Todd et al. (2014) have recently demonstrated the presence of vestibular dependent changes both in the morphology and in the intensity dependence of auditory evoked potentials (AEPs) when passing through the vestibular threshold as determined by vestibular evoked myogenic potentials (VEMPs). In this paper we extend this work by comparing left vs. right ear stimulation and by conducting a source analysis of the resulting evoked potentials of short and long latency. Ten healthy, right-handed subjects were recruited and evoked potentials were recorded to both left- and right-ear sound stimulation, above and below vestibular threshold. Below VEMP threshold, typical AEPs were recorded, consisting of mid-latency (MLR) waves Na and Pa followed by long latency AEPs (LAEPs) N1 and P2. In the supra-threshold condition, the expected changes in morphology were observed, consisting of: (1) short-latency vestibular evoked potentials (VsEPs) which have no auditory correlate, i.e. the ocular VEMP (OVEMP) and inion response related potentials; (2) a later deflection, labelled N42/P52, followed by the LAEPs N1 and P2. Statistical analysis of the vestibular dependent responses indicated a contralateral effect for inion related short-latency responses and a left-ear/right-hemisphere advantage for the long-latency responses. Source analysis indicated that the short-latency effects may be mediated by a contralateral projection to left cerebellum, while the long-latency effects were mediated by a contralateral projection to right cingulate cortex. In addition we found evidence of a possible vestibular contribution to the auditory T-complex in radial temporal lobe sources. These last results raise the possibility that acoustic activation of the otolith organs could potentially contribute to auditory processing.
Acoustic sensitivity of the vestibular apparatus is well-established, but the contribution of vestibular receptors to the late auditory evoked potentials of cortical origin is unknown. Evoked potentials from 500 Hz tone pips were recorded using 70 channel EEG at several intensities below and above the vestibular acoustic threshold, as determined by vestibular evoked myogenic potentials (VEMPs). In healthy subjects both auditory mid- and long-latency auditory evoked potentials (AEPs), consisting of Na, Pa, N1 and P2 waves, were observed in the sub-threshold conditions. However, in passing through the vestibular threshold, systematic changes were observed in the morphology of the potentials and in the intensity dependence of their amplitude and latency. These changes were absent in a patient without functioning vestibular receptors. In particular, for the healthy subjects there was a fronto-central negativity, which appeared at about 42 ms, referred to as an N42, prior to the AEP N1. Source analysis of both the N42 and N1 indicated involvement of cingulate cortex, as well as bilateral superior temporal cortex. Our findings are best explained by vestibular receptors contributing to what were hitherto considered as purely auditory evoked potentials and in addition tentatively identify a new component that appears to be primarily of vestibular origin.
Visually induced motion sickness (VIMS) is a common side effect in virtual environments and simulators. Several countermeasures against VIMS exist, but a reliable method to prevent or ease VIMS is unfortunately still missing. In the present study, we tested whether olfactory cues can alleviate VIMS. Sixty-two participants were exposed to a 15-min-long video showing a first-person-view bicycle ride that had successfully induced VIMS in previous studies. Participants were randomly assigned to one of three groups; the first group was exposed to a pleasant odor (rose) while watching the video, the second group was exposed to an unpleasant odor (leather), and the third group was not exposed to any odor. VIMS was measured using a verbal rating scale (0-20) and the Simulator Sickness Questionnaire. Results showed that only half of the participants who were exposed to the odor did notice it (n = 21), whereas the other half failed to detect the odor. However, among those participants who did notice the odor, the rose scent significantly reduced the severity of VIMS compared to the group that did not notice the odor. A moderate positive correlation between odor sensitivity and VIMS showed that participants with higher odor sensitivity also reported stronger VIMS. Our results demonstrate that olfaction can modulate VIMS and that a pleasant odor can potentially reduce VIMS. The relationship between olfactory perception, olfactory sensibility, and VIMS is discussed.
While there have been numerous studies of the vestibular system in mammals, less is known about the brain mechanisms of vestibular processing in humans. In particular, of the studies that have been carried out in humans over the last 30 years, none has investigated how vestibular stimulation (VS) affects cortical oscillations. Here we recorded high-density electroencephalography (EEG) in healthy human subjects and a group of bilateral vestibular loss patients (BVPs) undergoing transient and constant-velocity passive whole body yaw rotations, focusing our analyses on the modulation of cortical oscillations in response to natural VS. The present approach overcame significant technical challenges associated with combining natural VS with human electrophysiology and reveals that both transient and constant-velocity VS are associated with a prominent suppression of alpha power (8 -13 Hz). Alpha band suppression was localized over bilateral temporo-parietal scalp regions, and these alpha modulations were significantly smaller in BVPs. We propose that suppression of oscillations in the alpha band over temporo-parietal scalp regions reflects cortical vestibular processing, potentially comparable with alpha and mu oscillations in the visual and sensorimotor systems, respectively, opening the door to the investigation of human cortical processing under various experimental conditions during natural VS. EEG; vestibular processing; vestibular cortex THE VESTIBULAR SYSTEM encodes three-dimensional displacements of the head and its position relative to gravity. Vestibular signals are used for oculomotor and postural control but also underpin perceptual and cognitive functions, including visual perception according to internal models of gravity, spatial navigation, and bodily awareness (Brandt et al. 2005;Indovina et al. 2005;Lopez et al. 2010). In strong contrast with the growing number of functions shown to be under vestibular influence is the relative lack of data on the vestibular cortex in animals and humans (Angelaki and Cullen 2008;Brandt and Dieterich 1999;Lopez and Blanke 2011).Electrophysiological investigations in nonhuman primates have revealed vestibular responses in several areas of the cortex. These include the intraparietal sulcus and the somatosensory, temporal, frontal, and parieto-insular cortices (Bremmer et al. 2002;Grüsser et al. 1990aGrüsser et al. , 1990bGu et al. 2008;Liu et al. 2011;Schwarz and Fredrickson 1971). These areas form a cortical network of which the core is presumed to be located in the "parieto-insular vestibular cortex" (PIVC; Guldin and Grüsser 1998). Recently, descriptions of vestibular neurons' spatiotemporal tuning in these cortical regions have been achieved during three-dimensional passive rotations/ translations on motion platforms in nonhuman primates (e.g., Chen et al. 2011;Shinder and Newlands 2014;Takahashi et al. 2007).Investigations of the human vestibular cortex are challenging because neuroimaging techniques (fMRI, PET) do not allow head and body movements and thus the app...
The aim of this study was to test the validity of mirror neuron activity in humans through analysis of electroencephalographic (EEG) functional connectivity during an action not directed towards an object. We investigated changes in EEG interchannel synchronization prior to and during action execution and also prior to and during observation of the same action. Twelve participants observed a simple finger movement sequence. In a second testing session they physically executed the movement. EEGs were recorded from 19 active sites across the cortex. Activity was considered in four frequency bands (7-10 Hz, 10-13 Hz, 13-20 Hz, and 20-30 Hz) using a new measure: synchronization likelihood. This technique considers rapid changes in signal synchronization and spatiotemporal patterns of coherence. The results revealed no statistically significant difference in synchronization likelihood between the observation and execution data. We found an increase in synchronization over a broad frequency range during task processing and suggest that this may reflect interregional cortical coupling of intricately and hierarchically interconnected networks that are active in a similar way during both observation and execution of a movement. While EEG may be insensitive to differences present during the observation and execution of a movement, the results of the present study shed some light on the general mechanisms of cognitive integration.
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