Biology subjects

Kurotani, T.

Publications and source records attributed to Kurotani, T..

3 recordsLinked to original sources

bioRxiv2025

Prenatal valproic acid-exposed autism marmosets increase mutual gaze and reduce inter-individual distance during dyadic social interactions

Autism spectrum disorder (ASD) is associated with differences in social interaction, including alterations in gaze behavior and interpersonal distance. Although most assessments of ASD remain individual-centric, emerging human studies indicate that social difficulties may arise from atypical dyadic coordination rather than from reduced social interest alone. We examined dyadic coordination in a non-human primate model of ASD, focusing on gaze and inter-individual distance during minimally constrained first encounters between prenatal valproic acid-exposed marmosets (VPA) and unexposed conspecifics (UE). Markerless pose estimation quantified frame-by-frame gaze direction and spacing, comparing VPA-UE with UE-UE dyads. VPA-UE pairs exhibited a higher proportion of mutual-gaze events than UE-UE pairs. VPA individuals showed more rapid looks in response to the partners gaze, yet spent less time looking at the partner when unobserved. VPA-UE dyads maintained shorter inter-individual distances than UE-UE dyads, and closer spacing was associated with decreased stability of mutual gaze. These findings reveal a dyadic coordination pattern in VPA-UE pairs, with rapid responsiveness coupled with distance-dependent fragility, paralleling features reported in human ASD. Our dyad-centric, markerless framework yields ecologically grounded readouts and potential intervention targets that leverage intact social responsiveness while accommodating altered spatial coordination.

neuroscience↗

bioRxiv2024

Interval timing clock property in the rat granular retrosplenial cortex

The rodent granular retrosplenial cortex (gRSC), densely interconnected with the hippocampal formation and the anterior thalamic nuclei, plays an important role in learning and memory. We had revealed that small pyramidal neurons in the superficial layers of the rat gRSC exhibit late-spiking (LS) firing properties. It has been suggested that neural circuits containing LS neurons can encode time intervals on the order of seconds, known as "interval timing". To test the possibility that the rat gRSC is involved in the processing of interval timing, we employed a trace fear conditioning paradigm in which the conditioned stimulus (CS) and the unconditioned stimulus (US) were temporally separated. First, we examined the effect of cytotoxic lesions made in the RSC prior to trace fear conditioning. We found that intact rats exhibited freezing behavior after CS tone presentation, whereas lesioned rats did not exhibit such freezing behavior. Next, we conducted in vivo chronic or acute recordings of neural activity from the rat gRSC in a test session conducted one week after the conditioning. In both recordings, we observed a distinct spike activity in which there was a transient increase in the firing rate around the presentation of the CS tone, followed by a rapid suppression and then ramping activity (a gradual elevation of the firing rate) until the next CS presentation. This "ramping activity" is thought to be one way in which interval timing is represented in the brain. Post stimulus histogram analysis revealed the existence of ramping activity in the gRSC, which reached its peak at various time intervals after the onset of the CS tone. Interestingly, this activity was specifically observed in response to the CS tone but not to the non-CS tone. Moreover, in naive rat gRSC (no trace fear conditioning), no such ramping activity was observed. These results indicate that gRSC neurons can encode time information on the order of tens to hundreds of seconds, integrating incoming sensory input with past memory traces.

neuroscience↗

bioRxiv2020

Distinct synaptic and related transcriptional abnormalities in neonatal, childhood and mature autism model of primate: implications for early-age therapeutic intervention

Autism spectrum disorder (ASD) is a synapse-related disorder that is diagnosed at around 3 years of age. Earlier intervention is desirable for better ASD prognosis; however, there is limited biological literature regarding early-age ASD. This study aimed to assess altered cortical synapses and gene expression in the ASD model marmoset. There were distinct phenotypes in the model animals across the neonate, childhood, and mature stages in the dorsomedial prefrontal cortex (Brodmann area 8b/9). At the neonate stage, synapses were underdeveloped and modulated genes were enriched with synaptogenesis- and ASD-related genes. At the childhood stage, synaptic features and gene expressions associated with experience-dependent circuit remodeling were altered in model animals. At the mature stage, there were synapse overdevelopment and altered gene expression similar to those in human ASD. These early synaptic phenotypes and altered gene expressions could be novel targets of efficient therapy from a young age.

neuroscience↗