Cited by 22Neuropeptides and Animal PhysiologyIon Channels and ReceptorsCardiovascular, Neuropeptides, and Oxidative Stress Research

Pituitary adenylate cyclase‐activating polypeptide promotes eccrine gland sweat secretion

Sasaki, S., Watanabe, J., Ohtaki, H., Matsumoto, M., Murai, N., Nakamachi, T., Hannibal, J., Fahrenkrug, J. +6 more·2017·British Journal of Dermatology

Abstract

BACKGROUND: Sweat secretion is the major function of eccrine sweat glands; when this process is disturbed (paridrosis), serious skin problems can arise. To elucidate the causes of paridrosis, an improved understanding of the regulation, mechanisms and factors underlying sweat production is required. Pituitary adenylate cyclase-activating polypeptide (PACAP) exhibits pleiotropic functions that are mediated via its receptors [PACAP-specific receptor (PAC1R), vasoactive intestinal peptide (VIP) receptor type 1 (VPAC1R) and VPAC2R]. Although some studies have suggested a role for PACAP in the skin and several exocrine glands, the effects of PACAP on the process of eccrine sweat secretion have not been examined. OBJECTIVES: To investigate the effect of PACAP on eccrine sweat secretion. METHODS: Reverse transcriptase-polymerase chain reaction and immunostaining were used to determine the expression and localization of PACAP and its receptors in mouse and human eccrine sweat glands. We injected PACAP subcutaneously into the footpads of mice and used the starch-iodine test to visualize sweat-secreting glands. RESULTS: Immunostaining showed PACAP and PAC1R expression by secretory cells from mouse and human sweat glands. PACAP immunoreactivity was also localized in nerve fibres around eccrine sweat glands. PACAP significantly promoted sweat secretion at the injection site, and this could be blocked by the PAC1R-antagonist PACAP6-38. VIP, an agonist of VPAC1R and VPAC2R, failed to induce sweat secretion. CONCLUSIONS: This is the first report demonstrating that PACAP may play a crucial role in sweat secretion via its action on PAC1R located in eccrine sweat glands. The mechanisms underlying the role of PACAP in sweat secretion may provide new therapeutic options to combat sweating disorders.

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Authors
Sasaki, S., Watanabe, J., Ohtaki, H., Matsumoto, M., Murai, N., Nakamachi, T., Hannibal, J., Fahrenkrug, J., Hashimoto, H., Watanabe, H., Sueki, H., Honda, K., Miyazaki, A., & Shioda, S.
Affiliations
  • SHOWA Medical University (JP)
  • University of Toyama (JP)
  • University of Copenhagen (DK)
  • Kanazawa University (JP)
  • Hoshi University (JP)
Corresponding author
Shioda, S.
Venue
British Journal of Dermatology
Published
2017-01-24
Volume
176
Issue
2
Pages
413-422
ISSN
  • 0007-0963 (ISSN-L)
  • 1365-2133
OpenAlex
W2498123954
Cited by
22
References
0
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 1 · 2021: 2 · 2020: 3 · 2019: 3 · 2018: 5 · 2017: 2
FWCI
1.88
Type
journal article
Language
en
Open access
closed
Locations
  • British Journal of Dermatology (publishedVersion)
  • PubMed (publishedVersion)
  • Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
Funders
  • Japan Society for the Promotion of Science (15H01288, 15K15670, 23249079, 25861289, 26293020, 26670122)
  • Japan Society for the Promotion of Science London (S2603)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
  • Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
  • Health Sciences › Medicine › Surgery › Cardiovascular, Neuropeptides, and Oxidative Stress Research
Keywords
pituitary adenylate cyclase-activating polypeptide, PACAP, eccrine sweat glands, sweat secretion, PAC1 receptor, vasoactive intestinal peptide, VPAC1 receptor, VPAC2 receptor, sweat gland innervation, sweating disorders
MeSH terms
Adult, Animals, Eccrine Glands, Female, Foot, Humans, Male, Mice, Inbred C57BL, Nerve Fibers, RNA, Messenger, Sweat, Pituitary Adenylate Cyclase-Activating Polypeptide, Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Receptors, Vasoactive Intestinal Polypeptide, Type I, Receptors, Vasoactive Intestinal Peptide, Type II

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