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共轭和非共轭十八碳烯酸对肠道酰基辅酶A:胆固醇酰基转移酶活性的影响不同。

Conjugated and non-conjugated octadecaenoic acids affect differently intestinal acyl coenzyme A: cholesterol acyltransferase activity.

作者信息

Lam Cheuk Kai, Chen Jingnan, Cao Ying, Yang Lin, Wong Yin Mei, Yeung Sai Ying Venus, Yao Xiaoqiang, Huang Yu, Chen Zhen-Yu

机构信息

Food & Nutritional Sciences Programme of Department of Biochemistry, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.

出版信息

Atherosclerosis. 2008 May;198(1):85-93. doi: 10.1016/j.atherosclerosis.2007.11.001. Epub 2007 Dec 21.

DOI:10.1016/j.atherosclerosis.2007.11.001
PMID:18078940
Abstract

We investigated the relative hypocholesterolemic activity of linoleic acid (LA), conjugated linoleic acid (CLA), alpha-linolenic acid (LN) and conjugated linolenic acid (CLN) in hamsters. Five groups of hamsters (n=10 each) were fed either the control diet or one of the four fatty acids-supplemented diets for 6 weeks. Results demonstrated that the four octadecaenoic acids decreased plasma cholesterol differently, with CLA being the most effective. Western blotting and RT-PCR analysis demonstrated that the four octadecaenoic acids had no effect on sterol regulatory element binding protein-2 (SREBP-2), liver X receptor (LXR), 3-hydroxy-3-methylglutary-CoA reductase (HMGR), LDL receptor (LDLR), and cholesterol-7alpha-hydroxylase (CYP7A1). However, the four octadecaenoic acids increased the excretion of fecal neutral sterols with CLA being most effective followed by LN, LA and CLN, suggesting they all differentially affect cholesterol absorption. Dietary CLA was associated with the least intestinal acyl coenzyme A: cholesterol acyltransferase (ACAT) activity followed by LN, LA and CLN in a decreasing trend. Since esterification of cholesterol is catalyzed by intestinal ACAT, and is a rate-limiting step in cholesterol absorption, it was concluded that the varying effects of CLA, LN, LA and CLN on blood cholesterol were mediated, at least in part, by their inhibition on intestinal ACAT activity.

摘要

我们研究了亚油酸(LA)、共轭亚油酸(CLA)、α-亚麻酸(LN)和共轭亚麻酸(CLN)在仓鼠体内的相对降胆固醇活性。将五组仓鼠(每组n = 10)分别喂食对照饮食或四种补充脂肪酸饮食中的一种,持续6周。结果表明,这四种十八碳烯酸降低血浆胆固醇的效果不同,其中CLA最为有效。蛋白质免疫印迹法和逆转录-聚合酶链反应分析表明,这四种十八碳烯酸对固醇调节元件结合蛋白-2(SREBP-2)、肝脏X受体(LXR)、3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR)、低密度脂蛋白受体(LDLR)和胆固醇7α-羟化酶(CYP7A1)均无影响。然而,这四种十八碳烯酸均增加了粪便中性固醇的排泄,CLA最为有效,其次是LN、LA和CLN,表明它们对胆固醇吸收的影响各不相同。膳食CLA与最低的肠道酰基辅酶A:胆固醇酰基转移酶(ACAT)活性相关,其次是LN、LA和CLN,呈递减趋势。由于胆固醇的酯化由肠道ACAT催化,且是胆固醇吸收的限速步骤,因此得出结论,CLA、LN、LA和CLN对血液胆固醇的不同影响至少部分是由它们对肠道ACAT活性的抑制介导的。

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