Abstract

Functional recovery from central nervous system injury is likely to be partly due to a rearrangement of neural circuits. In this context, the corticobulbar (corticoreticular) motor projections onto different nuclei of the ponto‐medullary reticular formation (PMRF) were investigated in 13 adult macaque monkeys after either, primary motor cortex injury (MCI) in the hand area, or spinal cord injury (SCI) or Parkinson's disease‐like lesions of the nigro‐striatal dopaminergic system (PD). A subgroup of animals in both MCI and SCI groups was treated with neurite growth promoting anti‐Nogo‐A antibodies, whereas all PD animals were treated with autologous neural cell ecosystems (ANCE). The anterograde tracer BDA was injected either in the premotor cortex (PM) or in the primary motor cortex (M1) to label and quantify corticobulbar axonal boutons terminaux and en passant in PMRF. As compared to intact animals, after MCI the density of corticobulbar projections from PM was strongly reduced but maintained their laterality dominance (ipsilateral), both in the presence or absence of anti‐Nogo‐A antibody treatment. In contrast, the density of corticobulbar projections from M1 was increased following opposite hemi‐section of the cervical cord (at C7 level) and anti‐Nogo‐A antibody treatment, with maintenance of contralateral laterality bias. In PD monkeys, the density of corticobulbar projections from PM was strongly reduced, as well as that from M1, but to a lesser extent. In conclusion, the densities of corticobulbar projections from PM or M1 were affected in a variable manner, depending on the type of lesion/pathology and the treatment aimed to enhance functional recovery.

Highlights

  • The motor corticobulbar projections, acting in parallel with the corticospinal (CS) tract in the control of voluntary movements, terminate in brainstem nuclei, from which subsequent descending pathways arise to reach the spinal cord; one of these is the reticulospinal tract (RS; Kuypers, 1958, 1981; Lemon, 2008)

  • Thirteen animals were injected with the anterograde tracer biotinylated dextran amine (BDA) in either premotor cortex (PM) (n = 6) or primary motor cortex (M1) (n = 7), as listed in Table 1, in order to quantify the boutons emitted by the motor corticobulbar projections in ponto-­medullary reticular formation (PMRF)

  • All animals subjected to cortical M1 lesion (n = 4) were injected in PM; all animals subjected to spinal cord injury (SCI) (n = 5) were injected with BDA in M1, whereas, out of four animals subjected to parkinsonian lesion (n = 4), two were injected with BDA in PM (PMd and ventral premotor cortex (PMv)) and two in M1

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Summary

Introduction

The motor corticobulbar (corticoreticular) projections, acting in parallel with the corticospinal (CS) tract in the control of voluntary movements, terminate in brainstem nuclei, from which subsequent descending pathways arise to reach the spinal cord; one of these is the reticulospinal tract (RS; Kuypers, 1958, 1981; Lemon, 2008). The RS projection is involved in the control of posture and locomotion (Drew, Dubuc, & Rossignol, 1986; Lawrence & Kuypers, 1968a,b; Matsuyama & Drew, 1997; Matsuyama et al, 1999, 2004; Schepens & Drew, 2004, 2006; Schepens, Stapley, & Drew, 2008), as well as in the control of reaching movements (Buford & Davidson, 2004; Davidson & Buford, 2004, 2006; Davidson, Schieber, & Buford, 2007; Schepens & Drew, 2004, 2006; Schepens et al, 2008). Besides the role played by the RS projection in the control of hand movement, the main player for hand control remains the corticospinal tract (CST) mainly via its corticomotoneuronal (CM) system allowing sophisticated control of manual dexterity in nonhuman primates and humans (Courtine et al, 2007; Lawrence & Kuypers, 1968a,b; Lemon, 2008; Lemon & Griffiths, 2005; Rathelot & Strick, 2009; Schieber, 2007)

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