A heroin-, but not a cocaine-expecting, self-administration state preferentially alters endogenous brain peptides

Eur J Pharmacol. 1999 Jan 22;365(2-3):175-82. doi: 10.1016/s0014-2999(98)00874-7.

Abstract

The purpose of the current study was to assess neuropeptidergic alterations during a phase of the drug addiction cycle associated with drug craving as compared to a time period when the drug had been recently self-administered. Male Wistar rats were allowed to self-administer cocaine, heroin or saline for 6 h for 5 consecutive days. Immediately following the last self-administration session ('acute drug on board' state), and just before the next scheduled session ('drug expecting' state), the animals were decapitated and the levels of dynorphin A and B, [Met5]- and [Leu5]-enkephalin and substance P were measured in different brain areas. During the 'acute drug on board' state, peptide levels in animals that self-administered heroin or cocaine were not significantly changed. In contrast, during the 'drug expecting' state, heroin-treated animals had increased levels of dynorphin A, dynorphin B and [Met5]-enkephalin in the caudal striatum as compared to the cocaine- and saline-treated animals, and the level of [Leu5]-enkephalin was increased as compared to the cocaine-treated group. In the septum, an increase of [Met5]-enkephalin and substance P was observed in the animals expecting heroin as compared to the saline- and/or cocaine-treated animals. In the caudal striatum, substance P levels were elevated in the heroin- and cocaine-expecting animals. In conclusion, heroin, as compared to cocaine, appears to have a more pronounced effect on dynorphin, enkephalin and substance P levels in the caudal striatum and septum, especially during periods when self-administration of the drug is expected.

Publication types

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

MeSH terms

  • Animals
  • Behavior, Animal
  • Brain / metabolism*
  • Cocaine / pharmacology*
  • Dynorphins / metabolism
  • Enkephalins / metabolism
  • Heroin / pharmacology*
  • Injections, Intravenous
  • Male
  • Neuropeptides / metabolism*
  • Radioimmunoassay
  • Rats
  • Rats, Wistar
  • Self Administration
  • Substance P / metabolism
  • Substance Withdrawal Syndrome / metabolism*
  • Substance-Related Disorders / metabolism*
  • Time Factors

Substances

  • Enkephalins
  • Neuropeptides
  • Substance P
  • Heroin
  • Dynorphins
  • Cocaine