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Lipopolysaccharide Animal Models for Parkinson's Disease

Lipopolysaccharide (LPS), an endotoxin from Gram-negative bacteria, acts as a potent stimulator of microglia and has been used to study the inflammatory process in the pathogenesis of Parkinson's disease (PD) and anti-inflammatory therapy for PD treatment. Here, we review the growing body of li...

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Autores principales: Liu, Mei, Bing, Guoying
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096023/
https://www.ncbi.nlm.nih.gov/pubmed/21603177
http://dx.doi.org/10.4061/2011/327089
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author Liu, Mei
Bing, Guoying
author_facet Liu, Mei
Bing, Guoying
author_sort Liu, Mei
collection PubMed
description Lipopolysaccharide (LPS), an endotoxin from Gram-negative bacteria, acts as a potent stimulator of microglia and has been used to study the inflammatory process in the pathogenesis of Parkinson's disease (PD) and anti-inflammatory therapy for PD treatment. Here, we review the growing body of literature on both in vitro and in vivo LPS PD models. Primary cell cultures from mesencephalic tissue were exposed to LPS in vitro; LPS was stereotaxically injected into the substantia nigra, striatum, or globus pallidus of brain or injected into the peritoneal cavity of the animal in vivo. In conclusion, the LPS PD models are summarized as (1) local and direct LPS treatment and (2) systemic LPS treatment. Mechanisms underlying the PD models are investigated and indicated that LPS induces microglial activation to release a variety of neurotoxic factors, and damaged neurons may trigger reactive microgliosis, which lead to progressive dopaminergic neurodegeneration.
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spelling pubmed-30960232011-05-20 Lipopolysaccharide Animal Models for Parkinson's Disease Liu, Mei Bing, Guoying Parkinsons Dis Review Article Lipopolysaccharide (LPS), an endotoxin from Gram-negative bacteria, acts as a potent stimulator of microglia and has been used to study the inflammatory process in the pathogenesis of Parkinson's disease (PD) and anti-inflammatory therapy for PD treatment. Here, we review the growing body of literature on both in vitro and in vivo LPS PD models. Primary cell cultures from mesencephalic tissue were exposed to LPS in vitro; LPS was stereotaxically injected into the substantia nigra, striatum, or globus pallidus of brain or injected into the peritoneal cavity of the animal in vivo. In conclusion, the LPS PD models are summarized as (1) local and direct LPS treatment and (2) systemic LPS treatment. Mechanisms underlying the PD models are investigated and indicated that LPS induces microglial activation to release a variety of neurotoxic factors, and damaged neurons may trigger reactive microgliosis, which lead to progressive dopaminergic neurodegeneration. SAGE-Hindawi Access to Research 2011-04-27 /pmc/articles/PMC3096023/ /pubmed/21603177 http://dx.doi.org/10.4061/2011/327089 Text en Copyright © 2011 M. Liu and G. Bing. 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 Review Article
Liu, Mei
Bing, Guoying
Lipopolysaccharide Animal Models for Parkinson's Disease
title Lipopolysaccharide Animal Models for Parkinson's Disease
title_full Lipopolysaccharide Animal Models for Parkinson's Disease
title_fullStr Lipopolysaccharide Animal Models for Parkinson's Disease
title_full_unstemmed Lipopolysaccharide Animal Models for Parkinson's Disease
title_short Lipopolysaccharide Animal Models for Parkinson's Disease
title_sort lipopolysaccharide animal models for parkinson's disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096023/
https://www.ncbi.nlm.nih.gov/pubmed/21603177
http://dx.doi.org/10.4061/2011/327089
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