Kupffer细胞在肝缺血再灌注后中性粒细胞活化和浸润中的作用。

Circulatory shock Pub Date : 1994-04-01
S Suzuki, L H Toledo-Pereyra, F Rodriguez, F Lopez
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引用次数: 0

摘要

本研究旨在探讨Kupffer细胞在严重全肝缺血后多形核中性粒细胞(PMN)活化和浸润中的作用。生理盐水预处理雄性大鼠(NS组;N = 58)或氯化钆(7mg /kg;GC组(n = 57)肝缺血90 min,持续2 d。除7天存活率外,从缺血结束至再灌注后360 min,连续测定天冬氨酸转氨酶(AST)、PMN肝脏浸润、血浆髓过氧化物酶(MPO)、白细胞介素-1 (IL-1)水平。GC组的生存率显著提高至67% (P < 0.01),而NS组的生存率维持在20%。NS组AST水平极高(5372 +/- 231 IU/l),与肝坏死程度相关。NS组IL-1 (270.3 +/- 91.2 pg/ml)和MPO (1.7 +/- 0.4 U/ml)水平也非常高。与NS组相比,GC组显著抑制肝脏AST、IL-1、MPO水平升高及PMN浸润(P < 0.05)。我们的研究表明,Kupffer细胞激活通过IL-1的释放、PMN的激活和浸润,在肝脏全缺血后再灌注损伤的发生发展中具有重要作用。
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Role of Kupffer cells in neutrophil activation and infiltration following total hepatic ischemia and reperfusion.

This study was designed to examine the role of Kupffer cells in polymorphonuclear neutrophils (PMN) activation and infiltration after severe total hepatic ischemia. Male rats pretreated with either normal saline (NS group; n = 58) or gadolinium chloride (7 mg/kg; GC group, n = 57) for 2 days were subjected to 90 min total hepatic ischemia. In addition to 7-day survival rate, aspartate aminotransferase (AST), PMN liver infiltration, plasma myeloperoxidase (MPO), and interleukin-1 (IL-1) levels were serially measured from the end of ischemia to 360 min after reperfusion. Survival rate of the GC group significantly improved to 67% (P < 0.01), whereas that of the NS group remained at 20%. Extremely high AST levels (5,372 +/- 231 IU/liter) were obtained in the NS group, which correlated with the degree of hepatic necrosis. Very high IL-1 (270.3 +/- 91.2 pg/ml) and MPO (1.7 +/- 0.4 U/ml) levels were also seen in the NS group. The GC group significantly inhibited increases in AST, IL-1, and MPO levels as well as PMN infiltration in the liver compared to the NS group (P < 0.05). Our study demonstrated that Kupffer cell activation has an important role in the development of reperfusion injury after total hepatic ischemia through IL-1 release, and PMN activation and infiltration.

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