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Exploring the pharmacological mechanism of Shengjing capsule on male infertility by a network pharmacology approach
BACKGROUND: Shengjing capsule (SJC) is a traditional Chinese medicine (TCM) and has gained widespread clinical application for the treatment of male infertility (MI). However, the pharmacological mechanism of SJC against MI remains vague to date. METHOD: The active ingredients of SJC and their targe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675225/ https://www.ncbi.nlm.nih.gov/pubmed/36401273 http://dx.doi.org/10.1186/s12906-022-03774-z |
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author | Wang, Ming Wang, Qi Jiang, Hui Du, Yongqiang Zhang, Xiansheng |
author_facet | Wang, Ming Wang, Qi Jiang, Hui Du, Yongqiang Zhang, Xiansheng |
author_sort | Wang, Ming |
collection | PubMed |
description | BACKGROUND: Shengjing capsule (SJC) is a traditional Chinese medicine (TCM) and has gained widespread clinical application for the treatment of male infertility (MI). However, the pharmacological mechanism of SJC against MI remains vague to date. METHOD: The active ingredients of SJC and their targets were identified from the database, and MI-related genes were retrieved from several databases. Protein–protein interaction (PPI) data were obtained to construct the PPI networks. The candidate targets of SJC against MI were identified through topological analysis of the PPI network. Functional enrichment analysis of candidate targets was performed, and the key target genes were identified from the gene-pathway network. RESULTS: We identified 154 active ingredients and 314 human targets of SJC, as well as 564 MI-related genes. Eight pharmacological network diagrams illustrating the interactions among herbs, active ingredients, targets, and pathways, were constructed. The four dominating network maps included a compound-target network of SJC, a compound-anti-MI targets network, a candidate targets PPI network, a pathway-gene network, and a drug-key compounds-hub targets-pathways network. Systematic analysis indicated that the targets of SJC in the treatment of MI mainly involved RPS6, MAPK1, MAPK3, MDM2, and DDX5. Pathway enrichment analysis showed that SJC had the potential to impact multiple biological pathways, such as cancer-related pathways, viral/bacterial infection-related pathways, and signal transduction-related pathways. CONCLUSION: Our results preliminarily revealed the pharmacological basis and molecular mechanism SJC in treating MI, but further experimental research is required to verify these findings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-022-03774-z. |
format | Online Article Text |
id | pubmed-9675225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96752252022-11-20 Exploring the pharmacological mechanism of Shengjing capsule on male infertility by a network pharmacology approach Wang, Ming Wang, Qi Jiang, Hui Du, Yongqiang Zhang, Xiansheng BMC Complement Med Ther Research Article BACKGROUND: Shengjing capsule (SJC) is a traditional Chinese medicine (TCM) and has gained widespread clinical application for the treatment of male infertility (MI). However, the pharmacological mechanism of SJC against MI remains vague to date. METHOD: The active ingredients of SJC and their targets were identified from the database, and MI-related genes were retrieved from several databases. Protein–protein interaction (PPI) data were obtained to construct the PPI networks. The candidate targets of SJC against MI were identified through topological analysis of the PPI network. Functional enrichment analysis of candidate targets was performed, and the key target genes were identified from the gene-pathway network. RESULTS: We identified 154 active ingredients and 314 human targets of SJC, as well as 564 MI-related genes. Eight pharmacological network diagrams illustrating the interactions among herbs, active ingredients, targets, and pathways, were constructed. The four dominating network maps included a compound-target network of SJC, a compound-anti-MI targets network, a candidate targets PPI network, a pathway-gene network, and a drug-key compounds-hub targets-pathways network. Systematic analysis indicated that the targets of SJC in the treatment of MI mainly involved RPS6, MAPK1, MAPK3, MDM2, and DDX5. Pathway enrichment analysis showed that SJC had the potential to impact multiple biological pathways, such as cancer-related pathways, viral/bacterial infection-related pathways, and signal transduction-related pathways. CONCLUSION: Our results preliminarily revealed the pharmacological basis and molecular mechanism SJC in treating MI, but further experimental research is required to verify these findings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-022-03774-z. BioMed Central 2022-11-18 /pmc/articles/PMC9675225/ /pubmed/36401273 http://dx.doi.org/10.1186/s12906-022-03774-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Article Wang, Ming Wang, Qi Jiang, Hui Du, Yongqiang Zhang, Xiansheng Exploring the pharmacological mechanism of Shengjing capsule on male infertility by a network pharmacology approach |
title | Exploring the pharmacological mechanism of Shengjing capsule on male infertility by a network pharmacology approach |
title_full | Exploring the pharmacological mechanism of Shengjing capsule on male infertility by a network pharmacology approach |
title_fullStr | Exploring the pharmacological mechanism of Shengjing capsule on male infertility by a network pharmacology approach |
title_full_unstemmed | Exploring the pharmacological mechanism of Shengjing capsule on male infertility by a network pharmacology approach |
title_short | Exploring the pharmacological mechanism of Shengjing capsule on male infertility by a network pharmacology approach |
title_sort | exploring the pharmacological mechanism of shengjing capsule on male infertility by a network pharmacology approach |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675225/ https://www.ncbi.nlm.nih.gov/pubmed/36401273 http://dx.doi.org/10.1186/s12906-022-03774-z |
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