Life events-induced decrease of corticosteroid type I receptors is associated with reduced corticosterone feedback and enhanced vulnerability to amphetamine self-administration

Brain Res. 1991 Apr 26;547(1):7-12. doi: 10.1016/0006-8993(91)90568-g.

Abstract

In this study, we attempted to find out whether a social stress-induced increase in the vulnerability to acquire amphetamine self-administration was associated with a change in number of hippocampal corticosteroid receptors. This was examined in two types of sex-mixed colonies of rats. Animals were maintained for 4 weeks in: (1) 'stable social condition', membership did not change after constitution of the colony; (2) 'unstable social condition', the males were changed daily in a random design. The animals living in the 'stable social' conditions had: (1) a lower number of hippocampal type I corticosteroid receptors; (2) a longer duration of the increase in plasma corticosterone after exposure to novelty; (3) a higher vulnerability to acquire amphetamine self-administration. These findings suggest that a decrease in hippocampal type I corticosteroid receptors may be one of the biological mechanisms responsible for the impaired corticosterone feedback control observed in vulnerable animals. These findings throw more light on the role of hypothalamo-pituitary-adrenal axis in the modulation of adaptive behavior. The availability of drugs which are specific for corticosteroid receptors could represent a new approach to the therapy of certain behavioral disturbances.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenalectomy
  • Amphetamine / pharmacology*
  • Animals
  • Corticosterone / physiology*
  • Environment
  • Feedback
  • Female
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Hypothalamo-Hypophyseal System / physiopathology
  • Male
  • Pituitary-Adrenal System / physiopathology
  • Rats
  • Rats, Inbred Strains
  • Receptors, Glucocorticoid / metabolism*
  • Self Administration
  • Stress, Psychological / metabolism
  • Stress, Psychological / psychology*

Substances

  • Receptors, Glucocorticoid
  • Amphetamine
  • Corticosterone