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肿瘤坏死因子-α影响对乙酰氨基酚诱导的急性肝衰竭中的血脑屏障通透性。

Tumor necrosis factor-α affects blood-brain barrier permeability in acetaminophen-induced acute liver failure.

机构信息

Department of Infectious Diseases, the First Affiliated Hospital, China Medical University, No. 55 Nanjing Street, Shenyang, Liaoning Province, China.

出版信息

Eur J Gastroenterol Hepatol. 2011 Jul;23(7):552-8. doi: 10.1097/MEG.0b013e3283470212.

Abstract

OBJECTIVES

Cerebral edema is a major cause of death during acute liver failure (ALF), but the exact mechanism of this condition is still not entirely clear. The aim of this study was to investigate the role of tumor necrosis factor α (TNFα) in changing the permeability of the blood-brain barrier (BBB) during acetaminophen (APAP)-induced ALF.

MATERIALS AND METHODS

ALF animal models were generated by administering APAP. Anti-TNFα-IgG was intravenously injected (100 μg/mouse) 2 h after administration of APAP. We investigated BBB permeability with Evans blue staining, and structure with electron microscopy.

RESULTS

BBB permeability increased in APAP-induced ALF mice and correlated with elevated serum TNFα levels. Electron microscopy of mouse brain tissues revealed tight junction (TJ) disruptions and endothelial cell shrinkage, as well as increased vesicles and vacuoles. In addition, the expression of the TJ-associated protein, occludin, was significantly decreased in APAP-induced ALF mice. Changes in BBB permeability and occludin expression could be prevented by administering anti-TNFα-IgG 2 h after APAP challenge.

CONCLUSION

TNFα plays a critical role in the development of brain edema in APAP-induced ALF. Increased BBB permeability may be due to the loss of the TJ-associated protein occludin.

摘要

目的

脑水肿是急性肝衰竭(ALF)患者死亡的主要原因,但该疾病的确切机制尚不完全清楚。本研究旨在探讨肿瘤坏死因子α(TNFα)在乙酰氨基酚(APAP)诱导的 ALF 中改变血脑屏障(BBB)通透性中的作用。

材料与方法

通过给予 APAP 建立 ALF 动物模型。APAP 给药后 2 小时静脉注射抗 TNFα-IgG(100μg/只小鼠)。我们通过 Evans 蓝染色检测 BBB 通透性,并通过电子显微镜观察结构。

结果

APAP 诱导的 ALF 小鼠 BBB 通透性增加,与血清 TNFα 水平升高相关。小鼠脑组织的电子显微镜显示紧密连接(TJ)破坏和内皮细胞收缩,以及囊泡和空泡增加。此外,APAP 诱导的 ALF 小鼠 TJ 相关蛋白 occludin 的表达显著降低。APAP 挑战后 2 小时给予抗 TNFα-IgG 可预防 BBB 通透性改变和 occludin 表达。

结论

TNFα 在 APAP 诱导的 ALF 中脑水肿的发展中起关键作用。BBB 通透性增加可能是由于 TJ 相关蛋白 occludin 的丢失所致。

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