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首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Klotho Gene Delivery Prevents the Progression of Spontaneous Hypertension and Renal Damage
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Klotho Gene Delivery Prevents the Progression of Spontaneous Hypertension and Renal Damage

机译:Klotho基因递送可预防自发性高血压和肾损害的进展

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Klotho is a recently discovered antiaging gene. The objective of this study was to test the hypothesis that klotho gene delivery attenuates the progression of spontaneous hypertension and renal damage in spontaneous hypertensive rats (SHRs). An adeno-associated virus (AAV) carrying mouse klotho full-length cDNA (AAV.mKL) was constructed for in vivo expression of klotho. Four groups of male SHRs and 1 group of sex- and age-matched Wistar-Kyoto rats (5 rats per group) were used. Blood pressure was measured twice in all of the animals before gene delivery. Four groups of SHRs received an IV injection of AAV.mKL, AAV.LacZ, AAV.GFP, and PBS, respectively. The Wistar-Kyoto group received PBS and served as a control. AAV.mKL stopped the further increase in blood pressure in SHRs, whereas blood pressures continued to increase in other SHR groups. One single dose of AAV.mKL prevented the progression of spontaneous hypertension for at least 12 weeks (length of the study). Klotho expression and production were suppressed in SHRs, which were reverted by AAV.mKL. AAV.mKL increased plasma interleukin 10 levels but decreased Nox2 expression, NADPH oxidase activity, and superoxide production in kidneys and aortas in SHRs. AAV.mKL abolished renal tubular atrophy and dilation, tubular deposition of proteinaceous material, glomerular collapse, and collagen deposition seen in SHRs, indicating that klotho gene delivery attenuated renal damage. Therefore, the suppressed klotho expression may play a role in the progression of spontaneous hypertension and renal damage in SHRs. AAV delivery of klotho may offer a new approach for the long-term control of hypertension and for renoprotection.
机译:Klotho是最近发现的抗衰老基因。这项研究的目的是检验以下假设:klotho基因传递减弱了自发性高血压大鼠(SHRs)的自发性高血压和肾脏损害的进程。构建携带小鼠klotho全长cDNA(AAV.mKL)的腺相关病毒(AAV),用于体内表达klotho。使用四组雄性SHR和一组性别和年龄相匹配的Wistar-Kyoto大鼠(每组5只大鼠)。在基因递送之前,在所有动物中测量两次血压。四组SHR分别接受了AAV.mKL,AAV.LacZ,AAV.GFP和PBS的静脉注射。 Wistar-Kyoto组接受PBS并作为对照。 AAV.mKL阻止了SHR中血压的进一步升高,而其他SHR组中的血压继续升高。一剂AAV.mKL可以预防自发性高血压至少持续12周(研究持续时间)。在SHR中,Klotho的表达和产生受到抑制,而AHR.mKL恢复了SHR。 AAV.mKL增加了血浆白细胞介素10水平,但降低了SHRs肾脏和主动脉的Nox2表达,NADPH氧化酶活性和超氧化物生成。 AAV.mKL消除了SHR中出现的肾小管萎缩和扩张,蛋白质物质的小管沉积,肾小球塌陷和胶原蛋白沉积,表明klotho基因的传递减弱了肾脏损害。因此,抑制的klotho表达可能在SHRs的自发性高血压和肾脏损害的进展中起作用。 AAV递送克洛索可能为长期控制高血压和保护肾脏提供新的方法。

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