Kallai-Sanfacon M A, Cayen M N, Dubuc J, Greselin E, Dvornik D
Proc Soc Exp Biol Med. 1983 Jul;173(3):367-71. doi: 10.3181/00379727-173-41658.
The effect of the hypolipidemic agent AY-25,712 on liver catalase and carnitine acetyltransferase was studied in rats. At 250 mg/kg/day for 2 or 4 weeks, i.e., at least 125 times the minimum effective hypolipidemic dose, AY-25,712 had no effect on liver weight or liver catalase. Liver catalase was elevated after a 2-week treatment with clofibrate (+ 30%), bezafibrate (+71%), and fenofibrate (+77%) at doses of 250 mg/kg/day, and with ciprofibrate (+111%) at 25 mg/kg/day. Gemfibrozil at 250 mg/kg/day for 4 weeks increased catalase by 86%. The relative increase in liver weight induced by these compounds showed a good correlation to increased catalase. Nicotinic acid (250 mg/kg/day for 2 weeks) did not alter liver weight or catalase. Clofibrate increased carnitine acetyltransferase by 176% while AY-25,712 had no effect. The results show that AY-25,712 and nicotinic acid did not induce changes in the livers of rats which are associated with treatment by various other hypolipidemic agents.
在大鼠中研究了降血脂药物AY - 25712对肝脏过氧化氢酶和肉碱乙酰转移酶的影响。以250mg/kg/天的剂量给药2周或4周,即至少为最低有效降血脂剂量的125倍时,AY - 25712对肝脏重量或肝脏过氧化氢酶没有影响。以250mg/kg/天的剂量用氯贝丁酯治疗2周后,肝脏过氧化氢酶升高(+30%),苯扎贝特(+71%)、非诺贝特(+77%),以25mg/kg/天的剂量用环丙贝特治疗2周后过氧化氢酶升高(+111%)。以250mg/kg/天的剂量用吉非贝齐治疗4周后,过氧化氢酶增加86%。这些化合物诱导的肝脏重量相对增加与过氧化氢酶增加具有良好的相关性。烟酸(250mg/kg/天,共2周)未改变肝脏重量或过氧化氢酶。氯贝丁酯使肉碱乙酰转移酶增加176%,而AY - 25712没有影响。结果表明,AY - 25712和烟酸不会在大鼠肝脏中引起与其他各种降血脂药物治疗相关的变化。