4.5 Article

An amino acid mixture enhances insulin-stimulated glucose uptake in isolated rat epitrochlearis muscle

期刊

JOURNAL OF APPLIED PHYSIOLOGY
卷 111, 期 1, 页码 163-169

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.01368.2010

关键词

Akt substrate of 160 kDa; isoleucine; skeletal muscle

资金

  1. Abbott Nutrition, Abbott Laboratories

向作者/读者索取更多资源

Kleinert M, Liao Y-H, Nelson JL, Bernard JR, Wang W, Ivy JL. An amino acid mixture enhances insulin-stimulated glucose uptake in isolated rat epitrochlearis muscle. J Appl Physiol 111: 163-169, 2011. First published April 28, 2011; doi:10.1152/japplphysiol.01368.2010.-Protein and certain amino acids (AA) have been found to lower blood glucose. Although these glucose-lowering AA are important modulators of skeletal muscle metabolism, their impact on muscle glucose uptake remains unclear. We therefore examined how an AA mixture consisting of 2 mM isoleucine, 0.012 mM cysteine, 0.006 mM methionine, 0.0016 mM valine, and 0.014 mM leucine impacts skeletal muscle glucose uptake in the absence or presence of a submaximal (sINS) or maximal insulin (mINS) concentration. The AA mixture, sINS, and mINS significantly increased 2-[H-3] deoxyglucose (2-DG) uptake by 63, 79, and 298% above basal, respectively. When the AA mixture was combined with sINS and mINS, 2-DG uptake was further increased significantly by 26% (P = 0.028) and 14% (P = 0.032), respectively. Western blotting analysis revealed that the AA mixture increased basal and sINS Akt substrate of 160 kDa (AS160) phosphorylation, while AA mixture did not change phosphorylation of Akt or mammalian target of rapamycin (mTOR) under these conditions. Interestingly, addition of the AA mixture to mINS increased phosphorylation of mTOR, Akt as well as AS160, compared with mINS alone. These data suggest that certain AA increase glucose uptake in the absence of insulin and augment insulin-stimulated glucose uptake in an additive manner. Furthermore, these effects appear to be mediated via a pathway that is independent from the canonical insulin cascade and therefore may prove effective as an alternative therapeutic treatment for insulin resistance.

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