2025年第52卷第11期目录

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封面故事:该研究探究牛磺酸对二氢睾酮(DHT) 诱导的雄性C57BL/6小鼠雄激素性脱发(AGA) 的保护作用及机制,重点研究毛囊周期调节、细胞增殖/凋亡及相关信号通路。雌性小鼠实验中, 1%牛磺酸饮水可加速毛发生长,促进皮肤从休止期转生长期,增加毛囊数量与真皮厚度,增强毛 发基质角质细胞增殖;雄性小鼠实验中,采用DHT诱导构建AGA模型,高剂量牛磺酸能改善毛发 生长评分,恢复真皮厚度、毛囊数量、毛囊大小及毛球深度,减少毛囊细胞凋亡、促进增殖,还 可下调皮肤中雄激素受体、转化生长因子β1/2、Dickkopf-1的mRNA与蛋白质表达,降低DHT致病 影响。其机制涉及调节毛囊周期(促休止期转生长期)、细胞动力学(促增殖抑凋亡) 及抑制雄激 素致病通路。该研究为牛磺酸作为AGA新型候选药提供临床前证据,其安全性与多靶点优势可弥 补现有治疗缺陷,为脱发治疗提供新方向。
(吴晋强,郭果果,张欣婷,刘晋佳,王吉祥,赫晓燕,王海东. 牛磺酸通过调节毛囊周期及相关信号通路 减轻雄性C57BL/6 小鼠雄激素性脱发, 本期第2854~2868 页)

Cover Story:Objective This study aimed to comprehensively investigate the potential protective effects and underlying mechanisms of taurine against dihydrotestosterone (DHT)-induced androgenetic alopecia (AGA) in male C57BL/6 mice, with a focus on hair follicle cycle modulation, cellular proliferation/apoptosis, and key related signaling pathways.Methods Six-week-old female C57BL/6 mice were initially used to assess the hair growth-promoting potential of taurine. After acclimatization, they were randomly assigned to three groups (n=8): control (regular drinking water), taurine (drinking water containing 1% taurine), and minoxidil (topical 2% minoxidil, positive control). For the AGA study, male C57BL/6 mice were randomly divided into five groups (n=8): control (physiological saline), DHT (model group, 1 mg/d DHT), DHT+low-dose taurine (1 mg/d DHT+2 mg/d taurine), DHT+high-dose taurine (1 mg/d DHT+10 mg/d taurine), and DHT+minoxidil (positive control, 1 mg/d DHT+topical 2% minoxidil). One day before treatment initiation, dorsal hair was shaved with scissors, and residual hair was removed using a depilatory cream. DHT and taurine were administered via daily intraperitoneal injection. Hair regrowth was assessed by photographing the depilated area at regular intervals and quantified using a four-point grading system (0-3). Dorsal skin samples were collected on day 14 for histological analysis (H&E staining), immunofluorescence staining (Ki67 for proliferation, TUNEL for apoptosis), ELISA (DHT quantification), RT-qPCR, and Western blot analysis to evaluate the expression of key genes and proteins (androgen receptor (AR), transforming growth factor (TGF)-β1, TGF-β2, Dickkopf-1 (DKK1)).Results In female mice, taurine supplementation significantly accelerated hair growth, with effects comparable to minoxidil. This was evidenced by an earlier transition from pink (telogen) to black (anagen) skin and increased hair growth scores. Histological analysis showed that taurine increased hair follicle count and dermal thickness. Immunofluorescence confirmed enhanced keratinocyte proliferation in the hair matrix. In the DHT-induced AGA model, DHT significantly extended the telogen phase, inhibited hair growth, increased skin DHT content, and induced hair follicle miniaturization. Taurine treatment, particularly at the high dose, effectively counteracted these effects: it promoted the telogen-to-anagen transition and improved hair growth scores. Histomorphometric analysis showed that taurine significantly restored DHT-induced reductions in dermal thickness, hair follicle count, hair bulb depth, and follicle size. Taurine treatment also reduced apoptosis and promoted the proliferation of hair follicle cells, as demonstrated by Ki67 and TUNEL assays. Crucially, RT-qPCR and Western blot analyses revealed that DHT significantly up-regulated the expression of AR, TGF-β1, TGF-β2, and DKK1 at both mRNA and protein levels in dorsal skin. Taurine administration markedly down-regulated the expression of these pathogenic factors, bringing them closer to the levels observed in the control group.Conclusion Taurine demonstrates significant efficacy in alleviating DHT-induced AGA in male C57BL/6 mice. Its protective effects are mediated through multi-faceted mechanisms. (1) Promoting hair follicle cycle progression: it accelerates the transition from telogen to anagen, counteracting DHT-induced prolongation of the telogen phase. (2) Modulating cellular dynamics: it stimulates the proliferation of hair matrix keratinocytes and reduces DHT-induced apoptosis within hair follicle cells. (3) Suppressing androgen-driven pathogenic pathways: it downregulates the expression of critical molecules in the AGA pathway, including AR, the cytokines TGF-β1 and TGF-β2, and the Wnt pathway inhibitor DKK1. Given its favorable safety profile and multi-targeted action, taurine emerges as a promising novel therapeutic candidate or adjunct for treating AGA. Further investigation into its clinical potential and precise molecular mechanisms is warranted. This study provides a robust preclinical foundation for considering taurine supplementation or topical application in hair loss management strategies.

