Potential role of Kupffer cells in initiating liver injury during endotoxemia.

Journal of Experimental Pathology Pub Date : 1989-01-01
M Katoh, M Torisu
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Abstract

The potential contribution of Kupffer cells (KCs) to endotoxin-induced liver damage was evaluated by measuring the functional changes of KGs [Superoxide (O2-) generation, and chemotaxis (CTx)] isolated from such livers and comparing them with biochemical and histological changes of liver damage. Sublethal doses of endotoxin was daily administered to rats for 4 days. Liver damage was apparent in the rats treated with single administration of endotoxin and the maximal change was observed in the rats treated with endotoxin for 2 days in association with the marked enhancement of O2- release and CTx in vitro by KCs from these animals. However, liver injury decreased in the rats treated with endotoxin for 3 days and the rats treated with endotoxin for 4 days had shown almost no detectable injury. KCs' biological functions also diminished in group treated for 3 and 4 days. In particular, oxidative and chemotactic responses of KCs from rats treated for 4 days significantly decreased, compared with the cells from those treated for only two days. These results indicate that KCs are pivotal in the pathogenesis of liver injury during endotoxemia.

库普弗细胞在内毒素血症中引发肝损伤的潜在作用。
通过测量从这些肝脏中分离的KGs[超氧化物(O2-)生成和趋化性(CTx)]的功能变化,并将其与肝损伤的生化和组织学变化进行比较,评估KCs对内毒素诱导的肝损伤的潜在贡献。每天给大鼠亚致死剂量的内毒素,持续4天。单次内毒素处理的大鼠肝脏损伤明显,内毒素处理2天的大鼠肝脏损伤最大,并与这些动物的KCs显著增强体外O2-释放和CTx有关。然而,内毒素处理3天的大鼠肝损伤减轻,内毒素处理4天的大鼠几乎没有可检测到的损伤。治疗3 d和4 d组KCs的生物学功能也有所下降。特别是,与仅处理2天的大鼠相比,处理4天的大鼠KCs的氧化和趋化反应显著降低。这些结果表明,KCs在内毒素血症时肝损伤的发病机制中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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