Department of Pharmacology, Kyungpook National University School of Medicine, Daegu 700-422, Republic of Korea.
Biochem Biophys Res Commun. 2010 May 28;396(2):252-7. doi: 10.1016/j.bbrc.2010.04.074. Epub 2010 Apr 18.
The Na(+)-K(+)-2Cl(-) cotransporter 1 (NKCC1) is one of several transporters that have been implicated for development of hypertension since NKCC1 activity is elevated in hypertensive aorta and vascular contractions are inhibited by bumetanide, an inhibitor of NKCC1. We hypothesized that promoter hypomethylation upregulates the NKCC1 in spontaneously hypertensive rats (SHR). Thoracic aortae and mesenteric arteries were excised, cut into rings, mounted in organ baths and subjected to vascular contraction. The expression levels of nkcc1 mRNA and protein in aortae and heart tissues were measured by real-time PCR and Western blot, respectively. The methylation status of nkcc1 promoter region was analyzed by combined bisulfite restriction assay (COBRA) and bisulfite sequencing. Phenylephrine-induced vascular contraction in a dose-dependent manner, which was inhibited by bumetanide. The inhibition of dose-response curves by bumetanide was much greater in SHR than in Wistar Kyoto (WKY) normotensive rats. The expression levels of nkcc1 mRNA and of NKCC1 protein in aortae and heart tissues were higher in SHR than in WKY. Nkcc1 gene promoter was hypomethylated in aortae and heart than those of WKY. These results suggest that promoter hypomethylation upregulates the NKCC1 expression in aortae and heart of SHR.
钠钾 2 氯协同转运蛋白 1(NKCC1)是几种与高血压相关的转运蛋白之一,因为 NKCC1 活性在高血压主动脉中升高,而布美他尼(NKCC1 的抑制剂)可抑制血管收缩。我们假设启动子低甲基化会使自发性高血压大鼠(SHR)中的 NKCC1 上调。取出胸主动脉和肠系膜动脉,切成环,安装在器官浴中,并进行血管收缩。通过实时 PCR 和 Western blot 分别测量主动脉和心脏组织中 nkcc1 mRNA 和蛋白的表达水平。通过联合亚硫酸氢盐限制分析(COBRA)和亚硫酸氢盐测序分析 nkcc1 启动子区域的甲基化状态。苯肾上腺素以剂量依赖性方式诱导血管收缩,该收缩被布美他尼抑制。布美他尼对 SHR 比 Wistar Kyoto(WKY)正常血压大鼠的剂量-反应曲线的抑制作用更大。主动脉和心脏组织中 nkcc1 mRNA 和 NKCC1 蛋白的表达水平在 SHR 中高于 WKY。与 WKY 相比,NKCC1 基因启动子在主动脉和心脏中的甲基化程度较低。这些结果表明,启动子低甲基化会使 SHR 主动脉和心脏中的 NKCC1 表达上调。