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大鼠部分肝切除术后内毒素诱导的肝衰竭早期肝血窦内皮细胞的形态学和功能改变

Morphological and functional alterations to sinusoidal endothelial cells in the early phase of endotoxin-induced liver failure after partial hepatectomy in rats.

作者信息

Yachida S, Kokudo Y, Wakabayashi H, Maeba T, Kaneda K, Maeta H

机构信息

First Department of Surgery, Faculty of Medicine, Kagawa Medical University, Japan.

出版信息

Virchows Arch. 1998 Aug;433(2):173-81. doi: 10.1007/s004280050233.

Abstract

Liver failure following major hepatectomy is characterized pathologically by massive hepatic necrosis, which is thought to begin with injury of sinusoidal endothelial cells (SECs). To examine the early events of SECs leading to hepatic damage, we performed time-course analyses of the morphological and functional perturbation of SECs after endotoxin administration to hepatectomized rats. At 1.5 h after endotoxin injection, when hepatocellular damage was not yet evident, SECs showed augmented expression of intercellular adhesion molecule-1, with frequent adherence of infiltrating leucocytes and ultrastructural features of defenestration and hypertrophied cytoplasm enriched with cell organelles. The serum level of hyaluronate, as an indicator of the functional state of SECs, was significantly elevated. At 3 h, SECs underwent necrosis and disruption, accompanied by fibrin deposits with concomitant hepatocellular necrosis. The morphological and functional alterations of SECs precede necrotic changes in hepatocytes and SECs in endotoxin-induced liver failure after partial hepatectomy.

摘要

大肝切除术后肝衰竭的病理特征为大量肝坏死,据认为这始于肝窦内皮细胞(SECs)损伤。为了研究导致肝损伤的SECs早期事件,我们对内毒素给药后的肝切除大鼠进行了SECs形态和功能扰动的时间进程分析。在内毒素注射后1.5小时,当肝细胞损伤尚不明显时,SECs显示细胞间黏附分子-1表达增加,伴有浸润白细胞的频繁黏附以及窗孔消失和富含细胞器的肥大细胞质的超微结构特征。作为SECs功能状态指标的透明质酸血清水平显著升高。在3小时时,SECs发生坏死和破裂,伴有纤维蛋白沉积,同时肝细胞坏死。在部分肝切除术后内毒素诱导的肝衰竭中,SECs的形态和功能改变先于肝细胞和SECs的坏死变化。

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