Biology subjects

Morrone, M. C.

Publications and source records attributed to Morrone, M. C..

12 recordsLinked to original sources

bioRxiv2026

Residual cortical responses and network reorganization in inherited retinal degeneration: electrophysiological evidence

Retinitis pigmentosa (RP) progressively deprives the retina of input, but whether the responsiveness of the visual cortex declines in parallel, remains preserved, or increases through compensatory gain remains unclear. Indeed, a weaker visually evoked response cannot, on its own, distinguish these possibilities, since it is equally compatible with a passively degraded input and with an actively recalibrated cortex. We combined spatially resolved steady-state visual evoked potentials (SSVEPs), which index stimulus-driven activity, with transcranial magnetic stimulation combined with electroencephalography (TMS-EEG), which probes cortical reactivity independently of vision, in patients with RP and in healthy controls. Nine patients (PTs) with RP (five women, age range 28 to 69 years) and nineteen sex-, age-, and handedness-matched healthy controls (thirteen women, mean age 42.6 years) were tested. They underwent SSVEP recordings to stimuli presented at three eccentricities (central, intermediate, peripheral) and single-pulse TMS-EEG over the left and right occipital cortex and, as a non-visual control site, the dominant motor cortex. We quantified SSVEP amplitude and phase at 12 Hz, early TMS-evoked potentials, oscillatory power, inter-trial phase synchrony, and functional connectivity and graph-theoretical network measures derived from the weighted phase lag index. SSVEP amplitude followed the expected central-to-peripheral gradient: PTs were comparable to healthy controls at the center, reduced but still above their own resting baseline at intermediate eccentricity, and no longer distinguishable from baseline in the periphery; phase differed from controls in a quarter of the central and half of the intermediate sectors. Occipital stimulation elicited a larger early negative deflection after left-hemisphere stimulation in PTs compared to controls, a stronger beta-band event-related spectral perturbation after stimulation of either hemisphere, and stronger, more efficiently distributed post-stimulus connectivity, despite comparable pre-stimulus connectivity, resting motor threshold, and most early evoked components. The pattern was site- and hemisphere-specific: left occipital stimulation produced widespread, mainly contralateral effects; right occipital stimulation a more circumscribed ipsilateral one, and motor cortex stimulation showed altered alpha-band activity without the bilateral occipital beta effect. Together, these results show that progressive retinal deafferentation in RP does not produce a parallel decline in cortical responsiveness. Visually driven activity weakens with eccentricity, while direct cortical perturbation reveals preserved and, at selected sites, enhanced reactivity. This dissociation is consistent with a homeostatic increase in cortical gain rather than a uniform loss of cortical function, and indicates that the deafferented cortex retains, and in places strengthens, its capacity to respond as retinal input deteriorates.

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bioRxiv2025

Acute supplementation of beta-hydroxybutyrate increases visual cortical excitability in humans: a combined EEG and MRS study

Increasing plasma levels of ketone bodies via supplementation or dieting has been repeatedly used to ameliorate neurological symptoms and enhance cognitive performance. Here we aim to gain insight into the underlying mechanisms by characterizing the acute effects on visual cortical function of a single dose {beta}-hydroxybutyrate ({beta}HB) supplementation. Young human volunteers were orally administered a {beta}HB ester; we used EEG to assess cortical excitability and responsivity to visual stimulation, and Magnetic Resonance Spectroscopy to quantify glutamate and GABA+ concentrations in the occipital cortex. {beta}HB supplementation increased the amplitude of Visual Evoked Potentials and enhanced the resting-state EEG alpha rhythm. These electrophysiological changes were paralleled by a neurometabolic change in the occipital cortex, where glutamate (but not GABA+) concentration increased. The glutamate increase was correlated with the increased Visual Evoked Potential amplitude. This suggests that acute {beta}HB supplementation increases the excitability of the brain cortex, as assessed neurometabolically and electrophysiologically.

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bioRxiv2025

The pulvinar regulates plasticity in human visual cortex

In normally sighted human adults, two-hours of monocular deprivation is sufficient to transiently alter ocular dominance. Here we show that this is associated with a reduction of functional connectivity between the pulvinar and early visual cortex, selective for the pulvinar-to-V1 directionality. Across participants, the strength of the pulvinar-to-V1 connectivity was negatively correlated with the ocular dominance shift, implying less plasticity in participants with stronger influence of the pulvinar over V1. Our results support a revised model of adult V1 plasticity, where short-term reorganization is gated by modulatory signals relayed by the pulvinar. TeaserShort-term monocular deprivation triggers a reorganization of the visual processing network, measured with 7TfMRI in human adults.

