首页> 美国卫生研究院文献>Journal of Lipid Research >Western diet changes cardiac acyl-CoA composition in obese rats: a potential role for hepatic lipogenesis
【2h】

Western diet changes cardiac acyl-CoA composition in obese rats: a potential role for hepatic lipogenesis

机译:西方饮食改变肥胖大鼠心脏酰基辅酶A的组成:肝脂肪形成的潜在作用

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

The “lipotoxic footprint” of cardiac maladaptation in diet-induced obesity is poorly defined. We investigated how manipulation of dietary lipid and carbohydrate influenced potential lipotoxic species in the failing heart. In Wistar rats, contractile dysfunction develops at 48 weeks on a high-fat/high-carbohydrate “Western” diet, but not on low-fat/high-carbohydrate or high-fat diets. Cardiac content of the lipotoxic candidates—diacylglycerol, ceramide, lipid peroxide, and long-chain acyl-CoA species—was measured at different time points by high-performance liquid chromatography and biochemical assays, as was lipogenic capacity in the heart and liver by qRT-PCR and radiometric assays. Changes in membranes fluidity were also monitored using fluorescence polarization. We report that Western feeding induced a 40% decrease in myocardial palmitoleoyl-CoA content and a similar decrease in the unsaturated-to-saturated fatty acid ratio. These changes were associated with impaired cardiac mitochondrial membrane fluidity. At the same time, hepatic lipogenic capacity was increased in animals fed Western diet (+270% fatty acid elongase activity compared with high-fat diet), while fatty acid desaturase activity decreased over time. Our findings suggest that dysregulation of lipogenesis is a significant component of heart failure in diet-induced obesity.
机译:在饮食引起的肥胖中,心脏适应不良的“脂毒性足迹”定义不清。我们调查了饮食脂质和碳水化合物的处理如何影响衰竭心脏中潜在的脂毒性物质。在Wistar大鼠中,高脂/高碳水化合物“西方”饮食会在48周时出现收缩功能障碍,而低脂/高碳水化合物或高脂饮食则不会。通过高效液相色谱和生化测定,在不同时间点测量了脂毒性候选物的心脏含量(二酰甘油,神经酰胺,脂质过氧化物和长链酰基辅酶A物质),以及通过qRT在心脏和肝脏中的脂肪形成能力-PCR和放射分析。还使用荧光偏振监测膜流动性的变化。我们报道西方喂养引起心肌棕榈油酰辅酶A含量下降了40%,并且不饱和脂肪酸与饱和脂肪酸的比率也有相似的下降。这些变化与心脏线粒体膜流动性受损有关。同时,饲喂西方饮食的动物肝脏脂肪生成能力增加(与高脂饮食相比,脂肪延伸酶活性增加270%),而脂肪酸去饱和酶活性随时间下降。我们的研究结果表明,脂肪生成失调是饮食引起的肥胖中心力衰竭的重要组成部分。

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