4.6 Article

Transcranial magnetic stimulation and PAS-induced cortical neuroplasticity in the awake rhesus monkey

期刊

CLINICAL NEUROPHYSIOLOGY
卷 121, 期 12, 页码 2143-2151

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.clinph.2010.03.058

关键词

Rhesus monkey; Transcranial magnetic stimulation; Cortex representation; Cortical excitability; Paired associative stimulation; Neuroplasticity; Non-invasive brain stimulation

资金

  1. Deutsche Forschungsgemeinschaft [Li/1016/3-1]
  2. Walter and Ilse Rose Stiftung [T298/14375/2004]
  3. German Ministry for Research and Education [BMBF-1362873]

向作者/读者索取更多资源

Objective: Externally induced neuroplasticity may be of therapeutic value in several neuro-psychiatric disorders. To facilitate research on mechanisms and to make possible the design of prospective, advanced stimulation protocols without exposing human subjects to risk, we have developed a primate model which allows us to assess changes of motor cortical excitability using transcranial magnetic stimulation (TMS). Methods: TMS hand muscle representation and cortical excitability were determined in two awake trained rhesus monkeys. Neuroplastic changes of cortical excitability were established by 13 min of paired associative stimulation (PAS) with interstimulus intervals of either 15 or 5 ms. Results: The representational areas of FDI and APB muscles (3.02-4.96 cm(2)) were located between the spur of the arcuate and the superior precentral sulcus, indicating the potential to carry out spatially selective cortical stimulation. PAS with an interstimulus interval of 15 ms strongly increased cortical excitability for up to two hours, while 5 ms interval had no effect. Conclusions: This first systematic TMS and PAS primate study demonstrates that the trained rhesus monkeys represent an exceptional animal model that allows cortical TMS mapping as well as non-invasive assessment and induction of cortical neuroplasticity. Significance: This animal model offers additional advantageous options not possible with humans, namely an alternative to invasive, morphological or molecular analyses, making it highly suitable for preclinical development of advanced neuroplasticity paradigms without exposing human subjects to risk. (C) 2010 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.

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