Cargando…

Melatonin Attenuates Neuroinflammation by Down-Regulating NLRP3 Inflammasome via a SIRT1-Dependent Pathway in MPTP-Induced Models of Parkinson’s Disease

BACKGROUND: Inflammasome-induced neuroinflammation is a key contributor to the pathology of Parkinson’s disease (PD). NLR family pyrin domain-containing 3 (NLRP3) inflammasome activation has been implicated in PD in postmortem human PD brains, indicating it as a potential target for PD treatment. Me...

Descripción completa

Detalles Bibliográficos
Autores principales: Zheng, Ran, Ruan, Yang, Yan, Yiqun, Lin, Zhihao, Xue, Naijia, Yan, Yaping, Tian, Jun, Yin, Xinzhen, Pu, Jiali, Zhang, Baorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275196/
https://www.ncbi.nlm.nih.gov/pubmed/34267535
http://dx.doi.org/10.2147/JIR.S317672
_version_ 1783721684592754688
author Zheng, Ran
Ruan, Yang
Yan, Yiqun
Lin, Zhihao
Xue, Naijia
Yan, Yaping
Tian, Jun
Yin, Xinzhen
Pu, Jiali
Zhang, Baorong
author_facet Zheng, Ran
Ruan, Yang
Yan, Yiqun
Lin, Zhihao
Xue, Naijia
Yan, Yaping
Tian, Jun
Yin, Xinzhen
Pu, Jiali
Zhang, Baorong
author_sort Zheng, Ran
collection PubMed
description BACKGROUND: Inflammasome-induced neuroinflammation is a key contributor to the pathology of Parkinson’s disease (PD). NLR family pyrin domain-containing 3 (NLRP3) inflammasome activation has been implicated in PD in postmortem human PD brains, indicating it as a potential target for PD treatment. Melatonin, a multitasking molecule, has been found to have anti-inflammatory activities, mediated by silence information regulator 1 (SIRT1). However, whether and how melatonin is involved in inflammasome-induced neuroinflammation in PD pathogenesis remains unclear. METHODS: We investigated the potential anti-inflammatory effects of melatonin in vitro and in vivo, using 1-methyl-4-phenylpyridinium (MPP(+))-simulated BV2 and primary microglia cell models, and a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced murine PD model, with or without melatonin treatment. Rotarod, grip strength, and open-field tests were performed to measure the effects of melatonin on MPTP-induced motor disorders. Degeneration of dopaminergic neurons was evaluated by immunofluorescence. Changes in microglia were examined by immunofluorescence and Western blotting, and the expression levels of the involved signaling molecules were assessed by Western blotting and enzyme-linked immunosorbent assay (ELISA). Intracellular reactive oxygen species (ROS) was detected using fluorescent probes via flow cytometry. RESULTS: We found that melatonin significantly alleviated motor dysfunction and prevented MPTP-induced neurotoxicity in dopaminergic neurons. Additionally, melatonin reduced MPTP-induced microglial activation and suppressed NLRP3 inflammasome activity, and also inhibited IL-1β secretion. Moreover, in MPP(+)-primed BV2 cells, melatonin markedly restored the downregulation of SIRT1 and attenuated the activation of the NLRP3 inflammasome. This was reversed by SIRT1 inhibitor treatment. CONCLUSION: In conclusion, our data demonstrated that melatonin attenuates neuroinflammation by negatively regulating NLRP3 inflammasome activation via a SIRT1-dependent pathway in MPTP-induced PD models. These findings provide novel insights into the mechanism underlying the anti-inflammatory effects of melatonin in PD.
format Online
Article
Text
id pubmed-8275196
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-82751962021-07-14 Melatonin Attenuates Neuroinflammation by Down-Regulating NLRP3 Inflammasome via a SIRT1-Dependent Pathway in MPTP-Induced Models of Parkinson’s Disease Zheng, Ran Ruan, Yang Yan, Yiqun Lin, Zhihao Xue, Naijia Yan, Yaping Tian, Jun Yin, Xinzhen Pu, Jiali Zhang, Baorong J Inflamm Res Original Research BACKGROUND: Inflammasome-induced neuroinflammation is a key contributor to the pathology of Parkinson’s disease (PD). NLR family pyrin domain-containing 3 (NLRP3) inflammasome activation has been implicated in PD in postmortem human PD brains, indicating it as a potential target for PD treatment. Melatonin, a multitasking molecule, has been found to have anti-inflammatory activities, mediated