Physiopathology of the Neuronal Network Responsible for the Sleep-Waking Cycle Team, CNRS UMR5292, INSERM U1028, Lyon Neuroscience, Research Center, Lyon, F-69372, France.
Sleep. 2011 Apr 1;34(4):419-23. doi: 10.1093/sleep/34.4.419.
To determine whether sublaterodorsal tegmental nucleus (SLD) neurons triggering paradoxical (REM) sleep (PS) are glutamatergic.
Three groups of rats were used: controls, rats deprived of PS for 72 h, and rats allowed to recover for 3 h after deprivation. Brain sections were processed for double labeling combining Fos immunohistochemistry and vesicular glutamate transporter 2 (vGLUT2) in situ hybridization.
The number of single Fos+ and Fos/vGLUT2+ double-labeled neurons was counted for each experimental condition. A very large number of Fos+ neurons expressing vGLUT2 mRNA specifically after PS hypersomnia was counted in the SLD. These double-labeled cells accounted for 84% of the total number of Fos+ cells.
This finding adds further evidence to the concept that PS-on neurons of the SLD generating PS are of small size and glutamatergic in nature. By means of their descending projections to medullary and/or spinal glycinergic/GABAergic premotoneurons, they may be especially important for the induction of muscle atonia during PS, a disturbed phenomenon in narcolepsy and REM sleep behavior disorder.
确定触发反常(REM)睡眠(PS)的下丘脑背外侧被盖核(SLD)神经元是否为谷氨酸能性的。
使用了三组大鼠:对照组、PS 剥夺 72 h 组和剥夺后恢复 3 h 组。脑切片进行双重标记,结合 Fos 免疫组化和囊泡谷氨酸转运体 2(vGLUT2)原位杂交。
对每种实验条件下的单个 Fos+和 Fos/vGLUT2+双标记神经元的数量进行了计数。在 SLD 中,大量表达 vGLUT2 mRNA 的 Fos+神经元在 PS 过度嗜睡后特异性出现。这些双标记细胞占 Fos+细胞总数的 84%。
这一发现进一步证明了 SLD 中产生 PS 的 PS 神经元体积小,本质上为谷氨酸能性的观点。通过它们对延髓和/或脊髓甘氨酸/GABA 能前运动神经元的下行投射,它们可能对 PS 期间肌肉弛缓特别重要,而在发作性睡病和 REM 睡眠行为障碍中,这种现象受到干扰。