Interaction of carbohydrate and fat fuels in human skeletal muscle: Impact of obesity and NIDDM

Lawrence J. Mandarino, Agostino Consoli, Avanindra Jain, David E. Kelley

    Research output: Contribution to journalArticlepeer-review

    70 Scopus citations

    Abstract

    The current study was undertaken to examine the impact that obesity and non-insulin-dependent diabetes mellitus (NIDDM) have on the ability of glucose to stimulate its own uptake and oxidation in muscle. Euglycemic and hyperglycemic clamp experiments were performed with somatostatin infusions so that insulin could be replaced to basal levels or to physiological hyperinsulinemia. Arteriovenous leg balance methods were used to measure the pathways of leg muscle glucose uptake, oxidation, and storage. Percutaneous biopsies of the vastus lateralis muscle were taken to determine the pyruvate dehydrogenase complex or glycogen synthase activities. During basal insulin replacement, obese compared with lean nondiabetic subjects had higher values for glucose uptake, respiratory quotient, and glucose oxidation (all P < 0.05) and a higher proportion of leg energy expenditure derived from glucose. Obese NIDD patients had a greater reliance on fat calories than lean diabetics during basal insulin replacement (P < 0.05). Hyperinsulinemia increased leg glucose metabolism (P < 0.001) in all groups, but obese NIDD patients were significantly more insulin resistant. Hyperglycemia in NIDDM compensated for insulin resistance to the extent that rates of glucose metabolism were the same as those for nondiabetics studied at euglyemia. When nondiabetics were studied at hyperglycemia matched to the diabetics, the insulin resistance was still readily apparent.

    Original languageEnglish (US)
    Pages (from-to)E463-E470
    JournalAmerican Journal of Physiology - Endocrinology and Metabolism
    Volume270
    Issue number3 33-3
    DOIs
    StatePublished - 1996

    Keywords

    • non-insulin-dependent diabetes mellitus
    • substrate oxidation

    ASJC Scopus subject areas

    • Endocrinology, Diabetes and Metabolism
    • Physiology
    • Physiology (medical)

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