Open AccessDesign and Evaluation of a Rodent‐Specific Transcranial Magnetic Stimulation Coil: An In Silico and In Vivo Validation Study
Author(s) -
Boonzaier Julia,
Petrov Petar I.,
Otte Willem M.,
Smirnov Nickolay,
Neggers Sebastiaan F.W.,
Dijkhuizen Rick M.
Publication year - 2020
Publication title -
neuromodulation: technology at the neural interface
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.296
H-Index - 60
eISSN - 1525-1403
pISSN - 1094-7159
DOI - 10.1111/ner.13025
Subject(s) - transcranial magnetic stimulation , electromagnetic coil , neuroscience , motor cortex , rodent , stimulation , human brain , in vivo , rodent model , psychology , biology , physics , ecology , microbiology and biotechnology , quantum mechanics , endocrinology
Background Rodent models are fundamental in unraveling cellular and molecular mechanisms of transcranial magnetic stimulation (TMS)‐induced effects on the brain. However, proper translation of human TMS protocols to animal models have been restricted by the lack of rodent‐specific focal TMS coils. Objective We aimed to improve TMS focalization in rodent brain with a novel small, cooled, and rodent‐specific TMS coil. Methods A rodent‐specific 25‐mm figure‐of‐eight TMS coil was developed. Stimulation focalization was simulated in silico for the rodent coil and a commercial human 50‐mm figure‐of‐eight TMS coil. Both coils were also compared in vivo by electromyography measurements of brachialis motor evoked potential (MEP) responses to TMS at different brain sites in anesthetized rats ( n = 6). Focalization was determined from the coils' level of stimulation laterality. Differences in MEPs were statistically analyzed with repeated‐measures, within‐subjects, ANOVA. Results In silico simulation results deemed the human coil insufficient for unilateral stimulation of the rat motor cortex, whereas lateralized electrical field induction was projected attainable with the rodent coil. Cortical, in vivo MEP amplitude measurements from multiple points in each hemisphere, revealed unilateral activation of the contralateral brachialis muscle, in absence of ipsilateral brachialis activation, with both coils. Conclusion Computer simulations motivated the design of a smaller rodent‐specific TMS coil, but came short in explaining the capability of a larger commercial human coil to induce unilateral MEPs in vivo . Lateralized TMS, as demonstrated for both TMS coils, corroborates their use in translational rodent studies, to elucidate mechanisms of action of therapeutic TMS protocols.