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大鼠视交叉上核分子核心生物钟光周期同步化的个体发生

Ontogenesis of photoperiodic entrainment of the molecular core clockwork in the rat suprachiasmatic nucleus.

作者信息

Kováciková Z, Sládek M, Laurinová K, Bendová Z, Illnerová H, Sumová A

机构信息

Department of Neurohumoral Regulations, Institute of Physiology, Academy of Sciences of the Czech Republic, Vídenská 1083, 142 20 Prague 4, Czech Republic.

出版信息

Brain Res. 2005 Dec 7;1064(1-2):83-9. doi: 10.1016/j.brainres.2005.10.022. Epub 2005 Nov 14.

Abstract

The molecular mechanism underlying a generation of circadian rhythmicity within the suprachiasmatic nucleus (SCN) is based on interactive negative and positive feedback loops that drive the rhythmic transcription of clock genes and translation of their protein products. In adults, the molecular mechanism is affected by seasonal changes in day length, i.e., photoperiod. The photoperiod modulates phase, waveform, and amplitude of the rhythmic clock genes expression as well as the phase relationship between their profiles. To ascertain when and how the photoperiod affects the circadian core clock mechanism during ontogenesis, the rhythmic expression of clock genes, namely of Per1, Per2, Cry1 and Bmal1 was determined in 3-, 10- and 20-day-old rat pups maintained under either a long photoperiod with 16 h of light and 8 h of darkness per day (LD 16:8) or under a short, LD 8:16 photoperiod. The daily profiles in the level of clock genes mRNA were studied in constant darkness. The photoperiod affected the profile of Per1 and Per2 mRNA in 20- and 10- but not yet in 3-day-old pups. Expression of Cry1 was affected only in 20-day-old pups, whereas expression of Bmal1 was not yet affected even in 20-day-old rats. The results demonstrate no effect of the photoperiod on 3-day-old pups, only partial entrainment of the molecular core clockwork in 10-day-old pups and a more mature, though not yet fully complete, entrainment in 20-day-old pups as compared with adult animals. The developmental interval when the photoperiod begins to entrain the core clock mechanism completely might thus occur around the time of weaning.

摘要

视交叉上核(SCN)内昼夜节律产生的分子机制基于交互式负反馈和正反馈回路,这些回路驱动时钟基因的节律性转录及其蛋白质产物的翻译。在成年动物中,分子机制受日照长度季节性变化(即光周期)的影响。光周期调节节律性时钟基因表达的相位、波形和幅度,以及它们表达模式之间的相位关系。为了确定光周期在个体发育过程中何时以及如何影响昼夜节律核心时钟机制,在每天光照16小时、黑暗8小时的长光周期(LD 16:8)或短光周期LD 8:16条件下饲养的3日龄、10日龄和20日龄大鼠幼崽中,测定了时钟基因Per1、Per2、Cry1和Bmal1的节律性表达。在持续黑暗中研究了时钟基因mRNA水平的每日变化情况。光周期影响20日龄和10日龄幼崽中Per1和Per2 mRNA的表达模式,但不影响3日龄幼崽。Cry1的表达仅在20日龄幼崽中受到影响,而即使在20日龄大鼠中,Bmal1的表达也未受影响。结果表明,光周期对3日龄幼崽没有影响,10日龄幼崽的分子核心时钟机制只有部分被调节,与成年动物相比,20日龄幼崽的调节更成熟,但尚未完全完成。因此,光周期开始完全调节核心时钟机制的发育阶段可能在断奶时左右出现。

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