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Using Dual-Site Transcranial Magnetic Stimulation to Probe Connectivity between the Dorsolateral Prefrontal Cortex and Ipsilateral Primary Motor Cortex in Humans.
Brown, Matt J N; Goldenkoff, Elana R; Chen, Robert; Gunraj, Carolyn; Vesia, Michael.
Afiliación
  • Brown MJN; Department of Kinesiology and Health Science, California State University Sacramento, Sacramento, California, CA 95819-6073, USA.
  • Goldenkoff ER; Brain and Behavior Laboratory, School of Kinesiology University of Michigan, Ann Arbor, Michigan, MI 48109-2214, USA.
  • Chen R; Division of Brain, Imaging and Behaviour-Systems Neuroscience, Krembil Brain Institute, Toronto, ON M5T 2S8, Canada.
  • Gunraj C; Division of Neurology, Department of Medicine, University of Toronto, Toronto, ON M5G 2C4, Canada.
  • Vesia M; Division of Brain, Imaging and Behaviour-Systems Neuroscience, Krembil Brain Institute, Toronto, ON M5T 2S8, Canada.
Brain Sci ; 9(8)2019 Jul 26.
Article en En | MEDLINE | ID: mdl-31357468
ABSTRACT
Dual-site transcranial magnetic stimulation to the primary motor cortex (M1) and dorsolateral prefrontal cortex (DLPFC) can be used to probe functional connectivity between these regions. The purpose of this study was to characterize the effect of DLPFC stimulation on ipsilateral M1 excitability while participants were at rest and contracting the left- and right-hand first dorsal interosseous muscle. Twelve participants were tested in two separate sessions at varying inter-stimulus intervals (ISI 4, 5, 6, 7, 8, 9, 10, 11, 12, 15, and 20 ms) at two different conditioning stimulus intensities (80% and 120% of resting motor threshold). No significant effect on ipsilateral M1 excitability was found when applying a conditioning stimulus over DLPFC at any specific inter-stimulus interval or intensity in either the left or right hemisphere. Our findings suggest neither causal inhibitory nor faciliatory influences of DLPFC on ipsilateral M1 activity while participants were at rest or when performing an isometric contraction in the target hand muscle.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Brain Sci Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Brain Sci Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos
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