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Effect of Danggui-Shaoyao-San-Containing Serum on the Renal Tubular Epithelial-Mesenchymal Transition of Diabetic Nephropathy
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Objectives:
To investigate the effect of Danggui-Shaoyao-San (DSS)-containing serum on
the renal tubular Epithelial-Mesenchymal Transition (EMT) of Diabetic Nephropathy (DN) in high
glucose- induced HK-2 cells and its mechanism.
Methods:
20 rats were randomly divided into four groups: blank control group, DSS low dose group
(DSS-L), DSS middle dose group (DSS-M), and DSS high dose group (DSS-H). DSS was administrated
to the corresponding group (7g/kg/d, 14g/kg/d and 21g/kg/d) for 7 consecutive days, and the same
volume of saline was given to the blank control group by gavage. The rat drug-containing serum was
successfully prepared. HK-2 cells were divided into five groups: blank control group, model group,
DSS-L, DSS-M, DSS-H, according to the corresponding drug and dose of each treatment group. Protein
and mRNA levels of Jagged1, Notch1, Hes5, Notch Intracellular Domain (NICD), E-cadherin, alpha-
Smooth Muscle Actin (α-SMA) and vimentin at 24h, 48h and 72h were detected by Western Blot
and RT-qPCR.
Results:
The protein and mRNA levels of Jagged1, Notch1, Hes5, NICD, α-SMA and vimentin in the
treatment groups were remarkably decreased compared with the model group (P<0.05), and the protein
and mRNA levels of E-cadherin were notably increased (P<0.05) by Western Blot and RT-qPCR.
Conclusion:
Our results demonstrated that DSS could prevent DN by ameliorating renal tubular EMT
through inhibition of the Notch signaling pathway.
Bentham Science Publishers Ltd.
Title: Effect of Danggui-Shaoyao-San-Containing Serum on the Renal Tubular Epithelial-Mesenchymal Transition of Diabetic Nephropathy
Description:
Objectives:
To investigate the effect of Danggui-Shaoyao-San (DSS)-containing serum on
the renal tubular Epithelial-Mesenchymal Transition (EMT) of Diabetic Nephropathy (DN) in high
glucose- induced HK-2 cells and its mechanism.
Methods:
20 rats were randomly divided into four groups: blank control group, DSS low dose group
(DSS-L), DSS middle dose group (DSS-M), and DSS high dose group (DSS-H).
DSS was administrated
to the corresponding group (7g/kg/d, 14g/kg/d and 21g/kg/d) for 7 consecutive days, and the same
volume of saline was given to the blank control group by gavage.
The rat drug-containing serum was
successfully prepared.
HK-2 cells were divided into five groups: blank control group, model group,
DSS-L, DSS-M, DSS-H, according to the corresponding drug and dose of each treatment group.
Protein
and mRNA levels of Jagged1, Notch1, Hes5, Notch Intracellular Domain (NICD), E-cadherin, alpha-
Smooth Muscle Actin (α-SMA) and vimentin at 24h, 48h and 72h were detected by Western Blot
and RT-qPCR.
Results:
The protein and mRNA levels of Jagged1, Notch1, Hes5, NICD, α-SMA and vimentin in the
treatment groups were remarkably decreased compared with the model group (P<0.
05), and the protein
and mRNA levels of E-cadherin were notably increased (P<0.
05) by Western Blot and RT-qPCR.
Conclusion:
Our results demonstrated that DSS could prevent DN by ameliorating renal tubular EMT
through inhibition of the Notch signaling pathway.
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