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首页> 外文期刊>Inflammation >Elevated Expression of Liver X Receptor Alpha (LXRα) in Myocardium of Streptozotocin-Induced Diabetic Rats
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Elevated Expression of Liver X Receptor Alpha (LXRα) in Myocardium of Streptozotocin-Induced Diabetic Rats

机译:链脲佐菌素诱导的糖尿病大鼠心肌中肝脏X受体α(LXRα)的表达升高

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The present study was designed to investigate the myocardial expression of liver X receptor alpha (LXRα) in a streptozotocin (STZ)-induced diabetic rat model. Immunohistochemical staining, quantitative real-time RT-PCR, and Western blot analysis were used to determine the expression of LXRα in the myocardium of STZ-induced diabetic rats. The myocardial expression of LXRα target genes, long-chain acyl-CoA synthetase 3 (ACSL3), fatty acid transporter protein (FAT/CD36), ATP-binding cassette transporter A1 (ABCA1), and ABCG1 were also detected. Bisulfite sequencing analysis was employed to examine the methylation status of the CpG island at the LXRα promoter region in the myocardium of STZ-induced diabetic rats. We found that LXRα mRNA and protein expression in the left ventricles, right ventricles, and atria of diabetic rats were gradually increased during the progression of diabetic cardiomyopathy (DCM). The mRNA expression levels of ACSL3 and FAT/CD36 and the protein expression levels of ABCA1 and ABCG1 were also markedly increased in different heart chambers of diabetic rats. Moreover, there was a significant difference in the methylation status of LXRα gene between the ventricles of control and diabetic rats (P < 0.05). Our findings suggest that elevated expression of LXRα may be involved in the progression of DCM, and demethylation of LXRα is likely to be responsible for its increased expression in myocardial tissues.
机译:本研究旨在研究链脲佐菌素(STZ)诱导的糖尿病大鼠模型中肝脏X受体α(LXRα)的心肌表达。免疫组化染色,实时荧光定量RT-PCR和蛋白质印迹分析用于确定STZ诱导的糖尿病大鼠心肌中LXRα的表达。还检测了LXRα靶基因,长链酰基辅酶A合成酶3(ACSL3),脂肪酸转运蛋白(FAT / CD36),ATP结合盒转运蛋白A1(ABCA1)和ABCG1的心肌表达。亚硫酸氢盐测序分析用于检查STZ诱导的糖尿病大鼠心肌LXRα启动子区域CpG岛的甲基化状态。我们发现,在糖尿病性心肌病(DCM)进程中,糖尿病大鼠左心室,右心室和心房中的LXRαmRNA和蛋白表达逐渐增加。在糖尿病大鼠的不同心腔中,ACSL3和FAT / CD36的mRNA表达水平以及ABCA1和ABCG1的蛋白表达水平也明显升高。此外,在对照组和糖尿病大鼠的心室之间,LXRα基因的甲基化状态存在显着差异(P <0.05)。我们的发现表明,LXRα的表达升高可能与DCM的发展有关,LXRα的去甲基化可能是其在心肌组织中表达增加的原因。

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