The Possibility of IPC to Prevent Ischemic-Reperfusion Injury in Skeletal Muscle in a Rat

被引:4
|
作者
Morikawa, Takanori [1 ]
Shimasaki, Miyako [2 ]
Ichiseki, Toru [3 ]
Ueda, Shusuke [3 ]
Ueda, Yoshimichi [4 ]
Takahashi, Kan [1 ]
机构
[1] Kanazawa Med Univ, Dept Anesthesiol, Daigaku 1-1, Uchinada, Ishikawa 9200293, Japan
[2] Kanazawa Med Univ, Dept Pathol 2, Daigaku 1-1, Uchinada, Ishikawa 9200293, Japan
[3] Kanazawa Med Univ, Dept Orthopaed Surg, Daigaku 1-1, Uchinada, Ishikawa 9200293, Japan
[4] Keiju Med Ctr, Dept Pathol, 94,Tomiokamachi, Nanao, Ishikawa 9260816, Japan
关键词
ischemic preconditioning; reperfusion injury; apoptosis; vascular endothelial growth factor; cyclooxygenase; 2; 8-hydroxyguanosine; PERMEABILITY TRANSITION; MECHANISMS; TISSUE;
D O I
10.3390/jcm12041501
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Blood removal with air tourniquets for a long time induces muscle damage after reperfusion. Ischemic preconditioning (IPC) has a protective effect against ischemia-reperfusion injury in striated muscle and myocardium. However, the mechanism of action of IPC on skeletal muscle injury is unclear. Thus, this study aimed to investigate the effect of IPC in reducing skeletal muscle damage caused by ischemia-reperfusion injury. The hindlimbs of 6-month-old rats were wounded with air tourniquets at a carminative blood pressure of 300 mmHg on the thighs. Rats were divided into the IPC (-) group and the IPC (+) group. The vascular endothelial growth factor (VEGF), 8-hydroxyguanosine (8-OHdG), and cyclooxygenase 2 (COX-2) were investigated by protein levels. Quantitative analysis of apoptosis was performed using the TUNEL method. Compared with the IPC (-) group, the IPC (+) group retained the VEGF expression, and the COX-2 and 8-OHdG expressions were suppressed. The proportion of apoptosis cells decreased in the IPC (+) group compared with the IPC (-) group. IPC in skeletal muscles proliferated VEGF and suppressed inflammatory response and oxidative DNA damage. IPC has the potential to reduce muscle damage after ischemia-reperfusion.
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页数:13
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