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Ohira, H.

Publications and source records attributed to Ohira, H..

3 recordsLinked to original sources

Pre-movement respiration-action coupling is specific to self-initiated action: Evidence for action alignment with ongoing breathing

Voluntary actions are coupled with the respiratory cycle, yet whether this coupling reflects action timing aligning with breathing or breathing adjusting to anticipated action remains unclear. This pre-registered study compared respiration-action coupling across three conditions using a modified Libet clock task. Thirty participants performed key presses under Self-initiated (freely chosen timing), Delayed (predictable timing after one full clock rotation), and Immediate (speeded response to stimulus onset) conditions. Circular uniformity tests revealed significant respiratory phase concentration at key press exclusively in the Self-initiated condition, and time-resolved phase consistency analysis showed that coupling emerged before movement onset only in this condition. These findings suggest that action timing aligns with ongoing breathing rhythms, and that temporal freedom, rather than preparation time or predictability, is critical for this coupling to emerge. Additionally, actions performed during inhalation were followed by shorter and deeper subsequent breaths across all conditions, indicating greater perturbation of ongoing breathing when acting during inhalation. Participants reported a subjective preference for pressing during exhalation, which correlated with individual differences in exhalation bias during self-initiated actions. Body awareness, but not interoceptive awareness or trait anxiety, predicted coupling strength. These results suggest that pre-movement respiration-action coupling reflects an implicit process whereby self-chosen action timing exploits ongoing respiratory states, potentially minimizing action-related respiratory perturbation.

neuroscience↗

Behavioural and physiological evidence for the development of cardiac-exteroceptive integration during the first year of life

Continuous integration of environmental exteroceptive and internal interoceptive signals is fundamental for perception and adaptive behaviours, yet its developmental trajectory remains poorly understood. Here, we introduced a modified iBEATs paradigm, based on prior work, to investigate cardiac-exteroceptive integration in 3-8-month-old infants. Using behavioural measures of looking time and physiological measures of pupillometry, we found that the ability to detect cardiac-exteroceptive synchrony emerges during the first year of life. Critically, this was evident only when stimuli coincided with systole, the baroreceptor-active phase of the cardiac cycle, supporting central multimodal integration interpretable within a predictive coding framework. Furthermore, individual differences in behavioural sensitivity were accounted for by the degree of autonomic maturation. These findings provide the first evidence for the developmental emergence and mechanisms of cardiac-exteroceptive integration, and establish the modified iBEATs paradigm as a promising tool for assessing interoceptive development in early life.

neuroscience↗

A transgenic mutant mouse line accompanied by the complete deletion of interleukin-33 showed insulin and leptin resistances

Interleukin (IL) -33 has been identified as a member of the IL-1 family. Members of the IL-1 family have been reported to be involved in the regulation of energy homeostasis and glucose metabolism. Homozygous transgenic mutant mice of FLP14 line, that we previously generated, unexpectedly developed mature-onset obesity and diabetes. Through genetic investigations, we found that insertion of the transgenes had resulted in complete deletion of the Il33 gene. These obese male homozygous mutant mice exhibited hyperphagia with hyperleptinemia and insulin resistance caused by increased hepatic gluconeogenesis and decreased glucose uptake in skeletal muscle. As a result of examining preobese male homozygous mutant mice to investigate with the exclusion of the effect of obesity, hyperphagia with hyperleptinemina and insulin resistance caused by decreased glucose uptake in skeletal muscle were already observed, but the increased hepatic glucose production was not. To investigate whether the insulin resistance was caused by deletion of the Il33 gene, we treated these preobese homozygous mutant mice with recombinant IL-33 protein and noted a significant improvement in insulin resistance. Thus, insulin resistance in these homozygous mutant mice was caused, at least in part, by IL-33 deficiency, suggesting a favorable role of IL-33 for glucose metabolism in the skeletal muscle.

molecular biology↗