雌马酚用于抗真菌治疗的潜力与困境
The Antifungal Potential of Equol as a Selective Estrogen Receptor Modulator
DOI: 10.12677/amb.2025.144018, PDF,    科研立项经费支持
作者: 周 全, 吴天翔:西南医科大学药学院,四川 泸州;张 博:西南医科大学临床医学院,四川 泸州;杨圣威:大英县人民医院药剂科,四川 遂宁;周 浩:长宁县人民医院检验科,四川 宜宾
关键词: 雌马酚抗真菌药物老药新用侵袭性真菌病WHO真菌优先病原体清单Equol Antifungal Agents Drug Repurposing Invasive Fungal Disease WHO Fungal Priority Pathogens List
摘要: 侵袭性真菌感染及其耐药性已构成全球公共卫生重大威胁,世界卫生组织(WHO)于2022年首次发布《真菌优先病原体清单》(FPPL),突显其紧迫性。本文聚焦植物雌激素代谢产物雌马酚(equol)的治疗价值,探讨老药新用策略在抗真菌领域的应用前景。通过系统解析真菌耐药机制,结合雌马酚独特的双向雌激素调节特性,阐明其对白念珠菌的抑制机制。尽管该化合物在改善更年期综合征、骨质疏松及心血管保护等领域疗效明确,但其当前抗真菌谱仍局限于白念珠菌。本文主张拓展针对FPPL高危病原体(如耳念珠菌、烟曲霉)的研究,并探索与传统抗真菌药的协同作用,为耐药真菌感染提供创新解决方案。
Abstract: Invasive fungal diseases (IFDs) and their drug resistance pose a significant global public health threat. Highlighting its urgency, the World Health Organization (WHO) released its inaugural “Fungal Priority Pathogens List” (FPPL) in 2022. This review focuses on the therapeutic value of equol, a phytoestrogen metabolite, and explores the application prospects of drug repurposing strategies in antifungal fields. By systematically investigating fungal resistance mechanisms and leveraging equol’s unique dual-directional estrogenic regulatory properties, this study elucidates its inhibitory mechanism against Candida albicans. Although this compound demonstrates established efficacy in alleviating menopausal syndromes, osteoporosis, and cardiovascular protection, its current antifungal spectrum remains limited to C. albicans. This work calls for expanded research targeting high-risk FPPL pathogens (e.g., C. auris, Aspergillus fumigatus) and exploration of synergistic effects with conventional antifungals, thereby offering novel therapeutic solutions for drug-resistant fungal infections.
文章引用:周全, 张博, 吴天翔, 杨圣威, 周浩. 雌马酚用于抗真菌治疗的潜力与困境[J]. 微生物前沿, 2025, 14(4): 151-155. https://doi.org/10.12677/amb.2025.144018

参考文献

[1] Denning, D.W. (2024) Global Incidence and Mortality of Severe Fungal Disease. The Lancet Infectious Diseases, 24, e428-e438. [Google Scholar] [CrossRef] [PubMed]
[2] World Health Organization (2022) WHO Fungal Priority Pathogens List to Guide Research, Development and Public Health Action.
https://www.who.int/publications/i/item/9789240060241
[3] Kristanc, L., Božič, B., Jokhadar, Š.Z., Dolenc, M.S. and Gomišček, G. (2019) The Pore-Forming Action of Polyenes: From Model Membranes to Living Organisms. Biochimica et Biophysica Acta (BBA)—Biomembranes, 1861, 418-430. [Google Scholar] [CrossRef] [PubMed]
[4] Xia, Y., Sun, M., Huang, H. and Jin, W. (2024) Drug Repurposing for Cancer Therapy. Signal Transduction and Targeted Therapy, 9, Article No. 92. [Google Scholar] [CrossRef] [PubMed]
[5] Marrian, G.F. and Haslewood, G.A.D. (1932) Equol, a New Inactive Phenol Isolated from the Ketohydroxyoestrin Fraction of Mares’ Urine. Biochemical Journal, 26, 1227-1232. [Google Scholar] [CrossRef] [PubMed]
[6] 孙奥, 唐锐, 李文萱, 信彩岩, 王芬. 雌马酚抗菌作用的研究现状及前景展望[J]. 微生物前沿, 2022, 11(4): 191-195.
[7] Kawamoto, A., Sugano, N., Sakai, M., Ogisawa, S., Shiratsuchi, H., Seki, K., et al. (2024) Clinical Effect of Equol Supplementation in the Treatment of Desquamative Gingivitis with 1-Year Follow-Up. Journal of Oral Science, 66, 145-150. [Google Scholar] [CrossRef] [PubMed]
[8] Sekikawa, A., Wharton, W., Butts, B., Veliky, C.V., Garfein, J., Li, J., et al. (2022) Potential Protective Mechanisms of S-Equol, a Metabolite of Soy Isoflavone by the Gut Microbiome, on Cognitive Decline and Dementia. International Journal of Molecular Sciences, 23, Article 11921. [Google Scholar] [CrossRef] [PubMed]
[9] Jahan, N., Singh, L. and Sharma, J. (2025) Equol as a Multitarget Agent against Neurodegeneration: Mechanistic Insights into Its Molecular Modulation. NeuroMolecular Medicine, 27, Article No. 51. [Google Scholar] [CrossRef] [PubMed]
[10] Noda, K., Hattori, Y., Murata, H., Kokubo, Y., Higashiyama, A. and Ihara, M. (2024) Equol Nonproducing Status as an Independent Risk Factor for Acute Cardioembolic Stroke and Poor Functional Outcome. Nutrients, 16, Article 3377. [Google Scholar] [CrossRef] [PubMed]
[11] Lv, J., Jin, S., Zhang, Y., Zhou, Y., Li, M. and Feng, N. (2024) Equol: A Metabolite of Gut Microbiota with Potential Antitumor Effects. Gut Pathogens, 16, Article No. 35. [Google Scholar] [CrossRef] [PubMed]
[12] Jacobsen, I.D., Wilson, D., Wächtler, B., Brunke, S., Naglik, J.R. and Hube, B. (2012) Candida albicans Dimorphism as a Therapeutic Target. Expert Review of Anti-infective Therapy, 10, 85-93. [Google Scholar] [CrossRef] [PubMed]
[13] Lee, J.A. and Chee, H.Y. (2010) In vitro Antifungal Activity of Equol against Candida albicans. Mycobiology, 38, 328-330. [Google Scholar] [CrossRef] [PubMed]
[14] Wang, F., Zhang, J., Zhang, Q., Song, Z. and Xin, C. (2024) Antifungal Activities of Equol against Candida albicans in vitro and in vivo. Virulence, 15, Article ID: 2404256. [Google Scholar] [CrossRef] [PubMed]
[15] Ge, A., Zhou, H., Yang, X., Zhao, C., Xin, C. and Song, Z. (2025) The Antifungal Effects of Equol against Candida albicans Involve Mitochondrial Dysfunction. Journal of Fungi, 11, Article 339. [Google Scholar] [CrossRef] [PubMed]