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Inhibitory Potential of Shen-Shuai-Ling Formulation on Renal Interstitial Fibrosis via Upregulation of PLZF

BACKGROUND: Renal interstitial fibrosis (RIF) is an important cause of kidney disease, which seriously affects people's health. As a traditional Chinese medicine, Shen-Shuai-Ling Formulation (SSLF) has obvious kidney function. However, the therapeutic effect of SSLF on RIF and its molecular mec...

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Autores principales: Song, Na, Tu, Haitao, Li, Ying, Xiong, Weijian, Zhang, Ling, Liu, Hong, Ding, Weisen, Long, Mei, Ren, Dewei, Zhong, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991406/
https://www.ncbi.nlm.nih.gov/pubmed/35399631
http://dx.doi.org/10.1155/2022/5967804
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author Song, Na
Tu, Haitao
Li, Ying
Xiong, Weijian
Zhang, Ling
Liu, Hong
Ding, Weisen
Long, Mei
Ren, Dewei
Zhong, Jin
author_facet Song, Na
Tu, Haitao
Li, Ying
Xiong, Weijian
Zhang, Ling
Liu, Hong
Ding, Weisen
Long, Mei
Ren, Dewei
Zhong, Jin
author_sort Song, Na
collection PubMed
description BACKGROUND: Renal interstitial fibrosis (RIF) is an important cause of kidney disease, which seriously affects people's health. As a traditional Chinese medicine, Shen-Shuai-Ling Formulation (SSLF) has obvious kidney function. However, the therapeutic effect of SSLF on RIF and its molecular mechanism are still unclear. METHODS: First, the potential targets and pathways of SSLF for RIF were predicted by network pharmacology, and then, the binding of luteolin and target protein to SSLF was verified by molecular docking and Co-IP experiments. Finally, the effects of SSLF and luteolin on PLZF and (Pro) renin receptor (PRR) were verified by western blot and qPCR experiments. Angiotensin (Ang)-1, Ang-2, and transforming growth factor-β (TGF-β) were the indexes of renal interstitial fibrosis. RESULTS: Through the drug-active component-target network diagram, we found that luteolin has the most connections, and promyelocytic leukemia zinc finger (PLZF) is the target protein. GO analysis and KEGG pathway analysis of targets were performed using Cytoscape ClueGO. Molecular docking experiments and Co-IP are used to prove that luteolin and PLZF can be combined. Western blot and qPCR results showed that both SSLF and luteolin significantly upregulated the expression of PLZF and decreased the levels of PRR, Ang-1, Ang-2, and TGF-β. The overexpression of PLZF decreased the expression of PRR, the knockdown of PLZF increased the expression of PRR, and the overexpression of PRR decreased the expression of Ang-1, Ang-2, and TGF-β. CONCLUSIONS: SSLF inhibits PRR and renal interstitial fibers by the upregulation of PLZF levels.
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spelling pubmed-89914062022-04-09 Inhibitory Potential of Shen-Shuai-Ling Formulation on Renal Interstitial Fibrosis via Upregulation of PLZF Song, Na Tu, Haitao Li, Ying Xiong, Weijian Zhang, Ling Liu, Hong Ding, Weisen Long, Mei Ren, Dewei Zhong, Jin Evid Based Complement Alternat Med Research Article BACKGROUND: Renal interstitial fibrosis (RIF) is an important cause of kidney disease, which seriously affects people's health. As a traditional Chinese medicine, Shen-Shuai-Ling Formulation (SSLF) has obvious kidney function. However, the therapeutic effect of SSLF on RIF and its molecular mechanism are still unclear. METHODS: First, the potential targets and pathways of SSLF for RIF were predicted by network pharmacology, and then, the binding of luteolin and target protein to SSLF was verified by molecular docking and Co-IP experiments. Finally, the effects of SSLF and luteolin on PLZF and (Pro) renin receptor (PRR) were verified by western blot and qPCR experiments. Angiotensin (Ang)-1, Ang-2, and transforming growth factor-β (TGF-β) were the indexes of renal interstitial fibrosis. RESULTS: Through the drug-active component-target network diagram, we found that luteolin has the most connections, and promyelocytic leukemia zinc finger (PLZF) is the target protein. GO analysis and KEGG pathway analysis of targets were performed using Cytoscape ClueGO. Molecular docking experiments and Co-IP are used to prove that luteolin and PLZF can be combined. Western blot and qPCR results showed that both SSLF and luteolin significantly upregulated the expression of PLZF and decreased the levels of PRR, Ang-1, Ang-2, and TGF-β. The overexpression of PLZF decreased the expression of PRR, the knockdown of PLZF increased the expression of PRR, and the overexpression of PRR decreased the expression of Ang-1, Ang-2, and TGF-β. CONCLUSIONS: SSLF inhibits PRR and renal interstitial fibers by the upregulation of PLZF levels. Hindawi 2022-03-31 /pmc/articles/PMC8991406/ /pubmed/35399631 http://dx.doi.org/10.1155/2022/5967804 Text en Copyright © 2022 Na Song et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Song, Na
Tu, Haitao
Li, Ying
Xiong, Weijian
Zhang, Ling
Liu, Hong
Ding, Weisen
Long, Mei
Ren, Dewei
Zhong, Jin
Inhibitory Potential of Shen-Shuai-Ling Formulation on Renal Interstitial Fibrosis via Upregulation of PLZF
title Inhibitory Potential of Shen-Shuai-Ling Formulation on Renal Interstitial Fibrosis via Upregulation of PLZF
title_full Inhibitory Potential of Shen-Shuai-Ling Formulation on Renal Interstitial Fibrosis via Upregulation of PLZF
title_fullStr Inhibitory Potential of Shen-Shuai-Ling Formulation on Renal Interstitial Fibrosis via Upregulation of PLZF
title_full_unstemmed Inhibitory Potential of Shen-Shuai-Ling Formulation on Renal Interstitial Fibrosis via Upregulation of PLZF
title_short Inhibitory Potential of Shen-Shuai-Ling Formulation on Renal Interstitial Fibrosis via Upregulation of PLZF
title_sort inhibitory potential of shen-shuai-ling formulation on renal interstitial fibrosis via upregulation of plzf
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991406/
https://www.ncbi.nlm.nih.gov/pubmed/35399631
http://dx.doi.org/10.1155/2022/5967804
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