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Am J Physiol Regul Integr Comp Physiol 292: R328-R336, 2007. First published August 31, 2006; doi:10.1152/ajpregu.00561.2006
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INFLAMMATION AND CYTOKINES

Burn-induced increase in atrogin-1 and MuRF-1 in skeletal muscle is glucocorticoid independent but downregulated by IGF-I

Charles H. Lang, Danuta Huber, and Robert A. Frost

Department of Cellular and Molecular Physiology and Department of Surgery, Pennsylvania State University College of Medicine, Hershey, Pennsylvania

Submitted 8 August 2006 ; accepted in final form 30 August 2006

The present study determined whether thermal injury increases the expression of the ubiquitin (Ub) E3 ligases referred to as muscle ring finger (MuRF)-1 and muscle atrophy F-box (MAFbx; aka atrogin-1), which are muscle specific and responsible for the increased protein breakdown observed in other catabolic conditions. After 48 h of burn injury (40% total body surface area full-thickness scald burn) gastrocnemius weight was reduced, and this change was associated with an increased mRNA abundance for atrogin-1 and MuRF-1 (3.1- to 8-fold, respectively). Similarly, burn increased polyUb mRNA content in the gastrocnemius twofold. In contrast, there was no burn-induced atrophy of the soleus and no significant change in atrogin-1, MuRF-1, or polyUb mRNA. Burns also did not alter E3 ligase expression in heart. Four hours after administration of the anabolic agent insulin-like growth factor (IGF)-I to burned rats, the mRNA content of atrogin-1 and polyUb in gastrocnemius had returned to control values and the elevation in MuRF-1 was reduced 50%. In contrast, leucine did not alter E3 ligase expression. In a separate study, in vivo administration of the proteasome inhibitor Velcade prevented burn-induced loss of muscle mass determined at 48 h. Finally, administration of the glucocorticoid receptor antagonist RU-486 did not prevent burn-induced atrophy of the gastrocnemius or the associated elevation in atrogin-1, MuRF-1, or polyUb. In summary, the acute muscle wasting accompanying thermal injury is associated with a glucocorticoid-independent increase in the expression of several Ub E3 ligases that can be downregulated by IGF-I.

muscle atrophy F-box; muscle wasting; leucine



Address for reprint requests and other correspondence: C. H. Lang, Dept. of Cell and Molecular Physiology, H166, Penn State College of Medicine, 500 University Drive, Hershey, PA 17033 (e-mail: clang{at}psu.edu)




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