Cargando…
Protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa B signaling pathway
Spinal cord injury (SCI) is a high incident rate of central nervous system disease that usually causes paralysis below the injured level. The occurrence of chronic inflammation with the axonal regeneration difficulties are the underlying barriers for the recovery of SCI patients. Current studies hav...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524569/ https://www.ncbi.nlm.nih.gov/pubmed/36187352 http://dx.doi.org/10.3389/fnmol.2022.1013033 |
_version_ | 1784800529482776576 |
---|---|
author | Fan, Ruihua Wang, Lvxia Botchway, Benson O. A. Zhang, Yong Liu, Xuehong |
author_facet | Fan, Ruihua Wang, Lvxia Botchway, Benson O. A. Zhang, Yong Liu, Xuehong |
author_sort | Fan, Ruihua |
collection | PubMed |
description | Spinal cord injury (SCI) is a high incident rate of central nervous system disease that usually causes paralysis below the injured level. The occurrence of chronic inflammation with the axonal regeneration difficulties are the underlying barriers for the recovery of SCI patients. Current studies have paid attention to controlling the instigative and developmental process of neuro-inflammation. Ethyl pyruvate, as a derivative of pyruvate, has strong anti-inflammatory and neuroprotective functions. Herein, we reviewed the recent studies of ethyl pyruvate and high mobility group box-1 (HMGB1). We think HMGB1 that is one of the main nuclear protein mediators to cause an inflammatory response. This protein induces astrocytic activation, and promotes glial scar formation. Interestingly, ethyl pyruvate has potent inhibitory effects on HMGB1 protein, as it inhibits chronic inflammatory response by modulating the HMGB1/TLR4/NF-κB signaling pathway. This paper discusses the potential mechanism of ethyl pyruvate in inhibiting chronic inflammation after SCI. Ethyl pyruvate can be a prospective therapeutic agent for SCI. |
format | Online Article Text |
id | pubmed-9524569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95245692022-10-01 Protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa B signaling pathway Fan, Ruihua Wang, Lvxia Botchway, Benson O. A. Zhang, Yong Liu, Xuehong Front Mol Neurosci Molecular Neuroscience Spinal cord injury (SCI) is a high incident rate of central nervous system disease that usually causes paralysis below the injured level. The occurrence of chronic inflammation with the axonal regeneration difficulties are the underlying barriers for the recovery of SCI patients. Current studies have paid attention to controlling the instigative and developmental process of neuro-inflammation. Ethyl pyruvate, as a derivative of pyruvate, has strong anti-inflammatory and neuroprotective functions. Herein, we reviewed the recent studies of ethyl pyruvate and high mobility group box-1 (HMGB1). We think HMGB1 that is one of the main nuclear protein mediators to cause an inflammatory response. This protein induces astrocytic activation, and promotes glial scar formation. Interestingly, ethyl pyruvate has potent inhibitory effects on HMGB1 protein, as it inhibits chronic inflammatory response by modulating the HMGB1/TLR4/NF-κB signaling pathway. This paper discusses the potential mechanism of ethyl pyruvate in inhibiting chronic inflammation after SCI. Ethyl pyruvate can be a prospective therapeutic agent for SCI. Frontiers Media S.A. 2022-09-16 /pmc/articles/PMC9524569/ /pubmed/36187352 http://dx.doi.org/10.3389/fnmol.2022.1013033 Text en Copyright © 2022 Fan, Wang, Botchway, Zhang and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Neuroscience Fan, Ruihua Wang, Lvxia Botchway, Benson O. A. Zhang, Yong Liu, Xuehong Protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa B signaling pathway |
title | Protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa B signaling pathway |
title_full | Protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa B signaling pathway |
title_fullStr | Protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa B signaling pathway |
title_full_unstemmed | Protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa B signaling pathway |
title_short | Protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa B signaling pathway |
title_sort | protective role of ethyl pyruvate in spinal cord injury by inhibiting the high mobility group box-1/toll-like receptor4/nuclear factor-kappa b signaling pathway |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524569/ https://www.ncbi.nlm.nih.gov/pubmed/36187352 http://dx.doi.org/10.3389/fnmol.2022.1013033 |
work_keys_str_mv | AT fanruihua protectiveroleofethylpyruvateinspinalcordinjurybyinhibitingthehighmobilitygroupbox1tolllikereceptor4nuclearfactorkappabsignalingpathway AT wanglvxia protectiveroleofethylpyruvateinspinalcordinjurybyinhibitingthehighmobilitygroupbox1tolllikereceptor4nuclearfactorkappabsignalingpathway AT botchwaybensonoa protectiveroleofethylpyruvateinspinalcordinjurybyinhibitingthehighmobilitygroupbox1tolllikereceptor4nuclearfactorkappabsignalingpathway AT zhangyong protectiveroleofethylpyruvateinspinalcordinjurybyinhibitingthehighmobilitygroupbox1tolllikereceptor4nuclearfactorkappabsignalingpathway AT liuxuehong protectiveroleofethylpyruvateinspinalcordinjurybyinhibitingthehighmobilitygroupbox1tolllikereceptor4nuclearfactorkappabsignalingpathway |