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Spotlight on Nociceptin/Orphanin FQ Receptor in the Treatment of Pain

In our society today, pain has become a main source of strain on most individuals. It is crucial to develop novel treatments against pain while focusing on decreasing their adverse effects. Throughout the extent of development for new pain therapies, the nociceptin/orphanin FQ receptor (NOP receptor...

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Detalles Bibliográficos
Autores principales: El Daibani, Amal, Che, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838650/
https://www.ncbi.nlm.nih.gov/pubmed/35163856
http://dx.doi.org/10.3390/molecules27030595
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author El Daibani, Amal
Che, Tao
author_facet El Daibani, Amal
Che, Tao
author_sort El Daibani, Amal
collection PubMed
description In our society today, pain has become a main source of strain on most individuals. It is crucial to develop novel treatments against pain while focusing on decreasing their adverse effects. Throughout the extent of development for new pain therapies, the nociceptin/orphanin FQ receptor (NOP receptor) has appeared to be an encouraging focal point. Concentrating on NOP receptor to treat chronic pain with limited range of unwanted effects serves as a suitable alternative to prototypical opioid morphine that could potentially lead to life-threatening effects caused by respiratory depression in overdose, as well as generate abuse and addiction. In addition to these harmful effects, the uprising opioid epidemic is responsible for becoming one of the most disastrous public health issues in the US. In this article, the contributing molecular and cellular structure in controlling the cellular trafficking of NOP receptor and studies that support the role of NOP receptor and its ligands in pain management are reviewed.
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spelling pubmed-88386502022-02-13 Spotlight on Nociceptin/Orphanin FQ Receptor in the Treatment of Pain El Daibani, Amal Che, Tao Molecules Review In our society today, pain has become a main source of strain on most individuals. It is crucial to develop novel treatments against pain while focusing on decreasing their adverse effects. Throughout the extent of development for new pain therapies, the nociceptin/orphanin FQ receptor (NOP receptor) has appeared to be an encouraging focal point. Concentrating on NOP receptor to treat chronic pain with limited range of unwanted effects serves as a suitable alternative to prototypical opioid morphine that could potentially lead to life-threatening effects caused by respiratory depression in overdose, as well as generate abuse and addiction. In addition to these harmful effects, the uprising opioid epidemic is responsible for becoming one of the most disastrous public health issues in the US. In this article, the contributing molecular and cellular structure in controlling the cellular trafficking of NOP receptor and studies that support the role of NOP receptor and its ligands in pain management are reviewed. MDPI 2022-01-18 /pmc/articles/PMC8838650/ /pubmed/35163856 http://dx.doi.org/10.3390/molecules27030595 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
El Daibani, Amal
Che, Tao
Spotlight on Nociceptin/Orphanin FQ Receptor in the Treatment of Pain
title Spotlight on Nociceptin/Orphanin FQ Receptor in the Treatment of Pain
title_full Spotlight on Nociceptin/Orphanin FQ Receptor in the Treatment of Pain
title_fullStr Spotlight on Nociceptin/Orphanin FQ Receptor in the Treatment of Pain
title_full_unstemmed Spotlight on Nociceptin/Orphanin FQ Receptor in the Treatment of Pain
title_short Spotlight on Nociceptin/Orphanin FQ Receptor in the Treatment of Pain
title_sort spotlight on nociceptin/orphanin fq receptor in the treatment of pain
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838650/
https://www.ncbi.nlm.nih.gov/pubmed/35163856
http://dx.doi.org/10.3390/molecules27030595
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