Brain IRS2 Signaling Coordinates Life Span and Nutrient Homeostasis
Author(s) -
Akiko Taguchi,
Lynn M. Wartschow,
Morris F. White
Publication year - 2007
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1142179
Subject(s) - irs2 , insulin receptor , endocrinology , medicine , insulin , biology , glucose homeostasis , carbohydrate metabolism , superoxide dismutase , insulin receptor substrate , signal transduction , oxidative stress , microbiology and biotechnology , insulin resistance
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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