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基质金属蛋白酶抑制剂在Thy-1肾炎中的作用。

Participation of the matrix metalloproteinase inhibitor in Thy-1 nephritis.

作者信息

Mitani Osamu, Katoh Masahiro, Shigematsu Hidekazu

机构信息

Department of Pathology, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

Pathol Int. 2004 Apr;54(4):241-50. doi: 10.1111/j.1440-1827.2004.01615.x.

DOI:10.1111/j.1440-1827.2004.01615.x
PMID:15028025
Abstract

What influence would be shown in Thy-1 glomerulonephritis when the synthetic matrix metalloproteinase (MMP) inhibitor SI-27 is administered? Five groups of 80 male Wistar rats were studied: healthy group; treated healthy group; nephritic group; pretreated nephritic group; and post-treated nephritic group. SI-27 treatment of nephritic animals was initiated either 2 days before or 2 days after anti-Thy-1.1 antibody injection. On days 7, 14, 26 and 42 after disease induction, we examined renal histology, extracellular matrix (ECM) constituent, and MMP activity. SI-27 treated Thy-1 groups resulted in significant reduction of glomerular cells including alpha-smooth muscle actin (alpha-SMA) positive mesangial cells and suppressed expression of type IV collagen at 7 days. Moreover, type I collagen was also decreased by SI-27 at 42 days. However, glomerular cell numbers did not show any significant changes at 14, 26 and 42 days. In gelatin zymography, the gelatinolytic band for MMP-9 was expressed in SI-27 treated Thy-1 nephritis groups, although it was not expressed in the nephritic group at day 7. However, the expression of MMP-9 was no longer seen at 14, 26 and 42 days. The bands for an active form of MMP-2 were expressed throughout the experimental period in the Thy-1 nephritic groups. These results suggest that MMP plays an important role in the development of Thy-1 nephritis, and even if the synthetic MMP inhibitor intercepts the initial increase of glomerular cells and matrices, it does not inhibit recovery to normal glomerular capillary structures in Thy-1 nephritis.

摘要

给予合成基质金属蛋白酶(MMP)抑制剂SI-27时,Thy-1肾小球肾炎会表现出何种影响?对五组每组80只雄性Wistar大鼠进行了研究:健康组;经处理的健康组;肾炎组;预处理肾炎组;以及后处理肾炎组。在注射抗Thy-1.1抗体前2天或后2天开始对肾炎动物进行SI-27治疗。在疾病诱导后的第7、14、26和42天,我们检查了肾脏组织学、细胞外基质(ECM)成分和MMP活性。SI-27处理的Thy-1组在第7天时导致包括α-平滑肌肌动蛋白(α-SMA)阳性系膜细胞在内的肾小球细胞显著减少,并抑制了IV型胶原的表达。此外,在第42天时,I型胶原也因SI-27而减少。然而,在第14、26和42天时,肾小球细胞数量没有显示出任何显著变化。在明胶酶谱分析中,MMP-9的明胶分解带在SI-27处理的Thy-1肾炎组中表达,尽管在第7天时肾炎组中未表达。然而,在第14、26和42天时不再看到MMP-9的表达。在Thy-1肾炎组的整个实验期间,活性形式的MMP-2条带均有表达。这些结果表明,MMP在Thy-1肾炎的发展中起重要作用,并且即使合成的MMP抑制剂阻断了肾小球细胞和基质的最初增加,它也不会抑制Thy-1肾炎中肾小球毛细血管结构恢复正常。

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Renoprotective action of a matrix metalloproteinase inhibitor in progressive mesangioproliferative nephritis.基质金属蛋白酶抑制剂在进行性系膜增生性肾炎中的肾脏保护作用。
Nephron Extra. 2012 Jan;2(1):133-46. doi: 10.1159/000338801. Epub 2012 May 26.
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Matrix metalloproteinases in kidney homeostasis and diseases.
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Am J Physiol Renal Physiol. 2012 Jun 1;302(11):F1351-61. doi: 10.1152/ajprenal.00037.2012. Epub 2012 Apr 4.