A relationship between increased voluntary alcohol preference and basal hypercorticosteronemia associated with an attenuated rise in corticosterone output during stress

Alcohol. 1995 Jan-Feb;12(1):59-63. doi: 10.1016/0741-8329(94)00070-t.

Abstract

Some of the multiple biological effects of stress include activation of a variety of neuroendocrine systems, resulting in enhanced secretion of many hormones, including corticosterone, as well as facilitation of drug-seeking behavior. Therefore, we have examined the potential relationship between voluntary alcohol consumption (VAC) and corticosterone output profile using: (1) selectively bred alcohol-preferring (P) and nonpreferring (NP) rats; and (2) outbred male Holtzman Sprague-Dawley rats selected for (a) low basal corticosterone (< 2 micrograms/mg Cr) and high stimulation (> 250%) (L-H rats), and (b) high basal corticosterone (> 4 micrograms/mg Cr) and low stimulation of corticosterone output on 24-hour fasting stress (< 125%) (H-L rats). The results of this study show: (a) the corticosterone output profiles of P and NP rats were similar to those of H-L and L-H rats, respectively; and (b) the H-L rats exhibited significantly higher VAC than the L-H rats. In conclusion, these data suggest that basal hypercorticosteronemia associated with attenuated rise in corticosterone output during stress may be associated with increased VAC.

Publication types

  • Comparative Study

MeSH terms

  • Alcohol Drinking / genetics
  • Alcohol Drinking / psychology*
  • Animals
  • Corticosterone / blood*
  • Corticosterone / urine
  • Male
  • Radioimmunoassay
  • Rats
  • Rats, Sprague-Dawley
  • Species Specificity
  • Stress, Psychological / blood*

Substances

  • Corticosterone