Abstract
Introduction: Dopamine agonists are suggested to be more efficacious in treating Parkinson's disease (PD) as they have neuroprotective properties in addition to their receptor-related actions.
Aim of the study: The present study was designed to investigate the neuroprotective effects of rotigotine, a D-3/D-2/D-1 dopamine receptor agonist, against the two powerful complex I inhibitors, 1-methyl-4-phenylpyridinium (MPP+) and rotenone, in primary mesencephalic cell culture relevant to PD.
Material and methods: Primary mesencephalic cell cultures were prepared from embryonic mouse mesencephala at gestation day 14. Three sets of cultures were treated with rotigotine alone, rotigotine and MPP+, and rotigotine and rotenone to investigate the effect of rotigotine on the survival of dopaminergic neurons against age-, MPP+ and rotenone-induced cell death. At the end of each treatment, cultures were fixed and stained immunohistochemically against tyrosine hydroxylase (TH). The effect of rotigotine against rotenone-induced reactive oxygen species (ROS) production was measured using CH-H(2)DCFDA fluorescence dye.
Results: Rotigotine alone did not influence the survival of tyrosine hydroxylase immunoreactive (THir) neurons except at 10 mu M, it significantly decreased the number of THir neurons by 40% compared to untreated controls. Treatment of cultures with 0.01 mu M rotigotine rescued 10% of THir neurons against MPP+-induced cell death. Rotigotine was also found to significantly rescue 20% of THir neurons at 0.01 mu M of rotenone-treated cultures. Using of CH-H2DCFDA fluorescence dye, it was found that rotigotine significantly attenuated ROS production compared to rotenone-treated cultures.
Conclusions: Rotigotine provides minor protection against MPP+ and rescues a significant number of THir neurons against rotenone in primary mesencephalic cell cultures relevant to PD.