首页> 外文期刊>European Journal of Pharmacology: An International Journal >Edaravone protects against ischemia/reperfusion-induced oxidative damage to mitochondria in rat liver.
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Edaravone protects against ischemia/reperfusion-induced oxidative damage to mitochondria in rat liver.

机译:依达拉奉可预防缺血/再灌注引起的大鼠肝线粒体氧化损伤。

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摘要

This study investigated the effects of edaravone (3-methyl-1-phenyl-2-pyrazolin-5-one, MCI-186), a potent free radical scavenger, on the prevention of mitochondrial injury induced by hepatic ischemia and reperfusion. Mature male rats were subjected to 70 min of hepatic ischemia and 2 h of reperfusion. The rats received vehicle or edaravone (10 mg/kg body weight) intravenously prior to ischemia, before reperfusion and 1 h after reperfusion. In the vehicle-treated animals, the respiratory control index, ADP/O, State 3 respiration and dinitrophenol-induced uncoupled respiration decreased markedly after ischemia/reperfusion and were restored by edaravone administration. Mitochondrial lipid peroxidation was elevated in the vehicle-treated group, which was attenuated by edaravone, while mitochondrial glutathione peroxidase activity decreased in the vehicle-treated group, which was similarly abrogated by edaravone treatment. Electron microscopic observation demonstrated that treatment with edaravone restored the ischemia/reperfusion-induced disorganization of mitochondrial structures. Edaravone protects against mitochondrial injury, which prevents mitochondrial oxidative stress and improves ischemia/reperfusion-induced hepatic energy metabolism.
机译:这项研究调查了有效的自由基清除剂依达拉奉(3-甲基-1-苯基-2-吡唑啉-5-酮,MCI-186)在预防肝缺血和再灌注引起的线粒体损伤中的作用。成熟的雄性大鼠经历了70分钟的肝缺血和2小时的再灌注。大鼠在缺血前,再灌注前和再灌注后1 h静脉内接受赋形剂或依达拉奉(10 mg / kg体重)。在用媒介物治疗的动物中,缺血/再灌注后,呼吸控制指数,ADP / O,状态3呼吸和二硝基苯酚引起的非耦合呼吸显着下降,并通过依达拉奉给药得以恢复。媒介物处理组的线粒体脂质过氧化升高,被依达拉奉减弱,而线粒体谷胱甘肽过氧化物酶活性下降,在媒介物处理组被依达拉奉处理消除。电子显微镜观察表明,依达拉奉治疗可恢复缺血/再灌注引起的线粒体结构紊乱。依达拉奉可预防线粒体损伤,从而防止线粒体氧化应激并改善缺血/再灌注引起的肝能量代谢。

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