Derous Davina, Mitchell Sharon E, Green Cara L, Chen Luonan, Han Jing-Dong J, Wang Yingchun, Promislow Daniel E L, Lusseau David, Speakman John R, Douglas Alex
Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, Scotland, AB24 2TZ, UK.
Centre for Genome Enabled Biology and Medicine, University of Aberdeen, Aberdeen, Scotland, AB24 3RL, UK.
Aging (Albany NY). 2016 Apr;8(4):642-63. doi: 10.18632/aging.100895.
Food intake and circadian rhythms are regulated by hypothalamic neuropeptides and circulating hormones, which could mediate the anti-ageing effect of calorie restriction (CR). We tested whether these two signaling pathways mediate CR by quantifying hypothalamic transcripts of male C57BL/6 mice exposed to graded levels of CR (10 % to 40 %) for 3 months. We found that the graded CR manipulation resulted in upregulation of core circadian rhythm genes, which correlated negatively with circulating levels of leptin, insulin-like growth factor 1 (IGF-1), insulin, and tumor necrosis factor alpha (TNF-α). In addition, key components in the hunger signaling pathway were expressed in a manner reflecting elevated hunger at greater levels of restriction, and which also correlated negatively with circulating levels of insulin, TNF-α, leptin and IGF-1. Lastly, phenotypes, such as food anticipatory activity and body temperature, were associated with expression levels of both hunger genes and core clock genes. Our results suggest modulation of the hunger and circadian signaling pathways in response to altered levels of circulating hormones, that are themselves downstream of morphological changes resulting from CR treatment, may be important elements in the response to CR, driving some of the key phenotypic outcomes.
食物摄入和昼夜节律受下丘脑神经肽和循环激素调节,这些物质可能介导了热量限制(CR)的抗衰老作用。我们通过对暴露于分级CR水平(10%至40%)3个月的雄性C57BL/6小鼠的下丘脑转录本进行定量,来测试这两条信号通路是否介导CR。我们发现分级CR处理导致核心昼夜节律基因上调,这与瘦素、胰岛素样生长因子1(IGF-1)、胰岛素和肿瘤坏死因子α(TNF-α)的循环水平呈负相关。此外,饥饿信号通路中的关键成分以反映在更高限制水平下饥饿感增强的方式表达,并且也与胰岛素、TNF-α、瘦素和IGF-1的循环水平呈负相关。最后,诸如食物预期活动和体温等表型与饥饿基因和核心生物钟基因的表达水平相关。我们的结果表明,响应循环激素水平变化而对饥饿和昼夜信号通路进行的调节,这些激素本身是CR处理导致的形态变化的下游产物,可能是对CR反应的重要因素,驱动了一些关键的表型结果。