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Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain
Neuropathic pain is a chronic disease that severely afflicts the life and emotional status of patients, but currently available treatments are often ineffective. Novel therapeutic targets for the alleviation of neuropathic pain are urgently needed. Rhodojaponin VI, a grayanotoxin from Rhododendron m...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031280/ https://www.ncbi.nlm.nih.gov/pubmed/36970201 http://dx.doi.org/10.1016/j.apsb.2023.01.021 |
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author | Chen, Keliang Wang, Tao Li, Yong Wu, Jun Zhao, Cheng-Xiao Liu, Sheng Sun, Fengrun Fang, Yehong Hu, Jiahuan Hu, Jinping Zhang, Chong-Jing Yu, Haibo Ma, Chao Yu, Shi-Shan |
author_facet | Chen, Keliang Wang, Tao Li, Yong Wu, Jun Zhao, Cheng-Xiao Liu, Sheng Sun, Fengrun Fang, Yehong Hu, Jiahuan Hu, Jinping Zhang, Chong-Jing Yu, Haibo Ma, Chao Yu, Shi-Shan |
author_sort | Chen, Keliang |
collection | PubMed |
description | Neuropathic pain is a chronic disease that severely afflicts the life and emotional status of patients, but currently available treatments are often ineffective. Novel therapeutic targets for the alleviation of neuropathic pain are urgently needed. Rhodojaponin VI, a grayanotoxin from Rhododendron molle, showed remarkable antinociceptive efficacy in models of neuropathic pain, but its biotargets and mechanisms are unknown. Given the reversible action of rhodojaponin VI and the narrow range over which its structure can be modified, we perforwmed thermal proteome profiling of the rat dorsal root ganglion to determine the protein target of rhodojaponin VI. N-Ethylmaleimide-sensitive fusion (NSF) was confirmed as the key target of rhodojaponin VI through biological and biophysical experiments. Functional validation showed for the first time that NSF facilitated trafficking of the Cav2.2 channel to induce an increase in Ca(2+) current intensity, whereas rhodojaponin VI reversed the effects of NSF. In conclusion, rhodojaponin VI represents a unique class of analgesic natural products targeting Cav2.2 channels via NSF. |
format | Online Article Text |
id | pubmed-10031280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-100312802023-03-23 Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain Chen, Keliang Wang, Tao Li, Yong Wu, Jun Zhao, Cheng-Xiao Liu, Sheng Sun, Fengrun Fang, Yehong Hu, Jiahuan Hu, Jinping Zhang, Chong-Jing Yu, Haibo Ma, Chao Yu, Shi-Shan Acta Pharm Sin B Short Communication Neuropathic pain is a chronic disease that severely afflicts the life and emotional status of patients, but currently available treatments are often ineffective. Novel therapeutic targets for the alleviation of neuropathic pain are urgently needed. Rhodojaponin VI, a grayanotoxin from Rhododendron molle, showed remarkable antinociceptive efficacy in models of neuropathic pain, but its biotargets and mechanisms are unknown. Given the reversible action of rhodojaponin VI and the narrow range over which its structure can be modified, we perforwmed thermal proteome profiling of the rat dorsal root ganglion to determine the protein target of rhodojaponin VI. N-Ethylmaleimide-sensitive fusion (NSF) was confirmed as the key target of rhodojaponin VI through biological and biophysical experiments. Functional validation showed for the first time that NSF facilitated trafficking of the Cav2.2 channel to induce an increase in Ca(2+) current intensity, whereas rhodojaponin VI reversed the effects of NSF. In conclusion, rhodojaponin VI represents a unique class of analgesic natural products targeting Cav2.2 channels via NSF. Elsevier 2023-03 2023-02-03 /pmc/articles/PMC10031280/ /pubmed/36970201 http://dx.doi.org/10.1016/j.apsb.2023.01.021 Text en © 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting 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 | Short Communication Chen, Keliang Wang, Tao Li, Yong Wu, Jun Zhao, Cheng-Xiao Liu, Sheng Sun, Fengrun Fang, Yehong Hu, Jiahuan Hu, Jinping Zhang, Chong-Jing Yu, Haibo Ma, Chao Yu, Shi-Shan Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain |
title | Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain |
title_full | Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain |
title_fullStr | Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain |
title_full_unstemmed | Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain |
title_short | Rhodojaponin VI indirectly targets Cav2.2 channels via N-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain |
title_sort | rhodojaponin vi indirectly targets cav2.2 channels via n-ethylmaleimide-sensitive fusion protein to alleviate neuropathic pain |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031280/ https://www.ncbi.nlm.nih.gov/pubmed/36970201 http://dx.doi.org/10.1016/j.apsb.2023.01.021 |
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