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Amano, K.

Publications and source records attributed to Amano, K..

22 records · Page 2Linked to original sources

Atypical spatial frequency dependence of visual metacognition among schizophrenia patients

Although altered early stages of visual processing have been reported among schizophrenia patients, how such atypical visual processing may affect higher-level cognition remains largely unknown. Here we tested the hypothesis that metacognitive performance may be atypically modulated by spatial frequency (SF) of visual stimuli among individuals with schizophrenia, given their altered magnocellular function. To study the effect of SF on metacognitive performance, we asked patients and controls to perform a visual detection task on gratings with different SFs and report confidence, and analyzed the data using the signal detection theoretic measure meta-d. Control subjects showed better metacognitive performance after yes- (stimulus-presence) than after no- (stimulus-absence) responses ( yes-response advantage) for high SF (HSF) stimuli but not for low SF (LSF) stimuli. The patients, to the contrary, showed a yes-response advantage not only for HSF but also for LSF stimuli, indicating atypical SF dependency of metacognition. An fMRI experiment using the same task revealed that the dorsolateral prefrontal cortex (DLPFC), known to be crucial for metacognition, shows activity mirroring the behavioral results: decoding accuracy of perceptual confidence in DLPFC was significantly higher for HSF than for LSF stimuli in controls, whereas this decoding accuracy was independent of SF in patients. While individuals without schizophrenia may flexibly adapt metacognitive computations across SF ranges, patients may employ a different mechanism that is independent of SF. Because visual stimuli of low SF have been linked to top-down processing in predictive coding, this may reflect atypical functioning in these processes in schizophrenia. HighlightsO_LIVisual metacognition of controls was dependent on spatial frequency. C_LIO_LIVisual metacognition of schizophrenia patients was independent of spatial frequency. C_LIO_LIPatients and controls differently rely on the dorsolateral prefrontal cortex. C_LIO_LISensory inputs may reach metacognitive circuits in an atypical manner among patients. C_LI

neuroscience↗

Layer-specific ultra-high field 7T fMRI showing that threat anticipation is mediated by the pulvinar input to the superficial layers of primary visual cortex (V1)

The perceptual system gives priority to threat-relevant signals with survival value. Its mechanism may not only include the processing initiated in the presence of threat signals but also in the mere anticipation of such signals. Here, we show that the pulvinar modulates activity in the early visual cortex (V1) specifically in threat anticipation. Using ultra-high-field 7T fMRI, we examined the layer-specific interaction between V1 and the pulvinar, while taking advantage of the fact that the directionality of such interaction is anatomically constrained in specific V1 layers. Only in anticipation of a fearful face target, but not of a control happy face target, was false perception of anticipated-yet-unpresented target face accompanied by stronger activity in the V1 superficial-cortical-depth (layers 1-3), which was preceded by pre-target-onset pulvinar activity. The pulvinar may contribute to the visual processing initiated in the anticipation of threat, and play an important role in anxiety.

neuroscience↗

Microstructural properties of the vertical occipital fasciculus explain the variability in human stereoacuity

Stereopsis is a fundamental visual function that has been studied extensively. However, it is not clear why depth discrimination (stereoacuity) varies more significantly among people than other modalities. Previous studies reported the involvement of both dorsal and ventral visual areas in stereopsis, implying that not only neural computations in cortical areas but also the anatomical properties of white matter tracts connecting those areas can impact stereopsis and stereoacuity. Here, we studied how human stereoacuity relates to white matter properties by combining psychophysics, diffusion MRI (dMRI), and quantitative MRI (qMRI). We performed a psychophysical experiment to measure stereoacuity, and in the same participants we analyzed the microstructural properties of visual white matter tracts based on two independent measurements, dMRI (fractional anisotropy, FA) and qMRI (macromolecular tissue volume; MTV). Microstructural properties along the right vertical occipital fasciculus (VOF), a major tract connecting dorsal and ventral visual areas, were highly correlated with measures of stereoacuity. This result was consistent for both FA and MTV, suggesting that the structural-behavioral relationship reflects differences in neural tissue density, rather than differences in the morphological configuration of fibers. fMRI confirmed that binocular disparity stimuli activated the dorsal and ventral visual regions near VOF endpoints. No other occipital tracts explained the variance in stereoacuity. In addition, the VOF properties were not associated with differences in performance on a different psychophysical task (contrast detection). These series of experiments suggest that stereoscopic depth discrimination performance is, at least in part, constrained by dorso-ventral communication through the VOF.

neuroscience↗

Broadband spectral responses in visual cortex revealed by a new MEG denoising algorithm

Currently, non-invasive methods for studying the human brain do not reliably measure spike-rate-dependent signals, independent of other responses such as hemodynamic coupling (fMRI) and subthreshold neuronal synchrony (oscillations and event-related potentials). In contrast, invasive methods - animal microelectrode recordings and human electrocorticography (ECoG) - have recently measured broadband power elevation in field potentials (~50-200Hz) as a proxy for the locally averaged spike rates. Here, we sought to detect and quantify stimulus-related broadband responses using magnetoencephalography (MEG) in individual subjects. Because extracranial measurements like MEG have multiple global noise sources and a relatively low signal-to-noise ratio, we developed an automated denoising technique, adapted from (Kay et al., 2013), that helps reveal the broadband signal of interest. Subjects viewed 12-Hz contrast-reversing patterns in the left, right, or bilateral visual field. Sensor time series were separated into an evoked component (12-Hz amplitude) and a broadband component (60-150Hz, excluding stimulus harmonics). In all subjects, denoised broadband responses were reliably measured in sensors over occipital cortex. The spatial pattern of the broadband measure depended on the stimulus, with greater broadband power in sensors contralateral to the stimulus. Because we obtain reliable broadband estimates with relatively short experiments (~20 minutes), with a sufficient signal-to-noise-ratio to distinguish responses to different stimuli, we conclude that MEG broadband signals, denoised with our method, offer a practical, non-invasive means for characterizing spike-rate-dependent neural activity for a wide range of scientific questions about human brain function.\n\nSignificance StatementNeuronal activity causes perturbations in nearby electrical fields. These perturbations can be measured non-invasively in the living human brain using EEG and MEG. These techniques have emphasized two kinds of measurements: oscillations and event-related responses. A third type of signal, a stimulus-related increase in power spanning a wide range of frequencies ( broadband), is routinely measured in invasive recordings, but not with MEG and EEG. This broadband response is of great interest because unlike oscillations and event-related responses, it is correlated with neuronal spike rates. Here we report quantitative, spatially specific measurements of broadband fields in individual human subjects using MEG. These results demonstrate that a spike-rate-dependent measure of brain activity can be obtained non-invasively from the living human brain.

neuroscience↗