Amit Z, Levitan D E, Lindros K O
Arch Int Pharmacodyn Ther. 1976 Sep;223(1):114-9.
A comparison was made between the efficacy of action of dopamine-beta-hydroxylase and/or aldehyde dehydrogenase inhibition in suppressing voluntary ethanol consumption in rats. Calcium carbimide, which caused the largest increase in blood acetaldehyde levels following ethanol injections, was the least effective in reducing ethanol consumption, whereas FLA-63, which had a smaller effect on blood acetaldehyde levels, was the most potent suppressor of ethanol ingestion. Disulfiram, which inhibits both aldehyde dehydrogenase and dopamine-beta-hydroxylase had an intermediate effect in terms of raising blood acetaldehyde levels and in suppressing ethanol intake. It is suggested that the inhibition of dopamine-beta-hydroxylase may be at least partly responsible for the suppression of ethanol intake seen following disulfiram administration, and that disruption of catecholamine synthesis may prove to be a more effective method for suppressing ethanol consumption.
对多巴胺-β-羟化酶和/或醛脱氢酶抑制作用在抑制大鼠自愿乙醇摄入方面的功效进行了比较。在注射乙醇后导致血液乙醛水平升高幅度最大的卡巴咪嗪,在减少乙醇摄入方面效果最差,而对血液乙醛水平影响较小的FLA-63是最有效的乙醇摄入抑制剂。抑制醛脱氢酶和多巴胺-β-羟化酶的双硫仑在提高血液乙醛水平和抑制乙醇摄入方面具有中等效果。有人提出,多巴胺-β-羟化酶的抑制可能至少部分地导致了双硫仑给药后出现的乙醇摄入抑制,并且儿茶酚胺合成的破坏可能被证明是抑制乙醇消耗的一种更有效方法。