The expression of NR2B subunit of NMDA receptor in the suprachiasmatic nucleus of Wistar rats and its role in glutamate-induced CREB and ERK1/2 phosphorylation

被引:18
|
作者
Bendova, Zdenka [1 ,2 ]
Sladek, Martin [1 ]
Svobodova, Irena [1 ]
机构
[1] Acad Sci Czech Republic, Inst Physiol, Vvi, CR-14220 Prague 4, Czech Republic
[2] Charles Univ Prague, Dept Physiol, Fac Sci, Prague 2, Czech Republic
关键词
Circadian clock; NMDA receptor; NR2B subunit; Rat; Suprachiasmatic nucleus; D-ASPARTATE-RECEPTOR; ELEMENT-BINDING PROTEIN; PHASE-SHIFT; LIGHT; CLOCK; ACTIVATION; GENE; SCN; TRANSCRIPTION; ENTRAINMENT;
D O I
10.1016/j.neuint.2012.04.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most behavioral and physiological processes in living organisms exhibit periodic circadian rhythmicity. In mammals, these rhythms are coordinated by the circadian clock located in the suprachiasmatic nucleus (SCN) of the hypothalamus. In order to precisely synchronize free-running circadian oscillations to the 24 h solar cycle, signals from the external environment, primarily the light/dark cycle, must reach the circadian clock within the SCN. A light pulse elevates intracellular Ca2+ levels, and activates signaling cascades, leading to transcriptional activation of the clock genes mPer1 and mPer2 via phosphorylation of extracellular-signal-regulated kinases 1/2 (ERK1/2) and cyclic AMP-responsive element binding protein (CREB). Glutamate is the primary excitatory transmitter in retinal terminals in the SCN, and NMDA receptors (NMDAR) are the principal glutamate receptors that mediate the effect of light on resetting the circadian clock. Here we show the circadian rhythm in mRNA expression and protein level of the NMDAR 2B subunit (NR2B) in the SCN, with a peak at night. Also, we demonstrate ifenprodil inhibition of glutamate-induced phosphorylation of CREB (pCREB) and ERK1/2 (pERK1/2), and support thus the evidence for NR2B role in activation of signaling cascade involved in photic resetting of the circadian clock. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:43 / 47
页数:5
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