依普利酮对高糖和IL-1β诱导的心脏成纤维细胞MMP-2表达的影响

目的探讨依普利酮干预对高糖和白介素1β(IL-1B)诱导的人心脏成纤维细胞基质金属蛋白酶2(MMP-2)表达的影响。方法将人心脏成纤维细胞分别培养在正常葡萄糖浓度(正常对照组)、高浓度葡萄糖(高糖组)和等渗甘露醇(高渗对照组)的培养液中,分别添加IL-10和(或)盐皮质激素受体阻断剂依普利酮进行干预。明胶酶法测定细胞培养上清液中MMP-2的活性,RT—PCR测定成纤维细胞MMP-2和组织金属蛋白酶抑制因子2(TIMP-2)mRNA的表达。结果与正常对照组比较,高糖组MMP-2活性和mRNA的表达显著增高(P〈0.01),高渗对照组MMP-2活性和mRNA表达也增高但低于高糖组(P〈0.05)。...

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Published in上海交通大学学报(医学版) Vol. 32; no. 12; pp. 1571 - 1576
Main Author 池菊芳 郭航远 唐伟良 吕海涛 周妍 HiroyasuUZUI
Format Journal Article
LanguageChinese
Published 绍兴市人民医院心内科,绍兴,312000%日本福井大学医学院附属病院,福井910-1193 2012
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Summary:目的探讨依普利酮干预对高糖和白介素1β(IL-1B)诱导的人心脏成纤维细胞基质金属蛋白酶2(MMP-2)表达的影响。方法将人心脏成纤维细胞分别培养在正常葡萄糖浓度(正常对照组)、高浓度葡萄糖(高糖组)和等渗甘露醇(高渗对照组)的培养液中,分别添加IL-10和(或)盐皮质激素受体阻断剂依普利酮进行干预。明胶酶法测定细胞培养上清液中MMP-2的活性,RT—PCR测定成纤维细胞MMP-2和组织金属蛋白酶抑制因子2(TIMP-2)mRNA的表达。结果与正常对照组比较,高糖组MMP-2活性和mRNA的表达显著增高(P〈0.01),高渗对照组MMP-2活性和mRNA表达也增高但低于高糖组(P〈0.05)。与高糖组比较,高糖+IL-1p组MMP-2活性和mRNA的表达呈现叠加现象,高糖+依普利酮组和正常对照+IL.1β依普利酮组MMP-2活性和mRNA的表达分别显著低于高糖组和正常对照+IL-1B组(P〈0.05)。结论高糖可通过高渗外的作用诱导人心脏成纤维细胞MMP-2活性增强和mRNA表达增加,IL-1B对该诱导作用具有促进作用,而依普利酮则呈现抑制效应。
Bibliography:high glucose; interleuk'in-lβ; matrix metalloproteinase-2; mineralocorticoid receptor antagonist; fibroblast
CHI Ju-fang, GUO Hang-yuan, TANG Wei-liang, LU Hai-tao, ZHOU Yan, Hiroyasu UZUI (1. Department of Cardiology, Shaoxing People's Hospital, Shaoxing 312000, China; 2. Affiliated Hospital of Faculty of Medical Sciences, University of Fukui, Fuku 910 -1193, Japan)
31-1259/R
Objective To investigate the effect of eplerenone on the expression of matrix metalloproteinase-2 (MMP-2) in cardiac fibroblasts stimulated by high glucose and interleukin (IL)-113. Methods Human cardiac fibroblasts were cultured in fluid with normal glucose (normal control group), high glucose (high glucose group) and iso-osmotic mannitol (hyperosmotic control group) in the absence or presence of IL-Iβ and/or eplerenone. The activity of MMP-2 in the supernatant was assessed by gel zymography, and the expression of MMP-2 mRNA and tissue inhibitor of metalloproteinase- 2 (TIMP-2) mRNA was determined by RT-PCR. Results The activity of MMP-2
ISSN:1674-8115
DOI:10.3969/j.issn.1674-8115.2012.12.012