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3,3',4,4'-四溴联苯通过一种涉及不止肿瘤坏死因子的机制使大鼠对内毒素的肝毒性作用敏感。

3,3',4,4'-Tetrabromobiphenyl sensitizes rats to the hepatotoxic effects of endotoxin by a mechanism that involves more than tumor necrosis factor.

作者信息

Shedlofsky S I, Hoglen N C, Rodman L E, Honchel R, Robinson F R, Swim A T, McClain C J, Robertson L W

机构信息

Department of Medicine, University of Kentucky, Lexington.

出版信息

Hepatology. 1991 Dec;14(6):1201-8.

PMID:1660020
Abstract

To determine whether the cytokine tumor necrosis factor/cachectin might be a mediator of hepatotoxicity seen after exposure to polyhalogenated aromatic hydrocarbons, rats treated with a single dose of 3,3',4,4'-tetrabromobiphenyl (150 mumol/kg intraperitoneally) or corn oil vehicle were studied. The 3,3',4,4'-tetrabromobiphenyl caused the expected anorexia, alterations in organ weights and changes in cytochromes P-450 over 21 days. Although tumor necrosis factor could not be detected in the serum of rats at any time after 3,3',4,4'-tetrabromobiphenyl treatment alone (from 90 min to 21 days), 3,3',4,4'-tetrabromobiphenyl treatment significantly increased peak serum tumor necrosis factor concentrations after intravenous bacterial endotoxin (lipopolysaccharide, 1 mg/kg). This effect was seen with lipopolysaccharide given 24 hr, 48 hr, and 20 days after 3,3',4,4'-tetrabromobiphenyl treatment and increases in peak serum tumor necrosis factor levels ranged from threefold to eightfold over controls in various experiments with no significant differences between the three time points. However, a synergistic increase in hepatic damage (assessed by serum enzymes and liver histological findings 24 hr after lipopolysaccharide injection) was seen in rats given lipopolysaccharide 24 hr and 48 hr after 3,3',4,4'-tetrabromobiphenyl administration, with 75% and 25% lethality, respectively. There was no lethality with lipopolysaccharide given 20 days after 3,3',4,4'-tetrabromobiphenyl administration or with simultaneous administration. A lower dose of lipopolysaccharide (0.1 mg/kg) given 24 hr after 3,3',4,4'-tetrabromobiphenyl also enhanced hepatotoxicity and serum tumor necrosis factor but without lethality. Lipopolysaccharide decreased cytochromes P-450 concentrations and activities to similar extents at all time points tested in both control and 3,3'4,4'-tetrabromobiphenyl-treated rats.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了确定细胞因子肿瘤坏死因子/恶病质素是否可能是多卤代芳烃暴露后所见肝毒性的介质,对用单剂量3,3',4,4'-四溴联苯(150 μmol/kg腹腔注射)或玉米油载体处理的大鼠进行了研究。3,3',4,4'-四溴联苯在21天内引起了预期的厌食、器官重量改变和细胞色素P-450变化。虽然单独用3,3',4,4'-四溴联苯处理后任何时间大鼠血清中均未检测到肿瘤坏死因子(从90分钟到21天),但3,3',4,4'-四溴联苯处理显著增加了静脉注射细菌内毒素(脂多糖,1 mg/kg)后血清肿瘤坏死因子的峰值浓度。在3,3',4,4'-四溴联苯处理后24小时、48小时和20天给予脂多糖时均可见此效应,在各种实验中血清肿瘤坏死因子峰值水平比对照组增加了三到八倍,三个时间点之间无显著差异。然而,在3,3',4,4'-四溴联苯给药后24小时和48小时给予脂多糖的大鼠中,可见肝损伤协同增加(通过脂多糖注射后24小时血清酶和肝脏组织学检查结果评估),致死率分别为75%和25%。在3,3',4,4'-四溴联苯给药后20天给予脂多糖或同时给药时无致死率。在3,3',4,4'-四溴联苯处理后24小时给予较低剂量的脂多糖(0.1 mg/kg)也增强了肝毒性和血清肿瘤坏死因子,但无致死率。在对照大鼠和3,3',4,4'-四溴联苯处理的大鼠中,在所有测试时间点,脂多糖均以相似程度降低细胞色素P-450浓度和活性。(摘要截断于250字)

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