Abstract
5-HT plays a regulatory role in voluntary movements of the basal ganglia and has a major impact on disorders of the basal ganglia such as Parkinson's disease (PD). Clinical studies have suggested that 5-HT 2 receptor antagonists may be useful in the treatment of the motor symptoms of PD. We hypothesized that 5-HT 2A receptor antagonists may restore motor function by regulating glutamatergic activity in the striatum. Mice treated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) exhibited decreased performance on the beam-walking apparatus. Peripheral administration of the 5-HT 2A receptor antagonist M100907 improved performance of MPTP-treated mice on the beam-walking apparatus. In vivo microdialysis revealed an increase in striatal extracellular glutamate in MPTP-treated mice and local perfusion of M100907 into the dorsal striatum significantly decreased extracellular glutamate levels in saline and MPTP-treated mice. Our studies suggest that blockade of 5-HT 2A receptors may represent a novel therapeutic target for the motor symptoms of PD. © 2011 Ansah, Ferguson and Nayyar.
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Ansah, T. A., Ferguson, M. C., & Nayyar, T. (2011). The 5-HT 2A receptor antagonist M100907 produces antiparkinsonian effects and decreases striatal glutamate. Frontiers in Systems Neuroscience, (JUNE 2011). https://doi.org/10.3389/fnsys.2011.00048
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