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Long-term renal sympathetic denervation ameliorates renal fibrosis and delays the onset of hypertension in spontaneously hypertensive rats

机译:长期肾交感神经去神经改善自发性高血压大鼠的肾纤维化并延迟高血压的发作

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This study was designed to explore the effects of long-term renal denervation (RDN) on blood pressure and renal function in spontaneously hypertensive rats (SHR). RDN was performed in bilateral renal arteries with 10% phenol in absolute ethanol in SHR and Wistar-Kyoto rats (WKY) at 13 weeks. Age-matched SHR and WKY served as controls. Blood pressure was measured. Plasma, urine and kidneys were collected 8 months after the RDN operation. Plasma renin activity (PRA), aldosterone levels, reactive oxidative stress, renal function and structural remodeling were assessed. RDN-treated SHR demonstrated a lower spontaneous rise in systolic blood pressure than rats in the SHR-Sham group (P < 0.01, at 20, 27, 34 and 41 weeks), except at 48 weeks (198.2 ± 12.9 vs 209.4 ± 11.9 mmHg, P = 0.145). WKY were not affected by RDN. Renal tissue norepinephrine was decreased by RDN in both SHR and WKY. Plasma PRA activity, aldosterone levels, and NAD(P)H oxidase activity were reduced by the RDN in SHR. Plasma eNOS and NO were increased by RDN only in SHR. The renal nerve was destroyed by RDN with no regeneration after 8 months. The progression of renal dysfunction associated with urinary protein excretion, glomerular sclerosis, and tubulointerstitial fibrosis was attenuated by RDN only in SHR through downregulation of the ACE/Ang II/AT1R axis and upregulation of the ACE2/Ang-(1-7)/MasR axis in the kidney. Thus, RDN delays the onset of hypertension and ameliorates glomerular sclerosis and tubulointerstitial fibrosis in SHR.
机译:本研究旨在探讨长期肾脏去神经支配(RDN)对自发性高血压大鼠(SHR)血压和肾功能的影响。在第13周,在SHR和Wistar-Kyoto大鼠(WKY)中,在双侧肾动脉中用10%苯酚的无水乙醇溶液进行RDN。年龄匹配的SHR和WKY作为对照。测量血压。 RDN手术后8个月收集血浆,尿液和肾脏。评估血浆肾素活性(PRA),醛固酮水平,反应性氧化应激,肾功能和结构重塑。经RDN治疗的SHR的收缩压自发升高低于SHR-Sham组的大鼠(P <0.01,在20、27、34和41周时),但在48周时(198.2±12.9 vs 209.4±11.9 mmHg) ,P = 0.145)。 WKY不受RDN的影响。 RDN在SHR和WKY中均降低了肾组织去甲肾上腺素。 SHR中的RDN降低了血浆PRA活性,醛固酮水平和NAD(P)H氧化酶活性。 RDN仅在SHR中使血浆eNOS和NO增加。 8个月后RDN破坏了肾神经,没有再生。 RDN仅在SHR中通过下调ACE / Ang II / AT1R轴和上调ACE2 / Ang-(1-7)/ MasR上调,与尿蛋白排泄,肾小球硬化和肾小管间质纤维化相关的肾功能不全的进展得以缓解。肾中轴。因此,RDN可延缓高血压的发作,并改善SHR中的肾小球硬化和肾小管间质纤维化。

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