藿雪解毒汤能抑制巨噬细胞分泌的血管内皮生长因子-a对血管生成的影响,减轻单侧输尿管梗阻大鼠对侧肾脏的肾纤维化。

Gao Xiaomeng, Qiang Panpan, Chang Jingyue, Fan Lili, Yang Fan, X U Qingyou
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引用次数: 0

摘要

目的:阐明藿香正气水调节单侧输尿管梗阻(UUO)大鼠对侧肾血管生成的机制及其减轻肾脏纤维化的作用机制:雄性Wistar大鼠随机分为4组:假组、UUO组(左输尿管结扎180 d)、UUO加依普利酮(EPL)组和UUO加HJHR组。口服药物 180 天后,收集血液和对侧肾脏进行分析。检测血管生成和纤维化相关指标:结果:HJHR和EPL改善了对侧肾脏的结构损伤和肾间质纤维化,降低了α-平滑肌肌动蛋白(α-SMA)、波形蛋白和胶原蛋白I的蛋白表达水平。此外,HJHR 和 EPL 还能通过下调血管内皮生长因子-A 的产生来显著降低 CD34 和 CD105 的表达,从而抑制血管生成。最后,HJHR 组和 EPL 组 CD34、CD105 和 α-SMA 的共表达减少,表明内皮细胞向间质转化受到抑制:这些研究结果证实,HJHR 可通过抑制 VEGFA 诱导的血管生成缓解对侧肾脏纤维化,鼓励使用 HJHR 治疗肾间质纤维化,并为 CKD 患者的临床治疗提供理论依据。
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Huoxue Jiedu Huayu recipe inhibits macrophage-secreted vascular endothelial growth factor-a on angiogenesis and alleviates renal fibrosis in the contralateral kidneys of unilateral ureteral obstruction rats.

OBJECTIVE:To elucidate the mechanism by which Huoxue Jiedu Huayu recipe (, HJHR) regulates angiogenesis in the contralateral kidney of unilateral ureteral obstruction (UUO) rats and the mechanism by which it reduces of renal fibrosis.

Methods: Male Wistar rats were randomly divided into 4 groups: the sham group, UUO group (180 d of left ureter ligation), UUO plus eplerenone (EPL) group, and UUO plus HJHR group. After 180 d of oral drug administration, blood and contralateral kidneys were collected for analysis. Angiogenesis- and fibrosis-related indexes were detected.

Results: HJHR and EPL improved structural damage and renal interstitial fibrosis in the contralateral kidney and reduced the protein expression levels of α-smooth muscle actin (α-SMA), vimentin and collagen I. Moreover, these treatments could reduce the expression of vascular endothelial growth factor-A (VEGFA) by inhibiting the infiltration of macrophages. Furthermore, HJHR and EPL significantly reduced the expression of CD34 and CD105 by downregulating VEGFA production, which inhibited angiogenesis. Finally, the coexpressions of CD34, CD105 and α-SMA were decreased in the HJHR and EPL groups, indicating that endothelial-to-mesenchymal transition was inhibited.

Conclusions: These findings confirm that HJHR alleviates contralateral renal fibrosis by inhibiting VEGFA-induced angiogenesis, encourage the use of HJHR against renal interstitial fibrosis and provide a theoretical basis for the clinical management of patients with CKD.

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