Microinjection of oxytocin into limbic-mesolimbic brain structures disrupts heroin self-administration behavior: a receptor-mediated event?

Life Sci. 1987 Sep 7;41(10):1265-71. doi: 10.1016/0024-3205(87)90205-0.

Abstract

The systemic injection of oxytocin (OXT) decreases the self-administration of heroin in heroin-tolerant rats. Since OXT-ergic binding sites are present in limbic and mesolimbic brain regions, the effects of intracerebral microinjections of OXT were investigated. In heroin-tolerant rats, the microinjection of OXT (2 ng) into the anterodorsal part of the nucleus accumbens or into the ventral hippocampus disrupted the self-administration of heroin. The effect of intrahippocampal microinjections lasted longer than that of intraaccumbens injections. The administration of N alpha-acetyl-(2-0-methyltyrosine)-oxytocin (ACME-OXT), an inhibitor of oxytocin receptors, prevented the disruptive effect of intrahippocampal OXT injections on heroin self-administration. It is concluded that limbic-mesolimbic brain structures have an essential role in the expression of the disruptive action of OXT on heroin self-administration. It appears that OXT-ergic binding sites mediate the effects of OXT.

MeSH terms

  • Animals
  • Brain / drug effects
  • Brain / physiology*
  • Drug Tolerance
  • Heroin / administration & dosage*
  • Hippocampus / physiology
  • Limbic System / drug effects
  • Limbic System / physiology*
  • Male
  • Microinjections
  • Nucleus Accumbens / physiology
  • Oxytocin / administration & dosage
  • Oxytocin / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Angiotensin / physiology*
  • Receptors, Oxytocin
  • Self Administration
  • Self Stimulation / drug effects*

Substances

  • Receptors, Angiotensin
  • Receptors, Oxytocin
  • Oxytocin
  • Heroin