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Am J Physiol Endocrinol Metab 277: E176-E186, 1999;
0193-1849/99 $5.00
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Vol. 277, Issue 1, E176-E186, July 1999

Stimulation of both aerobic glycolysis and Na+-K+-ATPase activity in skeletal muscle by epinephrine or amylin

J. Howard James1, Kenneth R. Wagner2, Jy-Kung King1, Rebecca E. Leffler1, Radha Krishna Upputuri4, Ambikaipakan Balasubramaniam1, Lou Ann Friend1, Daniel A. Shelly3, Richard J. Paul3, and Josef E. Fischer1

1 Departments of Surgery, 2 Neurology, and 3 Molecular and Cellular Physiology, University of Cincinnati, Cincinnati 45267; Medical Research Service, Department of Veterans Affairs Medical Center, Cincinnati 45220; and 4 Shriners Hospital for Children, Cincinnati, Ohio 45229

Epinephrine and amylin stimulate glycogenolysis, glycolysis, and Na+-K+-ATPase activity in skeletal muscle. However, it is not known whether these hormones stimulate glycolytic ATP production that is specifically coupled to ATP consumption by the Na+-K+ pump. These studies correlated glycolysis with Na+-K+-ATPase activity in resting rat extensor digitorum longus and soleus muscles incubated at 30°C in well-oxygenated medium. Lactate production rose three- to fourfold, and the intracellular Na+-to-K+ ratio (Na+/K+) fell with increasing concentrations of epinephrine or amylin. In muscles exposed to epinephrine at high concentrations (5 × 10-7 and 5 × 10-6 M), ouabain significantly inhibited glycolysis by ~70% in either muscle and inhibited glycogenolysis by ~40 and ~75% in extensor digitorum longus and soleus, respectively. In the absence of ouabain, but not in its presence, statistically significant inverse correlations were observed between lactate production and intracellular Na+/K+ for each hormone. Epinephrine had no significant effect on oxygen consumption or ATP content in either muscle. These results suggest for the first time that stimulation of glycolysis and glycogenolysis in resting skeletal muscle by epinephrine or amylin is closely linked to stimulation of active Na+-K+ transport.

ouabain; lactate; oxygen consumption; metabolic compartmentation


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