Inhibition of neuropeptide degradation suppresses sweating but increases the area of the axon reflex flare
The neuropeptides CGRP (calcitonin gene‐elated peptide) and substance P (SP) mediate neurogenic inflammation. Both are degraded by the neutral endopeptidase (NEP) which can be blocked by phosphoramidon. The aim was to evaluate the effect of NEP inhibition on sweating and vasodilatation. Dermal micro...
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Published in | Experimental dermatology Vol. 22; no. 4; pp. 299 - 301 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Denmark
Blackwell Publishing Ltd
01.04.2013
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Subjects | |
Online Access | Get full text |
ISSN | 0906-6705 1600-0625 1600-0625 |
DOI | 10.1111/exd.12122 |
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Summary: | The neuropeptides CGRP (calcitonin gene‐elated peptide) and substance P (SP) mediate neurogenic inflammation. Both are degraded by the neutral endopeptidase (NEP) which can be blocked by phosphoramidon. The aim was to evaluate the effect of NEP inhibition on sweating and vasodilatation. Dermal microdialysis was performed on the skin of 39 subjects. Two fibres were perfused with phosphoramidon (0.01%, 0.02% or 0.2%), two with saline. Acetylcholine (ACh) was either added to the microdialysis perfusate (n = 30, 10−2 m) or thermoregulatory sweating was induced (n = 9). Co‐application of phosphoramidon reduced cholinergic and thermoregulatory sweating. However, the flare size – a localized increase in superficial blood flow after ACh‐application – was significantly increased. The increase in flare size is most probably due to increased CGRP levels. The inhibition of sweating by phosphoramidon may involve an increase in SP, a reduction in CGRP‐degradation fragments or a direct inhibitory action of phosphoramidon. |
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Bibliography: | Figure S1. Microdialysis.Figure S2. Stimulation paradigm. istex:429F9FB16978E54DF522B459AC41D065531858D2 ArticleID:EXD12122 ark:/67375/WNG-7Q741VWZ-N ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Correspondence-1 content type line 23 |
ISSN: | 0906-6705 1600-0625 1600-0625 |
DOI: | 10.1111/exd.12122 |