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J Appl Physiol 83: 67-73, 1997;
8750-7587/97 $5.00
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Journal of Applied Physiology
Vol. 83, No. 1, pp. 67-73, July 1997
EXERCISE AND MUSCLE

Functional deficits in medial gastrocnemius grafts in rats: relation to muscle metabolism and beta -AR regulation

Lisa M. Larkin1,2, John A. Faulkner2, Richard T. Hinkle2, Cheryl A. Hassett2, Mark A. Supiano1,2,3, and Jeffrey B. Halter1,2,3

1 Division of Geriatric Medicine, Department of Internal Medicine, and 2 Institute of Gerontology, University of Michigan, Ann Arbor 48105; and 3 Geriatric Research, Education, and Clinical Center, Department of Veterans Affairs Medical Center, Ann Arbor, Michigan 48109

Received 11 October 1996; accepted in final form 11 March 1997.

Larkin, Lisa M., John A. Faulkner, Richard T. Hinkle, Cheryl A. Hassett, Mark A. Supiano, and Jeffrey B. Halter. Functional deficits in medial gastrocnemius grafts in rats: relation to muscle metabolism and beta -AR regulation. J. Appl. Physiol. 83(1): 67-73, 1997.---This study tested the hypothesis that alterations in the metabolic integrity of grafted muscle contribute to its diminished ability to sustain power. Compared with control muscles, muscles studied 120 days after the grafting procedure had lower specific force and sustained power. The sustained power protocol resulted in a depletion of muscle glycogen in control (83%) and grafted (85%) animals. Grafts had lower pre- and poststimulation glycogen, diminished citrate synthase activity, and greater hexokinase activity. No differences were observed in phosphofructokinase activity, glucose transporter GLUT-4 content, fiber type, beta -adrenergic-receptor (beta -AR) density, or binding affinity. Isoproterenol-stimulated adenylyl cyclase activity was lower in grafted vs. control muscle, suggesting an uncoupling of the beta -AR-effector complex. Thus the diminished ability of the grafted muscle to sustain power may be explained, in part, by a decrease in energy available from glycogen stores and/or a decrease in oxidative capacity.

sustained power; hexokinase; citrate synthase; glycogen; GLUT-4; fiber type; beta -adrenergic-receptor function


0161-7567/97 $5.00 Copyright © 1997 the American Physiological Society




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