Graham E Scott, Littlewood Pauline, Turnbull Yvonne, Mercer Julian G, Morgan Peter J, Barrett Perry
Molecular Endocrinology Group, Aberdeen Centre for Energy Regulation and Obesity (ACERO), Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen AB21 9SB, UK.
Eur J Neurosci. 2005 Feb;21(3):814-9. doi: 10.1111/j.1460-9568.2005.03923.x.
Neuromedin-U (NMU) has been reported to drive several physiological or behavioural responses following i.c.v. injection of the peptide into the third ventricle of rodent brains. Many of these responses are mediated through a change in corticotrophin-releasing factor (CRF) output from the paraventricular nucleus (PVN). A number of the physiological or behavioural responses are regulated in a circadian manner, e.g. feeding. We have previously reported NMU gene expression in the suprachiasmatic nucleus (SCN) and NMU-2 receptor expression in the PVN, dorsal medial hypothalamus (DMH) and other regions of the mouse brain. We therefore hypothesized that NMU would be regulated by the circadian clock and may consequently drive a circadian rhythm of CRF expression in the PVN. Here we report that NMU is regulated in a circadian manner with peak expression during the light phase of a light-dark cycle. In C3H mice held in constant darkness, the NMU rhythm free runs with a period predicted by the free running period of locomotor activity in this mouse. The NMU mRNA transcript colocalizes with cells expressing AVP in the SCN and shows a coincident rhythm of expression with AVP. On the other hand, CRF did not express a circadian rhythm of expression in a light-dark cycle, although a rhythm was evident in constant darkness with a peak of expression prior to the rise of NMU in the same conditions. This would suggest that the circadian rhythm in NMU expression in the SCN does not drive a circadian rhythm in CRF in the PVN to be translated into physiological and behavioural responses mediated by NMU.
据报道,神经介素U(NMU)在将该肽脑室内注射到啮齿动物脑的第三脑室后,可引发多种生理或行为反应。其中许多反应是通过室旁核(PVN)促肾上腺皮质激素释放因子(CRF)输出的变化介导的。一些生理或行为反应以昼夜节律的方式受到调节,例如进食。我们之前报道过NMU基因在视交叉上核(SCN)中的表达以及NMU-2受体在PVN、下丘脑背内侧核(DMH)和小鼠脑其他区域中的表达。因此,我们推测NMU会受生物钟调节,进而可能驱动PVN中CRF表达的昼夜节律。在此我们报告,NMU以昼夜节律的方式受到调节,在明暗周期的光照阶段表达达到峰值。在持续黑暗环境中的C3H小鼠中,NMU节律自由运行,其周期由该小鼠运动活动的自由运行周期预测。NMU mRNA转录本与SCN中表达抗利尿激素(AVP)的细胞共定位,并与AVP呈现一致的表达节律。另一方面,CRF在明暗周期中未表现出表达的昼夜节律,尽管在持续黑暗中存在节律,且在相同条件下其表达峰值先于NMU升高。这表明SCN中NMU表达的昼夜节律不会驱动PVN中CRF的昼夜节律转化为NMU介导的生理和行为反应。