Chronic intermittent ethanol exposure in mice leads to an up-regulation of CRH/CRHR1 signaling

Alcohol Clin Exp Res. 2015 Apr;39(4):752-62. doi: 10.1111/acer.12686.

Abstract

Background: One of the most commonly used approaches to induce ethanol (EtOH) dependence in rodents is EtOH vapor inhalation. This procedure requires the co-administration of pyrazole-an inhibitor of the alcohol dehydrogenase-to obtain stable blood EtOH concentrations (BECs) during the entire induction course. However, pyrazole can produce unwanted side effects. Our goal was to obtain EtOH-dependent mice without pyrazole and to study their behavioral and molecular postdependent phenotype. In particular, we were interested in alterations in the corticotrophin-releasing hormone (CRH) and receptor (CRHR1 and CRHR2) system as a prominent role of CRH in driving the postdependent state via actions in the central extended amygdala (CeA) has been demonstrated in rats but not in postdependent mice.

Methods: We established an alternative model of chronic intermittent EtOH (CIE) inhalation without the use of pyrazole in C57BL/6N mice. Our CIE exposure protocol involved 8 cycles. One cycle consisted of 8 hours with EtOH inhalation and 8 hours without EtOH. We then examined withdrawal symptoms. After 2 weeks of abstinence, we studied relapse, reinstatement of EtOH-seeking, and stress-induced EtOH self-administration. We also did transcriptional analysis of components of the CRH system during CIE, protracted abstinence, and after stress-induced EtOH self-administration.

Results: CIE exposure without pyrazole resulted in reproducible BECs during the induction procedure. Mice showed strong withdrawal scores during 4 to 12 hours after the last CIE cycle and enhanced stress-induced EtOH self-administration. This postdependent phenotype during abstinence was accompanied by enhanced Crh and Crhr1 transcripts but no change in Crhr2 transcripts in the CeA. Cue-induced EtOH-seeking behavior and relapse (alcohol deprivation effect) were not affected by the inhalation procedure.

Conclusions: We have established a CIE inhalation protocol without pyrazole in mice and showed excessive EtOH self-administration under mild stress and enhanced CRH/CRHR1 signaling in the CeA.

Keywords: Corticotrophin-Releasing Hormone System; Ethanol; Inhalation; Postdependence Model; Pyrazole.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Inhalation
  • Amygdala / drug effects
  • Amygdala / metabolism
  • Animals
  • Corticotropin-Releasing Hormone / metabolism*
  • Disease Models, Animal
  • Drug-Seeking Behavior / drug effects
  • Ethanol / administration & dosage*
  • Ethanol / pharmacology*
  • Male
  • Mice
  • Receptors, Corticotropin-Releasing Hormone / metabolism*
  • Recurrence
  • Substance Withdrawal Syndrome / metabolism
  • Up-Regulation / drug effects*

Substances

  • CRF receptor type 2
  • Receptors, Corticotropin-Releasing Hormone
  • Ethanol
  • CRF receptor type 1
  • Corticotropin-Releasing Hormone