Alvira-Botero Maria Ximena, Garzón Miguel
Departamento de Anatomía, Histología y Neurociencia, Facultad de Medicina, Universidad Autónoma de Madrid, Calle Arzobispo Morcillo 4, 28029, Madrid, Spain.
Brain Res. 2006 Dec 6;1123(1):101-11. doi: 10.1016/j.brainres.2006.09.030. Epub 2006 Oct 13.
The ventral division of the reticular oral pontine nucleus (vRPO) is a pontine tegmentum region critically involved in REM sleep generation. Previous reports of morphine microinjections in the cat pontine tegmentum have shown that opioid receptor activation in this region modulates REM sleep. Even though opiate administration has marked effects on sleep-wake cycle architecture, the distribution of opioid receptors in vRPO has only been partially described. Using an antiserum directed against delta opioid receptor (DOR), to which morphine binds, in the present study, we use (1) light microscopy to determine DOR cellular distribution in the rostral pontine tegmentum and (2) electron microscopy to determine DOR subcellular distribution in the cat vRPO. In the dorsal pons, DOR immunoreactivity was evenly distributed throughout the neuropil of the reticular formation and was particularly intense in the parabrachial nuclei and locus coeruleus; the ventral and central areas of the RPO and locus coeruleus complex were especially rich in DOR-labeled somata. Within the vRPO, DOR was localized mainly in the cytoplasm and on plasma membranes of medium to large dendrites (47.8% of DOR-labeled profiles), which received both symmetric and asymmetric synaptic contacts mainly from non-labeled (82% of total inputs) axon terminals. Less frequently, DOR was distributed presynaptically in axon terminals (19% of DOR-labeled profiles). Our results suggest that DOR activation in vRPO regulates REM sleep occurrence by modulating postsynaptic responses to both excitatory and inhibitory afferents. DOR activation in vRPO could have, however, an additional role in direct modulation of neurotransmitter release from axon terminals.
脑桥嘴侧网状核腹侧部(vRPO)是脑桥被盖区的一个区域,在快速眼动睡眠产生过程中起关键作用。先前关于在猫脑桥被盖区微量注射吗啡的报道表明,该区域的阿片受体激活可调节快速眼动睡眠。尽管阿片类药物给药对睡眠-觉醒周期结构有显著影响,但vRPO中阿片受体的分布仅得到部分描述。在本研究中,我们使用一种针对吗啡所结合的δ阿片受体(DOR)的抗血清,(1)通过光学显微镜确定DOR在嘴侧脑桥被盖区的细胞分布,(2)通过电子显微镜确定猫vRPO中DOR的亚细胞分布。在脑桥背侧,DOR免疫反应性均匀分布于整个网状结构的神经毡,在臂旁核和蓝斑中尤其强烈;RPO和蓝斑复合体的腹侧和中央区域DOR标记的胞体特别丰富。在vRPO内,DOR主要定位于中到大型树突的细胞质和质膜上(47.8%的DOR标记轮廓),这些树突主要从未标记的轴突终末(占总输入的82%)接受对称和不对称突触联系。较少见的是,DOR分布于轴突终末的突触前(19%的DOR标记轮廓)。我们的结果表明,vRPO中DOR的激活通过调节对兴奋性和抑制性传入神经的突触后反应来调节快速眼动睡眠的发生。然而,vRPO中DOR的激活可能在直接调节轴突终末神经递质释放方面还有额外作用。