The influence of microglia on the pathogenesis of Parkinson's disease. Prog Neurobiol. 2009 Nov;89(3):277-87.

Typeset version

 

TY  - JOUR
  - Long-Smith, C., Sullivan, A.M., Nolan, Y.M.
  - 2009
  - November
  - Progress In Neurobiology
  - The influence of microglia on the pathogenesis of Parkinson's disease. Prog Neurobiol. 2009 Nov;89(3):277-87.
  - Validated
  - ()
  - 277
  - 287
  - Parkinson's disease (PD) is characterised by degeneration of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Inflammation may be associated with the neuropathology of PD due to the following accumulating evidence: excessive microglial activation and increased levels of the pro-inflammatory cytokines tumour necrosis factor-alpha and interleukin-1beta in the SNpc of patients with PD; the emergence of PD-like symptoms following influenza infection; the increased susceptibility to PD associated with bacterial vaginosis; the presence of inflammatory mediators and activators in animal models of PD; the ability of anti-inflammatory drugs to decrease susceptibility to PD; and the emerging possibility of the use of microglial activation inhibitors as a therapy in PD. In this review, we will discuss the role of inflammation in PD. We will focus on the influence of microglia in the pathogenesis of PD and discuss potential therapeutic interventions for PD, that target microglia.
  - 10.1016/j.pneurobio.2009.08.001
DA  - 2009/11
ER  - 
@article{V27579815,
   = {Long-Smith,  C. and  Sullivan,  A.M. and  Nolan,  Y.M. },
   = {2009},
   = {November},
   = {Progress In Neurobiology},
   = {The influence of microglia on the pathogenesis of Parkinson's disease. Prog Neurobiol. 2009 Nov;89(3):277-87.},
   = {Validated},
   = {()},
  pages = {277--287},
   = {{Parkinson's disease (PD) is characterised by degeneration of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Inflammation may be associated with the neuropathology of PD due to the following accumulating evidence: excessive microglial activation and increased levels of the pro-inflammatory cytokines tumour necrosis factor-alpha and interleukin-1beta in the SNpc of patients with PD; the emergence of PD-like symptoms following influenza infection; the increased susceptibility to PD associated with bacterial vaginosis; the presence of inflammatory mediators and activators in animal models of PD; the ability of anti-inflammatory drugs to decrease susceptibility to PD; and the emerging possibility of the use of microglial activation inhibitors as a therapy in PD. In this review, we will discuss the role of inflammation in PD. We will focus on the influence of microglia in the pathogenesis of PD and discuss potential therapeutic interventions for PD, that target microglia.}},
   = {10.1016/j.pneurobio.2009.08.001},
  source = {IRIS}
}
AUTHORSLong-Smith, C., Sullivan, A.M., Nolan, Y.M.
YEAR2009
MONTHNovember
JOURNAL_CODEProgress In Neurobiology
TITLEThe influence of microglia on the pathogenesis of Parkinson's disease. Prog Neurobiol. 2009 Nov;89(3):277-87.
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORD
VOLUME
ISSUE
START_PAGE277
END_PAGE287
ABSTRACTParkinson's disease (PD) is characterised by degeneration of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Inflammation may be associated with the neuropathology of PD due to the following accumulating evidence: excessive microglial activation and increased levels of the pro-inflammatory cytokines tumour necrosis factor-alpha and interleukin-1beta in the SNpc of patients with PD; the emergence of PD-like symptoms following influenza infection; the increased susceptibility to PD associated with bacterial vaginosis; the presence of inflammatory mediators and activators in animal models of PD; the ability of anti-inflammatory drugs to decrease susceptibility to PD; and the emerging possibility of the use of microglial activation inhibitors as a therapy in PD. In this review, we will discuss the role of inflammation in PD. We will focus on the influence of microglia in the pathogenesis of PD and discuss potential therapeutic interventions for PD, that target microglia.
PUBLISHER_LOCATION
ISBN_ISSN
EDITION
URL
DOI_LINK10.1016/j.pneurobio.2009.08.001
FUNDING_BODY
GRANT_DETAILS