2003Zhonghua ganzangbing zazhiRequires access

Gene expression of interstitial collagenase MMP-13 in progressive phase of rat liver fibrosis induced by ethanol

LI You-min

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Abstract

Objective To demonstrate the gene expression of MMP-13 in the progressive phase of ethanol-induced experimental liver fibrosis in rats. Methods 34 SD rats were randomized into two groups. The rats in experimental group (n = 24) were given ethanol (44%, 7 g/kg) every day, and the rats in control group (n = 10) were given equality normal saline. Liver samples were harvested from experimental rats at the 4th, 12th and 24th weeks respectively. The dynamic expression of MMP-13 mRNA was assayed by semi-quantity reverse transcription-polymerase chain reaction (RT-PCR). Results In normal rat liver, a faint band of MMP-13 mRNA was observed by RT-PCR (0.24 ± 0.41). The gene expression of MMP-13 increased in the livers of rats treated with ethanol for 4 weeks (0.62 ± 0.54), but it was not considered statistically, when compared with that in normal rats livers. And the livers from 12-week-treated rats showed a markedly MMP-13 mRNA expression (1.65 ± 0.47, t = -4.363, P 0.01). Once the 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, but it expresses in a distinct time frame.

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Objective To demonstrate the gene expression of MMP-13 in the progressive phase of ethanol-induced experimental liver fibrosis in rats. Methods 34 SD rats were randomized into two groups. The rats in experimental group (n = 24) were given ethanol (44%, 7 g/kg) every day, and the rats in control group (n = 10) were given equality normal saline. Liver samples were harvested from experimental rats at the 4th, 12th and 24th weeks respectively. The dynamic expression of MMP-13 mRNA was assayed by semi-quantity reverse transcription-polymerase chain reaction (RT-PCR). Results In normal rat liver, a faint band of MMP-13 mRNA was observed by RT-PCR (0.24 ± 0.41). The gene expression of MMP-13 increased in the livers of rats treated with ethanol for 4 weeks (0.62 ± 0.54), but it was not considered statistically, when compared with that in normal rats livers. And the livers from 12-week-treated rats showed a markedly MMP-13 mRNA expression (1.65 ± 0.47, t = -4.363, P 0.01). Once the 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, but it expresses in a distinct time frame.

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Available abstract

Objective To demonstrate the gene expression of MMP-13 in the progressive phase of ethanol-induced experimental liver fibrosis in rats. Methods 34 SD rats were randomized into two groups. The rats in experimental group (n = 24) were given ethanol (44%, 7 g/kg) every day, and the rats in control group (n = 10) were given equality normal saline. Liver samples were harvested from experimental rats at the 4th, 12th and 24th weeks respectively. The dynamic expression of MMP-13 mRNA was assayed by semi-quantity reverse transcription-polymerase chain reaction (RT-PCR). Results In normal rat liver, a faint band of MMP-13 mRNA was observed by RT-PCR (0.24 ± 0.41). The gene expression of MMP-13 increased in the livers of rats treated with ethanol for 4 weeks (0.62 ± 0.54), but it was not considered statistically, when compared with that in normal rats livers. And the livers from 12-week-treated rats showed a markedly MMP-13 mRNA expression (1.65 ± 0.47, t = -4.363, P 0.01). Once the 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, but it expresses in a distinct time frame.

Key concepts: Interstitial collagenase, Matrix metalloproteinase, Collagenase, Ethanol, Gene expression, Saline, Fibrosis, Messenger RNA

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