Granzer E, Ostrowski J
Arzneimittelforschung. 1984;34(2):191-3.
The antianginal drug N-ethoxycarbonyl-3-morpholinosydnonimine (molsidomine, Corvation) was orally administered (dose range 10(-5) - 10 mg/kg) to Wistar rats over 7 d once a day. The concentration of low density lipoprotein (LDL)-cholesterol in serum was decreased (40-45%) by therapeutic relevant dosages of molsidomine corresponding to an increase (80%) of the vasoprotective index high density lipoprotein (HDL)/LDL. HDL-cholesterol stayed unchanged. Clofibrate did not change the concentration of the lipoproteins in rat serum under equimolar conditions.
抗心绞痛药物N - 乙氧羰基 - 3 - 吗啉代西多胺(吗多明,可脉定)以10⁻⁵ - 10毫克/千克的剂量范围,每日一次口服给予Wistar大鼠,持续7天。与血管保护指数高密度脂蛋白(HDL)/低密度脂蛋白(LDL)增加80%相对应的治疗相关剂量的吗多明可使血清中低密度脂蛋白(LDL)胆固醇浓度降低(40 - 45%)。高密度脂蛋白(HDL)胆固醇保持不变。在等摩尔条件下,氯贝丁酯不会改变大鼠血清中脂蛋白的浓度。