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MUSCLE CELL BIOLOGY AND CELL MOTILITY

Potentiation of insulin-stimulated glucose transport by the AMP-activated protein kinase

Department of Biology, Saint Louis University, St. Louis, Missouri

Submitted 16 May 2006 ; accepted in final form 18 July 2006

Data from the use of activators and inhibitors of the AMP-activated protein kinase (AMPK) suggest that AMPK increases sensitivity of glucose transport to stimulation by insulin in muscle cells. We assayed insulin action after adenoviral (Ad) transduction of constitutively active (CA; a truncated form of AMPK₁) and dominant-negative (DN; which depletes endogenous AMPK) forms of AMPK (Ad-AMPK-CA and Ad-AMPK-DN, respectively) into C₂C₁₂ myotubes. Compared with control (Ad-green fluorescent protein), Ad-AMPK-CA increased the ability of insulin to stimulate glucose transport. The increased insulin action in cells expressing AMPK-CA was suppressed by compound C (an AMPK inhibitor). Exposure of cells to 5-aminoimidazole-4-carboxamide-1-D-ribofuranoside (an AMPK activator) increased insulin action in uninfected myotubes and myotubes transduced with green fluorescent protein but not in Ad-AMPK-DN-infected myotubes. In Ad-AMPK-CA-transduced cells, serine phosphorylation of insulin receptor substrate 1 was decreased at a mammalian target of rapamycin (or p70 S6 kinase) target site that has been reported to be associated with insulin resistance. These data suggest that, in myotubes, activated AMPK₁ is sufficient to increase insulin action and that the presence of functional AMPK is required for 5-aminoimidazole-4-carboxamide-1,D-ribofuranoside-related increases in insulin action.

compound C; AMPK; insulin sensitivity; Akt; mTOR

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