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AY-25,712对大鼠降血脂活性的评估。

Evaluation of the lipid-lowering activity of AY-25,712 in rats.

作者信息

Cayen M N, Kallai-Sanfacon M A, Dubuc J, Greselin E, Dvornik D

出版信息

Atherosclerosis. 1982 Dec;45(3):267-79. doi: 10.1016/0021-9150(82)90228-3.

Abstract

The effect of AY-25,712 (2-methyl-2-phenyl-3(2H)-furanone-5-carboxylic acid) on serum lipids, hepatic lipogenesis and biliary cholesterol was investigated in male rats. Based on one-week treatment, the minimal effective dose of AY-25,712 which lowered serum triglycerides was 1 mg/kg/day, and LDL-cholesterol, 5 mg/kg/day. Nicotinic acid produced a similar lipid-lowering profile albeit at 5 times higher doses. AY-25,712 at doses of 2 mg/kg/day and higher significantly increased the ratio of HDL to total cholesterol. Unlike clofibrate, AY-25,712 did not increase liver weight or liver mitochondrial alpha-glycerophosphate dehydrogenase, nor increase biliary cholesterol levels in rats fed a diet containing 2% cholesterol and 0.5% cholic acid. AY-25,712 lowered serum cholesterol, triglycerides and phospholipids in rats rendered hyperlipidemic with Triton WR-1339 and decreased the elevated serum triglycerides in streptozotocin-diabetic rats. [14C]Acetate incorporation into cholesterol by liver homogenate was suppressed in rats given AY-25,712 p.o. for 1 week. The results show that AY-25,712 is a potent LDL-cholesterol- and triglyceride-lowering agent in rats, and that its lipid-lowering profile differs from that of clofibrate but resembles that of nicotinic acid.

摘要

研究了AY - 25,712(2 - 甲基 - 2 - 苯基 - 3(2H)-呋喃酮 - 5 - 羧酸)对雄性大鼠血脂、肝脏脂肪生成及胆汁胆固醇的影响。基于为期一周的治疗,降低血清甘油三酯的AY - 25,712的最小有效剂量为1毫克/千克/天,降低低密度脂蛋白胆固醇的最小有效剂量为5毫克/千克/天。烟酸虽剂量高5倍但产生了类似的降脂效果。剂量为2毫克/千克/天及更高剂量的AY - 25,712显著提高了高密度脂蛋白与总胆固醇的比值。与氯贝丁酯不同,AY - 25,712不会增加喂食含2%胆固醇和0.5%胆酸饲料的大鼠的肝脏重量或肝脏线粒体α - 甘油磷酸脱氢酶,也不会增加胆汁胆固醇水平。AY - 25,712可降低经Triton WR - 1339诱导产生高脂血症的大鼠的血清胆固醇、甘油三酯和磷脂,并降低链脲佐菌素诱导的糖尿病大鼠升高的血清甘油三酯。口服AY - 25,712一周的大鼠肝脏匀浆中[14C]乙酸掺入胆固醇的过程受到抑制。结果表明,AY - 25,712是一种有效的降低大鼠低密度脂蛋白胆固醇和甘油三酯的药物,其降脂特性不同于氯贝丁酯,但类似于烟酸。

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