Shibata S, Watanabe A, Hamada T, Ono M, Watanabe S
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Am J Physiol. 1994 Aug;267(2 Pt 2):R360-4. doi: 10.1152/ajpregu.1994.267.2.R360.
The suprachiasmatic nucleus (SCN) acts as a pacemaker for mammalian circadian rhythms. Receptors for excitatory amino acids like N-methyl-D-aspartate (NMDA) and non-NMDA receptors have both been found to play an important role in the transmission of photic information from the retina to the SCN. Therefore, we investigated whether the application of glutamate receptor agonists could reset the phase of the circadian rhythm of SCN firing activity in vitro. Treatment with NMDA (0.1-10 microM) for 15 min or 1 h during the early part of the subjective night produced phase delay, whereas treatment during the late subjective night caused an advance in phase. The phase-response curve for NMDA was similar to that previously obtained in response to light pulses in vivo. Application of DL-alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid hydrobromide (AMPA) (1 or 10 microM), a non-NMDA-receptor agonist, also produced a dose-dependent phase delay of SCN activity. The NMDA-induced phase delay was antagonized by an NMDA-receptor antagonist MK-801. These findings suggest that both NMDA and non-NMDA receptors may be involved in the transmission of information to the SCN via the retinohypothalamic tract. In addition, both the advances and delays in phase caused by NMDA were potentiated by cotreatment with neuropeptide Y, whereas AMPA-induced phase delay was not potentiated by neuropeptide Y. This points to a functional link between NMDA and neuropeptide Y receptor-mediated mechanisms in the SCN.
视交叉上核(SCN)作为哺乳动物昼夜节律的起搏器。已发现兴奋性氨基酸如N-甲基-D-天冬氨酸(NMDA)的受体和非NMDA受体在从视网膜到SCN的光信息传递中均发挥重要作用。因此,我们研究了谷氨酸受体激动剂的应用是否能在体外重置SCN放电活动昼夜节律的相位。在主观夜间早期用NMDA(0.1 - 10 microM)处理15分钟或1小时会导致相位延迟,而在主观夜间晚期处理则会导致相位提前。NMDA的相位响应曲线与先前在体内对光脉冲的响应曲线相似。应用非NMDA受体激动剂DL-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸氢溴酸盐(AMPA)(1或10 microM)也会导致SCN活动出现剂量依赖性的相位延迟。NMDA诱导的相位延迟被NMDA受体拮抗剂MK-801拮抗。这些发现表明,NMDA和非NMDA受体可能都参与了通过视网膜下丘脑束向SCN传递信息。此外,NMDA引起的相位提前和延迟在与神经肽Y共同处理时都会增强,而AMPA诱导的相位延迟不会被神经肽Y增强。这表明在SCN中,NMDA和神经肽Y受体介导的机制之间存在功能联系。