Biology subjects

Sari, Z.

Publications and source records attributed to Sari, Z..

2 recordsLinked to original sources

bioRxiv2026

Retinal cell mosaics in the valproate-induced rat model of autism spectrum disorder

Valproic acid (VPA) is a widely used antiepileptic drug that also increases the risk of neurodevelopmental disorders in the offspring of exposed mothers. Prenatal exposure to VPA is a widely used rodent model of autism spectrum disorder (ASD). Anatomical, functional and molecular alterations in the retinas of various ASD model animals have been described in the literature, but the impact on the neural composition of the retina remains unclear. We examined whether and how the density and spatial regularity of selected retinal neurons are altered in the VPA induced model of ASD. Whole-mount retinas of 2-month-old VPA-treated and control animals were immunolabeled for S-cones, horizontal cells, AII amacrine cells, and parvalbumin-positive wide-field amacrines (PV-wfACs), and the positions of labelled cells mapped in various regions of interest (n = 39 for treated, n = 32 for control animals) across the retinas. Multivariate analysis of variance revealed a significant overall effect of VPA on cell densities (p = 6.1x10-7, 2 = 0.43), driven mainly by reduced AII amacrine density, while horizontal cells showed a modest reduction and S-cones were unaffected. After adjusting for retinal location, analysis of covariance indicated a 7% decrease in AII cells and a 15% increase in PV-wfACs. Regularity indices calculated from nearest neighbor distances or Voronoi-domain areas of cell mosaics were largely unchanged. These findings suggest that prenatal VPA exposure selectively alters inhibitory inner retinal circuitry in the rat ASD model at the time of cell differentiation, but self-organizing mechanisms responsible for spatial order are not affected. Lay SummaryValproic acid (VPA) is a medicine for epilepsy, but it can also raise the risk of autism in children when taken during pregnancy. In rats exposed to VPA before birth, we found changes in certain nerve cells of the retina: one type of cell important for night vision was reduced, while another type increased slightly, while most other cells stayed the same. This suggests that the changes in development that lead to autism may also be reflected in the structure and function of the eye.

neuroscience↗

bioRxiv2026

Conflicting binocular input triggers inhibition followed by rebound, explaining paradoxically fast reaction times

Binocular vision depends on the integration of matching visual features across the two eyes, while conflicting interocular signals can engage active inhibitory processes in the visual system. To investigate the temporal dynamics of these putative inhibitory processes, we examined how transitions between different binocular correlation states influence perceptual detectability and response speed. Using dynamic random-dot correlograms - free of monocular cues and allowing precise interocular manipulation - we presented brief target intervals embedded in longer background sequences. Stimuli varied in binocular correlation: correlated (C) patterns contained identical luminance profiles in both eyes, anticorrelated (A) patterns had inverted luminance dots, and uncorrelated (U) patterns had independent dot arrangements. Across three experiments, we measured (1) the presentation duration threshold required to detect a change in correlation, (2) simple reaction times (RTs) to the same transitions at suprathreshold levels, and (3) psychometric functions across durations for selected transitions. In Experiment 1, A[->]C transitions yielded significantly higher duration thresholds than C[->]A, indicating a suppressive influence associated with prior anticorrelation. In contrast, Experiment 2 showed that A[->]C transitions produced the shortest RTs, while C[->]U transitions were slowest, suggesting a rebound-like facilitation following prior suppression. Experiment 3 confirmed these temporal and contrast dependences, with opposite changes in contrast threshold and reaction times between transitions toward and away from the correlated fusional states. This divergence between perceptual onset and reaction time is consistent with a two-phase account in which binocular anticorrelation is associated with an initial suppressive phase followed by rebound-like facilitation that accelerates responses once the target becomes detectable. These findings are consistent with current models of binocular rivalry and fusion, and provide a temporally resolved behavioral perspective on how inhibitory control in sensory systems may dynamically influence subsequent responsiveness under conditions of perceptual ambiguity.

neuroscience↗