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Elimination of the Cortico-Subthalamic Hyperdirect Pathway Induces Motor Hyperactivity in Mice

Overview
Journal J Neurosci
Specialty Neurology
Date 2021 May 18
PMID 34001630
Citations 5
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Abstract

The substantia nigra pars reticulata (SNr) is the output station of the basal ganglia and receives cortical inputs by way of the following three basal ganglia pathways: the cortico-subthalamo (STN)-SNr hyperdirect, the cortico-striato-SNr direct, and the cortico-striato-external pallido-STN-SNr indirect pathways. Compared with the classical direct and indirect pathways via the striatum, the functions of the hyperdirect pathway remain to be fully elucidated. Here we used a photodynamic technique to selectively eliminate the cortico-STN projection in male mice and observed neuronal activity and motor behaviors in awake conditions. After cortico-STN elimination, cortically evoked early excitation in the SNr was diminished, while the cortically evoked inhibition and late excitation, which are delivered through the direct and indirect pathways, respectively, were unchanged. In addition, locomotor activity was significantly increased after bilateral cortico-STN elimination, and apomorphine-induced ipsilateral rotations were observed after unilateral cortico-STN elimination, suggesting that cortical activity was increased. These results are compatible with the notion that the cortico-STN-SNr hyperdirect pathway quickly conveys cortical excitation to the output station of the basal ganglia, resets or suppresses the cortical activity related to ongoing movements, and prepares for the forthcoming movement. The basal ganglia play a pivotal role in the control of voluntary movements, and their malfunctions lead to movement disorders, such as Parkinson's disease and dystonia. Understanding their functions is important to find better treatments for such diseases. Here we used a photodynamic technique to selectively eliminate the projection from the motor cortex to the subthalamic nucleus, the input station of the basal ganglia, and found greatly reduced early excitatory signals from the cortex to the output station of the basal ganglia and motor hyperactivity. These results suggest that the neuronal signals through the cortico-subthalamic hyperdirect pathway reset or suppress ongoing movements and that blockade of this pathway may be beneficial for Parkinson's disease, which is characterized by oversuppression of movements.

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References
1.
Scharff C, Kirn J, Grossman M, Macklis J, Nottebohm F . Targeted neuronal death affects neuronal replacement and vocal behavior in adult songbirds. Neuron. 2000; 25(2):481-92. DOI: 10.1016/s0896-6273(00)80910-1. View

2.
Iwamuro H, Tachibana Y, Ugawa Y, Saito N, Nambu A . Information processing from the motor cortices to the subthalamic nucleus and globus pallidus and their somatotopic organizations revealed electrophysiologically in monkeys. Eur J Neurosci. 2017; 46(11):2684-2701. PMC: 5725726. DOI: 10.1111/ejn.13738. View

3.
HUTCHINSON W, Levy R, Dostrovsky J, Lozano A, Lang A . Effects of apomorphine on globus pallidus neurons in parkinsonian patients. Ann Neurol. 1997; 42(5):767-75. DOI: 10.1002/ana.410420513. View

4.
Alexander G, Crutcher M . Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci. 1990; 13(7):266-71. DOI: 10.1016/0166-2236(90)90107-l. View

5.
Parent A, Hazrati L . Functional anatomy of the basal ganglia. II. The place of subthalamic nucleus and external pallidum in basal ganglia circuitry. Brain Res Brain Res Rev. 1995; 20(1):128-54. DOI: 10.1016/0165-0173(94)00008-d. View