Suppr超能文献

N-乙酰-L-半胱氨酸对小鼠部分肝缺血/再灌注后肝肺损伤的保护作用

[Protective effect of N-acetyl-L-cysteine on liver and lung injury in mice after partial hepatic ischemia/reperfusion].

作者信息

Wu He-shui, Jin Xin, Tian Yuan, Zhang Jing-hui, Wang Chun-you

机构信息

Center of Pancreatic Surgery, Affiliated Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei, China.

出版信息

Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2007 Jul;19(7):394-7.

Abstract

OBJECTIVE

To investigate the changes in Toll-like receptor 2/4(TLR2/4) gene expression in liver and lung in ischemia/reperfusion (I/R) injury with or without preconditioning of N-acetyl-L-cysteine (NAC).

METHODS

BALB/c mice were used in a model of partial hepatic I/R injury and randomly divided into sham-injury control group (SH group), hepatic I/R group and hepatic I/R with NAC pretreatment group (NAC group), each n=10. The level of tumor necrosis factor-alpha (TNF-alpha) in portal vein and plasma alanine aminotransferase (ALT) were measured at 1 hour and 3 hours respectively after reperfusion, the expressions of TLR2/4 mRNA and protein in liver and lung were observed with reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting at the same time points.

RESULTS

Compared with I/R group, the expressions of TLR2/4 mRNA and protein in liver and lung in NAC group were decreased at same time points (P<0.05 or P<0.01). The level of TNF-alpha in portal vein and plasma ALT increased continually in I/R group at 1 hour and 3 hours after reperfusion compared with SH group, however, they were significantly lowered in the group pretreated by NAC (P<0.05 or P<0.01).

CONCLUSION

TLR2/4 is activated in liver and lung in the process of partial hepatic I/R injury. NAC can inhibit the activation of TLR2/4 and the induction of TNF-alpha resulted from I/R injury via modulating the state of redox process; thus it might mitigate liver and lung injury following partial hepatic I/R in mice.

摘要

目的

研究在有或没有N-乙酰半胱氨酸(NAC)预处理的缺血/再灌注(I/R)损伤中,肝脏和肺组织中Toll样受体2/4(TLR2/4)基因表达的变化。

方法

将BALB/c小鼠用于部分肝脏I/R损伤模型,并随机分为假损伤对照组(SH组)、肝脏I/R组和NAC预处理的肝脏I/R组(NAC组),每组n = 10。再灌注后1小时和3小时分别测量门静脉中肿瘤坏死因子-α(TNF-α)水平和血浆丙氨酸氨基转移酶(ALT)水平,同时采用逆转录-聚合酶链反应(RT-PCR)和蛋白质印迹法观察肝脏和肺组织中TLR2/4 mRNA和蛋白的表达。

结果

与I/R组相比,NAC组在相同时间点肝脏和肺组织中TLR2/4 mRNA和蛋白的表达降低(P<0.05或P<0.01)。与SH组相比,I/R组再灌注后1小时和3小时门静脉中TNF-α水平和血浆ALT持续升高,然而,NAC预处理组的这些指标显著降低(P<0.05或P<0.01)。

结论

在部分肝脏I/R损伤过程中,肝脏和肺组织中的TLR2/4被激活。NAC可通过调节氧化还原状态抑制TLR2/4的激活以及I/R损伤诱导的TNF-α产生;因此它可能减轻小鼠部分肝脏I/R后的肝肺损伤。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验