GLUTAMINE PRESERVES SKELETAL MUSCLE FORCE DURING AN INFLAMMATORY INSULT

被引:15
作者
Meador, Benjamin M. [1 ]
Huey, Kimberly A. [1 ]
机构
[1] Univ Illinois, Dept Kinesiol, Urbana, IL 61801 USA
关键词
glutamine; heat shock proteins; lipopolysaccharide; muscle force; skeletal muscle; TUMOR-NECROSIS-FACTOR; CHRONIC HEART-FAILURE; SMALL STRESS PROTEINS; FACTOR-ALPHA; OXIDATIVE STRESS; TNF-ALPHA; GENE-EXPRESSION; SHOCK PROTEINS; CELL-DEATH; DIAPHRAGM CONTRACTILITY;
D O I
10.1002/mus.21430
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The purpose of this study was to test the hypothesis that acute glutamine (GLN) supplementation can counteract skeletal muscle contractile dysfunction occurring in response to inflammation by elevating muscle heat shock protein (Hsp) expression and reducing inflammatory cytokines. Mice received 5 mg/kg lipopolysaccharide (LPS) concurrently with 1 g/kg GLN or vehicle treatments. Plantarflexor isometric force production was measured at 2 hours post-injection. Blood and gastrocnemius muscles were collected, and serum and muscle tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) and muscle Hsp70 and Hsp25 were quantified. Saline/LPS treatment was associated with a 33% reduction in maximal force and elevated serum TNF-alpha and IL-6. GLN completely prevented this force decrement with LIPS. GLN was found to reduce muscle Hsp70 and IL-6, but only in the presence of LPS. GLN supplementation provides an effective, novel, clinically applicable means of preserving muscle force during acute inflammation. These data indicate that force preservation is not dependent on reductions in serum cytokines or muscle TNF-alpha, or elevated Hsp levels. Muscle Nerve 40: 1000-1007, 2009
引用
收藏
页码:1000 / 1007
页数:8
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