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SIRT1: A promising therapeutic target for chronic pain
Chronic pain remains an unresolved problem. Current treatments have limited efficacy. Thus, novel therapeutic targets are urgently required for the development of more effective analgesics. An increasing number of studies have proved that sirtuin 1 (SIRT1) agonists can relieve chronic pain. In this...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062570/ https://www.ncbi.nlm.nih.gov/pubmed/35396903 http://dx.doi.org/10.1111/cns.13838 |
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author | Song, Fan‐He Liu, Dai‐Qiang Zhou, Ya‐Qun Mei, Wei |
author_facet | Song, Fan‐He Liu, Dai‐Qiang Zhou, Ya‐Qun Mei, Wei |
author_sort | Song, Fan‐He |
collection | PubMed |
description | Chronic pain remains an unresolved problem. Current treatments have limited efficacy. Thus, novel therapeutic targets are urgently required for the development of more effective analgesics. An increasing number of studies have proved that sirtuin 1 (SIRT1) agonists can relieve chronic pain. In this review, we summarize recent progress in understanding the roles and mechanisms of SIRT1 in mediating chronic pain associated with peripheral nerve injury, chemotherapy‐induced peripheral neuropathy, spinal cord injury, bone cancer, and complete Freund's adjuvant injection. Emerging studies have indicated that SIRT1 activation may exert positive effects on chronic pain relief by regulating inflammation, oxidative stress, and mitochondrial dysfunction. Therefore, SIRT1 agonists may serve as potential therapeutic drugs for chronic pain. |
format | Online Article Text |
id | pubmed-9062570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90625702022-05-03 SIRT1: A promising therapeutic target for chronic pain Song, Fan‐He Liu, Dai‐Qiang Zhou, Ya‐Qun Mei, Wei CNS Neurosci Ther Reviews Chronic pain remains an unresolved problem. Current treatments have limited efficacy. Thus, novel therapeutic targets are urgently required for the development of more effective analgesics. An increasing number of studies have proved that sirtuin 1 (SIRT1) agonists can relieve chronic pain. In this review, we summarize recent progress in understanding the roles and mechanisms of SIRT1 in mediating chronic pain associated with peripheral nerve injury, chemotherapy‐induced peripheral neuropathy, spinal cord injury, bone cancer, and complete Freund's adjuvant injection. Emerging studies have indicated that SIRT1 activation may exert positive effects on chronic pain relief by regulating inflammation, oxidative stress, and mitochondrial dysfunction. Therefore, SIRT1 agonists may serve as potential therapeutic drugs for chronic pain. John Wiley and Sons Inc. 2022-04-09 /pmc/articles/PMC9062570/ /pubmed/35396903 http://dx.doi.org/10.1111/cns.13838 Text en © 2022 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Song, Fan‐He Liu, Dai‐Qiang Zhou, Ya‐Qun Mei, Wei SIRT1: A promising therapeutic target for chronic pain |
title | SIRT1: A promising therapeutic target for chronic pain |
title_full | SIRT1: A promising therapeutic target for chronic pain |
title_fullStr | SIRT1: A promising therapeutic target for chronic pain |
title_full_unstemmed | SIRT1: A promising therapeutic target for chronic pain |
title_short | SIRT1: A promising therapeutic target for chronic pain |
title_sort | sirt1: a promising therapeutic target for chronic pain |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062570/ https://www.ncbi.nlm.nih.gov/pubmed/35396903 http://dx.doi.org/10.1111/cns.13838 |
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