Zheng Ru-Jie, Lin Nan-Long, Zhang Meng-Long, Qiu Rui-Qin, Yu Feng-Qiang, Li Xu, Lin Jian-Bo
Department of Anesthesiology, First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
Department of Anesthesiology, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fuzhou 350005, China.
Mol Ther Nucleic Acids. 2025 May 16;36(2):102566. doi: 10.1016/j.omtn.2025.102566. eCollection 2025 Jun 10.
Primary focal hyperhidrosis (PFH) is a debilitating condition characterized by localized excessive sweating, yet its underlying mechanisms remain poorly understood. In this study, sweat gland tissues from PFH patients ( = 204) and healthy controls ( = 60) were analyzed to assess the mRNA and protein levels of plasminogen activator inhibitor 1 (PAI-1) and nicotinic acetylcholine receptor alpha 1 subunit (CHRNA1) using RT-qPCR and western blotting. Primary sweat gland cells were isolated for experiments, and a pilocarpine-induced hyperhidrosis mouse model was established to evaluate the therapeutic effect of recombinant human PAI-1 (rhPAI-1). PFH patients showed significantly reduced PAI-1 expression and elevated CHRNA1 expression compared to controls ( < 0.01). Treatment with rhPAI-1 downregulated CHRNA1 and aquaporin 5 (AQP5) expression in sweat gland cells and decreased sweat secretion and serum acetylcholine levels . These results suggest that PAI-1 negatively regulates CHRNA1 and AQP5 expression, offering new insights into the molecular pathology of PFH and identifying PAI-1 as a potential therapeutic target for hyperhidrosis.
原发性局灶性多汗症(PFH)是一种以局部多汗为特征的使人衰弱的病症,但其潜在机制仍知之甚少。在本研究中,对PFH患者(n = 204)和健康对照者(n = 60)的汗腺组织进行分析,使用逆转录定量聚合酶链反应(RT-qPCR)和蛋白质印迹法评估纤溶酶原激活物抑制剂1(PAI-1)和烟碱型乙酰胆碱受体α1亚基(CHRNA1)的mRNA和蛋白质水平。分离原代汗腺细胞进行实验,并建立毛果芸香碱诱导的多汗症小鼠模型以评估重组人PAI-1(rhPAI-1)的治疗效果。与对照组相比,PFH患者的PAI-1表达显著降低,CHRNA1表达升高(P < 0.01)。用rhPAI-1治疗可下调汗腺细胞中CHRNA1和水通道蛋白5(AQP5)的表达,并降低汗液分泌和血清乙酰胆碱水平。这些结果表明,PAI-1对CHRNA1和AQP5的表达具有负调控作用,为PFH的分子病理学提供了新的见解,并确定PAI-1为多汗症的潜在治疗靶点。