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bioRxiv2023

Serial Dependence in face-gender classification revealed in low-beta frequency EEG

Perception depends not only on current sensory input but is also heavily influenced by the immediate past perceptual experience, a phenomenon known as "serial dependence". It is particularly robust in face perception. We measured face-gender classification for a sequence of intermingled male, female and androgynous images. The classification showed strong serial dependence (androgynous images biased male when preceded by male and female when preceded by female). The strength of the bias oscillated over time in the beta range, at 14 Hz for female prior stimuli, 17 Hz for male. Using classification techniques, we were able to successfully classify the previous stimulus from current EEG activity. Classification accuracy correlated well with the strength of serial dependence in individual participants, confirming that the neural signal from the past trial biased face perception. Bandpass filtering of the signal within the beta range showed that the best information to classify gender was around 14 Hz when the previous response was "female", and around 17 Hz when it was "male", reinforcing the psychophysical results showing serial dependence to be carried at those frequencies. Overall, the results suggest that recent experience of face-gender is selectively represented in beta-frequency (14-20 Hz) spectral components of intrinsic neural oscillations. Significance StatementThe neurophysiological mechanisms of how past perceptual experience affects current perception are poorly understood. Using classification techniques, we demonstrate that the gender of face images can be decoded from the neural activity of the EEG response to the successive face stimulus, showing that relevant neural signals are maintained over trials. Classification accuracy was higher for participants with strong serial dependence, strongly implicating these signals as the neural substrate for serial dependence. The best information to classify gender was around 14 Hz for "female" faces, and around 17 Hz for "male", reinforcing the psychophysical results showing serial dependence to be carried at those beta-frequencies.

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bioRxiv2021

Short-term plasticity in the visual thalamus

While there is evidence that the visual cortex retains a potential for plasticity in adulthood, less is known about the subcortical stages of visual processing. Here we asked whether short-term ocular dominance plasticity affects the visual thalamus. We addressed this question in normally sighted adult humans, using ultra-high field (7T) magnetic resonance imaging combined with the paradigm of short-term monocular deprivation. With this approach, we previously demonstrated transient shifts of perceptual eye dominance and ocular dominance in visual cortex (Binda et al., 2018). Here we report evidence for short-term plasticity in the ventral division of the pulvinar (vPulv), where the deprived eye representation was enhanced over the non-deprived eye. This pulvinar plasticity effect was similar as previously seen in visual cortex and it was correlated with the ocular dominance shift measured behaviorally. In contrast, there was no short-term plasticity effect in Lateral Geniculate Nucleus (LGN), where results were reliably different from vPulv, despite their spatial proximity. We conclude that the visual thalamus retains potential for short-term plasticity in adulthood; the plasticity effect differs across thalamic subregions, possibly reflecting differences in their cortical connectivity.

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bioRxiv2021

Sleep Slow Oscillations and Spindles encode ocular dominance plasticity and promote its consolidation in adult humans

Sleep and plasticity are highly interrelated, as sleep slow oscillations and sleep spindles are associated with consolidation of Hebbian-based processes. However, in adult humans, visual cortical plasticity is mainly sustained by homeostatic mechanisms, for which the role of sleep is still largely unknown. Here we demonstrate that non-REM sleep stabilizes homeostatic plasticity of ocular dominance induced in adult humans by short-term monocular deprivation: the counter intuitive and otherwise transient boost of the deprived eye was preserved at the morning awakening (>6 hours after deprivation). Subjects exhibiting a stronger boost of the deprived eye after sleep had increased sleep spindle density in frontopolar electrodes, suggesting the involvement of distributed processes. Crucially, the individual susceptibility to visual homeostatic plasticity soon after deprivation correlated with the changes in sleep slow oscillations and spindle power in occipital sites, consistent with a modulation in early occipital visual cortex.

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bioRxiv2020

Propagation and update of auditory perceptual priors through alpha and theta rhythms

To maintain a continuous and coherent percept over time, the brain makes use of past sensory information to anticipate forthcoming stimuli. We recently showed that auditory experience in the immediate past is propagated through ear-specific reverberations, manifested as rhythmic fluctuations of decision bias at alpha frequency. Here, we apply the same time-resolved behavioural method to investigate how perceptual performance changes over time under conditions of high stimulus expectation, and to examine the effect of unexpected events on behaviour. As in our previous study, participants were required to discriminate the ear-of-origin of a brief monaural pure tone embedded in uncorrelated dichotic white noise. We manipulated stimulus expectation by increasing the target probability in one ear to 80%. Consistent with our earlier findings, performance did not remain constant across trials, but varied rhythmically with delay from noise onset. Specifically, decision bias showed a similar oscillation at ~9 Hz that depended on ear congruency between successive targets. This suggests rhythmic communication of auditory perceptual history occurs early and is not readily influenced by top-down expectations. In addition, we report a novel observation specific to infrequent, unexpected stimuli that gave rise to oscillations in accuracy at ~7.6 Hz one trial after the target occurred in the non-anticipated ear. This new behavioural oscillation may reflect a mechanism for updating the sensory representation once a prediction error has been detected.

