[Mechanisms of structural plasticity associated with photic synchronization of the circadian clock within the suprachiasmatic nucleus].

Journal de la Societe de biologie Pub Date : 2009-01-01 Epub Date: 2009-04-10 DOI:10.1051/jbio:2009004
Olivier Bosler, Clémence Girardet, Dominique Sage-Ciocca, Hélène Jacomy, Anne-Marie François-Bellan, Denis Becquet
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引用次数: 8

Abstract

The mammalian circadian clock, whose central component is located in the suprachiasmatic nucleus of the hypothalamus (SCN), orchestrates rhythmic events in metabolism, physiology and behavior. Adaptation of the organism to its environment requires precise adjustment of the clock to the 24 h astronomical time, primarily by the light/dark cycle. Photic synchronization acts on both the molecular loops which trigger circadian oscillations and the phasing of the multiple SCN cellular oscillators whose coordination permits elaboration of the rhythmic message that will be distributed throughout the organism. It is concomitant with structural plastic events characterized by day/night rearrangements of the SCN neuronal-glial network. The two main sources of SCN efferents, namely the VIP (vasoactive intestinal peptide)-synthesizing neurons which are major integrators of photic signals and the AVP (arginine-vasopressin)-synthesizing neurons which are known to importantly contribute to conveying rhythmic messages to brain targets, are involved in these mechanisms. Over the light/dark cycle, they indeed undergo ultrastructural changes in the extent of their membrane coverage by glial, axon terminal and/or somato-dendritic elements. These structural rearrangements appear to be dependent on light entrainment, as the rhythmic expression in SCN of glial fibrillary acidic protein (GFAP), a marker for brain astrocytes whose changing expression has proved to be a reliable index of neuronal-glial plasticity, is disrupted under constant darkness. Glucocorticoid hormones, which are known as important endocrine outputs of the clock, are required to maintain amplitude of the SCN GFAP rhythm to normal values, indicating that they modulate astrocytic plasticity within the SCN and, therefore, nycthemeral changes of the configuration of its neuronal-glial network. The view that such plastic events may subserve synchronization of the clock to the light-dark cycle is reinforced by other data showing that the daily fluctuations of circulating glucocorticoids actually are involved in modulation of light effects, contributing to the resistance of the circadian timing system to variations of the photoperiod. It is thus proposed that the capacity of the clock to integrate cyclic variations of the environment rely on the inherent capacity of the SCN to undergo neuronal-glial plasticity.

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[与视交叉上核生物钟光同步相关的结构可塑性机制]。
哺乳动物的生物钟,其中心成分位于下丘脑视交叉上核(SCN),协调代谢,生理和行为的节律事件。生物体对环境的适应需要将时钟精确地调整到24小时的天文时间,主要是通过光/暗周期。光同步作用于触发昼夜节律振荡的分子环和多个SCN细胞振荡子的相位,这些振荡子的协调允许在整个生物体中分布的节律信息的细化。它伴随着以SCN神经元-胶质网络的昼夜重排为特征的结构可塑性事件。SCN传出信号的两个主要来源,即合成VIP(血管活性肠肽)的神经元,它们是光信号的主要整合者,以及合成AVP(精氨酸-血管加压素)的神经元,它们在向大脑目标传递节律信息方面发挥着重要作用,参与了这些机制。在光/暗周期中,它们确实经历了由胶质细胞、轴突末端和/或体树突元件覆盖的膜的超微结构变化。这些结构重排似乎依赖于光干扰,因为SCN中胶质原纤维酸性蛋白(GFAP)的节律性表达在持续的黑暗下被破坏。GFAP是脑星形胶质细胞的标志,其表达变化已被证明是神经元-胶质可塑性的可靠指标。糖皮质激素被认为是生物钟重要的内分泌输出,它需要将SCN GFAP节律的振幅维持在正常值,这表明它们调节SCN内的星形细胞可塑性,从而调节其神经元-神经胶质网络结构的昼夜变化。这种可塑性事件可能支持生物钟与光暗周期同步的观点得到了其他数据的支持,这些数据表明,循环糖皮质激素的每日波动实际上参与了光效应的调节,有助于昼夜节律计时系统抵抗光周期的变化。因此,有人提出,生物钟整合环境周期性变化的能力依赖于SCN进行神经元-胶质可塑性的固有能力。
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