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缺血预处理预防大鼠骨骼肌缺血再灌注损伤的可能性

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

作者信息

Morikawa Takanori, Shimasaki Miyako, Ichiseki Toru, Ueda Shusuke, Ueda Yoshimichi, Takahashi Kan

机构信息

Department of Anesthesiology, Kanazawa Medical University, Daigaku 1-1, Uchinada, Kahoku-gun, Ishikawa 920-0293, Japan.

Department of Pathology 2, Kanazawa Medical University, Daigaku 1-1, Uchinada, Kahoku-gun, Ishikawa 920-0293, Japan.

出版信息

J Clin Med. 2023 Feb 14;12(4):1501. doi: 10.3390/jcm12041501.

Abstract

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.

摘要

长时间使用气压止血带放血会在再灌注后引发肌肉损伤。缺血预处理(IPC)对横纹肌和心肌的缺血再灌注损伤具有保护作用。然而,IPC对骨骼肌损伤的作用机制尚不清楚。因此,本研究旨在探讨IPC对减轻缺血再灌注损伤所致骨骼肌损伤的作用。将6月龄大鼠的后肢在大腿处以300 mmHg的驱血压力用气压止血带进行处理。大鼠被分为IPC(-)组和IPC(+)组。通过蛋白质水平检测血管内皮生长因子(VEGF)、8-羟基鸟苷(8-OHdG)和环氧合酶2(COX-2)。采用TUNEL法进行凋亡的定量分析。与IPC(-)组相比,IPC(+)组VEGF表达得以保留,COX-2和8-OHdG表达受到抑制。与IPC(-)组相比,IPC(+)组凋亡细胞比例降低。骨骼肌中的IPC使VEGF增殖,抑制炎症反应和氧化性DNA损伤。IPC具有减轻缺血再灌注后肌肉损伤的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a97a/9964745/f5a8b6878024/jcm-12-01501-g001.jpg

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