Mitochondrial Dysfunction in the Elderly: Possible Role in Insulin Resistance

Author:

Petersen Kitt Falk12345,Befroy Douglas12345,Dufour Sylvie12345,Dziura James12345,Ariyan Charlotte12345,Rothman Douglas L.12345,DiPietro Loretta12345,Cline Gary W.12345,Shulman Gerald I.12345

Affiliation:

1. Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.

2. Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06520, USA.

3. Department of Surgery, Yale University School of Medicine, New Haven, CT 06520, USA.

4. Department of Diagnostic Radiology, Yale University School of Medicine, New Haven, CT 06520, USA.

5. Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT 06520, USA.

Abstract

Insulin resistance is a major factor in the pathogenesis of type 2 diabetes in the elderly. To investigate how insulin resistance arises, we studied healthy, lean, elderly and young participants matched for lean body mass and fat mass. Elderly study participants were markedly insulin-resistant as compared with young controls, and this resistance was attributable to reduced insulin-stimulated muscle glucose metabolism. These changes were associated with increased fat accumulation in muscle and liver tissue assessed by 1 Hnuclear magnetic resonance (NMR) spectroscopy, and with a ∼40% reduction in mitochondrial oxidative and phosphorylation activity, as assessed by in vivo 13 C/ 31 P NMR spectroscopy. These data support the hypothesis that an age-associated decline in mitochondrial function contributes to insulin resistance in the elderly.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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