Interaction of chronic ethanol exposure and finasteride: Sex and strain differences

Deborah A. Finn, Season L. Long, Michelle A. Tanchuck, John C. Crabbe

Research output: Contribution to journalArticle

24 Scopus citations

Abstract

The neurosteroid allopregnanolone (ALLOP) is a very potent positive modulator of γ-aminobutyric acidA (GABAA) receptors that can modulate ethanol (EtOH) withdrawal. The 5α-reductase inhibitor finasteride blocks the formation of ALLOP from progesterone and was recently found to reduce some effects of EtOH. Thus, the present studies were conducted to determine the effect of finasteride on chronic EtOH withdrawal severity in male and female C57BL/6 (B6) and DBA/2 (D2) mice. The animals were exposed to 72 h EtOH vapor or air and received four injections of finasteride (50 mg/kg ip) 24 h prior to, and each day of, the EtOH vapor exposure. Upon removal from the inhalation chambers, handling-induced convulsions (HICs) were measured hourly for the first 12 h and then again at 24 h. EtOH withdrawal severity was significantly greater in D2 than in B6 mice. Pretreatment with finasteride significantly decreased EtOH withdrawal severity only in the female D2 mice, produced a nonselective suppressive effect on HIC in male B6 and D2 mice, and did not significantly alter HIC in female B6 mice. Finasteride pretreatment significantly decreased blood EtOH concentration (BEC) upon initiation of withdrawal, suggesting that finasteride may affect withdrawal severity via an alteration in EtOH pharmacokinetics.

Original languageEnglish (US)
Pages (from-to)435-443
Number of pages9
JournalPharmacology Biochemistry and Behavior
Volume78
Issue number3
DOIs
StatePublished - Jul 1 2004

Keywords

  • 5α-reductase
  • Allopregnanolone
  • C57BL/6
  • DBA/2
  • Handling-induced convulsions
  • Neurosteroid
  • Withdrawal

ASJC Scopus subject areas

  • Biochemistry
  • Toxicology
  • Pharmacology
  • Clinical Biochemistry
  • Biological Psychiatry
  • Behavioral Neuroscience

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