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Neurokinin 1 Receptor Antagonists for Pruritus
Pruritus, commonly known as itch, is a very common symptom in numerous dermatological disorders and systemic diseases. It can manifest as acute, or when lasting longer than 6 weeks, it is considered chronic and can lead to significant distress and reduced quality-of-life of those suffering. Current...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102458/ https://www.ncbi.nlm.nih.gov/pubmed/33675531 http://dx.doi.org/10.1007/s40265-021-01478-1 |
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author | Alam, Majid Buddenkotte, Joerg Ahmad, Fareed Steinhoff, Martin |
author_facet | Alam, Majid Buddenkotte, Joerg Ahmad, Fareed Steinhoff, Martin |
author_sort | Alam, Majid |
collection | PubMed |
description | Pruritus, commonly known as itch, is a very common symptom in numerous dermatological disorders and systemic diseases. It can manifest as acute, or when lasting longer than 6 weeks, it is considered chronic and can lead to significant distress and reduced quality-of-life of those suffering. Current therapeutics are limited and are lacking in efficacy, and the development of more effective treatments is needed. The neurokinin 1 receptor (NK1R) antagonists are a novel class of drugs that possess several properties such as antidepressant, anxiolytic and antiemetic activities. Recently, several studies have described the antipruritic activity of NK1R antagonists for treating chronic pruritus. In this review we outline the pathogenesis of chronic pruritus, the mechanism by which the neuropeptide substance P (SP) and its receptor NK1R may be targeted to inhibit pruritic activity, and the efficacy and tolerability of NK1R antagonists, which have been, or are currently being investigated for treating conditions where chronic pruritus is a major symptom. Increasing evidence from ongoing and completed studies demonstrates the importance of SP and NK1R signalling in mediating pruritic activity. Several NK1R antagonists have shown significant antipruritic activity and thus targeting the SP-NK1R pathway may provide a therapeutic option for treating chronic pruritus of certain origin/s in the foreseeable future. |
format | Online Article Text |
id | pubmed-8102458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-81024582021-05-11 Neurokinin 1 Receptor Antagonists for Pruritus Alam, Majid Buddenkotte, Joerg Ahmad, Fareed Steinhoff, Martin Drugs Leading Article Pruritus, commonly known as itch, is a very common symptom in numerous dermatological disorders and systemic diseases. It can manifest as acute, or when lasting longer than 6 weeks, it is considered chronic and can lead to significant distress and reduced quality-of-life of those suffering. Current therapeutics are limited and are lacking in efficacy, and the development of more effective treatments is needed. The neurokinin 1 receptor (NK1R) antagonists are a novel class of drugs that possess several properties such as antidepressant, anxiolytic and antiemetic activities. Recently, several studies have described the antipruritic activity of NK1R antagonists for treating chronic pruritus. In this review we outline the pathogenesis of chronic pruritus, the mechanism by which the neuropeptide substance P (SP) and its receptor NK1R may be targeted to inhibit pruritic activity, and the efficacy and tolerability of NK1R antagonists, which have been, or are currently being investigated for treating conditions where chronic pruritus is a major symptom. Increasing evidence from ongoing and completed studies demonstrates the importance of SP and NK1R signalling in mediating pruritic activity. Several NK1R antagonists have shown significant antipruritic activity and thus targeting the SP-NK1R pathway may provide a therapeutic option for treating chronic pruritus of certain origin/s in the foreseeable future. Springer International Publishing 2021-03-06 2021 /pmc/articles/PMC8102458/ /pubmed/33675531 http://dx.doi.org/10.1007/s40265-021-01478-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Leading Article Alam, Majid Buddenkotte, Joerg Ahmad, Fareed Steinhoff, Martin Neurokinin 1 Receptor Antagonists for Pruritus |
title | Neurokinin 1 Receptor Antagonists for Pruritus |
title_full | Neurokinin 1 Receptor Antagonists for Pruritus |
title_fullStr | Neurokinin 1 Receptor Antagonists for Pruritus |
title_full_unstemmed | Neurokinin 1 Receptor Antagonists for Pruritus |
title_short | Neurokinin 1 Receptor Antagonists for Pruritus |
title_sort | neurokinin 1 receptor antagonists for pruritus |
topic | Leading Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102458/ https://www.ncbi.nlm.nih.gov/pubmed/33675531 http://dx.doi.org/10.1007/s40265-021-01478-1 |
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