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Inflammatory process in Parkinson disease: neuroprotection by neuropeptide Y
Author(s) -
Pain Stéphanie,
Vergote Jackie,
Gulhan Zuhal,
Bodard Sylvie,
Chalon Sylvie,
Gaillard Afsaneh
Publication year - 2019
Publication title -
fundamental and clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.655
H-Index - 73
eISSN - 1472-8206
pISSN - 0767-3981
DOI - 10.1111/fcp.12464
Subject(s) - substantia nigra , neuroprotection , neuropeptide y receptor , neurodegeneration , dopaminergic , microglia , striatum , parkinson's disease , dopamine , translocator protein , medicine , endocrinology , inflammation , pars compacta , neuroscience , dopamine transporter , neuropeptide , biology , disease , receptor
Parkinson's disease (PD) is characterized by the degeneration of dopaminergic neurons in the nigro‐striatal pathway. Interestingly, it has already been shown that an intracerebral administration of neuropeptide Y (NPY) decreases the neurodegeneration induced by 6‐hydroxydopamine (6‐OHDA) in rodents and prevents loss of dopamine (DA) and DA transporter density. The etiology of idiopathic PD now suggest that chronic production of inflammatory mediators by activated microglial cells mediates the majority of DA‐neuronal tissue destruction. In an animal experimental model of PD, the present study shows that NPY inhibited the activation of microglia evaluated by the binding of the translocator protein (TSPO) ligand [3H]PK11195 in striatum and substantia nigra of 6‐OHDA rats. These results suggest a potential role for inflammation in the pathophysiology of the disease and a potential treatment by NPY in PD.

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