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Coumestrol Induces Mitochondrial Biogenesis by Activating Sirtl in Cultured Skeletal Muscle Cells

机译:香豆酚通过激活培养的骨骼肌细胞中的Sirtl诱导线粒体生物发生

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The mitochondrion is a central organelle in cellular energy homeostasis; thus, reduced mitochondrial activity has been associated with aging and metabolic disorders. This paper provides biological evidence that coumestrol, which is a natural isoflavone, activates mitochondrial biogenesis. In cultured myocytes, coumestrol activated the silent information regulator two ortholog 1 (Sirtl) through the elevation of the intracellular NAD+/NADH ratio. Coumestrol also increased the mitochondrial contents and induced the expression of key proteins in the mitochondrial electron transfer chain in cultured myocytes. A Sirtl inhibitor and Sirtl-targeting siRNAs abolished the effect of coumestrol on mitochondrial biogenesis. Similar to an increase in mitochondrial content, coumestrol improved myocyte function with increased ATP concentration. Taken together, the data suggest that coumestrol is a novel inducer of mitochondrial biogenesis through the activation of Sirtl.
机译:线粒体是细胞能量稳态的中心细胞器。因此,线粒体活性降低与衰老和代谢紊乱有关。本文提供了生物学证据,表明天然的异黄酮香豆酚可激活线粒体的生物发生。在培养的心肌细胞中,香豆甾醇通过升高细胞内NAD + / NADH比率激活了沉默信息调节剂2 ortholog 1(Sirtl)。香豆酚还增加了线粒体的含量,并诱导了培养的心肌细胞线粒体电子转移链中关键蛋白的表达。 Sirtl抑制剂和靶向Sirtl的siRNA消除了香豆酚对线粒体生物发生的影响。类似于线粒体含量的增加,香豆甾醇通过增加ATP浓度改善了肌细胞功能。两者合计,数据表明香豆酚是通过Sirtl激活的线粒体生物发生的新型诱导剂。

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