普伐他汀诱导豚鼠低密度脂蛋白受体代谢的变化。

Artery Pub Date : 1994-01-01
A Matsunaga, J Sasaki, K Hidaka, Y Takada, K Araki, K Moriyama, K Arakawa
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引用次数: 0

摘要

用豚鼠研究了HMG-CoA还原酶抑制剂普伐他汀对人低密度脂蛋白(LDL)代谢的影响。普伐他汀治疗显著降低血浆总胆固醇和低密度脂蛋白胆固醇水平,分别为15.6 mg/dl(38.8%)和12.7 mg/dl(42.9%)。我们通过同时静脉注射131i标记的LDL和125i标记的半乳糖处理的LDL,研究了普伐他汀处理和未处理的豚鼠LDL的代谢,以量化LDL受体途径。普伐他汀增加LDL受体依赖途径的分数分解代谢率(FCR)。普伐他汀治疗未改变LDL受体非依赖性通路的FCR。从普伐他汀治疗组中分离的LDL受体依赖通路的FCR高于从对照组分离的LDL。这些发现表明,普伐他汀主要通过加速LDL受体介导途径的FCR降低血浆胆固醇水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pravastatin-induced changes in receptor-mediated metabolism of low density lipoprotein in guinea pigs.

The effect of pravastatin, an inhibitor of HMG-CoA reductase, on the metabolism of human low density lipoprotein (LDL) was examined in guinea pigs. Pravastatin treatment significantly reduced plasma levels of total cholesterol and LDL-cholesterol by 15.6 mg/dl (38.8%) and 12.7 mg/dl (42.9%), respectively. We investigated the metabolism of LDL in pravastatin-treated and untreated guinea pigs using the simultaneous intravenous injection of 131I-labeled LDL and 125I-labeled, galactose-treated LDL to quantify the LDL receptor pathway. Pravastatin increased the fractional catabolic rate (FCR) of the LDL receptor-dependent pathway. The treatment with pravastatin did not alter the FCR of the LDL receptor-independent pathway. The FCR of the LDL receptor-dependent pathway was higher for LDL isolated from pravastatin-treated subjects than for LDL isolated from control subjects. These findings suggest that pravastatin mainly reduced plasma cholesterol levels by accelerated FCR of the LDL receptor-mediated pathway.

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