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首页> 外文期刊>The American Journal of the Medical Sciences >Finasteride Reduces Microvessel Density and Expression of Vascular Endothelial Growth Factor in Renal Tissue of Diabetic Rats
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Finasteride Reduces Microvessel Density and Expression of Vascular Endothelial Growth Factor in Renal Tissue of Diabetic Rats

机译:非那雄胺降低糖尿病大鼠肾脏组织中微血管的密度和血管内皮生长因子的表达

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Background: Vascular endothelial growth factor (VEGF) plays a critical role in the pathogenesis of diabetic microvascular complications. Finasteride has been confirmed to decrease VEGF expression in prostate and prostatic suburethral tissue resulting in limiting hematuria from human benign prostatic hyperplasia. The purpose of this study was to evaluate the effects of finasteride on microvessel density (MVD), VEGF protein and mRNA expressions in the renal tissue of diabetic rats. Methods: Diabetic rats induced by streptozotocin were intragastrically given finasteride at 30 mg/kg body weight once a day for 4 weeks. Histomorphologic changes in kidney were observed under light microscope. Immunohistochemistry for CD34 and VEGF on kidney sections was performed to assess MVD and VEGF protein expression in glomeruli of rats, respectively. The VEGF mRNA expression in the renal tissue was examined using reverse transcription polymerase chain reaction analysis. Results: The glomerular tuft area, glomerular volume, MVD, VEGF protein expression in glomeruli and VEGF mRNA expression in the renal cortex tissue were significantly increased in diabetic rats and finasteride-treated rats when compared with controls (P < 0.01, P < 0.05). When compared with diabetic rats, the glomerular tuft area, glomerular volume, MVD, VEGF protein expression in glomeruli and VEGF mRNA expression in the renal cortex tissue of finasteride-treated rats were significantly decreased (P < 0.05, P < 0.01). Conclusions: Finasteride reduces the VEGF expression and decreases the MVD in the renal tissue of diabetic rats, suggesting the therapeutic potential of finasteride on diabetic microvascular complications.
机译:背景:血管内皮生长因子(VEGF)在糖尿病微血管并发症的发病机理中起着至关重要的作用。非那雄胺已被证实能减少前列腺和前列腺下尿道组织中的VEGF表达,从而限制人良性前列腺增生引起的血尿。这项研究的目的是评估非那雄胺对糖尿病大鼠肾脏组织中微血管密度(MVD),VEGF蛋白和mRNA表达的影响。方法:链脲佐菌素诱导的糖尿病大鼠每天一次胃内给予非那雄胺30 mg / kg体重,持续4周。在光学显微镜下观察肾脏的组织形态学变化。对肾脏切片进行CD34和VEGF的免疫组织化学分析,分别评估大鼠肾小球中的MVD和VEGF蛋白表达。使用逆转录聚合酶链反应分析检查肾组织中的VEGF mRNA表达。结果:与对照组相比,糖尿病大鼠和非那雄胺治疗组大鼠的肾小球簇面积,肾小球体积,MVD,肾小球中的VEGF蛋白表达和肾皮质组织中的VEGF mRNA表达均显着升高(P <0.01,P <0.05)。 。与糖尿病大鼠相比,非那雄胺治疗组大鼠的肾小球簇面积,肾小球体积,MVD,肾小球中的VEGF蛋白表达和肾皮质组织中的VEGF mRNA表达显着降低(P <0.05,P <0.01)。结论:非那雄胺可降低糖尿病大鼠肾脏组织中VEGF的表达并降低MVD,提示非那雄胺对糖尿病微血管并发症具有治疗潜力。

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