Shibata S, Ono M, Tominaga K, Hamada T, Watanabe A, Watanabe S
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Neurosci Biobehav Rev. 1994 Winter;18(4):591-5. doi: 10.1016/0149-7634(94)90016-7.
Glutamate has been reported to be involved in the transmission of photic information from the retina to the suprachiasmatic nucleus (SCN). Therefore, we investigated whether the application of N-methyl-D-aspartate (NMDA), a glutamate receptor agonist could, reset the circadian rhythm of SCN firing activity in vitro. Treatment with NMDA for 1 h between projected zeitgeber time (ZT) 13-14 produced a phase delay in a concentration-dependent manner. The NMDA-induced phase delay was antagonized by an NMDA-receptor antagonist, MK-801 (100 microM). The retinohypothalamic tract has been reported to make terminals on neurons possessing vasoactive intestinal polypeptide (VIP). Therefore, we investigated the effect of NMDA on VIP release from the SCN and on VIP immunoreactivity in the SCN. Application of NMDA for 15 min between ZT 13-15 increased release of VIP from the SCN. In contrast to release, the content of VIP in the SCN tissue was reduced by application of NMDA. Immunohistochemical analysis revealed that application of NMDA for 4 h or 1 h reduced VIP immunoreactivity in the SCN. To investigate the possibility that VIP released by NMDA could reset SCN neuronal activity, we examined the effects of VIP on the SCN neuronal activity rhythm. Co-treatment with VIP (1 microM) and gastrin-releasing peptide (1 microM) for 1 h between ZT 13-14 caused a phase-delay of SCN activity rhythm. These findings suggest that activation of NMDA receptors during early subjective night causes a phase delay of the SCN neuronal activity via facilitation of VIP release in this nucleus.
据报道,谷氨酸参与了从视网膜到视交叉上核(SCN)的光信息传递。因此,我们研究了谷氨酸受体激动剂N-甲基-D-天冬氨酸(NMDA)的应用是否能在体外重置SCN放电活动的昼夜节律。在预计的授时时间(ZT)13至14之间用NMDA处理1小时会以浓度依赖的方式产生相位延迟。NMDA诱导的相位延迟被NMDA受体拮抗剂MK-801(100微摩尔)拮抗。据报道,视网膜下丘脑束在具有血管活性肠肽(VIP)的神经元上形成终末。因此,我们研究了NMDA对SCN中VIP释放和SCN中VIP免疫反应性的影响。在ZT 13至15之间应用NMDA 15分钟可增加SCN中VIP的释放。与释放情况相反,应用NMDA会降低SCN组织中VIP的含量。免疫组织化学分析显示,应用NMDA 4小时或1小时可降低SCN中的VIP免疫反应性。为了研究NMDA释放的VIP是否能重置SCN神经元活动的可能性,我们检查了VIP对SCN神经元活动节律的影响。在ZT 13至14之间用VIP(1微摩尔)和胃泌素释放肽(1微摩尔)共同处理1小时会导致SCN活动节律的相位延迟。这些发现表明,在主观夜间早期激活NMDA受体会通过促进该核中VIP的释放导致SCN神经元活动的相位延迟。