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基质金属蛋白酶-13在酒精性肝纤维化大鼠模型中的表达模式

Expression pattern of matrix metalloproteinases-13 in a rat model of alcoholic liver fibrosis.

作者信息

Yan Sheng, Chen Ge-Min, Yu Chao-Hui, Zhu Guo-Fang, Li You-Ming, Zheng Shu-Sen

机构信息

Department of Hepatobiliary Surgery, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.

出版信息

Hepatobiliary Pancreat Dis Int. 2005 Nov;4(4):569-72.

Abstract

BACKGROUND

Interstitial collagenase has been considered as an essential enzyme for collagenolysis in liver fibrosis, because type I and III collagens increase predominantly in liver fibrosis. The present study aimed to demonstrate the gene expression of matrix metalloproteinases-13 (MMP-13) in the progressive phases of ethanol induced experimental liver fibrosis in rats.

METHODS

Thirty-four Sprague-Dawley rats were randomly divided into two groups. The experimental group (24 rats) was given ethanol (44%, 7 g/kg) every day and the control group (10) was given normal saline. Liver samples were harvested from experimental rats at 4, 12 and 24 weeks respectively. The kinetics of MMP-13 mRNA expression was assayed by semi-quantity reverse transcriptase-polymerase chain reaction (RT-PCR).

RESULTS

In normal rat liver, a faint band for MMP-13 mRNA was observed by RT-PCR (0.24+/-0.41). The gene expression of MMP-13 was increased in the liver of the rats treated with ethanol for 4 weeks (0.62+/-0.54), but it was not considered statistically significant (P>0.05). And the livers from 12-week-treated rats showed a marked mRNA expression (1.65+/-0.47, P<0.01). Once fibrosis became prominent (24 weeks), a faint band of MMP-13 mRNA was observed (0.39+/-0.25).

CONCLUSION

MMP-13 participates in the degradation of newly-formed matrix in the early phase of rat liver fibrosis induced by ethanol, and it was induced in a distinct time frame.

摘要

背景

间质胶原酶被认为是肝纤维化中胶原蛋白分解的关键酶,因为在肝纤维化过程中I型和III型胶原蛋白含量主要增加。本研究旨在证明基质金属蛋白酶-13(MMP-13)在大鼠乙醇诱导的实验性肝纤维化进展阶段的基因表达。

方法

34只Sprague-Dawley大鼠随机分为两组。实验组(24只大鼠)每天给予乙醇(44%,7 g/kg),对照组(10只)给予生理盐水。分别在4周、12周和24周从实验组大鼠采集肝脏样本。采用半定量逆转录聚合酶链反应(RT-PCR)检测MMP-13 mRNA表达的动力学变化。

结果

在正常大鼠肝脏中,通过RT-PCR观察到MMP-13 mRNA的条带较淡(0.24±0.41)。乙醇处理4周的大鼠肝脏中MMP-13的基因表达增加(0.62±0.54),但差异无统计学意义(P>0.05)。12周处理的大鼠肝脏显示出明显的mRNA表达(1.65±0.47,P<0.01)。一旦纤维化变得明显(24周),观察到MMP-13 mRNA的条带较淡(0.39±0.25)。

结论

MMP-13参与乙醇诱导的大鼠肝纤维化早期新形成基质的降解,且在不同的时间框架内被诱导。

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