» Articles » PMID: 28674174

Cooperation Not Competition: Bihemispheric TDCS and FMRI Show Role for Ipsilateral Hemisphere in Motor Learning

Overview
Journal J Neurosci
Specialty Neurology
Date 2017 Jul 5
PMID 28674174
Citations 40
Authors
Affiliations
Soon will be listed here.
Abstract

What is the role of ipsilateral motor and premotor areas in motor learning? One view is that ipsilateral activity suppresses contralateral motor cortex and, accordingly, that inhibiting ipsilateral regions can improve motor learning. Alternatively, the ipsilateral motor cortex may play an active role in the control and/or learning of unilateral hand movements. We approached this question by applying double-blind bihemispheric transcranial direct current stimulation (tDCS) over both contralateral and ipsilateral motor cortex in a between-group design during 4 d of unimanual explicit sequence training in human participants. Independently of whether the anode was placed over contralateral or ipsilateral motor cortex, bihemispheric stimulation yielded substantial performance gains relative to unihemispheric or sham stimulation. This performance advantage appeared to be supported by plastic changes in both hemispheres. First, we found that behavioral advantages generalized strongly to the untrained hand, suggesting that tDCS strengthened effector-independent representations. Second, functional imaging during speed-matched execution of trained sequences conducted 48 h after training revealed sustained, polarity-independent increases in activity in both motor cortices relative to the sham group. These results suggest a cooperative rather than competitive interaction of the two motor cortices during skill learning and suggest that bihemispheric brain stimulation during unimanual skill learning may be beneficial because it harnesses plasticity in the ipsilateral hemisphere. Many neurorehabilitation approaches are based on the idea that is beneficial to boost excitability in the contralateral hemisphere while attenuating that of the ipsilateral cortex to reduce interhemispheric inhibition. We observed that bihemispheric transcranial direct current stimulation (tDCS) with the excitatory anode either over contralateral or ipsilateral motor cortex facilitated motor learning nearly twice as strongly as unihemispheric tDCS. These increases in motor learning were accompanied by increases in fMRI activation in both motor cortices that outlasted the stimulation period, as well as increased generalization to the untrained hand. Collectively, our findings suggest a cooperative rather than a competitive role of the hemispheres and imply that it is most beneficial to harness plasticity in both hemispheres in neurorehabilitation of motor deficits.

Citing Articles

Perceptual and Cognitive Effects of Focal Transcranial Direct Current Stimulation of Auditory Cortex in Tinnitus.

Leaver A Neuromodulation. 2024; 28(1):136-145.

PMID: 39396357 PMC: 11700759. DOI: 10.1016/j.neurom.2024.06.001.


Non-Dominant Hemisphere Excitability Is Unaffected during and after Transcranial Direct Current Stimulation of the Dominant Hemisphere.

Wilkins E, Young R, Houston D, Kawana E, Lopez Mora E, Sunkara M Brain Sci. 2024; 14(7).

PMID: 39061434 PMC: 11274959. DOI: 10.3390/brainsci14070694.


Kinematic descriptors of arm reaching movement are sensitive to hemisphere-specific immediate neuromodulatory effects of transcranial direct current stimulation post stroke.

Lowenthal-Raz J, Liebermann D, Friedman J, Soroker N Sci Rep. 2024; 14(1):11971.

PMID: 38796610 PMC: 11127956. DOI: 10.1038/s41598-024-62889-0.


Temporal Dynamics of Adverse Effects across Five Sessions of Transcranial Direct Current Stimulation.

Delicado-Miralles M, Flix-Diez L, Gurdiel-Alvarez F, Velasco E, Galan-Calle M, Lerma Lara S Brain Sci. 2024; 14(5).

PMID: 38790436 PMC: 11118034. DOI: 10.3390/brainsci14050457.


Transcutaneous auricular vagus nerve stimulation with task-oriented training improves upper extremity function in patients with subacute stroke: a randomized clinical trial.

Wang M, Wang Y, Xie M, Chen L, He M, Lin F Front Neurosci. 2024; 18:1346634.

PMID: 38525376 PMC: 10957639. DOI: 10.3389/fnins.2024.1346634.


References
1.
Ganguly K, Secundo L, Ranade G, Orsborn A, Chang E, Dimitrov D . Cortical representation of ipsilateral arm movements in monkey and man. J Neurosci. 2009; 29(41):12948-56. PMC: 3376707. DOI: 10.1523/JNEUROSCI.2471-09.2009. View

2.
Worsley K, Marrett S, Neelin P, Vandal A, Friston K, Evans A . A unified statistical approach for determining significant signals in images of cerebral activation. Hum Brain Mapp. 2010; 4(1):58-73. DOI: 10.1002/(SICI)1097-0193(1996)4:1<58::AID-HBM4>3.0.CO;2-O. View

3.
Nitsche M, Paulus W . Transcranial direct current stimulation--update 2011. Restor Neurol Neurosci. 2011; 29(6):463-92. DOI: 10.3233/RNN-2011-0618. View

4.
Stagg C, Bachtiar V, OShea J, Allman C, Bosnell R, Kischka U . Cortical activation changes underlying stimulation-induced behavioural gains in chronic stroke. Brain. 2011; 135(Pt 1):276-84. PMC: 3267983. DOI: 10.1093/brain/awr313. View

5.
Rahman A, Reato D, Arlotti M, Gasca F, Datta A, Parra L . Cellular effects of acute direct current stimulation: somatic and synaptic terminal effects. J Physiol. 2013; 591(10):2563-78. PMC: 3678043. DOI: 10.1113/jphysiol.2012.247171. View