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The Extract of Ilex cornuta Bark Promotes Bone Healing by Activating Adenosine A2A Receptor
INTRODUCTION: Bone fracture is a common reason causing human disability. The delay union and nonunion rates are approximately 5–10% despite patients receiving active treatment. Currently, there is a limited number of drugs directly accelerating bone healing, especially direct extracts from plants. M...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359408/ https://www.ncbi.nlm.nih.gov/pubmed/35959419 http://dx.doi.org/10.2147/DDDT.S362238 |
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author | Zheng, Xi Wang, Jingyi Zhou, Junlin Wang, Dong |
author_facet | Zheng, Xi Wang, Jingyi Zhou, Junlin Wang, Dong |
author_sort | Zheng, Xi |
collection | PubMed |
description | INTRODUCTION: Bone fracture is a common reason causing human disability. The delay union and nonunion rates are approximately 5–10% despite patients receiving active treatment. Currently, there is a limited number of drugs directly accelerating bone healing, especially direct extracts from plants. Moreover, the pharmacological effects of Ilex cornuta bark are still unknown. This study aimed to explore the effects and mechanisms of Ilex cornuta bark in bone healing. METHODS AND RESULTS: First, the promoting effects of Ilex cornuta bark on bone healing were verified by the mice femur fracture model as Ilex cornuta bark increased the callus formation and enhanced the biomechanical stability during the bone healing process. Second, the target gene of Ilex cornuta bark in bone healing identified by bioinformatics analysis and immunofluorescence validation was ADORA2A. Third, 410 main compound compositions of Ilex cornuta bark were explored by a non-target metabolomic analysis, where 190 of them were neg ion mode, and 220 were pos ion mode. Molecular docking was used to predict the regulatory effect of the compounds on adora2a (adenosine A2A receptor), and ursonic acid had the lowest binding energy with adora2a. Finally, nfkb1 was the transcription factor (TF) of adora2a, and ursonic acid also had the lowest binding energy by bioinformatic analysis and molecular docking. CONCLUSION: Overall, Ilex cornuta bark water extract was a new plant extract on promoting bone healing; in addition, the mechanism of it might be activating adora2a though Nfkb1. |
format | Online Article Text |
id | pubmed-9359408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-93594082022-08-10 The Extract of Ilex cornuta Bark Promotes Bone Healing by Activating Adenosine A2A Receptor Zheng, Xi Wang, Jingyi Zhou, Junlin Wang, Dong Drug Des Devel Ther Original Research INTRODUCTION: Bone fracture is a common reason causing human disability. The delay union and nonunion rates are approximately 5–10% despite patients receiving active treatment. Currently, there is a limited number of drugs directly accelerating bone healing, especially direct extracts from plants. Moreover, the pharmacological effects of Ilex cornuta bark are still unknown. This study aimed to explore the effects and mechanisms of Ilex cornuta bark in bone healing. METHODS AND RESULTS: First, the promoting effects of Ilex cornuta bark on bone healing were verified by the mice femur fracture model as Ilex cornuta bark increased the callus formation and enhanced the biomechanical stability during the bone healing process. Second, the target gene of Ilex cornuta bark in bone healing identified by bioinformatics analysis and immunofluorescence validation was ADORA2A. Third, 410 main compound compositions of Ilex cornuta bark were explored by a non-target metabolomic analysis, where 190 of them were neg ion mode, and 220 were pos ion mode. Molecular docking was used to predict the regulatory effect of the compounds on adora2a (adenosine A2A receptor), and ursonic acid had the lowest binding energy with adora2a. Finally, nfkb1 was the transcription factor (TF) of adora2a, and ursonic acid also had the lowest binding energy by bioinformatic analysis and molecular docking. CONCLUSION: Overall, Ilex cornuta bark water extract was a new plant extract on promoting bone healing; in addition, the mechanism of it might be activating adora2a though Nfkb1. Dove 2022-08-04 /pmc/articles/PMC9359408/ /pubmed/35959419 http://dx.doi.org/10.2147/DDDT.S362238 Text en © 2022 Zheng et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Zheng, Xi Wang, Jingyi Zhou, Junlin Wang, Dong The Extract of Ilex cornuta Bark Promotes Bone Healing by Activating Adenosine A2A Receptor |
title | The Extract of Ilex cornuta Bark Promotes Bone Healing by Activating Adenosine A2A Receptor |
title_full | The Extract of Ilex cornuta Bark Promotes Bone Healing by Activating Adenosine A2A Receptor |
title_fullStr | The Extract of Ilex cornuta Bark Promotes Bone Healing by Activating Adenosine A2A Receptor |
title_full_unstemmed | The Extract of Ilex cornuta Bark Promotes Bone Healing by Activating Adenosine A2A Receptor |
title_short | The Extract of Ilex cornuta Bark Promotes Bone Healing by Activating Adenosine A2A Receptor |
title_sort | extract of ilex cornuta bark promotes bone healing by activating adenosine a2a receptor |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359408/ https://www.ncbi.nlm.nih.gov/pubmed/35959419 http://dx.doi.org/10.2147/DDDT.S362238 |
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