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bioRxiv2020

Temporal binding of Visual and Motor cortical oscillations revealed by BOLD response in Humans

The mechanisms coordinating action and perception over time are poorly understood. The sensory cortex needs to prepare for upcoming changes contingent on action, and this requires temporally precise communication that takes into account the variable delays between sensory and motor processing. Several theorists1,2 have proposed synchronization of the endogenous oscillatory activity observed in most regions of the brain3 as the basis for an efficient and flexible communication protocol between distal brain areas2,4, a concept known as "communication through coherence". Synchronization of endogenous oscillations5,6 occurs after a salient sensory stimulus, such as a flash or a sound7-11, and after a voluntary action12-18, and this impacts directly on perception, causing performance to oscillate rhythmically over time. Here we introduce a novel fMRI paradigm to probe the neural sources of oscillations, based on the concept of perturbative signals, which overcomes the low temporal resolution of BOLD signals. The assumption is that a synchronized endogenous rhythm will modulate cortical excitability rhythmically, which should be reflected in the BOLD responses to brief stimuli presented at different phases of the oscillation cycle. We record rhythmic oscillations of V1 BOLD synchronized by a simple voluntary action, in phase with behaviourally measured oscillations in visual sensitivity in the theta range. The functional connectivity between V1 and M1 also oscillates at the same rhythm. By demonstrating oscillatory temporal coupling between primary motor and sensory cortices, our results strongly implicate communication through coherence to achieve precise coordination and to encode sensory-motor timing.

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bioRxiv2020

The visual white matter connecting human area prostriata and the thalamus is retinotopically organized

The human visual system is capable of processing visual information from fovea to the far peripheral visual field. Recent fMRI studies have shown a full and detailed retinotopic map in area prostriata, located ventro-dorsally and anterior to the calcarine sulcus along the parietooccipital sulcus with strong preference for peripheral and wide-field stimulation. Here, we report the anatomical pattern of white-matter connections between area prostriata and the thalamus encompassing the lateral geniculate nucleus (LGN). We observe a continuous and extended bundle of white matter fibers from which two subcomponents can be extracted: one passing ventrally parallel to the optic radiations (OR) and another passing dorsally circumventing the lateral ventricle. Interestingly, the loop travelling dorsally connects the thalamus with the central visual field representation of prostriata, while the other loop travelling more ventrally connects the LGN with the more peripheral visual field representation. This is consistent with a retinotopic segregation recently demonstrated in the OR, connecting the LGN and V1 in humans. Our results demonstrate for the first time a retinotopic segregation regarding the trajectory of a fiber bundle between the thalamus and an associative visual area.

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bioRxiv2019

Auditory perceptual history is communicated through alpha oscillations

Sensory expectations from the accumulation of information over time exert strong predictive biases on forthcoming perceptual decisions. These anticipatory mechanisms help to maintain a coherent percept in a noisy environment. Here we present novel behavioural evidence that past sensory experience biases perceptual decisions rhythmically through alpha oscillations. Participants identified the ear of origin of a brief sinusoidal tone masked by dichotic white noise, and response bias oscillated over time at [~]9 Hz. Importantly, the oscillations occurred only for trials preceded by a target to the same ear and lasted for at least two trials. These findings suggest that each stimulus elicits an oscillating memory trace, specific to the ear of origin, which subsequently biases perceptual decisions. This trace is phase-reset by the noise onset of the next trial, and remains within the circuitry of the ear in which it was elicited, modulating the sensory representations in that ear.

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bioRxiv2018

A new counter-intuitive therapy for adult amblyopia

Visual cortex plasticity is high during a critical period of early postnatal development, but rapidly diminishes with the transition to adulthood. Accordingly, visual disorders such as amblyopia (lazy eye), can be treated early in life by long-term occlusion of the non-amblyopic eye, but may become irreversible in adults, because of the decline in brain plasticity. Here we show that a novel counter-intuitive approach can promote the recovery of visual function in adult amblyopic patients: short-term occlusion of the amblyopic (not the fellow) eye, combined with physical exercise (cycling). After six brief (2h) training sessions, visual acuity improved in all ten patients (0.15{+/-}0.02 LogMar), and six of them also recovered stereopsis. The improvement was preserved for up to one year after training. A control experiment revealed that physical activity was crucial for the recovery of visual acuity and stereopsis. Thus, we propose a non-invasive therapeutic strategy for adult human amblyopia based an inverse-occlusion and physical exercise procedure.

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bioRxiv2018

Short-term plasticity of 7T BOLD ocular dominance and spatial frequency representation in adult human primary visual cortex

Visual cortex, particularly V1, is considered to be resilient to plastic changes in adults. In particular, ocular dominance is assumed to be hard-wired after the end of the critical period. We show that short-term (2h) monocular deprivation in adult humans boosts the BOLD response to the deprived eye, changing ocular dominance of V1 vertices, consistently with homeostatic plasticity. The boost is strongest in V1, present in V2, V3 & V4 but absent in V3a and MT. Assessment of spatial frequency tuning in V1 by a population Receptive-Field technique shows that deprivation primarily boosts high spatial frequencies, consistent with a primary involvement of the parvocellular pathway. Crucially, the V1 deprivation effect correlates across participants with the perceptual increase of the deprived eye dominance assessed with binocular rivalry, suggesting a common origin. Our results demonstrate that visual cortex, particularly the ventral pathway, retains a high potential for homeostatic plasticity in the human adult.

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