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Recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside Rb(1), a main active ingredient in Panax ginseng Meyer
Ginsenoside Rb(1) (Rb(1)), one of the most important ingredients in Panax ginseng Meyer, has been confirmed to have favorable activities, including reducing antioxidative stress, inhibiting inflammation, regulating cell autophagy and apoptosis, affecting sugar and lipid metabolism, and regulating va...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753521/ https://www.ncbi.nlm.nih.gov/pubmed/35058726 http://dx.doi.org/10.1016/j.jgr.2021.07.008 |
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author | Lin, Zuan Xie, Rongfang Zhong, Chenhui Huang, Jianyong Shi, Peiying Yao, Hong |
author_facet | Lin, Zuan Xie, Rongfang Zhong, Chenhui Huang, Jianyong Shi, Peiying Yao, Hong |
author_sort | Lin, Zuan |
collection | PubMed |
description | Ginsenoside Rb(1) (Rb(1)), one of the most important ingredients in Panax ginseng Meyer, has been confirmed to have favorable activities, including reducing antioxidative stress, inhibiting inflammation, regulating cell autophagy and apoptosis, affecting sugar and lipid metabolism, and regulating various cytokines. This study reviewed the recent progress on the pharmacological effects and mechanisms of Rb(1) against cardiovascular and nervous system diseases, diabetes, and their complications, especially those related to neurodegenerative diseases, myocardial ischemia, hypoxia injury, and traumatic brain injury. This review retrieved articles from PubMed and Web of Science that were published from 2015 to 2020. The molecular targets or pathways of the effects of Rb(1) on these diseases are referring to HMGB1, GLUT4, 11β-HSD1, ERK, Akt, Notch, NF-κB, MAPK, PPAR-γ, TGF-β1/Smad pathway, PI3K/mTOR pathway, Nrf2/HO-1 pathway, Nrf2/ARE pathway, and MAPK/NF-κB pathway. The potential effects of Rb(1) and its possible mechanisms against diseases were further predicted via Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway and disease ontology semantic and enrichment (DOSE) analyses with the reported targets. This study provides insights into the therapeutic effects of Rb(1) and its mechanisms against diseases, which is expected to help in promoting the drug development of Rb(1) and its clinical applications. |
format | Online Article Text |
id | pubmed-8753521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-87535212022-01-19 Recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside Rb(1), a main active ingredient in Panax ginseng Meyer Lin, Zuan Xie, Rongfang Zhong, Chenhui Huang, Jianyong Shi, Peiying Yao, Hong J Ginseng Res Review Article Ginsenoside Rb(1) (Rb(1)), one of the most important ingredients in Panax ginseng Meyer, has been confirmed to have favorable activities, including reducing antioxidative stress, inhibiting inflammation, regulating cell autophagy and apoptosis, affecting sugar and lipid metabolism, and regulating various cytokines. This study reviewed the recent progress on the pharmacological effects and mechanisms of Rb(1) against cardiovascular and nervous system diseases, diabetes, and their complications, especially those related to neurodegenerative diseases, myocardial ischemia, hypoxia injury, and traumatic brain injury. This review retrieved articles from PubMed and Web of Science that were published from 2015 to 2020. The molecular targets or pathways of the effects of Rb(1) on these diseases are referring to HMGB1, GLUT4, 11β-HSD1, ERK, Akt, Notch, NF-κB, MAPK, PPAR-γ, TGF-β1/Smad pathway, PI3K/mTOR pathway, Nrf2/HO-1 pathway, Nrf2/ARE pathway, and MAPK/NF-κB pathway. The potential effects of Rb(1) and its possible mechanisms against diseases were further predicted via Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway and disease ontology semantic and enrichment (DOSE) analyses with the reported targets. This study provides insights into the therapeutic effects of Rb(1) and its mechanisms against diseases, which is expected to help in promoting the drug development of Rb(1) and its clinical applications. Elsevier 2022-01 2021-07-30 /pmc/articles/PMC8753521/ /pubmed/35058726 http://dx.doi.org/10.1016/j.jgr.2021.07.008 Text en © 2021 The Korean Society of Ginseng. Publishing services by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Lin, Zuan Xie, Rongfang Zhong, Chenhui Huang, Jianyong Shi, Peiying Yao, Hong Recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside Rb(1), a main active ingredient in Panax ginseng Meyer |
title | Recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside Rb(1), a main active ingredient in Panax ginseng Meyer |
title_full | Recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside Rb(1), a main active ingredient in Panax ginseng Meyer |
title_fullStr | Recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside Rb(1), a main active ingredient in Panax ginseng Meyer |
title_full_unstemmed | Recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside Rb(1), a main active ingredient in Panax ginseng Meyer |
title_short | Recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside Rb(1), a main active ingredient in Panax ginseng Meyer |
title_sort | recent progress (2015–2020) in the investigation of the pharmacological effects and mechanisms of ginsenoside rb(1), a main active ingredient in panax ginseng meyer |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753521/ https://www.ncbi.nlm.nih.gov/pubmed/35058726 http://dx.doi.org/10.1016/j.jgr.2021.07.008 |
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