Sleep timing in flies from "adolescence" to adulthood.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Fly Pub Date : 2025-12-01 Epub Date: 2024-12-30 DOI:10.1080/19336934.2024.2448022
Esther D Domenie, Paola Cusumano, Sara Montagnese, Rodolfo Costa
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Abstract

The aim of the present study was to assess sleep timing in Drosophila melanogaster at different ages, within the setting of an enforced schedule of varying light-dark stimuli, simulating light exposure variations between four typical office working days and one free day spent outside by a human, for a total of 30 days. Locomotor activity recording started when male flies were 3 days old. Flies exhibited a bimodal activity pattern, with a morning and an evening peak, and clear anticipation of the lights on and lights off transitions. From experimental day 10 (i.e. 12-day-old flies) onwards, a decrease in activity counts/increase in sleep amount were observed. On free days, a rise in activity counts and a reduction in sleep amount during the lights on interval was observed and was also present, albeit less obvious, on the subsequent working day during the lights off interval. A progressive delay in sleep onset was observed in the first days of the experiment, peaking on day 4 (i.e. 6-day-old flies), after which sleep onset timing gradually advanced. A delay in sleep offset was also observed for the first 13 days of the experiment, after which sleep offset stabilized. In conclusion, 'adolescent' flies exhibited changes in sleep timing that were reminiscent of those of human adolescents.

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从“青春期”到成年期果蝇的睡眠时间。
本研究的目的是评估不同年龄的黑腹果蝇的睡眠时间,在不同的明暗刺激的强制时间表设置下,模拟四个典型的办公室工作日和一个人类在户外自由度过的一天之间的光暴露变化,总共30天。运动活动记录开始于雄蝇3天大时。苍蝇表现出双峰活动模式,有早晚高峰,对开灯和关灯的过渡有清晰的预期。从实验第10天(即12天大的果蝇)开始,观察到活动次数减少/睡眠量增加。在空闲的日子里,在开灯间隔期间观察到活动次数的增加和睡眠时间的减少,尽管不太明显,但在随后的工作日,在关灯间隔期间也出现了这种情况。在实验的头几天观察到睡眠开始逐渐延迟,在第4天(即6天大的苍蝇)达到峰值,之后睡眠开始时间逐渐提前。在实验的前13天也观察到睡眠偏移的延迟,之后睡眠偏移趋于稳定。总之,“青春期”果蝇表现出的睡眠时间变化让人想起人类青少年。
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来源期刊
Fly
Fly 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
>12 weeks
期刊介绍: Fly is the first international peer-reviewed journal to focus on Drosophila research. Fly covers a broad range of biological sub-disciplines, ranging from developmental biology and organogenesis to sensory neurobiology, circadian rhythm and learning and memory, to sex determination, evolutionary biology and speciation. We strive to become the “to go” resource for every researcher working with Drosophila by providing a forum where the specific interests of the Drosophila community can be discussed. With the advance of molecular technologies that enable researchers to manipulate genes and their functions in many other organisms, Fly is now also publishing papers that use other insect model systems used to investigate important biological questions. Fly offers a variety of papers, including Original Research Articles, Methods and Technical Advances, Brief Communications, Reviews and Meeting Reports. In addition, Fly also features two unconventional types of contributions, Counterpoints and Extra View articles. Counterpoints are opinion pieces that critically discuss controversial papers questioning current paradigms, whether justified or not. Extra View articles, which generally are solicited by Fly editors, provide authors of important forthcoming papers published elsewhere an opportunity to expand on their original findings and discuss the broader impact of their discovery. Extra View authors are strongly encouraged to complement their published observations with additional data not included in the original paper or acquired subsequently.
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