by silence information regulator 1 (SIRT1). However, whether and how melatonin is involved in inflammasome-induced neuroinflammation in PD pathogenesis remains unclear. METHODS: We investigated the potential anti-inflammatory effects of melatonin in vitro and in vivo, using 1-methyl-4-phenylpyridinium (MPP(+))-simulated BV2 and primary microglia cell models, and a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced murine PD model, with or without melatonin treatment. Rotarod, grip strength, and open-field tests were performed to measure the effects of melatonin on MPTP-induced motor disorders. Degeneration of dopaminergic neurons was evaluated by immunofluorescence. Changes in microglia were examined by immunofluorescence and Western blotting, and the expression levels of the involved signaling molecules were assessed by Western blotting and enzyme-linked immunosorbent assay (ELISA). Intracellular reactive oxygen species (ROS) was detected using fluorescent probes via flow cytometry. RESULTS: We found that melatonin significantly alleviated motor dysfunction and prevented MPTP-induced neurotoxicity in dopaminergic neurons. Additionally, melatonin reduced MPTP-induced microglial activation and suppressed NLRP3 inflammasome activity, and also inhibited IL-1β secretion. Moreover, in MPP(+)-primed BV2 cells, melatonin markedly restored the downregulation of SIRT1 and attenuated the activation of the NLRP3 inflammasome. This was reversed by SIRT1 inhibitor treatment. CONCLUSION: In conclusion, our data demonstrated that melatonin attenuates neuroinflammation by negatively regulating NLRP3 inflammasome activation via a SIRT1-dependent pathway in MPTP-induced PD models. These findings provide novel insights into the mechanism underlying the anti-inflammatory effects of melatonin in PD. Dove 2021-07-08 /pmc/articles/PMC8275196/ /pubmed/34267535 http://dx.doi.org/10.2147/JIR.S317672 Text en © 2021 Zheng et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zheng, Ran
Ruan, Yang
Yan, Yiqun
Lin, Zhihao
Xue, Naijia
Yan, Yaping
Tian, Jun
Yin, Xinzhen
Pu, Jiali
Zhang, Baorong
Melatonin Attenuates Neuroinflammation by Down-Regulating NLRP3 Inflammasome via a SIRT1-Dependent Pathway in MPTP-Induced Models of Parkinson’s Disease
title Melatonin Attenuates Neuroinflammation by Down-Regulating NLRP3 Inflammasome via a SIRT1-Dependent Pathway in MPTP-Induced Models of Parkinson’s Disease
title_full Melatonin Attenuates Neuroinflammation by Down-Regulating NLRP3 Inflammasome via a SIRT1-Dependent Pathway in MPTP-Induced Models of Parkinson’s Disease
title_fullStr Melatonin Attenuates Neuroinflammation by Down-Regulating NLRP3 Inflammasome via a SIRT1-Dependent Pathway in MPTP-Induced Models of Parkinson’s Disease
title_full_unstemmed Melatonin Attenuates Neuroinflammation by Down-Regulating NLRP3 Inflammasome via a SIRT1-Dependent Pathway in MPTP-Induced Models of Parkinson’s Disease
title_short Melatonin Attenuates Neuroinflammation by Down-Regulating NLRP3 Inflammasome via a SIRT1-Dependent Pathway in MPTP-Induced Models of Parkinson’s Disease
title_sort melatonin attenuates neuroinflammation by down-regulating nlrp3 inflammasome via a sirt1-dependent pathway in mptp-induced models of parkinson’s disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275196/
https://www.ncbi.nlm.nih.gov/pubmed/34267535
http://dx.doi.org/10.2147/JIR.S317672
work_keys_str_mv AT zhengran melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT ruanyang melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT yanyiqun melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT linzhihao melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT xuenaijia melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT yanyaping melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT tianjun melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT yinxinzhen melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT pujiali melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease
AT zhangbaorong melatoninattenuatesneuroinflammationbydownregulatingnlrp3inflammasomeviaasirt1dependentpathwayinmptpinducedmodelsofparkinsonsdisease