Duffield G E, Hastings M H, Ebling F J
Department of Anatomy, University of Cambridge, UK.
J Neuroendocrinol. 1998 Nov;10(11):871-84. doi: 10.1046/j.1365-2826.1998.00274.x.
Dopamine and melatonin have both been implicated in mediating maternal influences on the developing circadian system of altricial rodents. The aim of these studies was to investigate their role in the entrainment of the circadian system of the adult Siberian hamster (Phodopus sungorus). In-situ hybridization revealed that D1-dopamine receptor (D1-R) mRNA was expressed in the adult suprachiasmatic nucleus (SCN) at levels comparable to neonates. As dopamine has been postulated to mimic photic stimulation during early development, experiment 1 compared the effects of a D1-R agonist and a light pulse on free-running wheel running rhythms in hamsters maintained in constant dim red light. A phase response curve to light was generated, revealing clear phase delays early in the subjective night, and large phase advances in the late subjective night. However, the D1-R agonist (SKF 81297, 2 mg/kg, s.c.) did not produce consistent phase shifts at any circadian phase. Experiment 2 tested the ability of this dopaminergic agonist to modulate photic responses of the circadian system. Free-running animals were pre-treated with SKF 81297 (2 mg/kg, s.c.) 30 min before a 15 min light pulse given early or late in the subjective night. This agonist had no effect on the magnitude of phase shifts at either circadian time. In experiment 3, light pulses at CT13-15 induced expression of the immediate early gene c-fos in the SCN, as assessed by immunocytochemistry for the protein product. In contrast, SKF 81297 (2 mg/kg, s.c.) at the same phase did not induce c-fos in the SCN, despite marked c-fos induction in the caudate-putamen, nor did it affect photic induction of c-fos in the SCN. To investigate whether dopamine might be involved in nonphotic regulation of the circadian system in adult hamsters, experiment 4 compared the response of free-running hamsters to a series of injections of SKF 81297 (2 mg/kg, s.c.) or melatonin (1 mg/kg, s.c.), since melatonin receptor expression in the SCN also persists into adulthood. Animals were treated every 23.5 h for 6 days. The serial injections of melatonin produced cumulative phase advances of up to 3 h when delivered in late subjective day, but not when presented in late subjective night. Hamsters did not respond to SKF 81297 or vehicle treatment at either circadian phase. Moreover, pre-treatment with the dopaminergic agonist did not affect the phase-advancing effects of melatonin when both were given in the serial injection protocol. These results demonstrate clear phase-dependent effects of light pulses and melatonin on circadian rhythms in Siberian hamsters, but suggest that D1-Rs in the SCN no longer modulate photic or melatonin-dependent entrainment pathways in the adult.
多巴胺和褪黑素都被认为在介导母体对晚成性啮齿动物发育中的昼夜节律系统的影响方面发挥作用。这些研究的目的是调查它们在成年西伯利亚仓鼠(Phodopus sungorus)昼夜节律系统的同步化中的作用。原位杂交显示,D1-多巴胺受体(D1-R)mRNA在成年视交叉上核(SCN)中的表达水平与新生儿相当。由于多巴胺被假定在早期发育过程中模拟光刺激,实验1比较了D1-R激动剂和光脉冲对处于持续昏暗红光环境中的仓鼠自由活动的转轮节律的影响。生成了对光的相位响应曲线,结果显示在主观夜间早期有明显的相位延迟,在主观夜间后期有较大的相位提前。然而,D1-R激动剂(SKF 81297,2 mg/kg,皮下注射)在任何昼夜节律相位都没有产生一致的相位偏移。实验2测试了这种多巴胺能激动剂调节昼夜节律系统光反应的能力。在主观夜间早期或晚期给予15分钟光脉冲前30分钟,对自由活动的动物进行SKF 81297(2 mg/kg,皮下注射)预处理。该激动剂在两个昼夜节律时间点对相位偏移的幅度均无影响。在实验3中,通过对蛋白质产物进行免疫细胞化学评估发现,在CT13-15给予的光脉冲诱导了SCN中即刻早期基因c-fos的表达。相比之下,在相同相位给予的SKF 81297(2 mg/kg,皮下注射)在SCN中未诱导c-fos表达,尽管在尾状核-壳核中有明显的c-fos诱导,且它也不影响SCN中c-fos的光诱导。为了研究多巴胺是否可能参与成年仓鼠昼夜节律系统的非光调节,实验4比较了自由活动的仓鼠对一系列SKF 81297(2 mg/kg,皮下注射)或褪黑素(1 mg/kg,皮下注射)注射的反应,因为SCN中褪黑素受体的表达也持续到成年期。每隔23.5小时对动物进行一次处理,共处理6天。在主观白天后期给予褪黑素的系列注射会产生累计达3小时的相位提前,但在主观夜间后期给予时则不会。仓鼠在任何昼夜节律相位对SKF 81297或溶剂处理均无反应。此外,当二者都按照系列注射方案给予时,用多巴胺能激动剂进行预处理并不影响褪黑素的相位提前作用。这些结果表明,光脉冲和褪黑素对西伯利亚仓鼠的昼夜节律有明显的相位依赖性影响,但表明SCN中的D1-R在成年后不再调节光或褪黑素依赖性的同步化途径。