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Title: 7-Nitroindazole protects striatal dopaminergic neurons from MPP+- induced degeneration : an in vivo microdialysis study
Authors: Di Matteo, Vincenzo
Benigno, Arcangelo
Pierucci, Massimo
Giuliano, Davide Antonio
Crescimanno, Giuseppe
Esposito, Ennio
Di Giovanni, Giuseppe
Keywords: Microdialysis
Nitric oxide
Parkinson's disease -- Treatment
Corpus striatum
Issue Date: 2006
Publisher: Wiley-Blackwell Publishing Ltd.
Citation: Di Matteo, V., Benigno, A., Pierucci, M., Giuliano, D. A., Crescimanno, G., Esposito, E., & Di Giovanni G. (2006). 7-Nitroindazole protects striatal dopaminergic neurons from MPP+- induced degeneration : an in vivo microdialysis study. Annals of the New York Academy of Sciences. 1089(1), 462–471.
Abstract: The neuropathological hallmark of Parkinson's disease (PD) is the selective degeneration of dopaminergic (DAergic) neurons in the substantia nigra pars compacta (SNc). In this study, using a microdialysis technique, we investigated whether an inhibitor of neuronal nitric oxide synthase (nNOS), 7-nitrindazole (7-NI), could protect against DAergic neuronal damage induced by in vivo infusion of 1-methyl-4-phenylpiridinium iodide (MPP+) in freely moving rats. Experiments were performed over 2 days in three groups of rats: (a) nonlesioned, (b) MPP+-lesioned, and (c) 7-NI pretreated MPP+-lesioned rats. On day 1, control rats were perfused with an artificial CSF, while 1 mM MPP+ was infused into the striatum for 10 min in the other two groups. The infusion of the MPP+ produced a neurotoxic damage of the SNc DA neurons and increased striatal DA levels. On day 2, 1 mM MPP+ was reperfused for 10 min into the striata of each rat group and DA levels were measured as an index of neuronal cell integrity. The limited rise of DA following MPP+ reperfusion in the MPP+-lesioned rats was due to toxin-induced neuronal loss and was reversed by pretreatment with 7-NI (50 mg/kg, intraperitoneally) on day 1, indicating a neuroprotective effect by inhibiting NO formation. These results indicate that neuronally derived NO partially mediates MPP+-induced neurotoxicity. The similarity between the MPP+ model and PD suggests that NO may play a significant role in its etiology.
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