Department of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China.
Department of Pharmacy, Daping Hospital, Army Medical University, Chongqing, China; School of Medicine, Tibet University, Lhasa, China.
J Ethnopharmacol. 2025 Jan 30;337(Pt 1):118778. doi: 10.1016/j.jep.2024.118778. Epub 2024 Sep 3.
Terminalia bellirica (Gaertn.) Roxb. (TBR), a popular herbal remedy in India and Southeast Asia, has been demonstrated to possess multiple pharmacological activities. However, systematic studies on the medicinal effects and mechanism of TBR for the androgenetic alopecia (AGA) treatment are deficient.
Human Umbilical Vein Endothelial Cells (HUVECs) and testosterone-induced AGA mice were used to evaluate the hair regrowth activity of TBR extracts. Chemical constituents and potential active components of TBR extracts were analyed by UPLC-Q-TOF-MS in vitro/vivo. The hair regrowth mechanisms of TBR were elucidated through network pharmacology and experimental validation.
Totally 28 chemical constituents in TBR were identified, of which 15 were predicted as potential active components for AGA therapy. TBR could significantly scavenge ROS, promote VEGF level/cell migration of HUVECs, and inhibiting type II 5α-reductase activity (the inhibit rate: 82.35 ± 1.02 %). Pharmacodynamic evaluation suggested that TBR effectively led to hair regrowth in C57BL6 mice compared to minoxidil. TBR promoted the hair follicle (HF) transition from the telogen phase to anagen phase by decreasing MDA levels, increasing VEFG expression and up-regulating phosphorylated P38/ERK protein levels in the MAPK signalling pathway.
TBR reversed AGA via inhibiting SRD5A2 activity and stimulating the MAPK pathway. Meantime, TBR could remodel the follicle microenvironment by reducing oxidative stress and increasing angiogenesis.
Terminalia bellirica(Gaertn.)Roxb.(TBR),一种在印度和东南亚流行的草药疗法,已被证明具有多种药理学活性。然而,关于 TBR 治疗雄激素性脱发(AGA)的药效学和作用机制的系统研究还很缺乏。
用人脐静脉内皮细胞(HUVEC)和睾丸酮诱导的 AGA 小鼠评估 TBR 提取物的毛发生长活性。通过 UPLC-Q-TOF-MS 对 TBR 提取物的化学成分和潜在活性成分进行了体外/体内分析。通过网络药理学和实验验证阐明了 TBR 的毛发生长机制。
共鉴定出 TBR 中的 28 种化学成分,其中 15 种被预测为 AGA 治疗的潜在活性成分。TBR 能显著清除 ROS,促进 HUVEC 中 VEGF 水平/细胞迁移,并抑制 II 型 5α-还原酶活性(抑制率:82.35±1.02%)。药效学评价表明,与米诺地尔相比,TBR 能有效促进 C57BL6 小鼠的毛发生长。TBR 通过降低 MDA 水平、增加 VEGFA 表达和上调 MAPK 信号通路中磷酸化 P38/ERK 蛋白水平,促进毛囊(HF)从休止期向生长期的转变。
TBR 通过抑制 SRD5A2 活性和刺激 MAPK 通路逆转 AGA。同时,TBR 可以通过减少氧化应激和增加血管生成来重塑毛囊微环境。