PAI1 regulating CHRNA1 contributes to primary focal hyperhidrosis: Clinical and experimental studies

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 (<i>n</i> = 204) and healthy controls (<i>n</i> = 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 <i>in vitro</i> 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 (<i>p</i> < 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 <i>in vivo</i>. 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.

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Journal
Molecular Therapy — Nucleic Acids
Published
2025-05-16
DOI
https://doi.org/10.1016/j.omtn.2025.102566
Citations
1
Primary Topic
Sympathectomy and Hyperhidrosis Treatments
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article
Field-Weighted Citation Impact
1.16
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article

PAI1 regulating CHRNA1 contributes to primary focal hyperhidrosis: Clinical and experimental studies

M Zhang, Xu Li, Nanlong Lin, Runze Qiu et al.
1 citations
Molecular Therapy — Nucleic Acids
Sympathectomy and Hyperhidrosis Treatments
1.16
article

PAI1 regulating CHRNA1 contributes to primary focal hyperhidrosis: Clinical and experimental studies

M Zhang, Xu Li, Nanlong Lin, Runze Qiu, Fangqun Yu, Rongyuan Zheng, J Lin
article en
1 citations

Abstract

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 (<i>n</i> = 204) and healthy controls (<i>n</i> = 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 <i>in vitro</i> 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 (<i>p</i> < 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 <i>in vivo</i>. 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.

Molecular Therapy — Nucleic AcidsVol. 36(2)
Fujian Medical University (CN), First Affiliated Hospital of Fujian Medical University (CN)
Zero hunger
Openalex Percentile: Top 22%
Sympathectomy and Hyperhidrosis Treatments
1.16
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