Depletion of striatal DA in human PD and in the nonhuman primate model of MPTP-induced parkinsonism is associated with specific changes in neuronal activity patterns in the motor circuitry of the basal ganglia, including increased rates of neuronal discharge within the main output nucleus of the basal ganglia, Gpi, and in the STN, and minimally decreased discharge in the globus pallidus pars externa (GPe).186-188 Administration of dopaminergic

agents results in normalization of neuronal activity and reversal Inhibitors,research,lifescience,medical of motor impairment.188,189 Fiber-sparing ablation190 or muscimol-induced inactivation of STN191 reverses the motor deficits of monkeys made parkinsonian with MPTP. Radiofrequency lesioning192,193 or high-frequency electrical stimulation – deep brain stimulation (DBS) – of the motor territory of GPi194,195 provides effective treatment for ail of

the Inhibitors,research,lifescience,medical primary motor impairments of patients with PD. DBS applied to STN194,196,197 is also effective in restoring normal movement control to PD patients. Some patients have been treated successfully with subtotal STN lesions198-200 – however, Inhibitors,research,lifescience,medical the added risk of Selleck Lenvatinib persistent hemibailismus201,202 with this approach serves to lessen its appeal. It would be difficult to exaggerate the complexity of the interconnected Inhibitors,research,lifescience,medical cortical, basal ganglia, and thalamic neuronal networks affected by the depletion of striatal DA in PD. These networks comprise multiple layers and side loops, vast, numbers of neuronal elements, and a wide range of neurotransmitters, neuromodulators, axonal and dendritic branching patterns, and layer-to-layer connectivity. Nonetheless, from a large-scale perspective, these same networks can be viewed more simply as an Inhibitors,research,lifescience,medical array of contiguous but functionally specialized pathways linking basal

ganglia, thalamus, and cerebral cortex in circular fashion to form a corresponding family of parallel, partially closed and largely segregated basal ganglia-thalamocortical circuits or loops.203-207 According to this schema, each loop takes its origin from a particular set of anatomically and functionally related cortical fields (sensorimotor, Thymidine kinase oculomotor, dorsolateral prefrontal, ventromedial prefrontal, limbic), passing through the corresponding portions of the basal ganglia, and returning to parts of those same cortical fields by way of specific basal ganglia-recipient zones in the dorsal thalamus. To the extent that information processing remains functionally segregated throughout the course of each loop, each subserves a different set of behavioral functions.