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Biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans

Sensitive skin is a frequently mentioned cosmetic complaint. Addition of a biomimetic of neuromediator has recently appeared as a promising new way to cure skin care product problems. This study was aimed to assess the inhibitory effect of a biomimetic lipopeptide derived from proopiomelanocortin (b...

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Autores principales: Fatemi, Sayed Ali, Jafarian-Dehkordi, Abbas, Hajhashemi, Valiollah, Asilian-Mahabadi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168885/
https://www.ncbi.nlm.nih.gov/pubmed/28003842
http://dx.doi.org/10.4103/1735-5362.194890
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author Fatemi, Sayed Ali
Jafarian-Dehkordi, Abbas
Hajhashemi, Valiollah
Asilian-Mahabadi, Ali
author_facet Fatemi, Sayed Ali
Jafarian-Dehkordi, Abbas
Hajhashemi, Valiollah
Asilian-Mahabadi, Ali
author_sort Fatemi, Sayed Ali
collection PubMed
description Sensitive skin is a frequently mentioned cosmetic complaint. Addition of a biomimetic of neuromediator has recently appeared as a promising new way to cure skin care product problems. This study was aimed to assess the inhibitory effect of a biomimetic lipopeptide derived from proopiomelanocortin (bPOMC) on capsaicin-induced sensory irritation in human volunteers and also to compare its protective effect with that of the well-known anti irritant strontium chloride. The effect of each test compound was studied on 28 selected healthy volunteers with sensitive skin in accordance with a double-blind vehicle-controlled protocol. From day 1 to day 13 each group was applied the test compound (bPOMC or strontium chloride) to one wing of the nose and the corresponding placebo (vehicle) to the other side twice daily. On days 0 and 14, acute skin irritation was induced by capsaicin solution and quantified using clinical stinging test assessments. Following the application of capsaicin solution, sensory irritation was evaluated using a 4-point numeric scale. The sensations perceived before and after treatment (on days 0 and 14) was calculated for the two zones (test materials and vehicle). Ultimately the percentage of variation between each sample and the placebo and also the inhibitory effect of bPOMC compared to that of strontium chloride were reported. Clinical results showed that after two weeks treatment, the levels of skin comfort reported in the group treated with bPOMC were significantly higher than those obtained in the placebo group and the inhibitory effect of bPOMC was about 47% higher than that of strontium chloride. The results of the present study support the hypothesis that biomimetic peptides may be effective on sensitive skin.
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spelling pubmed-51688852016-12-21 Biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans Fatemi, Sayed Ali Jafarian-Dehkordi, Abbas Hajhashemi, Valiollah Asilian-Mahabadi, Ali Res Pharm Sci Original Article Sensitive skin is a frequently mentioned cosmetic complaint. Addition of a biomimetic of neuromediator has recently appeared as a promising new way to cure skin care product problems. This study was aimed to assess the inhibitory effect of a biomimetic lipopeptide derived from proopiomelanocortin (bPOMC) on capsaicin-induced sensory irritation in human volunteers and also to compare its protective effect with that of the well-known anti irritant strontium chloride. The effect of each test compound was studied on 28 selected healthy volunteers with sensitive skin in accordance with a double-blind vehicle-controlled protocol. From day 1 to day 13 each group was applied the test compound (bPOMC or strontium chloride) to one wing of the nose and the corresponding placebo (vehicle) to the other side twice daily. On days 0 and 14, acute skin irritation was induced by capsaicin solution and quantified using clinical stinging test assessments. Following the application of capsaicin solution, sensory irritation was evaluated using a 4-point numeric scale. The sensations perceived before and after treatment (on days 0 and 14) was calculated for the two zones (test materials and vehicle). Ultimately the percentage of variation between each sample and the placebo and also the inhibitory effect of bPOMC compared to that of strontium chloride were reported. Clinical results showed that after two weeks treatment, the levels of skin comfort reported in the group treated with bPOMC were significantly higher than those obtained in the placebo group and the inhibitory effect of bPOMC was about 47% higher than that of strontium chloride. The results of the present study support the hypothesis that biomimetic peptides may be effective on sensitive skin. Medknow Publications & Media Pvt Ltd 2016-12 /pmc/articles/PMC5168885/ /pubmed/28003842 http://dx.doi.org/10.4103/1735-5362.194890 Text en Copyright: © Research in Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Fatemi, Sayed Ali
Jafarian-Dehkordi, Abbas
Hajhashemi, Valiollah
Asilian-Mahabadi, Ali
Biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans
title Biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans
title_full Biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans
title_fullStr Biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans
title_full_unstemmed Biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans
title_short Biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans
title_sort biomimetic proopiomelanocortin suppresses capsaicin-induced sensory irritation in humans
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168885/
https://www.ncbi.nlm.nih.gov/pubmed/28003842
http://dx.doi.org/10.4103/1735-5362.194890
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