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Caloric restriction and growth hormone receptor knockout: effects on expression of genes involved in insulin action in the heart.


ABSTRACT: Blockade of growth hormone (GH), decreased insulin-like growth factor-1 (IGF1) action and increased insulin sensitivity are associated with life extension and an apparent slowing of the aging process. We examined expression of genes involved in insulin action, IR, IRS1, IRS2, IGF1, IGF1R, GLUT4, PPARs and RXRs in the hearts of normal and GHR-/- (KO) mice fed ad libitum or subjected to 30% caloric restriction (CR). CR increased the cardiac expression of IR, IRS1, IGF1, IGF1R and GLUT4 in normal mice and IRS1, GLUT4, PPARalpha and PPARbeta/delta in GHR-KO animals. Expression of IR, IRS1, IRS2, IGF1, GLUT4, PPARgamma and PPARalpha did not differ between GHR-KO and normal mice. These unexpected results suggest that CR may lead to major modifications of insulin action in the heart, but high insulin sensitivity of GHR-KO mice is not associated with alterations in the levels of most of the examined molecules related to intracellular insulin signaling.

SUBMITTER: Masternak MM 

PROVIDER: S-EPMC3082456 | biostudies-literature | 2006 Apr

REPOSITORIES: biostudies-literature

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Caloric restriction and growth hormone receptor knockout: effects on expression of genes involved in insulin action in the heart.

Masternak Michal M MM   Al-Regaiey Khalid A KA   Del Rosario Lim Marc Michael MM   Jimenez-Ortega Vanesa V   Panici Jacob A JA   Bonkowski Michael S MS   Bonkowski Michael S MS   Kopchick John J JJ   Wang Zhihui Z   Bartke Andrzej A  

Experimental gerontology 20060309 4


Blockade of growth hormone (GH), decreased insulin-like growth factor-1 (IGF1) action and increased insulin sensitivity are associated with life extension and an apparent slowing of the aging process. We examined expression of genes involved in insulin action, IR, IRS1, IRS2, IGF1, IGF1R, GLUT4, PPARs and RXRs in the hearts of normal and GHR-/- (KO) mice fed ad libitum or subjected to 30% caloric restriction (CR). CR increased the cardiac expression of IR, IRS1, IGF1, IGF1R and GLUT4 in normal m  ...[more]

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