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Network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil
Zedoary turmeric oil (ZTO) has been widely used in clinic. However, the unpleasant induced dyspnoea inevitably impedes its clinical application. Thus, it is urgent to elucidate the mechanism underlying the ZTO‐induced dyspnoea. In this study, network pharmacology was firstly performed to search the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313566/ https://www.ncbi.nlm.nih.gov/pubmed/35318816 http://dx.doi.org/10.1111/bcpt.13722 |
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author | Yang, Zhirui Wang, Zhenzhen Li, Jiangling Long, Jianglan Peng, Cheng Yan, Dan |
author_facet | Yang, Zhirui Wang, Zhenzhen Li, Jiangling Long, Jianglan Peng, Cheng Yan, Dan |
author_sort | Yang, Zhirui |
collection | PubMed |
description | Zedoary turmeric oil (ZTO) has been widely used in clinic. However, the unpleasant induced dyspnoea inevitably impedes its clinical application. Thus, it is urgent to elucidate the mechanism underlying the ZTO‐induced dyspnoea. In this study, network pharmacology was firstly performed to search the clue of ZTO‐induced dyspnoea. The key target genes of ZTO‐induced dyspnoea were analysed using GO enrichment analysis and KEGG pathway analysis. GO analysis suggested that haem binding could be a key molecular function involved in ZTO‐induced dyspnoea. Hence, the haemoglobin (Hb) was focused for its oxygen‐carrying capacity with haem as its critical component binding to the oxygen. Ultraviolet–visible absorption spectrum indicated that the ZTO injection (ZTOI) perturbed the Soret band of Hb, suggesting an interaction between ZTO and Hb. GC–MS analysis revealed that β‐elemene, germacrone, curdione and furanodiene were main components of ZTOI. Molecular docking was used to illustrate the high affinity between representative sesquiterpenes and Hb, which was finally confirmed by surface plasmon resonance, suggesting their potential roles in dyspnoea by ZTO. Following a network pharmacology‐driven strategy, our study revealed an intervened Hb‐based mechanism underlying the ZTO‐induced dyspnoea, providing a reference for elucidating mechanism underlying adverse drug reactions of herbal medicines in clinic. |
format | Online Article Text |
id | pubmed-9313566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93135662022-07-30 Network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil Yang, Zhirui Wang, Zhenzhen Li, Jiangling Long, Jianglan Peng, Cheng Yan, Dan Basic Clin Pharmacol Toxicol Basic Toxicology Zedoary turmeric oil (ZTO) has been widely used in clinic. However, the unpleasant induced dyspnoea inevitably impedes its clinical application. Thus, it is urgent to elucidate the mechanism underlying the ZTO‐induced dyspnoea. In this study, network pharmacology was firstly performed to search the clue of ZTO‐induced dyspnoea. The key target genes of ZTO‐induced dyspnoea were analysed using GO enrichment analysis and KEGG pathway analysis. GO analysis suggested that haem binding could be a key molecular function involved in ZTO‐induced dyspnoea. Hence, the haemoglobin (Hb) was focused for its oxygen‐carrying capacity with haem as its critical component binding to the oxygen. Ultraviolet–visible absorption spectrum indicated that the ZTO injection (ZTOI) perturbed the Soret band of Hb, suggesting an interaction between ZTO and Hb. GC–MS analysis revealed that β‐elemene, germacrone, curdione and furanodiene were main components of ZTOI. Molecular docking was used to illustrate the high affinity between representative sesquiterpenes and Hb, which was finally confirmed by surface plasmon resonance, suggesting their potential roles in dyspnoea by ZTO. Following a network pharmacology‐driven strategy, our study revealed an intervened Hb‐based mechanism underlying the ZTO‐induced dyspnoea, providing a reference for elucidating mechanism underlying adverse drug reactions of herbal medicines in clinic. John Wiley and Sons Inc. 2022-03-29 2022-05 /pmc/articles/PMC9313566/ /pubmed/35318816 http://dx.doi.org/10.1111/bcpt.13722 Text en © 2022 The Authors. Basic & Clinical Pharmacology & Toxicology published by John Wiley & Sons Ltd on behalf of Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Basic Toxicology Yang, Zhirui Wang, Zhenzhen Li, Jiangling Long, Jianglan Peng, Cheng Yan, Dan Network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil |
title | Network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil |
title_full | Network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil |
title_fullStr | Network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil |
title_full_unstemmed | Network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil |
title_short | Network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil |
title_sort | network pharmacology‐based dissection of the underlying mechanisms of dyspnoea induced by zedoary turmeric oil |
topic | Basic Toxicology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313566/ https://www.ncbi.nlm.nih.gov/pubmed/35318816 http://dx.doi.org/10.1111/bcpt.13722 |
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