期刊论文详细信息
The Journal of Physiological Sciences
Effect of Heat Shock Preconditioning on ROS Scavenging Activity in Rat Skeletal Muscle after Downhill Running
Katsuro Tomita1  Takeshi Tsuyama1  Yumiko Yoshiki2  Katsuhiko Kitaoka1  Yosuke Shima1  Yoshinobu Maruhashi1 
[1] Department of Orthopedic Surgery, Kanazawa University;Department of Environmental Bioremediation, Tohoku University
关键词: heat shock protein;    leukocyte infiltration;    muscle;    reactive oxygen species;    scavenging activity;   
DOI  :  10.2170/physiolsci.RP004808
学科分类:生理学
来源: Springer
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【 摘 要 】

References(38)Cited-By(7)The mechanisms of the protective effect conferred by heat shock preconditioning (HS) are currently unknown. The purpose of this study was to determine the effect of HS on muscle injury after downhill running and to address the mechanism of the effect. Female Wistar rats were assigned to three groups: HS, downhill running (E), and downhill running after heat shock preconditioning (HS + E). The HS and HS + E rats were placed in a heat chamber for 60 min (ambient temperature 42 ± 1.0°C) 48 h before downhill running. Reactive oxygen species (ROS) scavenging activity was determined by electron spin resonance (ESR), and heat shock protein 72 (HSP72) mRNA expression was measured in rat quadriceps femoris. Leukocyte infiltration and degenerated muscle fibers were determined histopathologically. ROS scavenging activity significantly increased at 3 days after HS (151 ± 18%) and HSP72 mRNA expression increased immediately after HS (1750 ± 1914%). No decrease in ROS scavenging activity was observed in the HS + E rats at 2 days after exercise compared with the E rats (102 ± 9% vs. 79 ± 5%). Degenerated muscle fibers in HS + E rats were significantly less than in E rats at 2, 3, and 7 days after exercise (0.8 ± 1.0 vs. 2.8 ± 1.6, 0.8 ± 1.0 vs. 1.8 ± 1.6, 0 vs. 0.3 ± 0.6, respectively). These data demonstrated that HS can reduce muscle injury after downhill running, and this effect may be mediated by increased ROS scavenging activity. Furthermore, HS may protect the antioxidant defense system in skeletal muscle by enhancing the adaptive HSP72 mRNA response.

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