Blum K, Briggs A H, Trachtenberg M C, Delallo L, Wallace J E
Department of Pharmacology, University of Texas Health Science Center, San Antonio 78234.
Alcohol. 1987 Nov-Dec;4(6):449-56. doi: 10.1016/0741-8329(87)90084-x.
This is the first report of alteration in alcohol intake in mice with a genetic predisposition to alcohol preference and known to have innate brain enkephalin deficiencies. We have been able to significantly attenuate both volitional and forced ethanol intake respectively by acute and chronic treatment with hydrocinnamic acid and D-phenylalanine, known carboxypeptidase (enkephalinase) inhibitors. Since these agents, through their enkephalinase inhibitory activity, raise brain enkephalin levels, we propose that excessive alcohol intake can be regulated by alteration of endogenous brain opioid peptides.
这是关于对酒精有偏好遗传倾向且已知存在先天性脑内脑啡肽缺乏的小鼠酒精摄入量变化的首次报告。我们已经能够分别通过用氢化肉桂酸和D-苯丙氨酸(已知的羧肽酶(脑啡肽酶)抑制剂)进行急性和慢性治疗,显著减弱自愿和强迫性乙醇摄入量。由于这些药物通过其脑啡肽酶抑制活性提高了脑内脑啡肽水平,我们提出过量饮酒可通过改变内源性脑阿片肽来调节。