» Articles » PMID: 21653716

Modules in the Brain Stem and Spinal Cord Underlying Motor Behaviors

Overview
Journal J Neurophysiol
Specialties Neurology
Physiology
Date 2011 Jun 10
PMID 21653716
Citations 79
Authors
Affiliations
Soon will be listed here.
Abstract

Previous studies using intact and spinalized animals have suggested that coordinated movements can be generated by appropriate combinations of muscle synergies controlled by the central nervous system (CNS). However, which CNS regions are responsible for expressing muscle synergies remains an open question. We address whether the brain stem and spinal cord are involved in expressing muscle synergies used for executing a range of natural movements. We analyzed the electromyographic (EMG) data recorded from frog leg muscles before and after transection at different levels of the neuraxis-rostral midbrain (brain stem preparations), rostral medulla (medullary preparations), and the spinal-medullary junction (spinal preparations). Brain stem frogs could jump, swim, kick, and step, while medullary frogs could perform only a partial repertoire of movements. In spinal frogs, cutaneous reflexes could be elicited. Systematic EMG analysis found two different synergy types: 1) synergies shared between pre- and posttransection states and 2) synergies specific to individual states. Almost all synergies found in natural movements persisted after transection at rostral midbrain or medulla but not at the spinal-medullary junction for swim and step. Some pretransection- and posttransection-specific synergies for a certain behavior appeared as shared synergies for other motor behaviors of the same animal. These results suggest that the medulla and spinal cord are sufficient for the expression of most muscle synergies in frog behaviors. Overall, this study provides further evidence supporting the idea that motor behaviors may be constructed by muscle synergies organized within the brain stem and spinal cord and activated by descending commands from supraspinal areas.

Citing Articles

Muscle synergy in several locomotor modes in chimpanzees and Japanese macaques, and its implications for the evolutionary origin of bipedalism through shared muscle synergies.

Goto R, Larson S, Shitara T, Hashiguchi Y, Nakano Y Sci Rep. 2024; 14(1):31134.

PMID: 39732749 PMC: 11682134. DOI: 10.1038/s41598-024-82479-4.


Nonnegative matrix factorization for analyzing state dependent neuronal network dynamics in calcium recordings.

Carbonero D, Noueihed J, Kramer M, White J Sci Rep. 2024; 14(1):27899.

PMID: 39537711 PMC: 11560946. DOI: 10.1038/s41598-024-78448-6.


Synergy quality assessment of muscle modules for determining learning performance using a realistic musculoskeletal model.

Fukunishi A, Kutsuzawa K, Owaki D, Hayashibe M Front Comput Neurosci. 2024; 18:1355855.

PMID: 38873285 PMC: 11171420. DOI: 10.3389/fncom.2024.1355855.


Rectified Latent Variable Model-Based EMG Factorization of Inhibitory Muscle Synergy Components Related to Aging, Expertise and Force-Tempo Variations.

Huang S, Guo X, Xie J, Lau K, Liu R, Mak A Sensors (Basel). 2024; 24(9).

PMID: 38732926 PMC: 11086352. DOI: 10.3390/s24092820.


Spatiotemporal modulation of a common set of muscle synergies during unpredictable and predictable gait perturbations in older adults.

Brull L, Santuz A, Mersmann F, Bohm S, Schwenk M, Arampatzis A J Exp Biol. 2024; 227(7).

PMID: 38506185 PMC: 11058090. DOI: 10.1242/jeb.247271.


References
1.
Lee D, Seung H . Learning the parts of objects by non-negative matrix factorization. Nature. 1999; 401(6755):788-91. DOI: 10.1038/44565. View

2.
Weiss E, Flanders M . Muscular and postural synergies of the human hand. J Neurophysiol. 2004; 92(1):523-35. DOI: 10.1152/jn.01265.2003. View

3.
Lockhart D, Ting L . Optimal sensorimotor transformations for balance. Nat Neurosci. 2007; 10(10):1329-36. DOI: 10.1038/nn1986. View

4.
Shinoda Y, Yokota J, Futami T . Divergent projection of individual corticospinal axons to motoneurons of multiple muscles in the monkey. Neurosci Lett. 1981; 23(1):7-12. DOI: 10.1016/0304-3940(81)90182-8. View

5.
Li Q, Martin J . Postnatal development of connectional specificity of corticospinal terminals in the cat. J Comp Neurol. 2002; 447(1):57-71. DOI: 10.1002/cne.10203. View