Department of Biology, University of Iowa, Iowa City, Iowa 52242.
Iowa Neuroscience Institute, University of Iowa, Iowa City, Iowa 52242.
eNeuro. 2022 Jan 19;9(1). doi: 10.1523/ENEURO.0443-21.2021. Print 2022 Jan-Feb.
In , molecular pathways affecting longevity have been extensively studied. However, corresponding neurophysiological changes underlying aging-related functional and behavioral deteriorations remain to be fully explored. We examined different motor circuits in across the life span and uncovered distinctive age-resilient and age-vulnerable trajectories in their established functional properties. In the giant fiber (GF) and downstream circuit elements responsible for the jump-and-flight escape reflex, we observed relatively mild deterioration toward the end of the life span. In contrast, more substantial age-dependent modifications were seen in the plasticity of GF afferent processing, specifically in use dependence and habituation properties. In addition, there were profound changes in different afferent circuits that drive flight motoneuron activities, including flight pattern generation and seizure spike discharges evoked by electroconvulsive stimulation. Importantly, in high-temperature (HT)-reared flies (29°C), the general trends in these age-dependent trajectories were largely maintained, albeit over a compressed time scale, lending support for the common practice of HT rearing for expediting aging studies. We discovered that shortened life spans in () mutant flies were accompanied by altered aging trajectories in motor circuit properties distinct from those in HT-reared flies, highlighting differential effects of oxidative versus temperature stressors. This work helps to identify several age-vulnerable neurophysiological parameters that may serve as quantitative indicators for assessing genetic and environmental influences on aging progression in .
在 中,影响寿命的分子途径已经得到了广泛的研究。然而,与衰老相关的功能和行为恶化相关的相应神经生理变化仍有待充分探索。我们在 中研究了不同的运动回路,并揭示了它们既定功能特性中具有年龄弹性和年龄脆弱性的独特轨迹。在负责跳跃和飞行逃避反射的巨大纤维 (GF) 和下游电路元件中,我们观察到它们在生命末期的恶化相对较轻。相比之下,GF 传入处理的可塑性中出现了更显著的年龄依赖性改变,特别是在使用依赖性和习惯化特性方面。此外,不同传入电路驱动飞行运动神经元活动的能力发生了深刻变化,包括飞行模式生成和电惊厥刺激引起的癫痫尖峰放电。重要的是,在高温 (HT) 饲养的苍蝇 (29°C) 中,这些年龄依赖性轨迹的总体趋势在很大程度上得到了维持,尽管时间尺度压缩,这为 HT 饲养加速 衰老研究的常见做法提供了支持。我们发现, () 突变苍蝇的寿命缩短伴随着运动回路特性的改变,这些改变与 HT 饲养的苍蝇不同,突出了氧化应激与温度应激因素的不同影响。这项工作有助于确定几个年龄脆弱的神经生理参数,这些参数可以作为评估遗传和环境因素对衰老进程影响的定量指标。