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表达显性负性 BMAL1 的转基因大鼠表现出昼夜节律钟振幅降低和从时差中快速恢复。

Transgenic rats expressing dominant negative BMAL1 showed circadian clock amplitude reduction and rapid recovery from jet lag.

机构信息

Department of Anatomy and Neurobiology, Faculty of Medicine, Kindai University, Osakasayama, Osaka, Japan.

Central Research Facilities, Faculty of Medicine Center for Animal Experiment, Kindai University Faculty of Medicine, Kindai University, Osakasayama, Osaka, Japan.

出版信息

Eur J Neurosci. 2021 Mar;53(6):1783-1793. doi: 10.1111/ejn.15085. Epub 2021 Feb 25.

DOI:10.1111/ejn.15085
PMID:33351992
Abstract

The circadian rhythms are endogenous rhythms of about 24 h, and are driven by the circadian clock. The clock centre locates in the suprachiasmatic nucleus. Light signals from the retina shift the circadian rhythm in the suprachiasmatic nucleus, but there is a robust part of the suprachiasmatic nucleus that causes jet lag after an abrupt shift of the environmental lighting condition. To examine the effect of attenuated circadian rhythm on the duration of jet lag, we established a transgenic rat expressing BMAL1 dominant negative form under control by mouse Prnp-based transcriptional regulation cassette [BMAL1 DN (+)]. The transgenic rats became active earlier than controls, just after light offset. Compared to control rats, BMAL1 DN (+) rats showed smaller circadian rhythm amplitudes in both behavioural and Per2 promoter driven luciferase activity rhythms. A light pulse during the night resulted in a larger phase shift of behavioural rhythm. Furthermore, at an abrupt shift of the light-dark cycle, BMAL1 DN (+) rat showed faster entrainment to the new light-dark cycle compared to controls. The circadian rhythm has been regarded as a limit cycle phenomenon, and our results support the hypothesis that modification of the amplitude of the circadian limit cycle leads to alteration in the length of the phase shift.

摘要

昼夜节律是大约 24 小时的内源性节律,由生物钟驱动。生物钟中心位于视交叉上核。来自视网膜的光信号会改变视交叉上核的昼夜节律,但视交叉上核中有一个强大的部分,会在环境光照条件突然改变后导致时差反应。为了研究减弱的昼夜节律对时差反应持续时间的影响,我们建立了一种转基因大鼠,该大鼠在由小鼠 Prnp 为基础的转录调控盒[BMAL1 DN(+)]控制下表达 BMAL1 显性负形式。转基因大鼠比对照大鼠更早地表现出活跃状态,就在光照结束后。与对照大鼠相比,BMAL1 DN(+)大鼠在行为和 Per2 启动子驱动的荧光素酶活性节律中表现出更小的昼夜节律幅度。夜间的光脉冲导致行为节律的相位偏移更大。此外,在光照-黑暗周期的突然改变中,与对照大鼠相比,BMAL1 DN(+)大鼠更快地适应新的光照-黑暗周期。昼夜节律被认为是一种极限环现象,我们的结果支持这样一种假设,即昼夜极限环幅度的改变会导致相位偏移长度的改变。

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