» Articles » PMID: 36693756

Loss of Motor Cortical Inputs to the Red Nucleus After CNS Disorders in Nonhuman Primates

Overview
Journal J Neurosci
Specialty Neurology
Date 2023 Jan 24
PMID 36693756
Authors
Affiliations
Soon will be listed here.
Abstract

The premotor (PM) and primary motor (M1) cortical areas broadcast voluntary motor commands through multiple neuronal pathways, including the corticorubral projection that reaches the red nucleus (RN). However, the respective contribution of M1 and PM to corticorubral projections as well as changes induced by motor disorders or injuries are not known in nonhuman primates. Here, we quantified the density and topography of axonal endings of the corticorubral pathway in RN in intact monkeys, as well as in monkeys subjected to either cervical spinal cord injury (SCI), Parkinson's disease (PD)-like symptoms or primary motor cortex injury (MCI). Twenty adult macaque monkeys of either sex were injected with the biotinylated dextran amine anterograde tracer either in PM or in M1. We developed a semiautomated algorithm to reliably detect and count axonal boutons within the magnocellular and parvocellular (pRN) subdivisions of RN. In intact monkeys, PM and M1 preferentially target the medial part of the ipsilateral pRN, reflecting its somatotopic organization. Projection of PM to the ipsilateral pRN is denser than that of M1, matching previous observations for the corticotectal, corticoreticular, and corticosubthalamic projections (Fregosi et al., 2018, 2019; Borgognon et al., 2020). In all three types of motor disorders, there was a uniform and strong decrease (near loss) of the corticorubral projections from PM and M1. The RN may contribute to functional recovery after SCI, PD, and MCI, by reducing direct cortical influence. This reduction possibly privileges direct access to the final output motor system, via emphasis on the direct corticospinal projection. We measured the corticorubral projection density arising from the PM or the M1 cortices in adult macaques. The premotor cortex sent denser corticorubral projections than the primary motor cortex, as previously observed for the corticotectal, corticoreticular, and corticosubthalamic projections. The premotor cortex may thus exert more influence than primary motor cortex onto subcortical structures. We next asked whether the corticorubral motor projections undergo lesion-dependent plasticity after either cervical spinal cord injury, Parkinson's disease-like symptoms, or primary motor cortex lesion. In all three types of pathology, there was a strong decrease of the corticorubral motor projection density, suggesting that the red nucleus may contribute to functional recovery after such motor system disorders based on a reduced direct cortical influence.

Citing Articles

Adaptation of the layer V supraspinal motor corticofugal projections from the primary (M1) and premotor (PM) cortices after CNS motor disorders in non-human primates: A survey.

Rouiller E Transl Neurosci. 2024; 15(1):20220342.

PMID: 38860225 PMC: 11163158. DOI: 10.1515/tnsci-2022-0342.


Anti-Nogo-A Antibody Therapy Improves Functional Outcome Following Traumatic Brain Injury.

Powers B, Ton S, Farrer R, Chaudhary S, Nockels R, Kartje G Neurorehabil Neural Repair. 2023; 37(10):682-693.

PMID: 37837331 PMC: 10843026. DOI: 10.1177/15459683231203194.


The effect of dorsal column lesions in the primary somatosensory cortex and medulla of adult rats.

Datta A IBRO Neurosci Rep. 2023; 14:466-482.

PMID: 37273897 PMC: 10238474. DOI: 10.1016/j.ibneur.2023.05.005.

References
1.
Brunet J, Redmond Jr D, Bloch J . Primate adult brain cell autotransplantation, a pilot study in asymptomatic MPTP-treated monkeys. Cell Transplant. 2009; 18(7):787-99. DOI: 10.3727/096368909X470847. View

2.
Bloch J, Kaeser M, Sadeghi Y, Rouiller E, Redmond Jr D, Brunet J . Doublecortin-positive cells in the adult primate cerebral cortex and possible role in brain plasticity and development. J Comp Neurol. 2011; 519(4):775-89. DOI: 10.1002/cne.22547. View

3.
Arshavsky Y, Orlovsky G, Perret C . Activity of rubrospinal neurons during locomotion and scratching in the cat. Behav Brain Res. 1988; 28(1-2):193-9. DOI: 10.1016/0166-4328(88)90096-4. View

4.
Brunet J, Pellerin L, Arsenijevic Y, Magistretti P, Villemure J . A novel method for in vitro production of human glial-like cells from neurosurgical resection tissue. Lab Invest. 2002; 82(6):809-12. DOI: 10.1097/01.lab.0000017166.26718.bb. View

5.
Fregosi M, Contestabile A, Hamadjida A, Rouiller E . Corticobulbar projections from distinct motor cortical areas to the reticular formation in macaque monkeys. Eur J Neurosci. 2017; 45(11):1379-1395. DOI: 10.1111/ejn.13576. View