Cargando…

A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury

BACKGROUND: Neuroinflammation is an essential player in many neurological diseases including traumatic brain injury (TBI). Recent studies have identified that inflammasome complexes are responsible for inflammatory responses in many pathological conditions. Inflammasomes are intracellular multiprote...

Descripción completa

Detalles Bibliográficos
Autores principales: Kuwar, Ram, Rolfe, Andrew, Di, Long, Xu, Hongyu, He, Liu, Jiang, Yuqi, Zhang, Shijun, Sun, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458637/
https://www.ncbi.nlm.nih.gov/pubmed/30975164
http://dx.doi.org/10.1186/s12974-019-1471-y
_version_ 1783410048019464192
author Kuwar, Ram
Rolfe, Andrew
Di, Long
Xu, Hongyu
He, Liu
Jiang, Yuqi
Zhang, Shijun
Sun, Dong
author_facet Kuwar, Ram
Rolfe, Andrew
Di, Long
Xu, Hongyu
He, Liu
Jiang, Yuqi
Zhang, Shijun
Sun, Dong
author_sort Kuwar, Ram
collection PubMed
description BACKGROUND: Neuroinflammation is an essential player in many neurological diseases including traumatic brain injury (TBI). Recent studies have identified that inflammasome complexes are responsible for inflammatory responses in many pathological conditions. Inflammasomes are intracellular multiprotein complexes which regulate the innate immune response, activation of caspase-1, production of pro-inflammatory cytokines IL-1β and IL-18, and induction of cell death (pyroptosis). Among inflammasome family members, the nucleotide-binding domain leucine-rich repeats family protein 3 (NLRP3) is the most extensively studied and its activation is induced following TBI. As a novel target, drug development targeting the formation and activation of NLRP3 inflammasome is a prospective therapy for TBI. We have recently developed a small molecule JC124 with specificity on NLRP3 inflammasome. In this study, we explored the therapeutic value of JC124 for TBI treatment. METHODS: Adult male Sprague-Dawley rats were subjected to a moderate cortical impact injury. Following TBI, animals received 4 doses of JC124 treatment with the first dose starting at 30 min, the second dose at 6 h after TBI, the third and fourth doses at 24 or 30 h following TBI, respectively. Animals were sacrificed at 2 days post-injury. Brain tissues were processed either for ELISA and western blotting analysis for inflammatory response, or for histological examination to assess degenerative neurons, acute inflammatory cell response and lesion volume. RESULTS: We found that post-injury treatment with JC124 significantly decreased the number of injury-induced degenerating neurons, inflammatory cell response in the injured brain, and cortical lesion volume. Injured animals treated with JC124 also had significantly reduced protein expression levels of NLRP3, ASC, IL-1 beta, TNFα, iNOS, and caspase-1. CONCLUSION: Our data suggest that our novel NLRP3 inhibitor has a specific anti-inflammatory effect to protect the injured brain following TBI.
format Online
Article
Text
id pubmed-6458637
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-64586372019-04-19 A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury Kuwar, Ram Rolfe, Andrew Di, Long Xu, Hongyu He, Liu Jiang, Yuqi Zhang, Shijun Sun, Dong J Neuroinflammation Research BACKGROUND: Neuroinflammation is an essential player in many neurological diseases including traumatic brain injury (TBI). Recent studies have identified that inflammasome complexes are responsible for inflammatory responses in many pathological conditions. Inflammasomes are intracellular multiprotein complexes which regulate the innate immune response, activation of caspase-1, production of pro-inflammatory cytokines IL-1β and IL-18, and induction of cell death (pyroptosis). Among inflammasome family members, the nucleotide-binding domain leucine-rich repeats family protein 3 (NLRP3) is the most extensively studied and its activation is induced following TBI. As a novel target, drug development targeting the formation and activation of NLRP3 inflammasome is a prospective therapy for TBI. We have recently developed a small molecule JC124 with specificity on NLRP3 inflammasome. In this study, we explored the therapeutic value of JC124 for TBI treatment. METHODS: Adult male Sprague-Dawley rats were subjected to a moderate cortical impact injury. Following TBI, animals received 4 doses of JC124 treatment with the first dose starting at 30 min, the second dose at 6 h after TBI, the third and fourth doses at 24 or 30 h following TBI, respectively. Animals were sacrificed at 2 days post-injury. Brain tissues were processed either for ELISA and western blotting analysis for inflammatory response, or for histological examination to assess degenerative neurons, acute inflammatory cell response and lesion volume. RESULTS: We found that post-injury treatment with JC124 significantly decreased the number of injury-induced degenerating neurons, inflammatory cell response in the injured brain, and cortical lesion volume. Injured animals treated with JC124 also had significantly reduced protein expression levels of NLRP3, ASC, IL-1 beta, TNFα, iNOS, and caspase-1. CONCLUSION: Our data suggest that our novel NLRP3 inhibitor has a specific anti-inflammatory effect to protect the injured brain following TBI. BioMed Central 2019-04-11 /pmc/articles/PMC6458637/ /pubmed/30975164 http://dx.doi.org/10.1186/s12974-019-1471-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kuwar, Ram
Rolfe, Andrew
Di, Long
Xu, Hongyu
He, Liu
Jiang, Yuqi
Zhang, Shijun
Sun, Dong
A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury
title A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury
title_full A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury
title_fullStr A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury
title_full_unstemmed A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury
title_short A novel small molecular NLRP3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury
title_sort novel small molecular nlrp3 inflammasome inhibitor alleviates neuroinflammatory response following traumatic brain injury
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458637/
https://www.ncbi.nlm.nih.gov/pubmed/30975164
http://dx.doi.org/10.1186/s12974-019-1471-y
work_keys_str_mv AT kuwarram anovelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT rolfeandrew anovelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT dilong anovelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT xuhongyu anovelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT heliu anovelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT jiangyuqi anovelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT zhangshijun anovelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT sundong anovelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT kuwarram novelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT rolfeandrew novelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT dilong novelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT xuhongyu novelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT heliu novelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT jiangyuqi novelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT zhangshijun novelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury
AT sundong novelsmallmolecularnlrp3inflammasomeinhibitoralleviatesneuroinflammatoryresponsefollowingtraumaticbraininjury