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首页> 外文期刊>The journals of gerontology.Series A. Biological sciences and medical sciences >The Effects of Aging on Rho-Kinase and Insulin Signaling in Skeletal Muscle and White Adipose Tissue of Rats
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The Effects of Aging on Rho-Kinase and Insulin Signaling in Skeletal Muscle and White Adipose Tissue of Rats

机译:老化对大鼠骨骼肌和白色脂肪组织的rho-激酶和胰岛素信号传导的影响

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摘要

The insulin receptor substrate 1 regulates insulin-mediated glucose uptake and is a target of Rho-kinase (Rock); however, the relationship between age-related insulin resistance and Rock signaling specifically in skeletal muscle and adipose tissue is unknown. We evaluated the content and activity of Rock in C2C12 myotubes, and in skeletal muscle and white adipose tissue (WAT) from two rodent models that differ in their patterns of body fat accumulation during aging (Wistar and Fischer 344 rats). Body fat gain in the Wistar rats was greater than in Fischer rats and only Wistar rats had impairment of whole-body insulin sensitivity. Rock activity and insulin signaling were impaired in skeletal muscle in both rat models, but only middle-aged Wistar rats had higher Rock activity in WAT. These data are consistent with a positive role of Rock in regulating insulin signaling in both skeletal muscle and its negative role in the adipose tissue, suggesting that Rock activity in adipose tissue is important in age-related insulin resistance.
机译:胰岛素受体底物1调节胰岛素介导的葡萄糖摄取,是RHO-激酶(岩石)的靶标;然而,年龄相关的胰岛素抵抗与岩石信号在骨骼肌和脂肪组织中的关系是未知的。我们评估了C2C12 Myotubes中岩石的含量和活性,以及​​来自两种啮齿动物模型的骨骼肌和白色脂肪组织(WAT),其在老化期间(Wistar和Fischer 344大鼠)的体脂积累模式不同。 Wistar大鼠的身体脂肪增益大于Fischer大鼠,只有Wistar大鼠患有全身胰岛素敏感性的损害。大鼠模型的骨骼肌中岩石活性和胰岛素信号传导损害,但只有中年Wistar大鼠在Wat中具有更高的岩石活性。这些数据与岩石在骨骼肌中调节胰岛素信号的积极作用以及其在脂肪组织中的负面作用中的作用,表明脂肪组织中的岩石活性在与年龄相关的胰岛素抵抗力中是重要的。

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