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Excess of Free Fatty Acids as a Cause of Metabolic Dysfunction in Skeletal Muscle

机译:游离脂肪酸过多是骨骼肌代谢功能异常的原因

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摘要

Obesity is often associated with metabolic impairments in peripheral tissues. Evidence suggests an excess of free fatty acids (FFA) as one factor linking obesity and related pathological conditions and the impact of FFA overload on skeletal muscle metabolism is described herein. Obesity is associated with dysfunctional adipose tissue unable to buffer the flux of dietary lipids. Resulting increased levels and fluxes of plasma FFA lead to ectopic lipid deposition and lipotoxicity. FFA accumulated in skeletal muscle are associated with insulin resistance and overall cellular dysfunction. Mechanisms supposed to be involved in these conditions include the Randle cycle, intracellular accumulation of lipid metabolites, inflammation and mitochondrial dysfunction or mitochondrial stress. These mechanisms are described and discussed in the view of current experimental evidence with an emphasis on conflicting theories of decreased vs. increased mitochondrial fat oxidation associated with lipid overload. Since different types of FFA may induce diverse metabolic responses in skeletal muscle cells, this review also focuses on cellular mechanisms underlying the different action of saturated and unsaturated FFA.
机译:肥胖症通常与周围组织的代谢受损有关。有证据表明,过量的游离脂肪酸(FFA)作为连接肥胖症和相关病理状况的一个因素,本文描述了FFA超载对骨骼肌代谢的影响。肥胖与功能失调的脂肪组织无法缓冲饮食中的脂质流量有关。血浆FFA的水平和流量增加导致异位脂质沉积和脂毒性。骨骼肌中积累的FFA与胰岛素抵抗和整体细胞功能障碍有关。推测与这些疾病有关的机制包括Randle循环,脂质代谢产物的细胞内积累,炎症和线粒体功能障碍或线粒体应激。这些机制的描述和讨论是基于当前的实验证据,重点是与脂质超负荷相关的线粒体脂肪氧化减少与增加的相互矛盾的理论。由于不同类型的FFA可能在骨骼肌细胞中诱导不同的代谢反应,因此本文也将重点放在饱和和不饱和FFA的不同作用基础的细胞机制上。

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