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自主神经系统与肠道源性内毒素:原位器官操作后参与库普弗细胞的激活

Autonomic nervous system and gut-derived endotoxin: involvement in activation of Kupffer cells after in situ organ manipulation.

作者信息

Schemmer P, Enomoto N, Bradford B U, Bunzendahl H, Raleigh J A, Thurman R G

机构信息

Laboratory of Hepatobiology and Toxicology, Department of Pharmacology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.

出版信息

World J Surg. 2001 Apr;25(4):399-406. doi: 10.1007/s002680020070.

Abstract

Gentle in situ organ manipulation rapidly causes disturbances in the hepatic microcirculation, hypoxia, and activation of Kupffer cells. Because the mechanisms of Kupffer cell activation after organ manipulation remain unclear, the possible role of the autonomic nervous system and gut-derived endotoxin were assessed. To mimic what occurs with major abdominal surgery, livers from female Sprague-Dawley rats (200-230 g) underwent minimal dissection for 12 minutes and were manipulated gently or were left alone for 13 subsequent minutes. Kupffer cells were activated 2 hours after manipulation, reflected by a significant increase in intracellular calcium ([Ca2+]i) from about 90 nM in unmanipulated controls to more than 180 nM in response to lipopolysaccharide (LPS 100 ng/ml). Furthermore, Kupffer cells from manipulated rats produced about threefold more tumor necrosis factor-alpha after LPS (100 ng/ml) than did the unmanipulated controls. Moreover, O2 uptake of ex situ perfused liver was increased from about 110 micromol/g/hr in unmanipulated controls to more than 160 micromol/g/hr 2 hours after organ manipulation. Binding of pimonidazole (120 mg/kg IV), a 2-nitroimidazole hypoxia marker given 2 hours after manipulation, increased about 2.5-fold, and hepatic glycogen was depleted. Two hours after organ manipulation gut permeability to horseradish peroxidase was elevated and endotoxin in the portal venous blood was increased twofold. Microsurgical hepatic denervation, ganglionic blockade, adrenalectomy, and antibiotics to sterilize the gut before manipulation prevented activation of Kupffer cells by organ manipulation. Hexamethonium and adrenalectomy prevented increases in gut permeability caused by manipulation. Although antibiotics blunted the increase in portal venous endotoxin significantly, there was no effect on gut permeability. These data indicate for the first time that both the autonomic nervous system and gut-derived endotoxin are involved in activation of Kupffer cells after organ manipulation.

摘要

轻柔的原位器官操作会迅速导致肝微循环紊乱、缺氧以及库普弗细胞激活。由于器官操作后库普弗细胞激活的机制尚不清楚,因此评估了自主神经系统和肠道源性内毒素的可能作用。为模拟大腹部手术时的情况,对雌性斯普拉格 - 道利大鼠(200 - 230克)的肝脏进行了12分钟的最小限度解剖,然后轻柔操作12分钟,随后13分钟不做处理。操作后2小时库普弗细胞被激活,表现为细胞内钙([Ca2+]i)显著增加,从未操作对照组的约90 nM增加到对脂多糖(LPS 100 ng/ml)反应时的超过180 nM。此外,操作大鼠的库普弗细胞在LPS(100 ng/ml)刺激后产生的肿瘤坏死因子 - α比未操作对照组多约三倍。而且,离体灌注肝脏的氧摄取量从未操作对照组的约110微摩尔/克/小时增加到器官操作后2小时的超过160微摩尔/克/小时。操作后2小时给予的2 - 硝基咪唑类缺氧标志物匹莫硝唑(120毫克/千克静脉注射)的结合增加了约2.5倍,肝糖原耗竭。器官操作后2小时,肠道对辣根过氧化物酶的通透性升高,门静脉血中的内毒素增加了两倍。在操作前进行显微手术肝去神经支配、神经节阻断、肾上腺切除术以及使用抗生素使肠道无菌,可防止器官操作激活库普弗细胞。六甲铵和肾上腺切除术可防止操作引起的肠道通透性增加。尽管抗生素显著减弱了门静脉内毒素的增加,但对肠道通透性没有影响。这些数据首次表明,自主神经系统和肠道源性内毒素均参与器官操作后库普弗细胞的激活。

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