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Doxazosin attenuates renal matrix remodeling mediated by anti-α1-adrenergic receptor antibody in a rat model of diabetes mellitus

机译:多沙唑嗪可减轻糖尿病大鼠模型中抗α1-肾上腺素能受体抗体介导的肾基质重塑

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摘要

Diabetic nephropathy is a major complication of diabetes mellitus (DM). Recent studies suggest that immunological mechanisms have a key role in the pathogenesis of DM, therefore these mechanisms may be important targets for diabetes therapy. The present study evaluated the effects of anti-α1-adrenergic receptor antibody (α1-R Ab) mediation and doxazosin treatment in a rat model of DM. It was observed that levels of 24-h urinary protein, serum creatinine and transforming growth factor-β1 in DM were significantly increased after α1-R Ab mediation (all P<0.05). In addition, electron microscopy identified severe damage in the renal tissue microstructures of DM rats following α1-R Ab mediation, while only mild abnormalities were observed in that of healthy rats mediated with α1-R Ab and of untreated DM rats. No marked abnormalities were observed in the renal tissue of healthy blank controls. Furthermore, in DM rats treated with α1-R Ab mediation + doxazosin intervention, the expression of TGF-β1 significantly decreased, and renal functions and renal matrix remodeling were significantly improved, relative to untreated DM controls (P<0.01). These results suggest that α1-R Ab may be involved in renal matrix remodeling during DM, and that kidney protection during DM may be achieved through treatment with corresponding receptor antagonists.
机译:糖尿病肾病是糖尿病(DM)的主要并发症。最近的研究表明,免疫机制在DM的发病机理中具有关键作用,因此这些机制可能是糖尿病治疗的重要靶标。本研究评估了抗-α1-肾上腺素能受体抗体(α1-RAb)介导和多沙唑嗪治疗DM大鼠的作用。观察到在α1-RAb介导后,DM中24小时尿蛋白,血清肌酐和转化生长因子-β1的水平显着升高(所有P <0.05)。此外,电子显微镜检查发现在α1-RAb介导后,DM大鼠的肾脏组织微观结构受到严重损害,而在以α1-RAb介导的健康大鼠和未治疗的DM大鼠中,仅观察到轻度异常。在健康空白对照组的肾脏组织中未观察到明显的异常。此外,与未经治疗的DM对照组相比,在接受α1-RAb介导+多沙唑嗪干预的DM大鼠中,TGF-β1的表达显着降低,肾功能和肾基质重塑明显改善(P <0.01)。这些结果表明,α1-RAb可能参与DM期间的肾基质重塑,而DM期间的肾脏保护可通过用相应的受体拮抗剂治疗来实现。

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