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在肾髓质中,NAD(P)H 氧化酶亚单位 p67(phox)的表达增加导致了过度的氧化应激和盐敏感型高血压。

Increased expression of NAD(P)H oxidase subunit p67(phox) in the renal medulla contributes to excess oxidative stress and salt-sensitive hypertension.

机构信息

Physiology Department, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Cell Metab. 2012 Feb 8;15(2):201-8. doi: 10.1016/j.cmet.2012.01.003.

Abstract

NAD(P)H oxidase has been shown to be important in the development of salt-sensitive hypertension. Here, we show that the expression of a subunit of NAD(P)H oxidase, p67(phox), was increased in response to a high-salt diet in the outer renal medulla of the Dahl salt-sensitive (SS) rat, an animal model for human salt-sensitive hypertension. The higher expression of p67(phox), not the other subunits observed, was associated with higher NAD(P)H oxidase activity and salt sensitivity in SS rats compared with a salt-resistant strain. Genetic mutations of the SS allele of p67(phox) were found in the promoter region and contributed to higher promoter activity than that of the salt-resistant strain. To verify the importance of p67(phox), we disrupted p67(phox) in SS rats using zinc-finger nucleases. These rats exhibited a significant reduction of salt-sensitive hypertension and renal medullary oxidative stress and injury. p67(phox) could represent a target for salt-sensitive hypertension therapy.

摘要

NAD(P)H 氧化酶在盐敏感性高血压的发展中起着重要作用。在这里,我们发现,在盐敏感(SS)大鼠的肾外髓质中,NAD(P)H 氧化酶的一个亚基 p67(phox)的表达在高盐饮食的刺激下增加,SS 大鼠是人类盐敏感性高血压的动物模型。与盐抵抗品系相比,p67(phox)的更高表达,而不是观察到的其他亚基,与 SS 大鼠中更高的 NAD(P)H 氧化酶活性和盐敏感性相关。在 p67(phox)的 SS 等位基因的启动子区域发现了遗传突变,导致启动子活性高于盐抵抗品系。为了验证 p67(phox)的重要性,我们使用锌指核酸酶在 SS 大鼠中破坏 p67(phox)。这些大鼠表现出盐敏感性高血压和肾髓质氧化应激和损伤的显著减少。p67(phox)可能成为盐敏感性高血压治疗的靶点。

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