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炔诺孕酮对大鼠极低密度脂蛋白和低密度载脂蛋白B代谢的不同影响。

Divergent effects of d-norgestrel on the metabolism of rat very low density and low density apolipoprotein B.

作者信息

Khokha R, Huff M W, Wolfe B M

出版信息

J Lipid Res. 1986 Jul;27(7):699-705.

PMID:3760708
Abstract

Rats treated with the contraceptive steroid d-norgestrel have lower plasma very low density lipoprotein (VLDL)-triglycerides and higher low density lipoprotein (LDL)-cholesterol than controls. To explain these results, the kinetics of VLDL and LDL turnover were studied by injecting 125I-labeled rat-VLDL and 131I-labeled rat-LDL simultaneously into rats treated with a small dose of d-norgestrel (4 micrograms per day per kg body weight0.75 for 18 days, n = 22) and their untreated controls (n = 22). VLDL- and LDL-apoB specific activity-time curves obtained over 50 hr best conformed to a three-pool model. VLDL-apoB clearance expressed as irreversible catabolic rate (k01) was markedly enhanced in the treated versus control rats (0.57 vs. 0.34 pools hr-1), leading to a marked reduction in VLDL-apoB pool size (270 vs. 420 micrograms). However, VLDL-apoB production rates were similar in the two groups (160 vs. 140 micrograms/hr, respectively). The 125I-labeled apoB specific activity-time curve derived from the catabolism of 125I-labeled VLDL-apoB also showed enhanced clearance in d-norgestrel-treated rats. 125I-Labeled IDL-apoB and 125I-labeled LDL-apoB specific activity-time curves failed to intersect the VLDL-apoB curve at maximal heights, suggesting input of intermediate density lipoprotein (IDL) and LDL independent of VLDL catabolism in both groups. However, the extent of independent LDL-apoB production was similar in both groups. Clearance of 131I-labeled LDL-apoB following injection of 131I-labeled rat-LDL was delayed in the d-norgestrel-treated versus control rats.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

用避孕类固醇炔诺孕酮治疗的大鼠,其血浆极低密度脂蛋白(VLDL)甘油三酯水平低于对照组,低密度脂蛋白(LDL)胆固醇水平高于对照组。为解释这些结果,通过将125I标记的大鼠VLDL和131I标记的大鼠LDL同时注射到用小剂量炔诺孕酮(每天每千克体重4微克,共18天,n = 22)治疗的大鼠及其未治疗的对照组(n = 22)中,研究了VLDL和LDL的周转动力学。在50小时内获得的VLDL-和LDL-载脂蛋白B特异性活性-时间曲线最符合三池模型。与对照大鼠相比,治疗组大鼠中以不可逆分解代谢率(k01)表示的VLDL-载脂蛋白B清除率明显提高(0.57对0.34池/小时),导致VLDL-载脂蛋白B池大小显著减少(270对420微克)。然而,两组的VLDL-载脂蛋白B产生率相似(分别为160对140微克/小时)。由125I标记的VLDL-载脂蛋白B分解代谢产生的125I标记的载脂蛋白B特异性活性-时间曲线也显示,炔诺孕酮治疗的大鼠清除率提高。125I标记的中间密度脂蛋白(IDL)-载脂蛋白B和125I标记的LDL-载脂蛋白B特异性活性-时间曲线在最大高度处未与VLDL-载脂蛋白B曲线相交,表明两组中中间密度脂蛋白(IDL)和LDL的输入均独立于VLDL分解代谢。然而,两组中独立的LDL-载脂蛋白B产生程度相似。与对照大鼠相比,注射131I标记的大鼠LDL后,炔诺孕酮治疗的大鼠中131I标记的LDL-载脂蛋白B清除延迟。(摘要截断于250字)

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