湖北农业科学 ›› 2026, Vol. 65 ›› Issue (4): 191-195.doi: 10.14088/j.cnki.issn0439-8114.2026.04.029

• 畜牧·兽医 • 上一篇    下一篇

千斤拔提取物在小鼠雄激素性脱发模型中的疗效研究

张文乐1, 胡一鸣1, 肖倩妮1, 肖红卫2, 尤祥宇1   

  1. 1.湖北工业大学生命科学与健康工程学院,武汉 430068;
    2.湖北省农业科学院畜牧兽医研究所/动物胚胎工程及分子育种湖北省重点实验室,武汉 430064
  • 收稿日期:2025-11-24 出版日期:2026-04-25 发布日期:2026-05-06
  • 通讯作者: 尤祥宇(1983-),男,福建南安人,副教授,主要从事传统中药新应用、天然高分子材料等领域研究,(电子信箱)youxiangyu@hbut.edu.cn。
  • 作者简介:张文乐(1992-),女,山东德州人,在读硕士研究生,研究方向为传统中药新应用,(电话)13375500913(电子信箱)22610079@qq.com。
  • 基金资助:
    湖北省科学技术厅湖北省科技创新人才计划项目(2025DJB038)

Evaluation of the therapeutic potential of Flemingia prostrata extract in the DHT-Induced mouse model of androgenetic alopecia

ZHANG Wen-le1, HU Yi-ming1, XIAO Qian-ni1, XIAO Hong-wei2, YOU Xiang-yu1   

  1. 1. School of Life and Health Sciences, Hubei University of Technology, Wuhan 430068, China;
    2. Key Laboratory of Animal Embryo Engineering and Molecular Breeding of Hubei Province,Institute of Animal Science and Veterinary Medicine, Hubei Academy of Agricultural Sciences, Wuhan 430064, China
  • Received:2025-11-24 Published:2026-04-25 Online:2026-05-06

摘要: 为研究千斤拔(Flemingia prostrata)提取物(Fle)对二氢睾酮(DHT)诱导的雌性C57BL/6小鼠雄激素性脱发(AGA)的治疗效果及潜在作用机制,随机选取3只8周龄小鼠用于评估毛发生长周期并确定AGA造模时间。其余小鼠随机分为3组(n=6):对照组(DHT)、米诺地尔组(DHT+外抹2%米诺地尔)、Fle组(DHT+口服Fle),每日定时在各组小鼠背部脱毛区涂抹DHT,持续15 d。在治疗21 d后处死小鼠,采集定点背部毛发测量毛干直径,并取背部皮肤进行HE染色分析;采集血清通过ELISA法测定其DHT含量。结果表明,在DHT诱导的AGA小鼠模型中,小鼠毛囊休止期明显延长,毛发生长受抑,并出现毛囊小型化。与对照组及米诺地尔组小鼠相比,口服Fle明显促进AGA小鼠毛发再生且毛干直径更粗。HE染色显示,口服Fle能显著恢复DHT所致的毛囊数量减少、毛球深度减小和毛囊体积缩小等病理变化。ELISA结果显示,口服Fle降低了AGA小鼠血清中DHT水平,可缩短AGA小鼠毛囊从休止期进入生长期的时间,促进毛发再生,增加毛发直径,降低体内DHT水平。

关键词: 雄激素性脱发(AGA), 千斤拔(Flemingia prostrata Roxb. f. ex Roxb.), 二氢睾酮(DHT)

Abstract: To investigate the therapeutic effects and potential mechanisms of Flemingia prostrata extract (Fle) on dihydrotestosterone (DHT)-induced androgenetic alopecia (AGA) in female C57BL/6 mice, twenty-one 8-week-old female mice were acclimated and randomly selected for three groups (n=6) after evaluating hair growth cycles and determining the AGA model establishment time: control group (DHT), minoxidil group (DHT + 2% topical minoxidil), and Fle group (DHT + oral Fle). DHT was applied topically on the shaved back of all mice daily for 15 days to induce hair loss. After the model was established, treatments were applied according to the schedule, with periodic photos taken to monitor hair regeneration. After 21 days of treatment, the mice were euthanized, and the hair diameter of back skin was measured. The back skin was collected for HE staining, and serum DHT levels were measured using ELISA. Results showed that in DHT-induced AGA mice, symptoms including a prolonged telogen phase, suppressed hair growth and follicular miniaturization were observed. Compared to the mice in control and minoxidil groups, oral Fle significantly promoted hair regeneration and increased hair shaft diameter in AGA mice. HE staining showed that oral Fle effectively restored the pathological changes caused by DHT, including reduced hair follicle count, decreased hair bulb depth, and smaller follicle volume. ELISA results indicated that oral Fle reduced serum DHT levels in AGA mice. Oral Fle shortened the time for AGA mice to transition from the telogen phase to anagen, promoted hair regeneration, increased hair shaft diameter, and lowered serum DHT levels.

Key words: androgenetic alopecia (AGA), Flemingia prostrata Roxb. f. ex Roxb., dihydrotestosterone (DHT)

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