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超氧化物歧化酶通过保护5'-核苷酸酶在犬缺血后再灌注期间不被降解,从而增强腺苷释放和冠脉充血性血流。

Superoxide dismutase enhances both adenosine release and coronary hyperemic flow through protection of 5'-nucleotidase against its degradation during reperfusion following ischemia in dogs.

作者信息

Kitakaze M, Hori M, Takashima S, Morioka T, Minamino T, Sato H, Okazaki Y, Inoue M, Kamada T

机构信息

First Department of Medicine, Osaka University School of Medicine, Suita, Japan.

出版信息

Biorheology. 1993 Sep-Dec;30(5-6):359-70. doi: 10.3233/bir-1993-305-607.

Abstract

Oxygen-derived free radicals are thought to inactivate ectosolic enzymes that regulate myocardial cellular functions. One such enzyme is ecto-5'-nucleotidase, which is responsible for adenosine production during coronary hyperemic flow. In the present study, we measured both reactive and hyperemic flow and adenosine release during reperfusion with and without superoxide dismutase. In 10 open chest dogs, the left anterior descending coronary artery was perfused through an extracorporeal bypass tube from the carotid artery. In the control hearts, a five-minute occlusion of the coronary artery caused the hyperemic flow with increased release of adenosine. In the superoxide dismutase-treated hearts, although administration of superoxide dismutase altered neither adenosine release nor coronary blood flow in the baseline, it augmented both peak coronary blood flow and repayment, and adenosine release during reperfusion. Therefore, we hypothesized that superoxide dismutase reduces generation of oxygen-derived free radicals during ischemia and reperfusion and attenuates the degradation of ecto-5'-nucleotidase. The administration of superoxide dismutase enhanced the increase in ecto-5'-nucleotidase activity at 10 minutes after reperfusion over the untreated group. Thus, we conclude that superoxide dismutase enhances reactive hyperemic flow and adenosine release during reperfusion following ischemia, which may be attributable to the protection of ecto-5'-nucleotidase by superoxide dismutase during ischemia and reperfusion.

摘要

氧衍生的自由基被认为会使调节心肌细胞功能的胞外酶失活。一种这样的酶是胞外5'-核苷酸酶,它在冠状动脉充血血流期间负责腺苷的产生。在本研究中,我们测量了在有和没有超氧化物歧化酶的再灌注过程中的反应性充血血流和腺苷释放。在10只开胸犬中,通过来自颈动脉的体外旁路管灌注左前降支冠状动脉。在对照心脏中,冠状动脉闭塞5分钟导致充血血流增加,腺苷释放增加。在超氧化物歧化酶处理的心脏中,虽然超氧化物歧化酶的给药在基线时既不改变腺苷释放也不改变冠状动脉血流,但它增加了再灌注期间的冠状动脉血流峰值和偿还以及腺苷释放。因此,我们假设超氧化物歧化酶减少了缺血和再灌注期间氧衍生自由基的产生,并减弱了胞外5'-核苷酸酶的降解。与未治疗组相比,超氧化物歧化酶的给药增强了再灌注后10分钟时胞外5'-核苷酸酶活性的增加。因此,我们得出结论,超氧化物歧化酶增强了缺血后再灌注期间的反应性充血血流和腺苷释放,这可能归因于超氧化物歧化酶在缺血和再灌注期间对胞外5'-核苷酸酶的保护。

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