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地塞米松对内毒素血症幼年大鼠心肌肌动蛋白及其mRNA表达的影响 被引量:1

Effect of dexamethasone on expressions of alpha-sarcomeric actin and its mRNA in myocardium of rats with endotoxemia
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摘要 目的:通过观察地塞米松(Dex)对内毒素血症幼年大鼠心肌肌动蛋白(α-SA)及其mRNA表达的影响,探讨Dex对内毒素血症大鼠心肌收缩功能的保护途径.方法:选健康18 d Wistar大鼠121只,按腹腔注射药物不同分成:生理盐水对照组,内毒素(LPS)组、Dex组,各组于加LPS后2,4,6,24及72 h分别将大鼠断头分离心脏,RT-PCR方法测定α-SA mRNA表达水平,用免疫组化方法测定α-SA.结果:LPS和Dex组各时点α-SA及其mRNA表达均较对照组明显减弱(P<0.01);Dex组最低点与LPS组一致在6~24 h,但明显高于LPS组(P<0.01).结论:α-SA及其mRNA表达在内毒素血症时明显受到抑制,心肌收缩功能受损;Dex可减轻LPS对d-SA及其mRNA表达的抑制作用. Objective: To study the effect of dexamethasone (Dex) on the expressions of alpha-sarcomeric actin (α-SA) and α-SA mRNA in myocardium of rats with endotoxemla, and to explore the protective effect of Dex on the systolic function of rat myocardium. Methods: We randomly divided 121 Wistar rats aged 18 days into 3 groups : saline control group ( intraperitoneal injection of saline of 1 ml/kg; n = 11 ), lipopolysaccharide (LPS) group ( intraperitoneal injection of LPS of 4 mg/kg; n = 55 ), and Dex group ( intraperitoneal injection of LPS of 4 mg/kg and Dex of 5 mg/kg; n =55). The rats in each group were killed 2, 4, 6, 24, and 72 hours after receiving LPS, respectively. The expressions of α-SA and α-SA mRNA in the myocardium were detected by using reverse transcription polymerase chain reaction and immunohistochemistry assay, respectively. Results: The expressions of α-SA and α-SA mRNA in LPS and Dex groups were significantly lower than those in control group at each time point ( P 〈 0.01 ), and in Dex group they were significantly higher than those in LPS group at hour 6 and hour 24 ( P 〈0.01). Conclusion: The expressions of α-SA and α-SA mRNA were inhibited and the systolic function of myocardium was damaged in rats with LPS-induced endotoxemia. Dex could relieve the inhibitory effect of LPS on the expressions of α-SA and α-SA mRNA.
出处 《中国医科大学学报》 CAS CSCD 北大核心 2006年第3期237-238,241,共3页 Journal of China Medical University
基金 辽宁省自然科学基金资助项目(20052091)
关键词 内毒素血症 地塞米松 心肌肌动蛋白 MRNA表达 endotoxemia dexamethasone alpha-sarcomeric actin mRNA expression
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