Inhibitory effect of oxymatrine on high glucose-induced rat renal tubular epithelial-mesenchymal transition
Liu Li-ron
Abstract
Liu Li-ron
Abstract
AIM: To investigate the inhibitory effect of oxymatrine( OM) on high glucose-induced rat renal tubular epithelial-mesenchymal transition( EMT). METHODS: The rat renal tubular epithelial NRK52E cells were cultured in vitro. The cells were divided into control group,high glucose group,high glucose + different concentrations of OM groups and high glucose + 0. 50 g / L OM dynamic observation group. The expression of TGF-β 1,Smad7,α-SMA and E-cadherin at mRNA and protein levels was detected by real-time PCR and Western blotting. The viability of NRK52E cells was determined by MTT assay. RESULTS:( 1) Compared with control group,the expression of TGF-β 1 and α-SMA at mRNA and protein levels in high glucose group gradually increased,and Smad7 protein and E-cadherin mRNA and protein gradually reduced,but the mRNA expression of Smad7 gradually increased.( 2) Compared with high glucose group,as increases in OM doses,the expression of TGF-β 1 and α-SMA at mRNA and protein levels in high glucose + different concentrations of OM groups gradually reduced,and Smad7 protein and E-cadherin mRNA and protein gradually increased,but the mRNA expression of Smad7 had no significant change.( 3) Compared with high glucose group,the expression of TGF-β 1 and αSMA at mRNA and protein levels was significantly reduced,the expression of E-cadherin at mRNA and protein levels significantly increased,and the protein expression of Smad7 significantly increased,but the mRNA expression of Smad7 had no significant change in high glucose + 0. 50 g / L OM dynamic observation group. CONCLUSION: In NRK52E cells, oxymatrine inhibits high glucose induced EMT by down-regulating TGF-β 1 and up-regulating Smad7,thus preventing the fibrosis effect of TGF-β 1 / Smads signaling.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
AIM: To investigate the inhibitory effect of oxymatrine( OM) on high glucose-induced rat renal tubular epithelial-mesenchymal transition( EMT). METHODS: The rat renal tubular epithelial NRK52E cells were cultured in vitro. The cells were divided into control group,high glucose group,high glucose + different concentrations of OM groups and high glucose + 0. 50 g / L OM dynamic observation group. The expression of TGF-β 1,Smad7,α-SMA and E-cadherin at mRNA and protein levels was detected by real-time PCR and Western blotting. The viability of NRK52E cells was determined by MTT assay. RESULTS:( 1) Compared with control group,the expression of TGF-β 1 and α-SMA at mRNA and protein levels in high glucose group gradually increased,and Smad7 protein and E-cadherin mRNA and protein gradually reduced,but the mRNA expression of Smad7 gradually increased.( 2) Compared with high glucose group,as increases in OM doses,the expression of TGF-β 1 and α-SMA at mRNA and protein levels in high glucose + different concentrations of OM groups gradually reduced,and Smad7 protein and E-cadherin mRNA and protein gradually increased,but the mRNA expression of Smad7 had no significant change.( 3) Compared with high glucose group,the expression of TGF-β 1 and αSMA at mRNA and protein levels was significantly reduced,the expression of E-cadherin at mRNA and protein levels significantly increased,and the protein expression of Smad7 significantly increased,but the mRNA expression of Smad7 had no significant change in high glucose + 0. 50 g / L OM dynamic observation group. CONCLUSION: In NRK52E cells, oxymatrine inhibits high glucose induced EMT by down-regulating TGF-β 1 and up-regulating Smad7,thus preventing the fibrosis effect of TGF-β 1 / Smads signaling.
Key concepts: Messenger RNA, Oxymatrine, Epithelial–mesenchymal transition, Internal medicine, Endocrinology, Chemistry, Blot, Gene expression