ABSTRACT
The motor cortex of 10 healthy subjects was stimulated by transcranial magnetic stimulation (TMS) before and after ethanol challenge (0.8 g/kg resulting in blood concentration of 0.77 +/- 0.14 ml/liter). The electrical brain activity resulting from the brief electromagnetic pulse was recorded with high-resolution electroencephalography (EEG) and located using inversion algorithms. Focal magnetic pulses to the left motor cortex were delivered with a figure-of-eight coil at the random interstimulus interval of 1.5-2.5 s. The stimulation intensity was adjusted to the motor threshold of abductor digiti minimi. Two conditions before and after ethanol ingestion (30 min) were applied: (1) real TMS, with the coil pressed against the scalp; and (2) control condition, with the coil separated from the scalp by a 2-cm-thick piece of plastic. A separate EMG control recording of one subject during TMS was made with two bipolar platinum needle electrodes inserted to the left temporal muscle. In each condition, 120 pulses were delivered. The EEG was recorded from 60 scalp electrodes. A peak in the EEG signals was observed at 43 ms after the TMS pulse in the real-TMS condition but not in the control condition or in the control scalp EMG. Potential maps before and after ethanol ingestion were significantly different from each other (P = 0.01), but no differences were found in the control condition. Ethanol changed the TMS-evoked potentials over right frontal and left parietal areas, the underlying effect appearing to be largest in the right prefrontal area. Our findings suggest that ethanol may have changed the functional connectivity between prefrontal and motor cortices. This new noninvasive method provides direct evidence about the modulation of cortical connectivity after ethanol challenge.
Subject(s)
Alcoholic Intoxication/physiopathology , Cerebral Cortex/drug effects , Electroencephalography/drug effects , Electromagnetic Fields , Ethanol/pharmacology , Motor Cortex/drug effects , Adult , Brain Mapping , Cerebral Cortex/physiopathology , Electromyography/drug effects , Ethanol/pharmacokinetics , Evoked Potentials, Motor/drug effects , Evoked Potentials, Motor/physiology , Humans , Image Processing, Computer-Assisted , Imaging, Three-Dimensional , Magnetic Resonance Imaging , Male , Motor Cortex/physiopathology , Prefrontal Cortex/drug effects , Prefrontal Cortex/physiopathology , Signal Processing, Computer-Assisted , Temporal Muscle/innervationABSTRACT
We studied event-related desynchronization (ERD) of the 8-13 Hz rhythm (mu rhythm) of the primary somatosensory cortex (SI) caused by contra- and ipsilateral median-nerve stimulation. We used whole-head magnetoencephalography (MEG) and wavelet analysis together with our newly developed color-coded single-trial ERD display. The somatosensory stimuli suppressed mu rhythm at both contra- and ipsilateral SI, but the attenuation was clearly lateralized, being at least 20% stronger contra- than ipsilaterally. Moreover, repeated stimulation significantly reduced mu-rhythm ERD in the ipsilateral but not in the contralateral hemisphere in the course of the experiment. The observed lateralization is in agreement with the classical concept of a dominant role of the contralateral hemisphere in the processing of somatosensory information. The strong ipsilateral ERD in the beginning of the experiment may reflect the presence of non-specific arousal-like activation, which attenuates toward the end of the experiment.
Subject(s)
Evoked Potentials, Somatosensory/physiology , Magnetoencephalography , Median Nerve/physiology , Adult , Analysis of Variance , Electric Stimulation/methods , Female , Humans , Magnetoencephalography/methods , Male , Statistics, NonparametricABSTRACT
OBJECTIVES: Brain responses to auditory and visual stimuli have been previously shown to depend on the level of spontaneous brain activity in the 8-13 Hz range. Our aim was to determine whether somatosensory evoked responses are influenced by ongoing rhythmic activity in the 8-13 Hz frequency range originating in the sensorimotor cortex (mu rhythm). METHODS: We used a whole-head 122 channel magnetoencephalography (MEG) system to record somatosensory evoked fields (SEFs) in response to median nerve stimulation in 11 subjects. Spontaneous oscillations in the 8-13 Hz band over the contralateral sensorimotor cortex were evaluated in 3 different pre-stimulus time intervals using wavelet analysis. RESULTS: The N20m SEF deflection did not depend on pre-stimulus activity, while the amplitude of the P35m deflection, and to a lesser extent that of the P60m deflection, showed a small positive correlation with the amplitude of the pre-stimulus mu rhythm. Although the amplitude of the mu rhythm varied by a factor of 2.3-5, the maximum variations in P35m and P60m amplitude were only 21 and 12%, respectively. The latencies of the peaks were not affected by the strength of the pre-stimulus mu rhythm. CONCLUSIONS: It appears that the first excitatory cortical response (N20m) is independent of the oscillatory state (8-13 Hz frequency range) of the sensorimotor cortex. Later parts of the response (P35m and P60m) are also relatively stable compared with the large variations in mu rhythm.
