Messiha F S, Pasi A
Texas Tech University Health Sciences Center, School of Medicine Lubbock.
Pharmacol Res. 1990 Nov-Dec;22(6):683-9. doi: 10.1016/s1043-6618(05)80094-5.
The effect of short-term oral administration of doxepin, a tricyclic antidepressant, on voluntary drinking of ethanol was studied in the rat as a function of sex. The effects of doxepin on ethanol and acetaldehyde metabolizing enzymes of hepatic and selected endocrine tissues were made in the presence and in the absence of ethanol. A reduction in voluntary ethanol intake was determined after the initial doxepin dose. This effect was not apparent during continued drug administration. Subsequently, a statistically insignificant reduction of ethanol drinking was noted 24 h and 72 h post-drug termination. Hepatic alcohol and aldehyde dehydrogenase were not altered from respective controls by doxepin in the presence and absence of ethanol. Epididymal and testicular adlehyde dehydrogenase were inhibited by doxepin from control in rats maintained on ethanol or water, respectively. The results suggest lack of adverse effect of doxepin on peripheral metabolism of alcohol metabolizing enzymes as compared to adverse interaction with acetaldehyde metabolizing enzyme in the endocrine tissues studied.
研究了三环类抗抑郁药多塞平短期口服给药对大鼠自愿饮用乙醇的影响,并将其作为性别函数进行研究。在有乙醇和无乙醇的情况下,研究了多塞平对肝脏及选定内分泌组织中乙醇和乙醛代谢酶的影响。在首次给予多塞平剂量后,测定了自愿乙醇摄入量的减少情况。在持续给药期间,这种作用并不明显。随后,在停药后24小时和72小时,观察到乙醇摄入量有统计学意义的轻微减少。在有乙醇和无乙醇的情况下,多塞平均未使肝脏酒精和醛脱氢酶与各自的对照组产生差异。在分别以乙醇或水喂养的大鼠中,多塞平分别抑制了附睾和睾丸醛脱氢酶。结果表明,与所研究的内分泌组织中与乙醛代谢酶的不良相互作用相比,多塞平对酒精代谢酶的外周代谢没有不良影响。