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脂肪酸和固醇合成对遗传性高脂血症和肥胖大鼠灌注肝脏甘油三酯和胆固醇分泌的作用。

Contributions of fatty acid and sterol synthesis to triglyceride and cholesterol secretion by the perfused rat liver in genetic hyperlipemia and obesity.

作者信息

Azain M J, Fukuda N, Chao F F, Yamamoto M, Ontko J A

出版信息

J Biol Chem. 1985 Jan 10;260(1):174-81.

PMID:3965446
Abstract

The relative importance of fatty acid synthesis in triglyceride secretion by perfused livers from lean (normal control) and obese Zucker rats was investigated. Livers from fed animals were perfused in a recirculating system with tritiated water and a constant infusion of oleic acid. Triglyceride secretion was 5 times greater and cholesterol secretion was 35% greater in the obese rat livers. The very-low-density lipoprotein hypersecreted by perfused livers from obese rats contained more apolipoprotein B and exhibited an increased B-48/B-100 ratio. Apo-B was also elevated in the hypertriglyceridemic plasma of obese rats in both fed and fasting states. The very-low-density lipoprotein isolated therefrom was likewise characterized by an increased B-48/B-100 ratio. Ketogenesis was depressed 40% in the obese rat livers and increased hepatic malonyl-CoA was implicated in this alteration. The de novo synthesis and secretion of newly synthesized cholesterol was moderately increased in the perfused livers from obese rats. Tritium incorporation into fatty acids was 15 times greater in the obese genotype. Most of the synthesized fatty acids remained in the liver and were recovered after perfusion in triglyceride and phospholipids. Newly synthesized fatty acids accounted for only 3 and 15% of the triglyceride secreted by the lean and obese rat livers, respectively. A large portion of the secreted triglyceride fatty acids was derived from endogenous liver lipids. When the turnover of newly synthesized fatty acids in these pools was considered, the contribution of de novo fatty acid synthesis to triglyceride secretion was estimated to be 9% in the lean and 44% in the obese rat livers. Therefore, the altered partition of free fatty acids (Fukuda, N., Azain, M. J., and Ontko, J. A. (1982) J. Biol. Chem. 257, 14066-14072) and increased fatty acid synthesis are both major determinants of the hypersecretion of triglyceride-rich lipoproteins by the liver in the genetically obese Zucker rat.

摘要

研究了脂肪酸合成在瘦型(正常对照)和肥胖型 Zucker 大鼠灌注肝脏甘油三酯分泌中的相对重要性。给食动物的肝脏在循环系统中用氚水和持续输注油酸进行灌注。肥胖大鼠肝脏的甘油三酯分泌量高 5 倍,胆固醇分泌量高 35%。肥胖大鼠灌注肝脏超量分泌的极低密度脂蛋白含有更多载脂蛋白 B,且 B-48/B-100 比值升高。在喂食和禁食状态下,肥胖大鼠的高甘油三酯血症血浆中载脂蛋白 B 也升高。从中分离出的极低密度脂蛋白同样具有升高的 B-48/B-100 比值。肥胖大鼠肝脏的生酮作用降低了 40%,肝丙二酰辅酶 A 增加被认为与这种改变有关。肥胖大鼠灌注肝脏中新合成胆固醇的从头合成和分泌适度增加。肥胖基因型中氚掺入脂肪酸的量高 15 倍。大多数合成脂肪酸留在肝脏中,并在灌注后在甘油三酯和磷脂中回收。新合成脂肪酸分别仅占瘦型和肥胖型大鼠肝脏分泌甘油三酯的 3%和 15%。分泌的甘油三酯脂肪酸的很大一部分来自肝脏内源性脂质。当考虑这些池中新合成脂肪酸的周转率时,脂肪酸从头合成对甘油三酯分泌的贡献估计在瘦型大鼠肝脏中为 9%,在肥胖型大鼠肝脏中为 44%。因此,游离脂肪酸分配的改变(福田,N.,阿赞,M. J.,和翁特科,J. A.(1982 年)《生物化学杂志》257,14066 - 14072)和脂肪酸合成增加都是遗传性肥胖 Zucker 大鼠肝脏中富含甘油三酯脂蛋白超量分泌的主要决定因素。

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