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1alpha,25-Dihydroxyvitamin D3 Protects Dopaminergic Neurons in Rodent Models of Parkinson's Disease through Inhibition of Microglial Activation
Journal of Clinical Neurology ; : 252-257, 2006.
Article in English | WPRIM | ID: wpr-224885
ABSTRACT

BACKGROUND:

Recent studies have demonstrated the molecular basis of the immunomodulatory and anti-inflammatory activities of 1,25-dihydroxyvitamin D3(1,25-(OH)2D3). This hormone improves behavioral deficits and normalizes the nigral dopamine levels in animal models of Parkinson's disease (PD).

METHODS:

We studied whether the administration of 1,25-(OH)2D3 would protect against 6-hydroxydopa (6-OHDA)- and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neuronal injury, and its potential regulatory effect on microglia activation.

RESULTS:

We found that 1,25-(OH)2D3 pretreatment significantly decreased 6-OHDA- and MPTP-induced dopaminergic neuronal loss in the substantia nigra pars compacta by preventing the activation of microglia. This observed neuroprotective effect in MPTP-treated mice that were given 1,25-(OH)2D3 may be attributable to inhibition of proinflammatory cytokine expression.

CONCLUSION:

These results suggest that 1,25-(OH)2D3 is a potentially valuable neuroprotective agent; it may therefore be considered for the treatment of pathologic conditions of the central nervous system, such as PD, where inflammation-induced neurodegeneration occurs.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Parkinson Disease / Rodentia / Vitamin D / Substantia Nigra / Dopamine / 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine / Central Nervous System / Microglia / Neuroprotective Agents / Models, Animal Limits: Animals Language: English Journal: Journal of Clinical Neurology Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Parkinson Disease / Rodentia / Vitamin D / Substantia Nigra / Dopamine / 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine / Central Nervous System / Microglia / Neuroprotective Agents / Models, Animal Limits: Animals Language: English Journal: Journal of Clinical Neurology Year: 2006 Type: Article