Tang Xueting, Wang Xueer, Zhang Yarui, Chen Qimei, Zhao Shan, Xu Xunhong, Yang Xinyu, Liu Xiaoran, Zhang Lin, Zhang Min
School of Public Health, Southern Medical University, Guangzhou 510515, China.
Department of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Int J Mol Sci. 2025 Apr 25;26(9):4068. doi: 10.3390/ijms26094068.
The etiopathogenesis and treatment response of sensitive skin remain poorly understood. We used 4-tert-butylcyclohexanol (4-TBLH) and 1% pimecrolimus ointment to treat sensitive skin in mice models constructed using tape stripping, propylene glycol, and capsaicin. This study aimed to further investigate the sensitivity and responsiveness of this sensitive mouse skin model. Sensitivity and responsiveness were assessed by measuring transepidermal water loss (TEWL), skin hydration, skin flakes, vascular dilatation, itching, stinging, and histological changes, including mast cell, lymphocyte, and granulocyte infiltration, tumor necrosis factor-α (TNF-α) expression, and transient receptor potential vanilloid 1 receptor (TRPV1) expression. The application of 4-TBLH and pimecrolimus revealed distinct responses in skin sensitivity indicators, including TEWL, capillary dilation, and mass cell activity, depending on the treatment timing and substance used. The prophylactic and therapeutic applications of 4-TBLH revealed distinct responses in skin sensitivity indicators, including skin flakes, TEWL, itching, stinging, epidermal thickness, mast cell activity, TNF-α, and TRPV1 expression. The prophylactic and therapeutic applications of pimecrolimus ointment revealed distinct responses in skin sensitivity indicators, including skin flakes, skin water content, itching, epidermal thickness, mast cell activity, CD45, CD11b, TNF-α, and TRPV1 expression. The mouse sensitive skin model demonstrates robust sensitivity and responsiveness to different treatment factors, and the model can be applied to the development of prophylactic and therapeutic medications for sensitive skin.
敏感性皮肤的发病机制和治疗反应仍未得到充分了解。我们使用4-叔丁基环己醇(4-TBLH)和1%吡美莫司软膏对通过胶带剥离、丙二醇和辣椒素构建的小鼠模型中的敏感性皮肤进行治疗。本研究旨在进一步探究这种敏感小鼠皮肤模型的敏感性和反应性。通过测量经表皮水分流失(TEWL)、皮肤水合作用、皮屑、血管扩张、瘙痒、刺痛以及组织学变化(包括肥大细胞、淋巴细胞和粒细胞浸润、肿瘤坏死因子-α(TNF-α)表达和瞬时受体电位香草酸亚型1受体(TRPV1)表达)来评估敏感性和反应性。根据治疗时间和所用物质的不同,4-TBLH和吡美莫司的应用在皮肤敏感性指标(包括TEWL、毛细血管扩张和肥大细胞活性)上显示出不同的反应。4-TBLH的预防性和治疗性应用在皮肤敏感性指标(包括皮屑、TEWL、瘙痒、刺痛、表皮厚度、肥大细胞活性、TNF-α和TRPV1表达)上显示出不同的反应。吡美莫司软膏的预防性和治疗性应用在皮肤敏感性指标(包括皮屑、皮肤含水量、瘙痒、表皮厚度、肥大细胞活性、CD45、CD11b、TNF-α和TRPV1表达)上显示出不同的反应。小鼠敏感性皮肤模型对不同治疗因素表现出较强的敏感性和反应性,该模型可应用于敏感性皮肤预防性和治疗性药物的研发。