Miyaso Hideaki, Morimoto Yoshinori, Ozaki Michitaka, Haga Sanae, Shinoura Susumu, Choda Yasuhiro, Iwagaki Hiromi, Tanaka Noriaki
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan.
J Gastroenterol Hepatol. 2005 Dec;20(12):1859-66. doi: 10.1111/j.1440-1746.2005.03953.x.
Patients with obstructive jaundice are prone to sepsis after biliary tract surgery. The present study was designed to determine the effect of biliary obstruction on cytokine responses to lipopolysaccharide (LPS).
Wister rats were allocated into two groups; the BDL group underwent bile duct ligation, followed 2 weeks later by administration of LPS into the duodenum. The control group underwent sham operation, and similarly received enteral LPS. Specimens were collected serially, and applied for the assays.
Serum aspartate aminotransferase and alanine aminotransferase levels were significantly increased in BDL rats. High tumor necrosis factor alpha (TNF-alpha) and interleukin (IL)-6 levels in peripheral blood were observed 2 h after LPS administration in BDL rats. In contrast, no increases in both cytokines were noted in peripheral and portal blood in control rats. Baseline HGF levels in portal and peripheral blood in BDL rats were significantly higher than in control rats. LPS significantly increased hepatocyte growth factor (HGF) levels in portal blood and decreased in peripheral blood in BDL rats, but not in control rats. Immunohistochemical analysis revealed that BDL increased expressions of Toll-like receptor (TLR)4, CD14 and CD68 both in the small intestine and liver. Both TLR4 and CD14 mRNAs were upregulated in the small intestine and liver after LPS administration in BDL rats.
Obstructive jaundice and LPS stimulation induced TLR4 upregulation both in the liver and small intestine, which led to increased TNF-alpha and IL-6 production in liver and HGF production in the small intestine. The upregulation of TLR4 may lead to pathological and host defense reactions in obstructive jaundice complicated with Gram-negative bacterial infection.
梗阻性黄疸患者在胆道手术后易发生脓毒症。本研究旨在确定胆道梗阻对细胞因子对脂多糖(LPS)反应的影响。
将Wistar大鼠分为两组;BDL组行胆管结扎术,2周后经十二指肠给予LPS。对照组行假手术,同样接受肠内LPS。连续收集标本并用于检测。
BDL大鼠血清天冬氨酸氨基转移酶和丙氨酸氨基转移酶水平显著升高。BDL大鼠在给予LPS后2小时外周血中观察到高肿瘤坏死因子α(TNF-α)和白细胞介素(IL)-6水平。相比之下,对照组大鼠外周血和门静脉血中两种细胞因子均未升高。BDL大鼠门静脉和外周血中的基线肝细胞生长因子(HGF)水平显著高于对照组大鼠。LPS显著增加BDL大鼠门静脉血中的肝细胞生长因子(HGF)水平,而外周血中则降低,但对照组大鼠未出现这种情况。免疫组织化学分析显示,BDL增加了小肠和肝脏中Toll样受体(TLR)4、CD14和CD68的表达。BDL大鼠在给予LPS后小肠和肝脏中TLR4和CD14 mRNA均上调。
梗阻性黄疸和LPS刺激诱导肝脏和小肠中TLR4上调,导致肝脏中TNF-α和IL-6产生增加以及小肠中HGF产生增加。TLR4的上调可能导致梗阻性黄疸合并革兰氏阴性菌感染时的病理和宿主防御反应。