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Huangqi decoction ameliorates kidney injury in db/db mice by regulating the BMP/Smad signaling pathway
PURPOSE: This study aims to investigate the mechanism underlying the beneficial effects of Huangqi decoction (HQD) on Diabetic kidney disease (DKD) in diabetic db/db mice. METHODS: Eight-week-old male diabetic db/db mice were randomly divided into four groups: Model (1% CMC), HQD-L (0.12 g/kg), HQD-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294356/ https://www.ncbi.nlm.nih.gov/pubmed/37365530 http://dx.doi.org/10.1186/s12906-023-04029-1 |
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author | Chen, Ying Rui, Rong Wang, Li Wang, Hao Zhu, Bingbing Cao, Aili |
author_facet | Chen, Ying Rui, Rong Wang, Li Wang, Hao Zhu, Bingbing Cao, Aili |
author_sort | Chen, Ying |
collection | PubMed |
description | PURPOSE: This study aims to investigate the mechanism underlying the beneficial effects of Huangqi decoction (HQD) on Diabetic kidney disease (DKD) in diabetic db/db mice. METHODS: Eight-week-old male diabetic db/db mice were randomly divided into four groups: Model (1% CMC), HQD-L (0.12 g/kg), HQD-M (0.36 g/kg), and HQD-H (1.08 g/kg) groups. Non-diabetic db/m mice were served as the control group. These mice received HQD treatment for 8 weeks. After treatment, the kidney function, histopathology, micro-assay, and protein expression levels were assessed. RESULTS: HQD treatment improved the albumin/creatine ratio (ACR) and 24 h urinary albumin excretion, prevented the pathological phenotypes of increased glomerular volume, widened mesangial areas, the of mesangial matrix proliferation, foot process effacement, decreased nephrin expression and reduced number of podocytes. Expression profiling analysis revealed global transcriptional changes that predicted related functions, diseases and pathways. HQD treatment activated protein expressions of BMP2, BMP7, BMPR2, and active-Rap1, while inhibiting Smad1 and phospho-ERK. In addition, HQD was associated with improvements in lipid deposition in the kidneys of db/db mice. CONCLUSION: HQD ameliorated the progression of DKD in db/db mice by regulating BMP transcription and downstream targets, inhibiting the phosphorylation of ERK and the expression of Smad1, promoting Rap1 binding to GTP, and regulating the lipid metabolism. These findings provide a potential therapeutic approach for treating DKD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-023-04029-1. |
format | Online Article Text |
id | pubmed-10294356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102943562023-06-28 Huangqi decoction ameliorates kidney injury in db/db mice by regulating the BMP/Smad signaling pathway Chen, Ying Rui, Rong Wang, Li Wang, Hao Zhu, Bingbing Cao, Aili BMC Complement Med Ther Research PURPOSE: This study aims to investigate the mechanism underlying the beneficial effects of Huangqi decoction (HQD) on Diabetic kidney disease (DKD) in diabetic db/db mice. METHODS: Eight-week-old male diabetic db/db mice were randomly divided into four groups: Model (1% CMC), HQD-L (0.12 g/kg), HQD-M (0.36 g/kg), and HQD-H (1.08 g/kg) groups. Non-diabetic db/m mice were served as the control group. These mice received HQD treatment for 8 weeks. After treatment, the kidney function, histopathology, micro-assay, and protein expression levels were assessed. RESULTS: HQD treatment improved the albumin/creatine ratio (ACR) and 24 h urinary albumin excretion, prevented the pathological phenotypes of increased glomerular volume, widened mesangial areas, the of mesangial matrix proliferation, foot process effacement, decreased nephrin expression and reduced number of podocytes. Expression profiling analysis revealed global transcriptional changes that predicted related functions, diseases and pathways. HQD treatment activated protein expressions of BMP2, BMP7, BMPR2, and active-Rap1, while inhibiting Smad1 and phospho-ERK. In addition, HQD was associated with improvements in lipid deposition in the kidneys of db/db mice. CONCLUSION: HQD ameliorated the progression of DKD in db/db mice by regulating BMP transcription and downstream targets, inhibiting the phosphorylation of ERK and the expression of Smad1, promoting Rap1 binding to GTP, and regulating the lipid metabolism. These findings provide a potential therapeutic approach for treating DKD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-023-04029-1. BioMed Central 2023-06-26 /pmc/articles/PMC10294356/ /pubmed/37365530 http://dx.doi.org/10.1186/s12906-023-04029-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Chen, Ying Rui, Rong Wang, Li Wang, Hao Zhu, Bingbing Cao, Aili Huangqi decoction ameliorates kidney injury in db/db mice by regulating the BMP/Smad signaling pathway |
title | Huangqi decoction ameliorates kidney injury in db/db mice by regulating the BMP/Smad signaling pathway |
title_full | Huangqi decoction ameliorates kidney injury in db/db mice by regulating the BMP/Smad signaling pathway |
title_fullStr | Huangqi decoction ameliorates kidney injury in db/db mice by regulating the BMP/Smad signaling pathway |
title_full_unstemmed | Huangqi decoction ameliorates kidney injury in db/db mice by regulating the BMP/Smad signaling pathway |
title_short | Huangqi decoction ameliorates kidney injury in db/db mice by regulating the BMP/Smad signaling pathway |
title_sort | huangqi decoction ameliorates kidney injury in db/db mice by regulating the bmp/smad signaling pathway |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294356/ https://www.ncbi.nlm.nih.gov/pubmed/37365530 http://dx.doi.org/10.1186/s12906-023-04029-1 |
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