacology*
  • Kinetics
  • Male
  • Motor Activity / drug effects*
  • Pentobarbital / pharmacology*
  • Rats
  • Serotonin / metabolism*
  • Tryptophan / pharmacology

Substances

  • Serotonin
  • Ethanol
  • Tryptophan
  • Pentobarbital
  • Fenclonine