Kurmukov A G, Aĭzikov M I, Rasulova S A, Makhmudov O Kh
Farmakol Toksikol. 1986 Nov-Dec;49(6):54-7.
Amorphin--24-vicyanoside (C34H4O16(2)H2O)--in a dose of 10 mg/kg orally decreases the content of cholesterol, total lipids, atherogenic lipoproteids in the blood and organs of intact rats and rats with endogenous or ethanol hyperlipemia, inhibits the development of experimental atherosclerosis in rabbits induced by the combination of risk factors (cholesterol + glucose + hypodynamia), decreases the content of lipids in the blood and organs (especially in aorta), prevents the development of morphological manifestations of the aorta atherosclerosis.
阿吗啡 - 24 - 氰糖苷（C34H40O16·2H2O），口服剂量为10毫克/千克时，可降低正常大鼠以及内源性或乙醇性高脂血症大鼠血液和器官中胆固醇、总脂质、致动脉粥样硬化脂蛋白的含量，抑制由危险因素（胆固醇+葡萄糖+运动不足）组合诱导的家兔实验性动脉粥样硬化的发展，降低血液和器官（尤其是主动脉）中的脂质含量，防止主动脉动脉粥样硬化形态学表现的发展。
