草药小柴胡汤(TJ - 9)可增加大鼠星状细胞中基质金属蛋白酶(MMPs)的表达,同时降低金属蛋白酶组织抑制剂(TIMPs)的表达。

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.

作者信息

Sakaida Isao, Hironaka Koji, Kimura Teruaki, Terai Shuji, Yamasaki Takahiro, Okita Kiwamu

机构信息

Department of Gastroenterology and Hepatology, Yamaguchi University, School of Medicine, Minami-Kogushi 1-1-1, Ube, Yamaguchi 755-8505, Japan.

出版信息

Life Sci. 2004 Mar 19;74(18):2251-63. doi: 10.1016/j.lfs.2003.09.059.

Abstract

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 metalloproteinases (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 microg/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 microg/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-1 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.

摘要

我们曾报道过小柴胡汤(TJ - 9)可在体内预防肝纤维化。为了进一步深入了解TJ - 9的作用效果,我们检测了基质金属蛋白酶(MMPs)/金属蛋白酶组织抑制剂(TIMPs)的平衡。从雄性Wistar大鼠中分离出肝星状细胞(HSCs),并在未包被的塑料培养皿中用TJ - 9(0 - 1000微克/毫升)培养4天。为阐明TJ - 9对MMPs/TIMPs平衡的影响,我们进行了IV型胶原降解活性的定量分析、明胶酶谱分析和反向酶谱分析。采用Northern印迹分析来确定MMP - 2、13和TIMP - 1 mRNA的表达。TJ - 9处理导致MMP - 2、13 mRNA呈剂量依赖性上调,TIMP - 1 mRNA在高达500微克/毫升时呈剂量依赖性下调。明胶酶谱分析、反向酶谱分析以及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MMP - 2活性并抑制TIMP - 1、2活性。SB203580减弱了TJ - 9对TIMP - 1 mRNA的减少作用及其活性,以及对MMP - 2 mRNA的诱导作用及其活性。这些结果表明,TJ - 9可能通过P38途径增加HSCs上MMP - 2、13的活性,同时降低TIMP - 1、2的活性。

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