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Nyrhinen, M.

Publications and source records attributed to Nyrhinen, M..

3 recordsLinked to original sources

Mapping of individual somatosensory representations - comparison of fMRI and TMS

Invasive brain mapping, functional magnetic resonance imaging (fMRI) and navigated transcranial magnetic stimulation (nTMS) results indicate that somatosensory representations vary between individuals. However, it is unknown how well somatosensory representations determined using nTMS and fMRI correspond. Here, we used single-pulse nTMS and fMRI in 17 right-handed subjects to determine the S1 representation of the tip of the right index finger stimulated mechanically with a Braille device. In an nTMS mapping experiment, the S1 site at which tactile sensation was blocked by nTMS, was considered the S1 representation site (S1HS) of the fingertip. The location of S1HS varied up to 36 mm between subjects. In the fMRI experiment, passive and oddball tactile tasks were employed. The location of the somatosensory peak fMRI activation varied up to 39 mm between subjects in the passive condition and up to 84 mm in the oddball condition. Within subjects, the mean distance between the S1HS and the peak fMRI activation was 10 + 2 mm (S.E.M.) in the passive condition and 14 + 3 mm in the oddball task. Taken together, our findings underscore the importance of multimodal approaches to brain mapping in future studies.

neuroscience↗

A multi-channel TMS system enabling accurate stimulus orientation control during concurrent ultra-high-field MRI for preclinical applications

Monitoring cortical responses to neuromodulation protocols on preclinical models can elucidate fundamental mechanisms of brain function. Concurrent brain stimulation and imaging is challenging, usually compromising spatiotemporal resolution, accuracy, and versatility. Here we report a non-invasive brain stimulation system with electronic control of neuromodulation parameters in a 9.4-T magnetic resonance imaging (MRI) environment. In the imaging scanner, transcranial magnetic stimulation is delivered with a set of two coils and the MRI signals are recorded with a radiofrequency coil. The coil set provides millisecond-scale electronic control of the stimulus orientation with 1{degrees} resolution. Without physically rotating the coils, we evoked orientation-specific muscle responses after cortical stimulation on an anesthetized rat. We show that the stimulation pulses do not affect the anatomical imaging quality, and imaging signals are disrupted only if recorded before 10 ms after pulse delivery. Concurrent electronically targeted brain stimulation and neuroimaging sets the stage for the causal investigation of whole-brain network functions, endorsing more efficient treatment protocols.

neuroscience↗

Hemodynamic changes in response to excitatory and inhibitory modulations by transcranial magnetic stimulation at the human sensorimotor cortex

Transcranial magnetic stimulation (TMS) can non-invasively induce both excitatory and inhibitory neuronal activity. However, the neurophysiological basis for both kinds of modulation remains elusive. In this study, with a controlled dosage over the 30-s interval, we elicited excitatory and inhibitory TMS modulations over the human primary motor cortex (M1) with TMS bursts of high (10-Hz and 30-Hz) and low frequency (0.5-Hz), respectively, and took functional magnetic resonance images (fMRI). Excitatory and inhibitory modulations were evidenced by changes in motor evoked potentials (MEP). Significantly increased fMRI signal at M1 was only detected under excitatory high-frequency TMS but not during inhibitory low-frequency TMS. The supplementary motor area (SMA) had significant fMRI signal changes after both excitatory and inhibitory TMS. The topology of the activated M1 and SMA matched the activated sensorimotor network during voluntary movement. The precuneus was selectively activated with bursts of five TMS pulses. These findings demonstrated the asymmetric hemodynamic responses to excitatory and inhibitory TMS modulations with region-dependent relationships between the local fMRI signal changes and TMS dosage over different time scales.

neuroscience↗