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01 February 2010

Melatonin MT1 and MT2 receptor expression in Parkinson's disease

Nikhil AdiABCDEF, Deborah C MashACEFG, Yousuf AliBCDEF, Carlos SingerADG, Lina ShehadehBCDF, Spyridon PapapetropoulosABCDEFG

Med Sci Monit 2010; 16(2): BR61-67 :: ID: 878353


Idiopathic Parkinson disease (PD) is a multi-system disorder with a multifactorial etiology and diverse clinical phenotype. Selective, regional dopaminergic neuronal degeneration in the substantia nigra and other CNS areas including the amygdala are observed in all patients. Apoptotic mechanisms resulting from oxidative stress and mitochondrial dysfunction have been implicated in the pathogenesis of the disease. Although the role of melatonin, a potent endogenous antioxidant, has been highlighted in PD there is no data on the expression of melatonin receptors in affected CNS regions.
Material and Method
We conducted an RT-PCR-based study to determine the MT1 and MT2 receptors expression in whole brain post-mortem tissue from the amygdala and substantia nigra of well-characterized PD and control subjects.
PD cases showed a statistically significant decrease of MT1 receptor expression in both substantia nigra (FC=5.11; p<0.05) and the amygdala (FC=3.11; p<0.001) versus normal controls. The expression of MT2 receptor expression was also decreased in both substantia nigra (FC=3.90; p<0.0001) and the amygdala (FC=1.91; p<0.001) versus normal controls.
The results demonstrate a down-regulation of melatonin receptors in regions affected by PD, suggesting their possible involvement in the disease process. Future studies are needed to elucidate the role of melatonin and its receptors in the treatment/pathogenesis of PD.

Keywords: Reverse Transcriptase Polymerase Chain Reaction, Receptor, Melatonin, MT2 - metabolism, Receptor, Melatonin, MT1 - metabolism, Parkinson Disease - pathology, Cohort Studies, Case-Control Studies, Amygdala - pathology, Aged, 80 and over, Substantia Nigra - pathology

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Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750