Obacunone improves dihydrotestosterone-induced androgen alopecia by inhibiting androgen receptor dimerization.

Androgen receptor Androgenetic alopecia Nuclear translocation Obacunone, Dermal papilla cells

Journal

Phytomedicine : international journal of phytotherapy and phytopharmacology
ISSN: 1618-095X
Titre abrégé: Phytomedicine
Pays: Germany
ID NLM: 9438794

Informations de publication

Date de publication:
14 Sep 2024
Historique:
received: 11 06 2024
revised: 02 09 2024
accepted: 11 09 2024
medline: 23 9 2024
pubmed: 23 9 2024
entrez: 22 9 2024
Statut: aheadofprint

Résumé

Dihydrotestosterone-induced androgen receptor activation and nuclear translocation was identified as the key event in androgen alopecia, which led to dermal papilla cell damage and hair growth cycle arrest. Inhibiting androgen receptor activation or nuclear translocation thus represents a potential therapeutic strategy for reducing dermal papilla cell damage and treating androgen alopecia. To evaluate the effects of obacunone androgen alopecia and explore the potential underlying mechanisms. The effects of obacunone on androgen receptor activation and changes in the properties of dermal papilla cells were investigated. Meanwhile, the effects of obacunone on transforming growth factor-β-induced hair follicle stem cell damage and on androgen alopecia mice induced by dihydrotestosterone were evaluated. Obacunone can competitively bind to androgen receptors with dihydrotestosterone, thereby alleviating the androgen receptor dimerization and nuclear translocation. The negative effects of dihydrotestosterone on dermal papilla cell apoptosis, senescence, and cycle arrest were alleviated by obacunone. Obacunone also counteracted the proliferation and apoptosis of transforming growth factor-β-mediated hair follicle stem cells. In mice with androgen alopecia, treatment with obacunone promoted mice hair growth and inhibited TGF-β/smad signaling. Thus, inhibiting androgen receptor dimerization was found to be an effective strategy for alleviating androgen alopecia. Obacunone follows a novel mechanism and holds potential as a drug candidate for androgen alopecia through inhibition of the dimerization of the androgen receptor. This targeting strategy may provide a new avenue for the development of new drugs different from the existing therapeutic approaches.

Sections du résumé

BACKGROUND BACKGROUND
Dihydrotestosterone-induced androgen receptor activation and nuclear translocation was identified as the key event in androgen alopecia, which led to dermal papilla cell damage and hair growth cycle arrest. Inhibiting androgen receptor activation or nuclear translocation thus represents a potential therapeutic strategy for reducing dermal papilla cell damage and treating androgen alopecia.
PURPOSE OBJECTIVE
To evaluate the effects of obacunone androgen alopecia and explore the potential underlying mechanisms.
METHODS METHODS
The effects of obacunone on androgen receptor activation and changes in the properties of dermal papilla cells were investigated. Meanwhile, the effects of obacunone on transforming growth factor-β-induced hair follicle stem cell damage and on androgen alopecia mice induced by dihydrotestosterone were evaluated.
RESULTS RESULTS
Obacunone can competitively bind to androgen receptors with dihydrotestosterone, thereby alleviating the androgen receptor dimerization and nuclear translocation. The negative effects of dihydrotestosterone on dermal papilla cell apoptosis, senescence, and cycle arrest were alleviated by obacunone. Obacunone also counteracted the proliferation and apoptosis of transforming growth factor-β-mediated hair follicle stem cells. In mice with androgen alopecia, treatment with obacunone promoted mice hair growth and inhibited TGF-β/smad signaling.
CONCLUSION CONCLUSIONS
Thus, inhibiting androgen receptor dimerization was found to be an effective strategy for alleviating androgen alopecia. Obacunone follows a novel mechanism and holds potential as a drug candidate for androgen alopecia through inhibition of the dimerization of the androgen receptor. This targeting strategy may provide a new avenue for the development of new drugs different from the existing therapeutic approaches.

Identifiants

pubmed: 39306884
pii: S0944-7113(24)00699-8
doi: 10.1016/j.phymed.2024.156042
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

156042

Informations de copyright

Copyright © 2024. Published by Elsevier GmbH.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Jianxing Liu (J)

China Pharmaceutical University, PR China.

Shanshan Chen (S)

China Pharmaceutical University, PR China.

Wenjing Yan (W)

China Pharmaceutical University, PR China.

Jiakun Liu (J)

China Pharmaceutical University, PR China.

Qianqian Jin (Q)

China Pharmaceutical University, PR China.

Yanfeng Zhang (Y)

China Pharmaceutical University, PR China.

Fangfang Zhang (F)

China Pharmaceutical University, PR China.

Yi Pan (Y)

China Pharmaceutical University, PR China.

Wenjun Hu (W)

China Pharmaceutical University, PR China. Electronic address: wjhu@cpu.edu.cn.

Liang Jin (L)

China Pharmaceutical University, PR China. Electronic address: ljstemcell@cpu.edu.cn.

Classifications MeSH