首页> 美国卫生研究院文献>Cholesterol >The Influence of an Obesogenic Diet on Oxysterol Metabolism in C57BL/6J Mice
【2h】

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

机译:致肥胖饮食对C57BL / 6J小鼠体内氧固醇代谢的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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 4β-hydroxycholesterol, 5,6α-epoxycholesterol, 5,6β-epoxycholesterol, 7α-hydroxycholesterol, 7β-hydroxycholesterol, and 27-hydroxycholesterol were significantly (P < 0.05) increased. In the liver and adipose tissue of the obese mice, 4β-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 4β-hydroxylase, 27-hydroxylase, or 7α-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.
机译:目前我们对肥胖和血脂异常等不同疾病状态下氧固醇代谢的了解有限。因此,本研究的目的是确定饮食引起的肥胖对各种氧固醇的组织分布以及参与氧固醇代谢的关键酶的mRNA表达的影响。为了诱发肥胖,给雄性C57BL / 6J小鼠饲喂高脂胆固醇饮食24周。饮食引起的肥胖后,血浆中的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-羟基胆固醇水平显着增加(P <0.05)。在肥胖小鼠的肝脏和脂肪组织中,4β-羟基胆固醇显着增加(P <0.05),而27-羟基胆固醇仅在脂肪组织中增加。氧固醇合成酶4β-羟化酶,27-羟化酶或7 α -羟化酶的肝脏或脂肪组织mRNA表达均未见明显变化。 SULT2B1b是参与氧固醇解毒的关键酶,其肝脏mRNA表达在肥胖小鼠中显着升高( P <0.05)。有趣的是,在肥胖期间观察到大的HDL1脂蛋白的出现,其中氧固醇的合成增加。在饮食诱发的肥胖小鼠中,饮食摄入和氧固醇的内源性酶促合成不能解释氧固醇水平的升高,这表明非酶促胆固醇氧化途径可能是氧固醇代谢变化的原因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号