加味二至丸通过调节SIRT1/JNK/p38 MAPK信号通路改善雄激素性脱发
Jiawei Erzhiwan Ameliorates Androgenetic Alopecia by Regulating the SIRT1/JNK/p38 MAPK Pathway.
作者信息
Huang Zhiguang, Li Yuanyuan, Xie Yixin, Fu Hangjie, Weng Zhiwei, Yuan Jianchang, Wu Lan, Lin Weizhou, Cao Yi, Ding Bin
机构信息
School of Life Sciences, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.
Academy of Chinese Medical Science, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.
出版信息
Drug Des Devel Ther. 2025 Apr 1;19:2393-2409. doi: 10.2147/DDDT.S501823. eCollection 2025.
PURPOSE
Androgenetic alopecia (AGA) is a type of hair loss. Our previous study showed AGA ameliorating capability of water extract of an herbal prescription, "Jiawei Erzhiwan" (WJWE), which was derived from the traditional formula "Erzhiwan". However, the underlying mechanisms is still unknown.
PATIENTS AND METHODS
In this study, the phytochemical ingredients in WJWE were characterized via UPLC‒MS/MS analysis. The dihydrotestosterone (DHT)-induced murine model and dermal papilla cells (DPCs) assays were used to evaluate and elucidate the beneficial effects and mechanisms of WJWE on AGA.
RESULTS
WJWE promoted hair growth and hair follicle regeneration in AGA mice, improved DPCs growth and dose-dependently protected DHT-reduced DPCs viability in vitro by stimulating the Wnt5A/β-Catenin pathway. Additionally, WJWE reduced DHT-induced oxidative stress in AGA model murine skin and DHT-treated DPCs. To elucidate the regulative mechanism, we found that WJWE treatment significantly and dose-dependently increased the expression of SIRT1 and reduced the phosphorylation of JNK and p38 MAPK in both DHT-treated DPCs and AGA model mice. And the application of EX527 (a SIRT1 inhibitor) could the effect of WJWE.
CONCLUSION
Our study provided some evidence of WJWE on AGA treatment, by which SIRT1/JNK/p38 MAPK signaling pathway might be the major target.
目的
雄激素性脱发(AGA)是一种脱发类型。我们之前的研究表明,源自传统方剂“二至丸”的中药方剂“加味二至丸”(WJWE)的水提取物具有改善AGA的能力。然而,其潜在机制仍不清楚。
患者和方法
在本研究中,通过超高效液相色谱-串联质谱(UPLC-MS/MS)分析对WJWE中的植物化学成分进行了表征。使用二氢睾酮(DHT)诱导的小鼠模型和真皮乳头细胞(DPCs)实验来评估和阐明WJWE对AGA的有益作用和机制。
结果
WJWE促进了AGA小鼠的毛发生长和毛囊再生,改善了DPCs的生长,并通过刺激Wnt5A/β-连环蛋白途径在体外剂量依赖性地保护DHT降低的DPCs活力。此外,WJWE降低了AGA模型小鼠皮肤和DHT处理的DPCs中DHT诱导的氧化应激。为了阐明调节机制,我们发现WJWE处理在DHT处理的DPCs和AGA模型小鼠中均显著且剂量依赖性地增加了SIRT1的表达,并降低了JNK和p38丝裂原活化蛋白激酶(MAPK)的磷酸化。并且应用EX527(一种SIRT1抑制剂)可以消除WJWE的作用。
结论
我们的研究为WJWE治疗AGA提供了一些证据,其中SIRT1/JNK/p38 MAPK信号通路可能是主要靶点。