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Bushen-Yizhi Formula Alleviates Neuroinflammation via Inhibiting NLRP3 Inflammasome Activation in a Mouse Model of Parkinson's Disease

Parkinson's disease (PD), the second most common neurodegenerative disease, is characterized by the progressive loss of dopaminergic neurons in the substantia nigra. Although the molecular mechanisms underlying dopaminergic neuronal degeneration in PD remain unclear, neuroinflammation is consid...

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Autores principales: Mo, Yousheng, Xu, Erjin, Wei, Renrong, Le, Baoluu, Song, Lei, Li, Dongli, Chen, Yonggen, Ji, Xiaotian, Fang, Shuhuan, Shen, Jiangang, Yang, Cong, Wang, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129340/
https://www.ncbi.nlm.nih.gov/pubmed/30224927
http://dx.doi.org/10.1155/2018/3571604
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author Mo, Yousheng
Xu, Erjin
Wei, Renrong
Le, Baoluu
Song, Lei
Li, Dongli
Chen, Yonggen
Ji, Xiaotian
Fang, Shuhuan
Shen, Jiangang
Yang, Cong
Wang, Qi
author_facet Mo, Yousheng
Xu, Erjin
Wei, Renrong
Le, Baoluu
Song, Lei
Li, Dongli
Chen, Yonggen
Ji, Xiaotian
Fang, Shuhuan
Shen, Jiangang
Yang, Cong
Wang, Qi
author_sort Mo, Yousheng
collection PubMed
description Parkinson's disease (PD), the second most common neurodegenerative disease, is characterized by the progressive loss of dopaminergic neurons in the substantia nigra. Although the molecular mechanisms underlying dopaminergic neuronal degeneration in PD remain unclear, neuroinflammation is considered as the vital mediator in the pathogenesis and progression of PD. Bushen-Yizhi Formula (BSYZ), a traditional Chinese medicine, has been demonstrated to exert antineuroinflammation in our previous studies. However, it remains unclear whether BSYZ is effective for PD. Here, we sought to assess the neuroprotective effects and explore the underlying mechanisms of BSYZ in a 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine- (MPTP-) induced mouse model of PD. Our results indicate that BSYZ significantly alleviates the motor impairments and dopaminergic neuron degeneration of MPTP-treated mice. Furthermore, BSYZ remarkably attenuates microglia activation, inhibits NLPR3 activation, and decreases the levels of inflammatory cytokines in MPTP-induced mouse brain. Also, BSYZ inhibits NLRP3 activation and interleukin-1β production of the 1-methyl-4-phenyl-pyridinium (MPP(+)) stimulated BV-2 microglia cells. Taken together, our results indicate that BSYZ alleviates MPTP-induced neuroinflammation probably via inhibiting NLRP3 inflammasome activation in microglia. Collectively, BSYZ may be a potential therapeutic agent for PD and the related neurodegeneration diseases.
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spelling pubmed-61293402018-09-17 Bushen-Yizhi Formula Alleviates Neuroinflammation via Inhibiting NLRP3 Inflammasome Activation in a Mouse Model of Parkinson's Disease Mo, Yousheng Xu, Erjin Wei, Renrong Le, Baoluu Song, Lei Li, Dongli Chen, Yonggen Ji, Xiaotian Fang, Shuhuan Shen, Jiangang Yang, Cong Wang, Qi Evid Based Complement Alternat Med Research Article Parkinson's disease (PD), the second most common neurodegenerative disease, is characterized by the progressive loss of dopaminergic neurons in the substantia nigra. Although the molecular mechanisms underlying dopaminergic neuronal degeneration in PD remain unclear, neuroinflammation is considered as the vital mediator in the pathogenesis and progression of PD. Bushen-Yizhi Formula (BSYZ), a traditional Chinese medicine, has been demonstrated to exert antineuroinflammation in our previous studies. However, it remains unclear whether BSYZ is effective for PD. Here, we sought to assess the neuroprotective effects and explore the underlying mechanisms of BSYZ in a 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine- (MPTP-) induced mouse model of PD. Our results indicate that BSYZ significantly alleviates the motor impairments and dopaminergic neuron degeneration of MPTP-treated mice. Furthermore, BSYZ remarkably attenuates microglia activation, inhibits NLPR3 activation, and decreases the levels of inflammatory cytokines in MPTP-induced mouse brain. Also, BSYZ inhibits NLRP3 activation and interleukin-1β production of the 1-methyl-4-phenyl-pyridinium (MPP(+)) stimulated BV-2 microglia cells. Taken together, our results indicate that BSYZ alleviates MPTP-induced neuroinflammation probably via inhibiting NLRP3 inflammasome activation in microglia. Collectively, BSYZ may be a potential therapeutic agent for PD and the related neurodegeneration diseases. Hindawi 2018-08-26 /pmc/articles/PMC6129340/ /pubmed/30224927 http://dx.doi.org/10.1155/2018/3571604 Text en Copyright © 2018 Yousheng Mo et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mo, Yousheng
Xu, Erjin
Wei, Renrong
Le, Baoluu
Song, Lei
Li, Dongli
Chen, Yonggen
Ji, Xiaotian
Fang, Shuhuan
Shen, Jiangang
Yang, Cong
Wang, Qi
Bushen-Yizhi Formula Alleviates Neuroinflammation via Inhibiting NLRP3 Inflammasome Activation in a Mouse Model of Parkinson's Disease
title Bushen-Yizhi Formula Alleviates Neuroinflammation via Inhibiting NLRP3 Inflammasome Activation in a Mouse Model of Parkinson's Disease
title_full Bushen-Yizhi Formula Alleviates Neuroinflammation via Inhibiting NLRP3 Inflammasome Activation in a Mouse Model of Parkinson's Disease
title_fullStr Bushen-Yizhi Formula Alleviates Neuroinflammation via Inhibiting NLRP3 Inflammasome Activation in a Mouse Model of Parkinson's Disease
title_full_unstemmed Bushen-Yizhi Formula Alleviates Neuroinflammation via Inhibiting NLRP3 Inflammasome Activation in a Mouse Model of Parkinson's Disease
title_short Bushen-Yizhi Formula Alleviates Neuroinflammation via Inhibiting NLRP3 Inflammasome Activation in a Mouse Model of Parkinson's Disease
title_sort bushen-yizhi formula alleviates neuroinflammation via inhibiting nlrp3 inflammasome activation in a mouse model of parkinson's disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129340/
https://www.ncbi.nlm.nih.gov/pubmed/30224927
http://dx.doi.org/10.1155/2018/3571604
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