» Articles » PMID: 8815929

Spinal Cord Terminations of the Medial Wall Motor Areas in Macaque Monkeys

Overview
Journal J Neurosci
Specialty Neurology
Date 1996 Oct 15
PMID 8815929
Citations 130
Authors
Affiliations
Soon will be listed here.
Abstract

We used anterograde transport of wheat germ agglutinin-horseradish peroxidase to examine the pattern of spinal termination of efferents from the supplementary motor area (SMA) and the two caudal cingulate motor areas (CMAd and CMAv). Our analysis was limited to cervical segments of the macaque. For comparison, we also examined the pattern of termination of efferents from the primary motor cortex (M1). The SMA, CMAd, CMAv, and M1 all terminate in the ventral horn (lamina IX). Thus, all of these motor areas appear to have direct connections with spinal motoneurons, particularly those innervating muscles of the fingers and wrist. All of the motor areas also terminate in the intermediate zone of the spinal cord (laminae V-VIII). Terminations from the SMA and M1 were densest in three regions: (1) dorsolaterally within laminae V-VII; (2) dorsomedially within lamina VI; and (3) ventromedially within lamina VII and adjacent lamina VIII. In contrast, efferents from the CMAd terminate most densely in the dorsolateral portion of the intermediate zone, whereas those from the CMAv were concentrated in the dorsomedial region. Thus, the CMAd and CMAv may innervate distinct sets of interneurons that project directly to motoneurons, and thereby influence specific aspects of segmental motor control. These results suggest that corticospinal projections from the SMA, CMAd, and CMAv are in many respects similar to those of efferents from M1. Consequently, each of the motor areas on the medial wall has the potential to generate and control movement at the level of the spinal cord and may provide an anatomical substrate for the recovery of motor function that follows damage to M1.

Citing Articles

Corticospinal and corticoreticulospinal projections have discrete but complementary roles in chronic motor behaviors after stroke.

Taga M, Hong Y, Charalambous C, Raju S, Hayes L, Lin J J Neurophysiol. 2024; 132(6):1917-1936.

PMID: 39503588 PMC: 11687835. DOI: 10.1152/jn.00301.2024.


Differential Modulation of Local Field Potentials in the Primary and Premotor Cortices during Ipsilateral and Contralateral Reach to Grasp in Macaque Monkeys.

Falaki A, Quessy S, Dancause N J Neurosci. 2024; 44(21).

PMID: 38589229 PMC: 11112639. DOI: 10.1523/JNEUROSCI.1161-23.2024.


Contribution of the subthalamic nucleus to motor, cognitive and limbic processes: an electrophysiological and stimulation study in monkeys.

Bertrand M, Chabardes S, Fontanier V, Procyk E, Bastin J, Piallat B Front Neurosci. 2024; 18:1257579.

PMID: 38456146 PMC: 10918855. DOI: 10.3389/fnins.2024.1257579.


Preparatory activity and the expansive null-space.

Churchland M, Shenoy K Nat Rev Neurosci. 2024; 25(4):213-236.

PMID: 38443626 DOI: 10.1038/s41583-024-00796-z.


Association between activity in the ventral premotor cortex and spinal cord activation during force generation-A combined cortico-spinal fMRI study.

Braass H, Feldheim J, Chu Y, Tinnermann A, Finsterbusch J, Buchel C Hum Brain Mapp. 2023; 44(18):6471-6483.

PMID: 37873743 PMC: 10681651. DOI: 10.1002/hbm.26523.


References
1.
Heffner R, Masterton B . Variation in form of the pyramidal tract and its relationship to digital dexterity. Brain Behav Evol. 1975; 12(3):161-200. DOI: 10.1159/000124401. View

2.
Kwan H, Mackay W, Murphy J, Wong Y . Spatial organization of precentral cortex in awake primates. II. Motor outputs. J Neurophysiol. 1978; 41(5):1120-31. DOI: 10.1152/jn.1978.41.5.1120. View

3.
Macpherson J, Marangoz C, Miles T, WIESENDANGER M . Microstimulation of the supplementary motor area (SMA) in the awake monkey. Exp Brain Res. 1982; 45(3):410-6. DOI: 10.1007/BF01208601. View

4.
SPRAGUE J . A study of motor cell localization in the spinal cord of the rhesus monkey. Am J Anat. 1948; 82(1):1-26. DOI: 10.1002/aja.1000820102. View

5.
Gibson A, Hansma D, Houk J, ROBINSON F . A sensitive low artifact TMB procedure for the demonstration of WGA-HRP in the CNS. Brain Res. 1984; 298(2):235-41. DOI: 10.1016/0006-8993(84)91423-9. View