Title
Inflammatory mechanisms and oxidative stress as key factors responsible for progression of neurodegeneration: Role of brain innate immune system
Date Issued
01 April 2016
Access level
metadata only access
Resource Type
journal article
Author(s)
Leszek J.
Gąsiorowski K.
Koutsouraki E.
Ávila-Rodrigues M.
Aliev G.
Pontificia Universidad Javeriana
Publisher(s)
Bentham Science Publishers B.V.
Abstract
Chronic inflammation is characterized by longstanding microglial activation followed by sustained release of inflammatory mediators, which aid in enhanced nitrosative and oxidative stress. The sustained release of inflammatory mediators propels the inflammatory cycle by increased microglial activation, promoting their proliferation and thus stimulating enhanced release of inflammatory factors. Elevated levels of several cytokines and chronic neuroinflammation have been associated with many neurodegenerative disorders of central nervous system like age-related macular degeneration, Alzheimer disease, multiple sclerosis, Parkinson’s disease, Huntington’ disease, and tauopathies. This review highlights the basic mechanisms of neuroinflammation, the characteristics of neurodegenerative diseases, and the main immunologic responses in CNS neurodegenerative disorders. A comprehensive outline for the crucial role of microglia in neuroinflammation and neurodegeneration and the role of Toll-like receptor signalling in coexistence of inflammatory mechanisms and oxidative stress as major factors responsible for progression of neurodegeneration have also been presented.
Start page
329
End page
336
Volume
15
Issue
3
Language
English
OCDE Knowledge area
Neurociencias Inmunología
Scopus EID
2-s2.0-84961577153
PubMed ID
Source
CNS and Neurological Disorders - Drug Targets
ISSN of the container
18715273
Sponsor(s)
This study was supported by the GALLY International Biomedical Research Consulting LLC, San Antonio, Texas, USA, and Russian Science Foundation (RSCF: ? 14-23-00160). GEB work is supported by Pontificia Universidad Javeriana and Universidad Autonoma de Chile.
Sources of information: Directorio de Producción Científica Scopus