Modulation and neural correlates of postmating sleep plasticity in Drosophila females.

IF 8.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Current Biology Pub Date : 2023-07-10 Epub Date: 2023-06-22 DOI:10.1016/j.cub.2023.05.054
José M Duhart, Joseph R Buchler, Sho Inami, Kyle J Kennedy, B Peter Jenny, Dinis J S Afonso, Kyunghee Koh
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引用次数: 0

Abstract

Sleep is essential, but animals may forgo sleep to engage in other critical behaviors, such as feeding and reproduction. Previous studies have shown that female flies exhibit decreased sleep after mating, but our understanding of the process is limited. Here, we report that postmating nighttime sleep loss is modulated by diet and sleep deprivation, demonstrating a complex interaction among sleep, reproduction, and diet. We also find that female-specific pC1 neurons and sleep-promoting dorsal fan-shaped body (dFB) neurons are required for postmating sleep plasticity. Activating pC1 neurons leads to sleep suppression on standard fly culture media but has little sleep effect on sucrose-only food. Published connectome data suggest indirect, inhibitory connections among pC1 subtypes. Using calcium imaging, we show that activating the pC1e subtype inhibits dFB neurons. We propose that pC1 and dFB neurons integrate the mating status, food context, and sleep drive to modulate postmating sleep plasticity.

雌性果蝇交配后睡眠可塑性的调节和神经相关性。
睡眠是必不可少的,但动物可能会放弃睡眠,从事其他关键行为,如喂养和繁殖。先前的研究表明,雌蝇交配后睡眠减少,但我们对这一过程的了解有限。在这里,我们报道了夜间睡眠不足受饮食和睡眠剥夺的调节,表明睡眠、生殖和饮食之间存在复杂的相互作用。我们还发现,女性特异性pC1神经元和促进睡眠的背侧扇形体(dFB)神经元是后期睡眠可塑性所必需的。激活pC1神经元在标准苍蝇培养基上导致睡眠抑制,但在纯蔗糖食物上几乎没有睡眠影响。已发表的连接组数据表明pC1亚型之间存在间接的抑制性连接。通过钙成像,我们发现激活pC1e亚型可以抑制dFB神经元。我们提出pC1和dFB神经元整合交配状态、食物环境和睡眠驱动,以调节交配后的睡眠可塑性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Biology
Current Biology 生物-生化与分子生物学
CiteScore
11.80
自引率
2.20%
发文量
869
审稿时长
46 days
期刊介绍: Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.
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