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Chrysophanol Inhibits the Progression of Diabetic Nephropathy via Inactivation of TGF-β Pathway
BACKGROUND: Diabetic nephropathy (DN) is a common form of diabetic complication which threatens the health of patients with diabetes. It has been reported that chrysophanol (CHR) can alleviate the progression of diabetes; however, the role of CHR in DN remains unclear. METHODS: To mimic DN in vitro,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678702/ https://www.ncbi.nlm.nih.gov/pubmed/33235436 http://dx.doi.org/10.2147/DDDT.S274191 |
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author | Guo, Chuan Wang, Yarong Piao, Yuanlin Rao, Xiangrong Yin, Dehai |
author_facet | Guo, Chuan Wang, Yarong Piao, Yuanlin Rao, Xiangrong Yin, Dehai |
author_sort | Guo, Chuan |
collection | PubMed |
description | BACKGROUND: Diabetic nephropathy (DN) is a common form of diabetic complication which threatens the health of patients with diabetes. It has been reported that chrysophanol (CHR) can alleviate the progression of diabetes; however, the role of CHR in DN remains unclear. METHODS: To mimic DN in vitro, human podocytes (AB8/13 cells) were treated with high glucose (HG). Meanwhile, Western blot was performed to detect protein expressions. CCK-8 assay was used to test cell viability and cell proliferation was detected by Ki-67 staining. In addition, flow cytometry was performed to investigate cell apoptosis and cycle and cell migration was tested by transwell assay. Moreover, in vivo model of DN was established to detect the effect of CHR on DN in vivo. RESULTS: HG-induced AB8/13 cell growth inhibition was significantly rescued by CHR. In addition, HG notably promoted the migration of AB8/13 cells, while this phenomenon was obviously reversed by CHR. Moreover, CHR inhibited the progression of DN via inactivation of TGF-β/EMT axis. Furthermore, CHR alleviated the symptom of DN in vivo. CONCLUSION: CHR significantly alleviated the progression of DN via inactivation of TGF-β/EMT signaling in vitro and in vivo. Our findings were helpful to uncover the mechanism by which CHR regulates DN, as well as inspire the development of novel therapy against DN. |
format | Online Article Text |
id | pubmed-7678702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-76787022020-11-23 Chrysophanol Inhibits the Progression of Diabetic Nephropathy via Inactivation of TGF-β Pathway Guo, Chuan Wang, Yarong Piao, Yuanlin Rao, Xiangrong Yin, Dehai Drug Des Devel Ther Original Research BACKGROUND: Diabetic nephropathy (DN) is a common form of diabetic complication which threatens the health of patients with diabetes. It has been reported that chrysophanol (CHR) can alleviate the progression of diabetes; however, the role of CHR in DN remains unclear. METHODS: To mimic DN in vitro, human podocytes (AB8/13 cells) were treated with high glucose (HG). Meanwhile, Western blot was performed to detect protein expressions. CCK-8 assay was used to test cell viability and cell proliferation was detected by Ki-67 staining. In addition, flow cytometry was performed to investigate cell apoptosis and cycle and cell migration was tested by transwell assay. Moreover, in vivo model of DN was established to detect the effect of CHR on DN in vivo. RESULTS: HG-induced AB8/13 cell growth inhibition was significantly rescued by CHR. In addition, HG notably promoted the migration of AB8/13 cells, while this phenomenon was obviously reversed by CHR. Moreover, CHR inhibited the progression of DN via inactivation of TGF-β/EMT axis. Furthermore, CHR alleviated the symptom of DN in vivo. CONCLUSION: CHR significantly alleviated the progression of DN via inactivation of TGF-β/EMT signaling in vitro and in vivo. Our findings were helpful to uncover the mechanism by which CHR regulates DN, as well as inspire the development of novel therapy against DN. Dove 2020-11-16 /pmc/articles/PMC7678702/ /pubmed/33235436 http://dx.doi.org/10.2147/DDDT.S274191 Text en © 2020 Guo et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Guo, Chuan Wang, Yarong Piao, Yuanlin Rao, Xiangrong Yin, Dehai Chrysophanol Inhibits the Progression of Diabetic Nephropathy via Inactivation of TGF-β Pathway |
title | Chrysophanol Inhibits the Progression of Diabetic Nephropathy via Inactivation of TGF-β Pathway |
title_full | Chrysophanol Inhibits the Progression of Diabetic Nephropathy via Inactivation of TGF-β Pathway |
title_fullStr | Chrysophanol Inhibits the Progression of Diabetic Nephropathy via Inactivation of TGF-β Pathway |
title_full_unstemmed | Chrysophanol Inhibits the Progression of Diabetic Nephropathy via Inactivation of TGF-β Pathway |
title_short | Chrysophanol Inhibits the Progression of Diabetic Nephropathy via Inactivation of TGF-β Pathway |
title_sort | chrysophanol inhibits the progression of diabetic nephropathy via inactivation of tgf-β pathway |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678702/ https://www.ncbi.nlm.nih.gov/pubmed/33235436 http://dx.doi.org/10.2147/DDDT.S274191 |
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