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Cell Signaling Pathways Related to Pain Receptors in the Degenerated Disk

Many of the causes of low back pain are still unknown; sufficient evidence indicates that both degenerative and mechanical change within the intervertebral disk (IVD) is a relevant factor. This article reviews intracellular signaling pathways related to pain receptors in the degenerated IVD. Several...

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Detalles Bibliográficos
Autores principales: Hiyama, Akihiko, Sakai, Daisuke, Mochida, Joji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856443/
https://www.ncbi.nlm.nih.gov/pubmed/24436867
http://dx.doi.org/10.1055/s-0033-1345036
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author Hiyama, Akihiko
Sakai, Daisuke
Mochida, Joji
author_facet Hiyama, Akihiko
Sakai, Daisuke
Mochida, Joji
author_sort Hiyama, Akihiko
collection PubMed
description Many of the causes of low back pain are still unknown; sufficient evidence indicates that both degenerative and mechanical change within the intervertebral disk (IVD) is a relevant factor. This article reviews intracellular signaling pathways related to pain receptors in the degenerated IVD. Several reports have demonstrated the number of nerve fibers in the IVD was increased in degenerated disks. In recent years, some groups have reported that an increase in nerve fibers is associated with the presence of inflammatory mediators and/or neurotrophins in the IVD. Cell signaling events, which are regulated by inflammatory mediators and neurotrophins, must be identified to clarify the mechanism underlying low back pain. Major intracellular signaling pathways (nuclear factor kappa β, mitogen-activated protein kinases, and Wnts) potentially play vital roles in mediating the molecular events responsible for the initiation and progression of IVD degeneration. These signaling pathways may represent therapeutic targets for the treatment of IVD degeneration and its associated back pain.
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spelling pubmed-38564432014-06-01 Cell Signaling Pathways Related to Pain Receptors in the Degenerated Disk Hiyama, Akihiko Sakai, Daisuke Mochida, Joji Global Spine J Article Many of the causes of low back pain are still unknown; sufficient evidence indicates that both degenerative and mechanical change within the intervertebral disk (IVD) is a relevant factor. This article reviews intracellular signaling pathways related to pain receptors in the degenerated IVD. Several reports have demonstrated the number of nerve fibers in the IVD was increased in degenerated disks. In recent years, some groups have reported that an increase in nerve fibers is associated with the presence of inflammatory mediators and/or neurotrophins in the IVD. Cell signaling events, which are regulated by inflammatory mediators and neurotrophins, must be identified to clarify the mechanism underlying low back pain. Major intracellular signaling pathways (nuclear factor kappa β, mitogen-activated protein kinases, and Wnts) potentially play vital roles in mediating the molecular events responsible for the initiation and progression of IVD degeneration. These signaling pathways may represent therapeutic targets for the treatment of IVD degeneration and its associated back pain. Georg Thieme Verlag KG 2013-05-09 2013-06 /pmc/articles/PMC3856443/ /pubmed/24436867 http://dx.doi.org/10.1055/s-0033-1345036 Text en © Thieme Medical Publishers
spellingShingle Article
Hiyama, Akihiko
Sakai, Daisuke
Mochida, Joji
Cell Signaling Pathways Related to Pain Receptors in the Degenerated Disk
title Cell Signaling Pathways Related to Pain Receptors in the Degenerated Disk
title_full Cell Signaling Pathways Related to Pain Receptors in the Degenerated Disk
title_fullStr Cell Signaling Pathways Related to Pain Receptors in the Degenerated Disk
title_full_unstemmed Cell Signaling Pathways Related to Pain Receptors in the Degenerated Disk
title_short Cell Signaling Pathways Related to Pain Receptors in the Degenerated Disk
title_sort cell signaling pathways related to pain receptors in the degenerated disk
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856443/
https://www.ncbi.nlm.nih.gov/pubmed/24436867
http://dx.doi.org/10.1055/s-0033-1345036
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