综述与专论

蛋白质聚集路径的分子机制:成核-延伸与液固转变梁雨涵,程婉茹,杨硕,冯爽,牛铮  [摘要][PDF][HTML]

癌基因与抑癌基因对肿瘤免疫微环境的调控作用谭舒祎,张建  [摘要][PDF][HTML]

子宫内膜异位性疾病中的糖酵解亢进:从分子机制到精准干预杜霖,王美玲,周双双,付先芸,石文洁,陶奕丹,周昊鑫  [摘要][PDF][HTML]

线粒体AAA+蛋白酶的结构与功能及其在神经系统疾病中的作用李茹茹,张叶,卫涛涛,朱笠  [摘要][PDF][HTML]

鸢尾素改善糖尿病心肌病的细胞机制颜雪茹,张跃军,李佳悦,张浩达,何恩鹏  [摘要][PDF][HTML]

超声靶向微泡破坏技术:神经退行性疾病治疗的新手段李玲妍,郑若泉,胡火军,尤程程,杨轶,盛德乔,周军,黄益玲  [摘要][PDF][HTML]

精神分裂症核心认知损伤的非药物治疗冯家欣,谢彦鸿,李伊,林佛香,黄敏芳,王钦文,王正春  [摘要][PDF][HTML]

帕金森病精准运动干预的多维体系:基于遗传分型、运动亚型、临床分期和可穿戴数字生物标志物的动态调控周子贵,颜敏,温潇,王慧,刘国强,田雪文  [摘要][PDF][HTML]

天然孢子/花粉微载体的制备及其在新型药物递送系统中的应用袁晨曼,史秀艳,柳佳,王晶晶  [摘要][PDF][HTML]

面向核酸适配体的人工智能方法与应用刘上华,张洪旗,刘入铭,曾红娟,邓科君,鄢丹,汤丽霞,林昊  [摘要][PDF][HTML]

研究快报

梓醇通过小窝蛋白1依赖途径在3D微流控芯片中促进神经干细胞向少突胶质细胞分化王亚辰,王亮,沈丽明,刘晶  [摘要][PDF][HTML]

研究报告

牛磺酸通过调节毛囊周期及相关信号通路减轻雄性C57BL/6小鼠雄激素性脱发吴晋强,郭果果,张欣婷,刘晋佳,王吉祥,赫晓燕,王海东  [摘要][PDF][HTML]

基于正则化U-net分割模型的脑胶质瘤精准密度估计方法夏瑞晨,叶臣,赵来定,刘凯,潘敏鸿,姚佳烽  [摘要][PDF][HTML]

微波热声和超声双模态显微成像研究迟子惠,聂银强,郭翔文,杜爽,方秋潮,吴丹,蒋华北  [摘要][PDF][HTML]

技术与方法

基于双分支残差网络的多组织RNA m6A甲基化位点预测郭晓甜,高伟,陈丹,李慧敏,谭学文  [摘要][PDF][HTML]

科教融合

新医科视域下“教-学-研一体化”生理学混合式课程构建与实践研究徐佳,张俊芳,李丽萍,刘昊,郭蕾,徐淑君,陈晓薇  [摘要][PDF][HTML]

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