Department of Neuroscience, the Farber Institute for Neurosciences, and Synaptic Biology Center, Thomas Jefferson University, Philadelphia, PA 19107, USA; Laboratorio de Genética del Comportamiento, Fundación Instituto Leloir-IIBBA-CONICET, Buenos Aires C1405BWE, Argentina; Universidad Nacional de Quilmes, Quilmes B1876BXD, Argentina.
Department of Neuroscience, the Farber Institute for Neurosciences, and Synaptic Biology Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Curr Biol. 2023 Jul 10;33(13):2702-2716.e3. doi: 10.1016/j.cub.2023.05.054. Epub 2023 Jun 22.
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.
睡眠是必不可少的,但动物可能会放弃睡眠来从事其他关键行为,如进食和繁殖。先前的研究表明,雌性苍蝇在交配后睡眠减少,但我们对这一过程的理解有限。在这里,我们报告说,交配后夜间睡眠损失受饮食和睡眠剥夺的调节,表明睡眠、繁殖和饮食之间存在复杂的相互作用。我们还发现,雌性特异性 pC1 神经元和促进睡眠的背扇形体(dFB)神经元对于交配后睡眠可塑性是必需的。激活 pC1 神经元会导致在标准果蝇培养基上的睡眠抑制,但对仅蔗糖的食物几乎没有睡眠效果。已发表的连接组数据表明 pC1 亚型之间存在间接抑制性连接。使用钙成像,我们表明激活 pC1e 亚型会抑制 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力来调节交配后睡眠可塑性。