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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Multiple mechanisms of hypocholesterolemic action of pactimibe, a novel acyl-coenzyme A:cholesterol acyltransferase inhibitor.
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Multiple mechanisms of hypocholesterolemic action of pactimibe, a novel acyl-coenzyme A:cholesterol acyltransferase inhibitor.

机译:Pactimibe(一种新型的酰基辅酶A:胆固醇酰基转移酶抑制剂)的降胆固醇作用的多种机制。

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摘要

Novel acyl-coenzyme A:cholesterol acyltransferase inhibitor pactimibe has been evaluated in vivo; it exhibited significant serum cholesterol lowering activities in hamsters and monkeys without affecting non-high density lipoprotein cholesterol levels. The mechanism of the hypocholesterolemic action of pactimibe was examined in normocholesterolemic hamsters in this study. Results with the dual-isotope plasma ratio method indicated that pactimibe inhibits cholesterol absorption from the intestine, reduces cholesteryl ester formation in the liver, and enhances its elimination from the body. The Triton WR-1339 experiment showed that pactimibe inhibited secretion of very low density lipoprotein cholesterol from the liver. These results suggest that pactimibe is likely to have multiple mechanisms of action responsible for its effectiveness in reducing serum cholesterol.
机译:已在体内评估了新型酰基辅酶A:胆固醇酰基转移酶抑制剂倍他米布。它在仓鼠和猴子中表现出显着的血清胆固醇降低活性,而不会影响非高密度脂蛋白胆固醇水平。在这项研究中,在正常胆固醇的仓鼠中检查了拟杆菌的降胆固醇作用的机制。双同位素血浆比例法的结果表明,倍他米布抑制肠中胆固醇的吸收,减少肝脏中胆固醇酯的形成,并增强其从体内的清除。 Triton WR-1339实验表明,拟除虫菊酯抑制了肝脏中非常低密度脂蛋白胆固醇的分泌。这些结果表明,拟除虫菊酯可能具有多种作用机制,这归因于其降低血清胆固醇的有效性。

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