Disruption of growth hormone releasing hormone results in extended longevity with increased insulin sensitivity in mice. Yet, less is known about tissue-specific insulin action and insulin signaling pathway in growth hormone releasing hormone knock-out mice (GHRH-/-). In this study, our hyperinsulinemic-euglycemic clamp data showed that glucose infusion rate to maintain euglycemia was dramatically elevated in GHRH-/- mice. Insulin-mediated hepatic glucose production was suppressed whereas glucose uptake in skeletal muscle and brown adipose tissue were significantly increased in GHRH-/- mice compared to WT littermates. Furthermore, growth hormone deficiency further enhanced insulin sensitivity in metabolically active tissues via activated PI3K-AKT and MAPK-ERK1/2 signaling cascades. Altered tissue-specific insulin response is likely to mediate the prolonged longevity and healthy-aging effects of growth hormone deficiency in mice.

Disclosure

F. Zhang: None. M. Icyuz: None. L. Sun: None.

Funding

National Institutes of Health (R01AG057734)

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