ABSTRACT
The beneficial effects of drugs that act via nicotinic acetylcholine receptors (nAChRs) on Parkinson's disease (PD) symptomatology may explain the negative correlation between cigarette smoking and risk of this neurological condition. Varenicline, an α4β2 nAChR partial agonist approved for smoking cessation treatments, could be valuable for PD treatment. Here, we investigated varenicline effects in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) PD mouse model. From postnatal day (PN) 90 to PN119, male C57BL/6 mice were exposed daily to varenicline (2 mg/kg) by gavage. After that, MPTP was injected (30 mg/kg, ip) once a day for five days. At PN125, locomotor and anxiety-like effects were assessed with the open field test. At PN126, immobile behavior was assessed with the forced swimming test. At PN127, the frontal cerebral cortex was collected to evaluate dopamine and DOPAC levels. To verify whether varenicline was protective during the MPTP insult, a separate group of MPTP animals received varenicline from PN90 to PN124. MPTP reduced cortical dopamine content and increased dopamine turnover. Those effects were not reversed by varenicline treatment. Interestingly, varenicline reversed the MPTP-induced hyperactivity in the open field. Both maintenance of varenicline treatment during MPTP exposure or its interruption before MPTP exposure elicited similar results. No alterations were observed in anxiety-like behavior or in immobility time. Altogether, these findings suggested that varenicline treatment reduced the MPTP-induced hyperactivity, but did not protect against dopaminergic damage. Based on this partial protective effect, varenicline could exert neuroprotective effects on circuits that control motor activity in PD.
ABSTRACT
The development of the corpus callosum of male Swiss mice was perturbed by exposure to gamma radiation at embryonic day 16 with total doses of 2 Gy (N = 48) or 3 Gy (N = 26). At adulthood paw preference was studied in these callosal defective animals and in 93 control nonirradiated male Swiss mice. The analysis of directional laterality indicated a populational tendency for right paw use in the 2 Gy group (60 per cent ) that was markedly increased in the 3 Gy group (95 per cent ). In the 3 Gy group, directional laterality was significantly different from chance in contrast to that observed in normal controls (49 per cent ). In the three groups most mice presented a significant individual paw preference. These data are consistent with our hypothesis that the early absence of the corpus callosum disrupts the normal pattern of directional asymmetries