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Vitamin D Deficiency Aggravates the Renal Features of Moderate Chronic Kidney Disease in 5/6 Nephrectomized Rats

机译:维生素D缺乏症加重5/6肾切除大鼠的中度慢性肾脏病的肾脏特征

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The pathogenesis of chronic kidney disease (CKD) involves a very complex interaction between hemodynamic and inflammatory processes, leading to glomerular/vascular sclerosis, and fibrosis formation with subsequent evolution to end-stage of renal disease. Despite efforts to minimize the progression of CKD, its incidence and prevalence continue to increase. Besides cardiovascular diseases and infections, several studies demonstrate that vitamin D status could be considered as a non-traditional risk factor for the progression of CKD. Therefore, we investigated the effects of vitamin D deficiency (VDD) in the course of moderate CKD in 5/6 nephrectomized rats (Nx). Adult male Wistar rats underwent Sham surgery or Nx and were subdivided into the following four groups: Sham, receiving standard diet (Sham); Sham VDD, receiving vitamin D-free diet (VDD); Nx, receiving standard diet (Nx); and VDD+Nx, receiving vitamin D-free diet (VDD+Nx). Sham or Nx surgeries were performed 30 days after standard or vitamin D-free diets administration. After validation of vitamin D depletion, we considered only Nx and VDD+Nx groups for the following studies. Sixty days after surgeries, VDD+Nx rats exhibited hypertension, a greater decline in renal function and plasma FGF-23 levels, renal hypertrophy, as well as higher plasma levels of PTH and aldosterone. In addition, those animals presented more significant chronic tubulointerstitial changes (cortical interstitial expansion/inflammation/fibrosis), higher expression of collagen IV, fibronectin and α-smooth muscle actin, and lower expressions of JG12 and M2 macrophages. Also, VDD+Nx rats had greater infiltration of inflammatory cells (M1 macrophages and T-cells). Such changes were accompanied by higher expression of TGF-β1 and angiotensinogen and decreased expression of VDR and Klotho protein. Our observations indicate that vitamin D deficiency impairs the renal function and worsens the renovascular and morphological changes, aggravating the features of moderate CKD in 5/6 nephrectomized rats.
机译:慢性肾脏病(CKD)的发病机制涉及血液动力学和炎症过程之间非常复杂的相互作用,从而导致肾小球/血管硬化和纤维化形成,随后发展为肾脏疾病的终末期。尽管努力使CKD的进展减至最小,但其发病率和患病率仍在增加。除心血管疾病和感染外,多项研究表明,维生素D的状态也可被视为CKD病情的非传统危险因素。因此,我们在5/6肾切除大鼠(Nx)中度CKD过程中研究了维生素D缺乏症(VDD)的影响。成年雄性Wistar大鼠接受了Sham手术或Nx手术,分为以下四组:Sham,接受标准饮食(Sham);假VDD,接受不含维生素D的饮食(VDD); Nx,接受标准饮食(Nx);和VDD + Nx,接受不含维生素D的饮食(VDD + Nx)。在标准或无维生素D饮食管理后30天进行假手术或Nx手术。在验证维生素D的消耗量后,我们在以下研究中仅考虑了Nx和VDD + Nx组。手术后六十天,VDD + Nx大鼠表现出高血压,肾脏功能和血浆FGF-23水平下降更大,肾脏肥大以及血浆PTH和醛固酮水平升高。此外,这些动物表现出更显着的慢性肾小管间质改变(皮质间质扩张/炎症/纤维化),胶原蛋白IV,纤连蛋白和α-平滑肌肌动蛋白的较高表达,以及JG12和M2巨噬细胞的较低表达。此外,VDD + Nx大鼠具有更大的炎症细胞(M1巨噬细胞和T细胞)浸润。这些变化伴随着TGF-β1和血管紧张素原的高表达以及VDR和Klotho蛋白的表达降低。我们的观察结果表明,维生素D缺乏会损害肾功能并恶化肾血管和形态学变化,从而加剧5/6肾切除大鼠的中度CKD的特征。

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