Losartan treating podocyte injury induced by Ang II via downregulation of TRPC6 in podocytes
Chi-Xianggeng, Hu-Bo, SY Yu, Yin-Lianghong, Mengyu Mengyu, Wang-Boxun, Yang-Jinsheng, Lin-Jiahui, Huang-Dexu, Chen-lanlan
Abstract
Chi-Xianggeng, Hu-Bo, SY Yu, Yin-Lianghong, Mengyu Mengyu, Wang-Boxun, Yang-Jinsheng, Lin-Jiahui, Huang-Dexu, Chen-lanlan
Abstract
OBJECTIVE: In this study, we investigated the molecule mechanisms of podocyte injury and proteinuria and the protective effects of losartan. METHODS: This study set up three groups: a control group; an Ang II group (Ang II 10(-6) mol/l, Sigma); and a losartan group (losartan 10(-6) mol/l, Sigma). We used RT-PCR assay to detect TRPC6 mRNA expression, and Western blot to detect TRPC6 protein expression. RESULTS: TRPC6 overexpression was the basic change of podocyte injury and proteinuria occurrence. Losartan can treat podocyte injury and proteinuria induced by Ang II via downregulation of TRPC6 in podocytes. CONCLUSION: These findings maybe provide an ideal drug target for the diagnosis and treatment of acquired glomerular diseases.
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OBJECTIVE: In this study, we investigated the molecule mechanisms of podocyte injury and proteinuria and the protective effects of losartan. METHODS: This study set up three groups: a control group; an Ang II group (Ang II 10(-6) mol/l, Sigma); and a losartan group (losartan 10(-6) mol/l, Sigma). We used RT-PCR assay to detect TRPC6 mRNA expression, and Western blot to detect TRPC6 protein expression. RESULTS: TRPC6 overexpression was the basic change of podocyte injury and proteinuria occurrence. Losartan can treat podocyte injury and proteinuria induced by Ang II via downregulation of TRPC6 in podocytes. CONCLUSION: These findings maybe provide an ideal drug target for the diagnosis and treatment of acquired glomerular diseases.
Key concepts: TRPC6, Podocyte, Losartan, Downregulation and upregulation, Proteinuria, Western blot, Angiotensin II, Nephrin