首页> 外文期刊>Kidney and blood pressure research >Fosinopril and Losartan Regulate Klotho Gene and Nicotinamide Adenine Dinucleotide Phosphate Oxidase Expression in Kidneys of Spontaneously Hypertensive Rats
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Fosinopril and Losartan Regulate Klotho Gene and Nicotinamide Adenine Dinucleotide Phosphate Oxidase Expression in Kidneys of Spontaneously Hypertensive Rats

机译:福辛普利和洛沙坦调节自发性高血压大鼠肾脏的Klotho基因和烟酰胺腺嘌呤二核苷酸磷酸氧化酶表达。

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Background/Aims: Klotho, a newly identified antiaging gene, predominantly detected in the kidney, has pleiotropic protective effects on kidney diseases. Several studies have confirmed the association between Klotho and oxidative stress. The present studies were performed to explore effects of fosinopril (Fos) and losartan (Los) on Klotho and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase expression in kidneys of spontaneously hypertensive rats (SHR). Methods: Twenty-four male 22-week-old SHR were randomly divided into three groups: model group, Fos group and Los group. Wistar-Kyoto rats were taken as control. After 8 weeks, urinary N-acetyl-β-D-glucosaminidase (NAGase), 24 h urinary protein (Upro), serum creatinine (Scr), blood urea nitrogen (BUN) and renal pathological changes were detected. Renal mRNA and protein expression of Klotho and three subunits of NADPH oxidase protein expression were evaluated. Results: As compared to the model group, NAGase, Upro, Scr and BUN were decreased; the typical renal pathological damage was relieved in the Fos or Los group. Fos or Los inhibited the reduction of Klotho expression, and reduced the elevation of NADPH oxidase expression. Conclusion: Abnormal expression of Klotho and NADPH oxidase plays important roles in progression of hypertensive renal damage. Fos and Los can increase Klotho expression, and inhibit NADPH oxidase expression, which may be one of the mechanisms of their protective effects in hypertensive renal damage.
机译:背景/目的:Klotho是一种新发现的抗衰老基因,主要在肾脏中发现,对肾脏疾病具有多效保护作用。多项研究已证实Klotho与氧化应激之间的关联。本研究旨在探讨福辛普利(Fos)和氯沙坦(Los)对自发性高血压大鼠(SHR)肾脏中Klotho和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶表达的影响。方法:将24名22周龄男性SHR随机分为三组:模型组,Fos组和Los组。以Wistar-Kyoto大鼠为对照。 8周后,检测尿N-乙酰基-β-D-氨基葡萄糖苷酶(NAGase),24 h尿蛋白(Upro),血清肌酐(Scr),血尿素氮(BUN)和肾脏病理变化。评估肾脏的Klotho mRNA和蛋白质表达以及NADPH氧化酶三个亚基的蛋白质表达。结果:与模型组相比,NAGase,Upro,Scr和BUN均降低; Fos或Los组可减轻典型的肾脏病理损害。 Fos或Los抑制Klotho表达的降低,并降低NADPH氧化酶表达的升高。结论:Klotho和NADPH氧化酶的异常表达在高血压肾损害的进展中起重要作用。 Fos和Los可以增加Klotho的表达,并抑制NADPH氧化酶的表达,这可能是它们在高血压肾损害中的保护作用机制之一。

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