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首页> 外文期刊>Journal of the American Society of Nephrology: JASN >Vascular endothelial growth factor165 resolves glomerular inflammation and accelerates glomerular capillary repair in rat anti-glomerular basement membrane glomerulonephritis.
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Vascular endothelial growth factor165 resolves glomerular inflammation and accelerates glomerular capillary repair in rat anti-glomerular basement membrane glomerulonephritis.

机译:血管内皮生长因子165可解决大鼠抗肾小球基底膜肾小球肾炎的肾小球炎症并加速肾小球毛细血管修复。

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Vascular endothelial growth factor (VEGF) is essential for maintenance of the glomerular capillary network. The present study investigated the effects of VEGF in rats with progressive crescentic glomerulonephritis (GN). Necrotizing and crescentic GN was induced in rats by injection of anti-rat glomerular basement membrane (GBM) antibody. The alterations of glomerular capillaries and glomerular VEGF expression were assessed. In addition, the effects of continuous VEGF165 administration (10 microg/100 g per d) on glomerular capillaries, glomerular inflammation, and the course of crescentic GN were examined. The appropriate timing of VEGF administration in progressive GN also was evaluated. In anti-GBM GN, necrotizing and crescentic glomerular lesions occurred by day 7, and newly formed necrotizing lesions reoccurred by week 3. Expression of VEGF was markedly reduced in necrotizing and crescentic lesions. Capillary repair was impaired after capillary destruction in necrotizing and crescentic glomeruli, which rapidly progressed to sclerotic glomeruli with chronic renal failure. In contrast, in the rats that received VEGF165 administration from day 7, the necrotizing and crescentic lesions recovered and renal function significantly improved in week 4. This was evident by proliferating endothelial cells and glomerular capillary repair. In addition, VEGF administration decreased intercellular adhesion molecule-1 and monocyte chemoattractant protein-1 expression in glomeruli (particularly on endothelial cells), reduced glomerular infiltrating CD8-postive and ED-1-positive cells, and inhibited the newly formed necrotizing lesions. VEGF administration was apparently effective against both the inflammatory and necrotizing glomerular lesions. These results suggest that VEGF administration resolves glomerular inflammation and accelerates glomerular recovery in the progressive necrotizing and crescentic GN. The therapeutic application of VEGF may be clinically useful for severe GN accompanied by extensive glomerular inflammation and endothelial injury.
机译:血管内皮生长因子(VEGF)对于维持肾小球毛细血管网络至关重要。本研究调查了VEGF在进行性新月形肾小球肾炎(GN)大鼠中的作用。通过注射抗大鼠肾小球基底膜(GBM)抗体在大鼠中诱发坏死性新月形GN。评估肾小球毛细血管和肾小球VEGF表达的变化。此外,检查了连续给予VEGF165(10微克/ 100克/天)对肾小球毛细血管,肾小球发炎和新月形GN病程的影响。还评估了进行性GN中VEGF给药的适当时机。在抗GBM GN中,坏死和新月型肾小球病变发生在第7天,新形成的坏死性肾小球病变在第3周时再次出现。在坏死和新月形病变中,VEGF的表达显着降低。坏死性和新月形肾小球毛细血管破坏后,毛细血管修复受损,后者迅速发展为硬化性肾小球,伴有慢性肾功能衰竭。相反,在从第7天开始接受VEGF165给药的大鼠中,坏死和新月形病变得以恢复,并且肾功能在第4周显着改善。这可以通过内皮细胞的增殖和肾小球毛细血管修复来体现。此外,VEGF的给药降低了肾小球(尤其是内皮细胞)中细胞间粘附分子1和单核细胞趋化蛋白1的表达,减少了肾小球浸润性CD8阳性和ED-1阳性细胞,并抑制了新形成的坏死性病变。显然,VEGF的给药对炎性和坏死性肾小球病变均有效。这些结果表明,在进行性坏死性和新月形GN中,VEGF的给药可解决肾小球炎症并加速肾小球的恢复。 VEGF的治疗应用对于严重的GN伴有广泛的肾小球炎症和内皮损伤可能在临床上有用。

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