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Association between circadian clock gene expressions and meal timing in young and older adults

昼夜节律 生物钟 联想(心理学) 时钟 生物 心理学 医学 生理学 内分泌学 老年学 内科学 心理治疗师
作者
Masaki Takahashi,Mayuko Fukazawa,Yu Tahara,Hyeon‐Ki Kim,Kumpei Tanisawa,Tomoko Ito,Takashi Nakaoka,Mitsuru Higuchi,Shigenobu Shibata
出处
期刊:Chronobiology International [Taylor & Francis]
卷期号:40 (9): 1235-1243 被引量:1
标识
DOI:10.1080/07420528.2023.2256855
摘要

Ageing is associated with a decline in circadian clock systems, which correlates with the development of ageing-associated diseases. Chrononutrition is a field of chronobiology that examines the relationship between the timing of meal/nutrition and circadian clock systems. Although there is growing evidence regarding the role of chrononutrition in the prevention of lifestyle and ageing-related diseases, the optimal timing of meal intake to regulate the circadian clock in humans remains unknown. In this study, we investigated the relationship between clock gene expression and meal timing in young and older adults. In this cross-sectional study, we enrolled 51 healthy young men and 35 healthy older men (age, mean±standard deviation: 24 ± 4 and 70 ± 4 y, respectively). Under daily living conditions, beard follicle cells were collected at 4-h intervals over a 24-h period to evaluate clock gene expression. Participants were asked to record the timing of habitual sleep and wake-up, breakfast, lunch, and dinner. From these data, we calculated “From bedtime to breakfast time,” “From wake up to first meal time,” and “From dinner to bed time.” NR1D1 and PER3 expressions in older adults at 06:00 h were significantly higher than those in young adults (P = 0.001). There were significant differences in the peak time for NR1D2 (P = 0.003) and PER3 (P = 0.049) expression between young and older adults. “From bedtime to breakfast time” was significantly longer in older adults than in young adults. In contrast, “From dinner to bed time” was significantly shorter in older adults than in young adults. Moreover, higher rhythmicity of NR1D1 correlated with longer “From bedtime to breakfast time” (r = −0.470, P = 0.002) and shorter “From wake up to first meal time” in young adults (r = 0.302, P = 0.032). Higher rhythmicity of PER3 correlated with longer “From bedtime to breakfast time” in older adults (r = −0.342, P = 0.045). These results suggest that the peak time of clock gene expression in older adults may be phase-advanced compared to that in young adults. In addition, a longer fasting duration from bedtime to breakfast in both young and older adults and earlier intake of meals after waking up in young adults may correlate with robust clock gene expression rhythms.
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