首页> 外文期刊>Life sciences >Herbal medicine Sho-saiko-to (TJ-9) increases expression matrix metalloproteinases (MMPs) with reduced expression of tissue inhibitor of metalloproteinases (TIMPs) in rat stellate cell
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Herbal medicine Sho-saiko-to (TJ-9) increases expression matrix metalloproteinases (MMPs) with reduced expression of tissue inhibitor of metalloproteinases (TIMPs) in rat stellate cell

机译:草药Sho-saiko-to(TJ-9)在大鼠星状细胞中增加了表达基质金属蛋白酶(MMP)的表达,并减少了组织金属蛋白酶(TIMPs)的表达

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We have reported that Sho-saiko-to (TJ-9) prevents liver fibrosis in vivo. To gain further insights into the effect of TJ-9, the matrix metalloprotemases (MMPs)/tissue inhibitors of metalloproteinases (TIMPs) balance was examined. Hepatic stellate cells (HSCs) were isolated from male Wistar rats and cultured with TJ-9 (0-1000 mug/ml) on uncoated plastic dishes for 4 days. To elucidate the effects on the MMPs/TIMPs balance by TJ-9, quantitative analysis of type IV collagen-degrading activity, gelatin zymography and reverse zymography were carried out. Northern blot analysis was performed to determine the expression of MMP-2, 13 and TIMP-1 mRNAs. TJ-9 treatment resulted in dose-dependent upregulation of MMP-2, 13 mRNA and downregulation of TIMP-1 mRNA up to 500 mug/ml. Gelatin zymography, reverse zymography and quantitative analysis of type IV collagen-degrading activity confirmed that TJ-9 increased MMP-2 activity and prevented TIMP-1, 2 activities in a dose-dependent manner. SB203580 diminished the reduction of mRNA as well as the activity of TIMP-I by TJ-9 and induction of mRNA as well as the activity of MMP-2. These results show that TJ-9 increased MMP-2, 13 activity with reduced TIMP-1, 2 activities on HSCs possibly via P38 pathway. (C) 2004 Elsevier Inc. All rights reserved. [References: 44]
机译:我们已经报道说Sho-saiko-to(TJ-9)可以在体内预防肝纤维化。为了进一步了解TJ-9的作用,研究了基质金属蛋白酶(MMP)/金属蛋白酶组织抑制剂(TIMPs)平衡。从雄性Wistar大鼠中分离出肝星状细胞(HSC),并在未涂覆的塑料皿中与TJ-9(0-1000杯/毫升)一起培养4天。为了阐明TJ-9对MMP / TIMPs平衡的影响,对IV型胶原降解活性,明胶酶谱和反向酶谱进行了定量分析。进行Northern印迹分析以确定MMP-2、13和TIMP-1 mRNA的表达。 TJ-9处理导致MMP-2、13 mRNA的剂量依赖性上调和TIMP-1 mRNA的下调,直至500 mug / ml。明胶酶谱,反向酶谱和IV型胶原降解活性的定量分析证实,TJ-9以剂量依赖性方式增加了MMP-2活性并阻止了TIMP-1、2活性。 SB203580减少了TJ-9对mRNA的还原以及TIMP-1的活性以及对mRNA的诱导以及MMP-2的活性。这些结果表明,TJ-9可能通过P38途径增加了HSC的MMP-2、13活性和TIMP-1、2活性。 (C)2004 Elsevier Inc.保留所有权利。 [参考:44]

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