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普伐他汀钠对大鼠肝脏和原代肝细胞脂肪酸合成的诱导作用。

Induction of fatty acid synthesis by pravastatin sodium in rat liver and primary hepatocytes.

作者信息

Fujioka T, Tsujita Y, Shimotsu H

机构信息

Pharmacology and Molecular Biology Research Laboratories, Sankyo Co., Ltd., Shinagawa-ku, Tokyo, Japan.

出版信息

Eur J Pharmacol. 1997 Jun 11;328(2-3):235-9. doi: 10.1016/s0014-2999(97)83050-6.

Abstract

We examined the effect of pravastatin sodium (pravastatin), a 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor, on fatty acid synthesis in rat liver. The repeated administration of pravastatin to rats at 250 mg/kg for 7 days led to a 2.8-fold increase in fatty acid synthesis in the liver. The diurnal change of fatty acid synthesis was not affected by the treatment. Hepatic fatty acid synthase activity was increased 3.2-fold, while acetyl-CoA carboxylase activity was not changed by the repeated administration of pravastatin. In rat hepatocytes, the incubation with 2 microg/ml pravastatin for 24 h increased fatty acid synthase activity 1.5-fold, as well as HMG-CoA reductase activity 2.8-fold. These results suggest that HMG-CoA reductase inhibitors might increase fatty acid synthesis in vivo through the induction of hepatic fatty acid synthase.

摘要

我们研究了3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂普伐他汀钠(普伐他汀)对大鼠肝脏脂肪酸合成的影响。以250mg/kg的剂量给大鼠重复给药普伐他汀7天,导致肝脏脂肪酸合成增加了2.8倍。脂肪酸合成的昼夜变化不受该处理的影响。重复给予普伐他汀后,肝脏脂肪酸合酶活性增加了3.2倍,而乙酰辅酶A羧化酶活性未发生变化。在大鼠肝细胞中,用2μg/ml普伐他汀孵育24小时,脂肪酸合酶活性增加了1.5倍,HMG-CoA还原酶活性增加了2.8倍。这些结果表明,HMG-CoA还原酶抑制剂可能通过诱导肝脏脂肪酸合酶来增加体内脂肪酸合成。

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