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致肥胖饮食对C57BL/6J小鼠氧化甾醇代谢的影响

The Influence of an Obesogenic Diet on Oxysterol Metabolism in C57BL/6J Mice.

作者信息

Wooten Joshua S, Wu Huaizhu, Raya Joe, Perrard Xiaoyuan Dai, Gaubatz John, Hoogeveen Ron C

机构信息

Division of Atherosclerosis and Vascular Medicine, Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA ; Department of Kinesiology and Health Education, Southern Illinois University Edwardsville, Campus Box 1126, Edwardsville, IL 62026-1126, USA.

Division of Atherosclerosis and Vascular Medicine, Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Cholesterol. 2014;2014:843468. doi: 10.1155/2014/843468. Epub 2014 Feb 5.

Abstract

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.

摘要

我们目前对肥胖和血脂异常等不同疾病状态下氧化甾醇代谢的了解有限。因此,本研究的目的是确定饮食诱导的肥胖对各种氧化甾醇组织分布以及氧化甾醇代谢关键酶mRNA表达的影响。为诱导肥胖,给雄性C57BL/6J小鼠喂食高脂高胆固醇饮食24周。饮食诱导肥胖后,4β-羟基胆固醇、5,6α-环氧胆固醇、5,6β-环氧胆固醇、7α-羟基胆固醇、7β-羟基胆固醇和27-羟基胆固醇的血浆水平显著(P<0.05)升高。在肥胖小鼠的肝脏和脂肪组织中,4β-羟基胆固醇显著(P<0.05)升高,而27-羟基胆固醇仅在脂肪组织中升高。氧化甾醇合成酶4β-羟化酶、27-羟化酶或7α-羟化酶在肝脏或脂肪组织中的mRNA表达均未观察到显著变化。参与氧化甾醇解毒的关键酶SULT2B1b的肝脏mRNA表达在肥胖小鼠中显著(P<0.05)升高。有趣的是,在肥胖期间随着氧化甾醇合成增加观察到了大HDL1脂蛋白的出现。在饮食诱导的肥胖小鼠中,氧化甾醇的饮食摄入和内源性酶促合成无法解释氧化甾醇水平的升高,这表明非酶促胆固醇氧化途径可能是氧化甾醇代谢变化的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d2/3941159/b42db2b934a5/CHOLESTEROL2014-843468.001.jpg

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