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 its plasticity following motor disorders or injuries are not known in non-human 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 (BDA) anterograde tracer either in PM or in M1. We developed a semi-automated algorithm to reliably detect and count axonal boutons within the magnocellular (mRN) 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. PM’s projection to the ipsilateral pRN is denser than M1’s, 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.
SIGNIFICANCE STATEMENT:
We measured the corticorubral projection density arising from the premotor (PM) or the primary motor (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 strong decrease of the corticorubral motor projections density, suggesting that the red nucleus may contribute to functional recovery after such motor system disorders, based on a reduced direct cortical influence.
Footnotes
The authors declare no competing interest, except the anti-Nogo-A antibody provided by Novartis AG, as reported in previous own publications.
We thank Prof. Joceylne Bloch, Prof. Patrick Freund, Dr. Jean-Francois Brunet, Dr. Simon Badoud and Dr. Eric Schmidlin for surgical assistance; Prof. Martin Schwab, Prof. Joceylne Bloch, Prof. Patrick Freund, Dr. Anis Mir, Dr. T. Wannier, Dr. Eric Schmidlin, Dr. Marie-Laure Beaud, Dr. Alexander Wyss, Dr. Shahid Bashir, Dr. Adjia Hamadjida, Dr. Aderraouf Belhaj-Saif, Dr. Mélanie Kaeser, Dr. J. Savidan, Dr. Anne-Dominique Gindrat, Dr. Yu Liu, Dr. Michela Fregosi, Dr. Simon Badoud, Mr. Alessandro Contestabile and Mr. Jérôme Cottet for contributions to experimental sessions and elaborations of experimental protocols; Mr. L. Bossy, Mr. J. Maillard, Mr. B. Bapst, Mr. B. Morandi and Mr. J. Corpataux for animal care assistance; Mrs. Christine Roulin, Mrs. Véronique Moret and Mrs. Christiane Marti for tissue processing. Mr. Felix Meyenhofer for technical microscopical assistance. Finally, we thank Dr. Erinn M. Grigsby for the proof-reading. This work was financially supported by Swiss National Science Foundation Grants No 110005, 132465, 144990, 149643, Sinergia CRSII3_160696, Sinergia PROMETHEUS CRSI33_125408 (to EMR), postdoc mobility No 210986 (to SB) and the Swiss Primate Competence Centre for Research (SPCCR: www.unifr.ch/spccr).