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5-Aminoimidazole-4-carboxamide ribonucleoside (AICAR) has previously been reported to be taken up into cells and phosphorylated to form ZMP, an analog of 5'-AMP. This study was designed to determine whether AICAR can activate AMP-activated protein kinase (AMPK) in skeletal muscle with consequent phosphorylation of acetyl-CoA carboxylase (ACC), decrease in malonyl-CoA, and increase in fatty acid oxidation. Rat hindlimbs were perfused with Krebs-Henseleit bicarbonate containing 4% bovine serum albumin, washed bovine red blood cells, 200 microU/ml insulin, and 10 mM glucose with or without AICAR (0.5-2.0 mM). Perfusion with medium containing AICAR was found to activate AMPK in skeletal muscle, inactivate ACC, and decrease malonyl-CoA. Hindlimbs perfused with 2 mM AICAR for 45 min exhibited a 2.8-fold increase in fatty acid oxidation and a significant increase in glucose uptake. No difference was observed in oxygen uptake in AICAR vs. control hindlimb. These results provide evidence that decreases in muscle content of malonyl-CoA can increase the rate of fatty acid oxidation.
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Gary F. Merrill
Rutgers, The State University of New Jersey
E. J. Kurth
Brigham Young University
D. Grahame Hardie
Brigham Young University
AJP Endocrinology and Metabolism
Rutgers, The State University of New Jersey
University of Dundee
Brigham Young University
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Merrill et al. (Mon,) studied this question.
synapsesocial.com/papers/6a208ae5f9c5f638e0cc42a8 — DOI: https://doi.org/10.1152/ajpendo.1997.273.6.e1107
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