Infante R
Nouv Presse Med. 1980 Oct 30;9(40):2976-80.
The mechanism of action of probucol is discussed after human and animal studies. This drug seems to have a poor or no effect on the overall cholesterol synthesis in the body and does not produce any storage of cholesterol or its metabolic intermediates (i.e. desmosterol) in the tissues. The main effect of probucol could be a decreased synthesis and/or an acceleration of plasma lipoprotein turnover; disappearance of xanthomatous lesions under traitement suggest a facilitation of cholesterol transferred from tissues to the excretion or catabolic pathways; its relevance in atheroma lesions is to be proved. Probucol seems to be a non hepatotoxic drug and induces a decrease of lithogenic index of bile.
在人体和动物研究之后,对普罗布考的作用机制进行了讨论。这种药物似乎对体内整体胆固醇合成的影响很小或没有影响,并且不会在组织中产生胆固醇或其代谢中间体(即胆甾烯醇)的任何蓄积。普罗布考的主要作用可能是降低合成和/或加速血浆脂蛋白周转;治疗后黄色瘤病变的消失表明促进了胆固醇从组织转移至排泄或分解代谢途径;其在动脉粥样硬化病变中的相关性尚待证实。普罗布考似乎是一种无肝毒性的药物,并可降低胆汁的致石指数。