Feillet Céline A, Albrecht Urs, Challet Etienne
Department of Neurobiology of Rhythms, Institute of Cellular and Integrative Neurosciences, University Louis Pasteur and CNRS, 67084 Strasbourg, France.
J Physiol Paris. 2006 Nov-Dec;100(5-6):252-60. doi: 10.1016/j.jphysparis.2007.05.002. Epub 2007 Jun 7.
Circadian clocks are autonomous time-keeping mechanisms that allow living organisms to predict and adapt to environmental rhythms of light, temperature and food availability. At the molecular level, circadian clocks use clock and clock-controlled genes to generate rhythmicity and distribute temporal signals. In mammals, synchronization of the master circadian clock located in the suprachiasmatic nuclei of the hypothalamus is accomplished mainly by light stimuli. Meal time, that can be experimentally modulated by temporal restricted feeding, is a potent synchronizer for peripheral oscillators with no clear synchronizing influence on the suprachiasmatic clock. Furthermore, food-restricted animals are able to predict meal time, as revealed by anticipatory bouts of locomotor activity, body temperature and plasma corticosterone. These food anticipatory rhythms have long been thought to be under the control of a food-entrainable clock (FEC). Analysis of clock mutant mice has highlighted the relevance of some, but not all of the clock genes for food-entrainable clockwork. Mutations of Clock or Per1 do not impair expression of food anticipatory components, suggesting that these clock genes are not essential for food-entrainable oscillations. By contrast, mice mutant for Npas2 or deficient for Cry1 and Cry2 show more or less altered responses to restricted feeding conditions. Moreover, a lack of food anticipation is specifically associated with a mutation of Per2, demonstrating the critical involvement of this gene in the anticipation of meal time. The actual location of the FEC is not yet clearly defined. Nevertheless, current knowledge of the putative brain regions involved in food-entrainable oscillations is discussed. We also describe several neurochemical pathways, including orexinergic and noradrenergic, likely to participate in conveying inputs to and outputs from the FEC to control anticipatory processes.
昼夜节律时钟是自主的计时机制,使生物体能够预测并适应光照、温度和食物可利用性等环境节律。在分子水平上,昼夜节律时钟利用时钟基因和受时钟控制的基因来产生节律性并分配时间信号。在哺乳动物中,位于下丘脑视交叉上核的主昼夜节律时钟的同步主要通过光刺激来完成。进食时间(可通过限时进食进行实验调节)是外周振荡器的有效同步器,对视交叉上核时钟没有明显的同步影响。此外,食物受限的动物能够预测进食时间,这通过运动活动、体温和血浆皮质酮的预期发作得以体现。长期以来,这些食物预期节律一直被认为受食物可调节时钟(FEC)的控制。对时钟突变小鼠的分析突出了某些但并非所有时钟基因与食物可调节时钟机制的相关性。Clock或Per1的突变不会损害食物预期成分的表达,这表明这些时钟基因对于食物可调节振荡并非必不可少。相比之下,Npas2突变或Cry1和Cry2缺陷的小鼠对受限进食条件的反应或多或少有所改变。此外,缺乏食物预期与Per2的突变特别相关,这表明该基因在进食时间的预期中起关键作用。FEC的实际位置尚未明确界定。然而,本文讨论了目前关于参与食物可调节振荡的假定脑区的知识。我们还描述了几种神经化学途径,包括食欲素能和去甲肾上腺素能途径,它们可能参与将输入传递至FEC并从FEC输出,以控制预期过程。