Neuroinflammation in the pathophysiology of Parkinson's disease: Evidence from animal models to human in vivo studies with [11C]‐PK11195 PET
Identifieur interne : 003C46 ( Main/Merge ); précédent : 003C45; suivant : 003C47Neuroinflammation in the pathophysiology of Parkinson's disease: Evidence from animal models to human in vivo studies with [11C]‐PK11195 PET
Auteurs : Anna L. Bartels [Pays-Bas] ; Klaus L. Leenders [Pays-Bas]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-10-15.
English descriptors
- KwdEn :
- Animals, Anti-Inflammatory Agents, Non-Steroidal (pharmacology), Brain (immunology), Brain (radionuclide imaging), COX‐2 inhibition, Cyclooxygenase 2 (blood), Cytokines (blood), Disease Models, Animal, Humans, Inflammation Mediators (blood), Isoquinolines (diagnostic use), Microglia (immunology), Nerve Degeneration (immunology), Nerve Degeneration (radionuclide imaging), Nitric Oxide Synthase Type II (blood), PK11195 PET, Parkinson's disease, Parkinsonian Disorders (immunology), Parkinsonian Disorders (radionuclide imaging), Positron-Emission Tomography, Reactive Oxygen Species (immunology), microglia, neuroinflammation, neuroprotection.
- MESH :
- chemical , blood : Cyclooxygenase 2, Cytokines, Inflammation Mediators, Nitric Oxide Synthase Type II.
- chemical , diagnostic use : Isoquinolines.
- chemical , immunology : Reactive Oxygen Species.
- chemical , pharmacology : Anti-Inflammatory Agents, Non-Steroidal.
- immunology : Brain, Microglia, Nerve Degeneration, Parkinsonian Disorders.
- radionuclide imaging : Brain, Nerve Degeneration, Parkinsonian Disorders.
- Animals, Disease Models, Animal, Humans, Positron-Emission Tomography.
Abstract
Increasing evidence suggests that neuroinflammation is an active process in Parkinson's disease (PD) that contributes to ongoing neurodegeneration. PD brains and experimental PD models show elevated cytokine levels and up‐regulation of inflammatory‐associated factors as cyclo‐oxygenase‐2 and inducible nitric oxide oxidase. Antiinflammatory treatment reduced neuronal degeneration in experimental models. In this review, we summarize the place of neuroinflammation in the pathophysiology of PD. In vivo PET studies are discussed. These methods provide a means to monitor in vivo potential clinical relevance of antiinflammatory treatment strategies in PD. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21552
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