Wednesday, April 24th, 2024

Time	Event
5:32p	Characterising time-on-task effects on oscillatory and aperiodic EEG components and their co-variation with visual task performance. Fluctuations in oscillatory brain activity have been shown to co-occur with variations in task performance. More recently, part of these fluctuations has been attributed to long-term (>1hr) monotonous trends in the power and frequency of alpha oscillations (8-13 Hz). Here we tested whether these time-on-task changes in EEG activity are limited to activity in the alpha band and whether they are linked to task performance. Thirty-six participants performed 900 trials of a two-alternative forced choice visual discrimination task with confidence ratings. Pre- and post-stimulus spectral power (1-40Hz) and aperiodic (i.e., non-oscillatory) components were compared across blocks of the experimental session and tested for relationships with behavioural performance. We found that time-on-task effects on oscillatory EEG activity were primarily localised within the alpha band, with alpha power increasing and peak alpha frequency decreasing over time, even when controlling for aperiodic contributions. Aperiodic, broadband activity on the other hand did not show time-on-task effects in our data set. Importantly, time-on-task effects in alpha frequency and power explained variability in single-trial reaction times. Moreover, controlling for time-on-task effectively removed the relationships between alpha activity and reaction times. However, time-on-task effects did not affect other EEG signatures of behavioural performance, including post-stimulus predictors of single-trial decision confidence. Therefore, our results dissociate alpha-band brain-behaviour relationships that can be explained away by time-on-task from those that remain after accounting for it - thereby further specifying the potential functional roles of alpha in human visual perception. (Comment on this)
10:03p	Anatomical circuits for flexible spatial mapping by single neurons in posterior parietal cortex Primate lateral intraparietal area (LIP) is critical for cognitive processing. Its contribution to categorization and decision-making has been causally linked to neurons' spatial sensorimotor selectivity. We reveal the intrinsic anatomical circuits and neuronal responses within LIP that provide the substrate for this flexible generation of motor responses to sensory targets. Retrograde tracers delineate a loop between two distinct operational compartments, with a sensory-like, point-to-point projection from ventral to dorsal LIP and an asymmetric, more widespread projection in reverse. Neurophysiological recordings demonstrate that especially more ventral LIP neurons exhibit motor response fields that are spatially distinct from its sensory receptive field. The different associations of response and receptive fields in single neurons tile visual space. These anatomical circuits and neuronal responses provide the basis for the flexible allocation of attention and motor responses to salient or instructive visual input across the visual field. (Comment on this)
10:03p	Epg5 links proteotoxic stress due to defective autophagic clearance and epileptogenesis in Drosophila and Vici Syndrome patients Epilepsy is a common neurological condition that arises from dysfunctional neuronal circuit control due to either acquired or innate disorders. Autophagy is an essential neuronal housekeeping mechanism, which causes severe proteotoxic stress when impaired. Autophagy impairment has been associated to epileptogenesis through a variety of molecular mechanisms. Vici Syndrome (VS) is the paradigmatic congenital autophagy disorder in humans due to recessive variants in the ectopic P-granules autophagy tethering factor 5 (EPG5) gene that is crucial for autophagosome-lysosome fusion and ultimately for effective autophagic clearance. VS is characterized by a wide range of neurodevelopmental, neurodegenerative, and neurological features, including epilepsy. Here, we used Drosophila melanogaster to study the importance of epg5 in development, ageing, and seizures. Our data indicate that proteotoxic stress due to impaired autophagic clearance and seizure-like behaviors correlate and are commonly regulated, suggesting that seizures occur as a direct consequence of proteotoxic stress and age-dependent neurodegenerative progression in epg5 Drosophila mutants, in the absence of evident neurodevelopmental abnormalities. We provide complementary evidence from EPG5-mutated patients demonstrating an epilepsy phenotype consistent with Drosophila predictions and propose autophagy stimulating diets as a feasible approach to control EPG5-related pharmacoresistant seizures. (Comment on this)

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