IRS2
胰岛素受体
内分泌学
内科学
胰岛素
生物
葡萄糖稳态
碳水化合物代谢
超氧化物歧化酶
胰岛素受体底物
信号转导
氧化应激
细胞生物学
医学
胰岛素抵抗
作者
Akiko Taguchi,Lynn M. Wartschow,Morris F. White
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2007-07-20
卷期号:317 (5836): 369-372
被引量:484
标识
DOI:10.1126/science.1142179
摘要
Reduced insulin-like signaling extends the life span of Caenorhabditis elegans and Drosophila . Here, we show that, in mice, less insulin receptor substrate–2 (Irs2) signaling throughout the body or just in the brain extended life span up to 18%. At 22 months of age, brain-specific Irs2 knockout mice were overweight, hyperinsulinemic, and glucose intolerant; however, compared with control mice, they were more active and displayed greater glucose oxidation, and during meals they displayed stable superoxide dismutase–2 concentrations in the hypothalamus. Thus, less Irs2 signaling in aging brains can promote healthy metabolism, attenuate meal-induced oxidative stress, and extend the life span of overweight and insulin-resistant mice.
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