致肥性饮食对C57BL/6J小鼠氧甾醇代谢的影响

Cholesterol Pub Date : 2014-01-01 Epub Date: 2014-02-05 DOI:10.1155/2014/843468
Joshua S Wooten, Huaizhu Wu, Joe Raya, Xiaoyuan Dai Perrard, John Gaubatz, Ron C Hoogeveen
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引用次数: 25

摘要

我们目前对不同疾病状态(如肥胖和血脂异常)中氧甾醇代谢的了解有限。因此,本研究的目的是确定饮食性肥胖对各种氧甾醇的组织分布和参与氧甾醇代谢的关键酶mRNA表达的影响。为了诱导肥胖,雄性C57BL/6J小鼠喂食高脂高胆固醇饮食24周。饮食性肥胖后,血浆4 β -羟基胆固醇、5,6 α -环氧胆固醇、5,6 β -环氧胆固醇、7 α -羟基胆固醇、7 β -羟基胆固醇和27-羟基胆固醇水平显著升高(P < 0.05)。肥胖小鼠肝脏和脂肪组织中4 β -羟胆固醇显著升高(P < 0.05), 27-羟胆固醇仅在脂肪组织中升高(P < 0.05)。肝脏和脂肪组织中氧甾醇合成酶4 β -羟化酶、27-羟化酶和7 α -羟化酶的mRNA表达均无显著变化。肥胖小鼠肝脏中参与氧甾醇解毒的关键酶SULT2B1b mRNA表达显著升高(P < 0.05)。有趣的是,在肥胖期间观察到大HDL1脂蛋白的出现与增加的氧固醇合成。在饮食诱导的肥胖小鼠中,饮食摄入和内源性酶促合成的氧甾醇不能解释氧甾醇水平的增加,这表明非酶促胆固醇氧化途径可能是导致氧甾醇代谢变化的原因。
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The Influence of an Obesogenic Diet on Oxysterol Metabolism in C57BL/6J Mice.

Our current understanding of oxysterol metabolism during different disease states such as obesity and dyslipidemia is limited. Therefore, the aim of this study was to determine the effect of diet-induced obesity on the tissue distribution of various oxysterols and the mRNA expression of key enzymes involved in oxysterol metabolism. To induce obesity, male C57BL/6J mice were fed a high fat-cholesterol diet for 24 weeks. Following diet-induced obesity, plasma levels of 4 β -hydroxycholesterol, 5,6 α -epoxycholesterol, 5,6 β -epoxycholesterol, 7 α -hydroxycholesterol, 7 β -hydroxycholesterol, and 27-hydroxycholesterol were significantly (P < 0.05) increased. In the liver and adipose tissue of the obese mice, 4 β -hydroxycholesterol was significantly (P < 0.05) increased, whereas 27-hydroxycholesterol was increased only in the adipose tissue. No significant changes in either hepatic or adipose tissue mRNA expression were observed for oxysterol synthesizing enzymes 4 β -hydroxylase, 27-hydroxylase, or 7 α -hydroxylase. Hepatic mRNA expression of SULT2B1b, a key enzyme involved in oxysterol detoxification, was significantly (P < 0.05) elevated in the obese mice. Interestingly, the appearance of the large HDL1 lipoprotein was observed with increased oxysterol synthesis during obesity. In diet-induced obese mice, dietary intake and endogenous enzymatic synthesis of oxysterols could not account for the increased oxysterol levels, suggesting that nonenzymatic cholesterol oxidation pathways may be responsible for the changes in oxysterol metabolism.

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