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缺血预处理可减轻缺血后白细胞的黏附和迁移。

Ischemic preconditioning attenuates postischemic leukocyte adhesion and emigration.

作者信息

Akimitsu T, Gute D C, Korthuis R J

机构信息

Department of Physiology and Biophysics, School of Medicine in Shreveport, Louisiana State University 71130, USA.

出版信息

Am J Physiol. 1996 Nov;271(5 Pt 2):H2052-9. doi: 10.1152/ajpheart.1996.271.5.H2052.

Abstract

Intravital microscopy was used to determine whether ischemic preconditioning (IPC; 5 min ischemia and 10 min reperfusion) would attenuate leukocyte adhesion and emigration induced by subsequent prolonged ischemia (60 min) and reperfusion (60 min) (I/R) in murine cremaster muscle and whether adenosine produced during IPC and/or reperfusion contributed to these beneficial effects. I/R elicited a marked increase in the number of adherent and emigrated leukocytes compared with the nonischemic control muscles, an effect that was largely prevented by IPC. Superfusion of the cremaster with adenosine deaminase only during IPC or only during 60-min reperfusion attenuated the inhibitory effect of IPC on postischemic leukocyte adhesion and emigration. However, the beneficial effects of IPC were mimicked in cremaster muscles preconditioned with adenosine (topical application for 10 min beginning 20 min before the onset of prolonged ischemia). Similar results were obtained in experiments in which adenosine was topically applied to the cremaster only during the 60-min reperfusion period. Our findings suggest that the ability of IPC to attenuate postischemic leukocyte adhesion and emigration may be mediated by adenosine released during IPC and during reperfusion after prolonged ischemia.

摘要

采用活体显微镜检查法,以确定缺血预处理(IPC;5分钟缺血和10分钟再灌注)是否会减弱小鼠提睾肌中后续长时间缺血(60分钟)和再灌注(60分钟)(I/R)诱导的白细胞黏附和移出,以及IPC和/或再灌注期间产生的腺苷是否促成了这些有益效应。与非缺血对照肌肉相比,I/R使黏附和移出的白细胞数量显著增加,而IPC在很大程度上可防止这种效应。仅在IPC期间或仅在60分钟再灌注期间用腺苷脱氨酶灌注提睾肌,会减弱IPC对缺血后白细胞黏附和移出的抑制作用。然而,在用腺苷预处理的提睾肌(在长时间缺血开始前20分钟开始局部应用10分钟)中,IPC的有益效应得到了模拟。在仅在60分钟再灌注期将腺苷局部应用于提睾肌的实验中也获得了类似结果。我们的研究结果表明,IPC减弱缺血后白细胞黏附和移出的能力可能由IPC期间以及长时间缺血后的再灌注期间释放的腺苷介导。

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