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Effects of ubiquitin-proteasome inhibitor on the expression levels of TNF-α and TGF-β1 in mice with viral myocarditis

机译:泛素蛋白酶体抑制剂对病毒性心肌炎小鼠TNF-α和TGF-β1表达水平的影响

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摘要

Effects of ubiquitin-proteasome system (UPS) inhibitor MG-132 on the expression levels of tumor necrosis factor-α (TNF-α) and transforming growth factor-β1 (TGF-β1) in mice with viral myocarditis were investigated to analyze the correlation of myocardial tissue score of mice between TNF-α and TGF-β1. Eighty healthy male SPF mice aged 6 weeks were selected and 20 mice were randomly selected as the blank group. The blank group did not receive any intervention. Mortality rates of each group were recorded and compared on day 8 of modeling, and heart specimens from the remaining mice were histopathologically examined and the expression of mRNA and protein of TNF-α and TGF-β1 in myocardial tissues were detected by western blot analysis. Correlation between mouse myocardial histopathologic scores and expression of protein of TNF-α and TGF-β1 in myocardial tissues, as well as the expression of TNF-α and TGF-β1 in myocardial tissue in VMC mice was analyzed. The expression levels of myocardial histopathological scores, mRNA and protein of TNF-α and TGF-β1 in the blank and control group were significantly lower than those in the VMC and the MG-132 group. The myocardial histopathological scores, mRNA and TNF-α and TGF-β1 protein in the MG-132 group were significantly lower than those in the VMC group (P<0.05). The expression of TNF-α and TGF-β1 protein in myocardial tissues was positively correlated with the pathological score in myocardial tissue of mice (r=0.843, P<0.05; r=0.763, P<0.05), and there was a positive correlation between the expression of TNF-α and TGF-β1 protein in myocardial tissues of VMC mice (r=0.672, P<0.05). UPS inhibitor MG-132, which can significantly alleviate the myocardial injury of VMC mice, reduced the expression of inflammatory factors in myocardial tissues, and improved the survival rate of mice, thus it is a potential new treatment for VMC.
机译:研究了泛素-蛋白酶体系统(UPS)抑制剂MG-132对病毒性心肌炎小鼠肿瘤坏死因子-α(TNF-α)和转化生长因子-β1(TGF-β1)表达水平的影响,以分析其相关性。在小鼠TNF-α和TGF-β1之间的心肌组织评分。选择80只健康的6周龄雄性SPF小鼠,并随机选择20只小鼠作为空白组。空白组未接受任何干预。在建模的第8天,记录每组的死亡率并进行比较,并且对其余小鼠的心脏标本进行组织病理学检查,并通过western blot分析检测心肌组织中TNF-α和TGF-β1的mRNA和蛋白的表达。分析了小鼠心肌组织病理学评分与心肌组织中TNF-α和TGF-β1蛋白表达以及VMC小鼠心肌组织中TNF-α和TGF-β1表达的相关性。空白和对照组的心肌组织病理学评分,TNF-α和TGF-β1的mRNA和蛋白的表达水平明显低于VMC和MG-132组。 MG-132组的心肌组织病理学评分,mRNA,TNF-α和TGF-β1蛋白明显低于VMC组(P <0.05)。心肌组织中TNF-α和TGF-β1蛋白的表达与小鼠心肌组织病理评分呈正相关(r = 0.843,P <0.05; r = 0.763,P <0.05),且呈正相关。小鼠心肌组织中TNF-α和TGF-β1蛋白的表达变化(r = 0.672,P <0.05)。 UPS抑制剂MG-132可以明显减轻VMC小鼠的心肌损伤,减少心肌组织中炎性因子的表达,提高小鼠的成活率,因此是VMC的潜在新疗法。

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