Eccentric muscle contractions induce greater oxidative stress than concentric contractions in skeletal muscle

被引:25
作者
Kon, Michihiro
Tanabe, Kai
Lee, Hoseong
Kimura, Fuminori
Akimoto, Takayuki
Kono, Ichiro
机构
[1] Univ Tsukuba, Grad Sch Comprehens Human Sci, Doctoral Program Sports Med, Tsukuba, Ibaraki 3058574, Japan
[2] Univ Dankook, Taekwondo Major Sch Sports Sci, Cheonan Si Choongnam 330714, South Korea
[3] Waseda Univ, Inst Biomed Engn, Consolidated Res Inst Adv Sci & Med Care, Shinjuku Ku, Tokyo 1620041, Japan
关键词
TBARS; neutrophil; macrophage; muscle damage; muscle inflammation; ROS;
D O I
10.1139/H06-115
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The purpose of this study was to examine oxidative stress in skeletal muscle after eccentric and concentric muscle contractions. Eight-week-old Institute of Cancer Research (ICR) mice (n = 90) were divided into 3 groups: eccentric muscle contraction group (ECC, n = 42), concentric muscle contraction group (CON, n = 42), and control group (pre, n = 6). The tibialis anterior muscle was stimulated via the peroneal nerve to contract either eccentrically or concentrically. The tibialis anterior muscle was isolated before and 0, 6, 12, 18, 24, 72, and 168 h after muscle contraction. Immediately after muscle contractions, thiobarbituric acid reactive substances (TBARS) in skeletal muscle significantly increased (p < 0.05) in both ECC and CON conditions. However, in the ECC group alone, the TBARS level peaked at 12 and 72 h after the contractions. There was greater migration of mononuclear cells in ECC than in CON muscle. In addition, there was a correlation between TBARS in skeletal muscle and migration of mononuclear cells in ECC muscle (r = 0.773, p < 0.01), but this correlation was not apparent in CON muscle (r = 0.324, p = 0.12). The increased mononuclear cells may reflect inflammatory cells. These data suggest that eccentric muscle contraction induces greater oxidative stress in skeletal muscle, which may in turn be due to enhanced generation of reactive oxygen species (ROS) by migrating inflammatory cells.
引用
收藏
页码:273 / 281
页数:9
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