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11β-羟类固醇脱氢酶2基因启动子的表观遗传调控与人类高血压相关。

Epigenetic control of 11 beta-hydroxysteroid dehydrogenase 2 gene promoter is related to human hypertension.

作者信息

Friso Simonetta, Pizzolo Francesca, Choi Sang-Woon, Guarini Patrizia, Castagna Annalisa, Ravagnani Viviana, Carletto Antonio, Pattini Patrizia, Corrocher Roberto, Olivieri Oliviero

机构信息

Department of Clinical and Experimental Medicine, University of Verona School of Medicine, Verona, Italy.

出版信息

Atherosclerosis. 2008 Aug;199(2):323-7. doi: 10.1016/j.atherosclerosis.2007.11.029. Epub 2008 Feb 7.

Abstract

BACKGROUND

Lower activity of 11 beta-hydroxysteroid dehydrogenase 2 (11beta-HSD2) classically induces hypertension by leading to an altered tetrahydrocortisol- versus tetrahydrocortisone-metabolites (THFs/THE) shuttle. Recent cell culture and animal studies suggest a role for promoter methylation, a major epigenetic feature of DNA, in regulation of HSD11B2 expression. Little is known, however, of human HSD11B2 epigenetic control and its relationship with the onset of hypertension.

OBJECTIVE

To explore the possible relevance of HSD11B2 promoter methylation, by examining human peripheral blood mononuclear cell (PBMC) DNA and urinary THFs/THE ratio as a biochemical indicator of 11beta-HSD2 activity, in blood pressure control.

METHODS

Twenty-five essential hypertensives and 32 subjects on prednisone therapy were analyzed, the latter to investigate 11beta-HSD2 function in the development of hypertension.

RESULTS

Elevated HSD11B2 promoter methylation was associated with hypertension developing in glucocorticoid-treated patients in parallel with a higher urinary THFs/THE ratio. Essential hypertensives with elevated urinary THFs/THE ratio also showed higher HSD11B2 promoter methylation.

CONCLUSIONS

These results show a clear link between the epigenetic regulation through repression of HSD11B2 in PBMC DNA and hypertension.

摘要

背景

11β-羟类固醇脱氢酶2(11β-HSD2)活性降低通常通过导致四氢皮质醇与四氢可的松代谢物(THFs/THE)穿梭改变而诱发高血压。最近的细胞培养和动物研究表明,启动子甲基化(DNA的一种主要表观遗传特征)在HSD11B2表达调控中发挥作用。然而,关于人类HSD11B2的表观遗传调控及其与高血压发病的关系知之甚少。

目的

通过检测人类外周血单个核细胞(PBMC)DNA和尿THFs/THE比值(作为11β-HSD2活性的生化指标),探讨HSD11B2启动子甲基化在血压控制中的可能相关性。

方法

分析了25例原发性高血压患者和32例接受泼尼松治疗的受试者,后者用于研究11β-HSD2在高血压发生中的作用。

结果

HSD11B2启动子甲基化升高与糖皮质激素治疗患者发生高血压相关,同时尿THFs/THE比值升高。尿THFs/THE比值升高的原发性高血压患者也表现出较高的HSD11B2启动子甲基化。

结论

这些结果表明,PBMC DNA中HSD11B2的表观遗传调控与高血压之间存在明确联系。

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