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Am J Physiol Endocrinol Metab 287: E934-E938, 2004. First published June 22, 2004; doi:10.1152/ajpendo.00054.2004
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Neutralization of tumor necrosis factor-{alpha} reverses insulin resistance in skeletal muscle but not adipose tissue

Stephen E. Borst,1,2 Youngil Lee,1 Christine F. Conover,2 Eugene W. Shek,2 and Gregory J. Bagby3

1Department of Applied Physiology and Kinesiology, University of Florida, Gainesville 32611; 2Malcom Randall Veterans Affairs Medical Center, Gainesville, Florida 32608; and 3Department of Physiology, Louisiana State University Health Science Center, New Orleans, Louisiana 70112

Submitted 3 February 2004 ; accepted in final form 15 June 2004

We examined the possible role of tumor necrosis factor-{alpha} (TNF-{alpha}) as a mediator of insulin resistance in maturing male Sprague-Dawley rats. Rats were treated either with goat anti-murine TNF-{alpha} IgG (anti-TNF-{alpha}) or goat nonimmune IgG (NI) for 7 days. Vascular catheters were implanted, and rats were fasted overnight before hyperinsulinemic euglycemic clamp (HUC) studies were performed. TNF-{alpha} neutralization increased the rate of glucose infusion required to maintain euglycemia by 68%. Insulin-stimulated glucose transport into individual tissues was measured after bolus administration of 2-deoxy-[14C]glucose during HUC. Anti-TNF-{alpha} administration increased glucose transport in muscles composed predominantly of fast-twitch fibers: white gastrocnemius muscle (68% increase) and tibialis anterior muscle (64% increase). There were nonsignificant trends for increased glucose transport in the slow-twitch soleus muscle and in the mixed-fiber red gastrocnemius muscle. Glucose transport was unchanged in visceral and subcutaneous fat. Anti-TNF treatment did not alter body weight, muscle mass, or fat mass. Anti-TNF-{alpha} did not alter the distribution of the 17-kDa and 26-kDa forms of TNF-{alpha} in either muscle or fat. However, anti-TNF-{alpha} treatment caused an ~50% reduction in the secretion of TNF-{alpha} bioactivity in vitro by explants of visceral and subcutaneous fat. We conclude that TNF-{alpha} neutralization reversed insulin resistance substantially in fast-twitch muscle and may have done so in other muscles, while having little effect in fat. TNF-{alpha} neutralization was accompanied by reduced TNF-{alpha} bioactivity without tissue depletion of TNF-{alpha} protein.

glucose transport; muscle fiber type; soluble tumor necrosis factor-{alpha}; membrane tumor necrosis factor-{alpha}



Address for reprint requests and other correspondence: S. Borst, VA Medical Center, GRECC-182, 1601 SW Archer Rd., Gainesville, FL 32608-1197 (E-mail: seborst{at}ufl.edu)




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