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吉非贝齐给药对兔极低密度脂蛋白受体mRNA水平的影响。

Effects of gemfibrozil administration on very low density lipoprotein receptor mRNA levels in rabbits.

作者信息

Matsuoka N, Jingami H, Masuzaki H, Mizuno M, Nakaishi S, Suga J, Tanaka T, Yamamoto T, Nakao K

机构信息

Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Japan.

出版信息

Atherosclerosis. 1996 Oct 25;126(2):221-6. doi: 10.1016/0021-9150(96)05910-2.

Abstract

To elucidate the regulation of very low density lipoprotein (VLDL) receptor gene expression, we administered to rabbits for 14 days gemfibrozil, a fabric acid derivative and a lipid lowering drug that is also included among peroxisome proliferators. VLDL receptor mRNA levels were examined by Northern blot analysis. The VLDL receptor mRNA levels in retroperitoneal adipose tissue and in gastrocnemius muscle were increased 6.9-fold and 3.7-fold, respectively, with gemfibrozil treatment, but no marked changes were observed in the heart, the organ in which VLDL receptor is most highly expressed. In the liver, VLDL receptor mRNA was not detected either before or after gemfibrozil administration. Lipoprotein lipase (LPL) and long-chain acyl coenzyme A synthetase (ACS) mRNA levels were also increased in parallel in adipose tissue. The enhanced expression of VLDL receptor mRNA may contribute to the increase of triglyceride-rich lipoprotein catabolism in peripheral tissues such as adipose tissue and muscles.

摘要

为阐明极低密度脂蛋白(VLDL)受体基因表达的调控机制,我们对兔子连续14天给予吉非贝齐,它是一种贝特类衍生物,也是一种降脂药物,同时也属于过氧化物酶体增殖剂。通过Northern印迹分析检测VLDL受体mRNA水平。用吉非贝齐治疗后,腹膜后脂肪组织和腓肠肌中VLDL受体mRNA水平分别增加了6.9倍和3.7倍,但在VLDL受体表达最高的器官——心脏中未观察到明显变化。在肝脏中,无论在给予吉非贝齐之前还是之后,均未检测到VLDL受体mRNA。脂肪组织中的脂蛋白脂肪酶(LPL)和长链酰基辅酶A合成酶(ACS)mRNA水平也同时升高。VLDL受体mRNA表达的增强可能有助于富含甘油三酯的脂蛋白在诸如脂肪组织和肌肉等外周组织中的分解代谢增加。

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