The University of Osaka · Psychology
Professor Shota Nishitani's research lab focuses on the neurobiological and epigenetic mechanisms underlying maternal behavior, child maltreatment, and stress responses, particularly in the context of early life adversity. The lab integrates neuroimaging, epigenetic analysis (especially DNA methylation in saliva), and psychosocial assessments to explore how early stressors affect brain development and oxytocin-related systems. A key focus is on understanding the interplay between biological aging, mental health, and parenting stress during global crises such as the COVID-19 pandemic. The lab also investigates the role of oxytocin and its epigenetic regulation in maternal-infant bonding and breastfeeding outcomes.
Figures are computed from collected data and may differ slightly.
Mothers are attracted by infant cues of a variety of different modalities. To clarify the possible neural mechanisms underlying maternal attraction to infant odor cues, we used near-infrared spectroscopy to examine prefrontal cortex (PFC) activity during odor detection tasks in which 19 mothers and 19 nulliparous females (nonmothers) were presented with infant or adult male odors. They were instructed to make a judgment about whether they smelled an odor during each task. We estimated the PFC ac
Saliva is a non-invasive, easily accessible tissue, which is regularly collected in large epidemiological studies to examine genetic questions. Recently, it is becoming more common to use saliva to assess DNA methylation. However, DNA extracted from saliva is a mixture of both bacterial and human DNA derived from epithelial and immune cells in the mouth. Thus, there are unique challenges to using salivary DNA in methylation studies that can influence data quality. This study assesses: (1) quanti
Child maltreatment dysregulates the brain's oxytocinergic system, resulting in dysfunctional attachment patterns. However, how the oxytocinergic system in children who are maltreated (CM) is epigenetically affected remains unknown. We assessed differences in salivary DNA methylation of the gene encoding oxytocin (OXT) between CM (n = 24) and non-CM (n = 31), alongside its impact on brain structures and functions using multi-modal brain imaging (voxel-based morphometry, diffusion tensor imaging,
<b>Background:</b> In a previous study, we demonstrated that the accumulation of parenting stress during prolonged school closures and restrictions on daily activities due to the COVID-19 pandemic in Japan indicates the need for mental health intervention for parents at higher risk of parenting stress. However, few studies have focused on parenting stress in other Asian countries, although they have experienced higher numbers of infections. The aim of the present study was to investigate whether
Accelerated biological aging, such as early onset of pubertal development, is a phenomenon that presents in children exposed to early life adversity, especially child maltreatment (CM).1 Recently, two studies2, 3 used DNA methylation-based age (mAge) and reported that age acceleration was correlated with the number of exposures to maltreatment. Jovanovic et al. rated violence exposure to children (6–13 years) using the Violence Exposure Scale for Children – Revised.3 Sumner et al. assessed expos
Breastfeeding in early postpartum days could be accompanied by the frequent release of oxytocin and lower state anxiety, potentially contributing to exclusive breastfeeding.
Child maltreatment can adversely affect brain development, leading to vulnerabilities in brain structure and function and various psychiatric disorders. Among the various types of child maltreatment, neglect has the highest incidence rate (76.0%); however, data on its sole adverse influence on the brain remain limited. This case-control brain magnetic resonance imaging (MRI) study identified the changes in gray matter structure and function that distinguish neglected children with no other type
Reproductive efforts, such as pregnancy, delivery, and interaction with children, make maternal brains optimized for child-rearing. However, extensive studies in non-human species revealed a tradeoff between reproductive effort and life expectancy. In humans, large demographic studies have shown that this is the case for the most part; however, molecular marker studies regarding aging remain controversial. There are no studies simultaneously evaluating the relationship between reproductive effor
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