Nielsen H S, Hannibal J, Knudsen S M, Fahrenkrug J
Department of Clinical Biochemistry, Bispebjerg Hospital, University of Copenhagen, DK-2400 NV, Copenhagen, Denmark.
Neuroscience. 2001;103(2):433-41. doi: 10.1016/s0306-4522(00)00563-7.
The suprachiasmatic nucleus generates circadian rhythms which are synchronized to the environmental light-dark cycle via the retinohypothalamic tract. Pituitary adenylate cyclase-activating polypeptide and glutamate, two neurotransmitters co-stored in the retinohypothalamic tract of the rat, are able to phase shift the endogenous rhythm similar to light. The "clock genes" period1 (per1) and per2, which show circadian oscillation within the suprachiasmatic nucleus, have been attributed a role in light-induced resetting of the mammalian circadian clock due to rapid induction of the period (per) genes after light stimulation at night. Using a rat in vitro brain slice model, we demonstrate by quantitative in situ hybridization histochemistry that the diurnal alteration in expression of both per genes in the suprachiasmatic nucleus was retained in vitro. In the model, we examined the effects of pituitary adenylate cyclase-activating polypeptide and glutamate alone and in combination on per1 and per2 gene expression at late subjective night (circadian time 19). Glutamate administration (10(-3)M) induced both per1 and per2 gene expression in the suprachiasmatic nucleus of the brain slice within 1h. The per gene responses were similar to the induction of gene expression observed after light stimulation in vivo at late night. Pituitary adenylate cyclase-activating polypeptide (10(-6)M) administered alone had no effect on the per gene expression, but when pituitary adenylate cyclase-activating polypeptide in micromolar concentration was applied before glutamate, the neuropeptide blocked the glutamate-induced per1 and per2 gene expression in the suprachiasmatic nucleus. In contrast to the lack of effect of pituitary adenylate cyclase-activating polypeptide itself in micromolar concentration, pituitary adenylate cyclase-activating polypeptide (10(-9)M) induced both per1 and per2 gene expression, an effect which was not augmented by co-application of glutamate. Our results provide the molecular substrate for the previous electrophysiological findings that pituitary adenylate cyclase-activating polypeptide in high concentration is able to block glutamate-induced phase advance at late night, and that the peptide in low concentration can induce a phase advance similar to light and glutamate.
视交叉上核产生昼夜节律,该节律通过视网膜下丘脑束与环境光暗周期同步。垂体腺苷酸环化酶激活多肽和谷氨酸是共同储存在大鼠视网膜下丘脑束中的两种神经递质,它们能够使内源性节律发生相移,类似于光的作用。“时钟基因”period1(per1)和per2在视交叉上核内呈现昼夜振荡,由于夜间光照刺激后周期(per)基因的快速诱导,它们在哺乳动物昼夜节律时钟的光诱导重置中发挥作用。使用大鼠体外脑片模型,我们通过定量原位杂交组织化学证明,视交叉上核中两个per基因表达的昼夜变化在体外得以保留。在该模型中,我们研究了垂体腺苷酸环化酶激活多肽和谷氨酸单独及联合应用对主观夜间晚期(昼夜时间19)per1和per2基因表达的影响。给予谷氨酸(10⁻³M)在1小时内诱导了脑片视交叉上核中per1和per2基因的表达。per基因的反应类似于深夜体内光照刺激后观察到的基因表达诱导。单独给予垂体腺苷酸环化酶激活多肽(10⁻⁶M)对per基因表达没有影响,但当在谷氨酸之前应用微摩尔浓度的垂体腺苷酸环化酶激活多肽时,该神经肽阻断了视交叉上核中谷氨酸诱导的per1和per2基因表达。与微摩尔浓度的垂体腺苷酸环化酶激活多肽本身缺乏作用相反,垂体腺苷酸环化酶激活多肽(10⁻⁹M)诱导了per1和per2基因表达,谷氨酸共同应用并未增强该作用。我们的结果为先前的电生理研究结果提供了分子基础,即高浓度的垂体腺苷酸环化酶激活多肽能够在深夜阻断谷氨酸诱导的相位提前,而低浓度的该多肽能够诱导类似于光和谷氨酸的相位提前。