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Purpose: This study aimed to determine the effects of yoga on the recovery of the cardiac autonomic nervous system and immunosuppression after intense exercise., Methods: Seven healthy adult men were enrolled in two trials: rest for 30 min in a seated position (CON) and yoga for 30 min (YOG) after a treadmill running for 60 min at 75% V˙ O2max in a randomized crossover design. Natural killer (NK) cell activity, salivary secretory immunoglobulin A (SIgA), cortisol, testosterone, and indicators related to heart rate variability, mood states, and muscle soreness were measured before exercise (Pre), immediately (P0) and 60 min (P1) after rest or yoga, and the following morning (P2)., Results: NK cell activity was significantly decreased in the CON trial (P < 0.05) but not in the YOG trial. The decrease in NK cell activity from Pre at P0, P1, and P2 in the CON trial was significantly larger than that in the YOG trial (P < 0.05). Testosterone secretion rate tended to be higher after yoga than at rest (P = 0.052). The square root of the mean squared difference of successive normal-to-normal intervals (RMSSD) at P0 in the YOG trial was significantly higher than that in the CON trial (P < 0.05). Changes in NK cell activity correlated with changes in RMSSD (r = 0.445, P < 0.05)., Conclusion: This study showed that yoga can alleviate the decline of NK cell activity after intense exercise by enhancing parasympathetic nerve activity, thus suggesting that yoga may be an effective recovery method for athlete conditioning.

Autism spectrum disorder (ASD) is characterized by social deficits and restricted behaviors, with developmental defects in GABAergic circuits proposed as a key underlying etiology. Here, we introduce the V-Y assay, a novel space preference test in which one arm of the Y-maze is initially hidden and later revealed as a novel space. Using an ASD mouse model with FOXG1 haploinsufficiency, which exhibits ASD-like social impairments that can be either exacerbated or ameliorated by GABAergic circuit manipulations, we observed impaired novel space preference and exploratory behavior in the V-Y assay. Interestingly, unlike social phenotypes, novel space preference was initially established by 3 weeks of age but regressed by 6 weeks. Furthermore, alterations in GABAergic signaling via Gad2 mutation did not affect novel space preference, in contrast to their impact on social behaviors. These findings reveal that the regression of novel space preference in ASD follows a distinct developmental trajectory from GABA-driven social impairments, providing new insights into the mechanisms underlying ASD., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision., (Copyright © 2025 Asano, Arai, Narita, Kuroiwa, Fukuchi, Yoshimoto, Oya and Miyoshi.)