Henny Pablo, Jones Barbara E
Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada.
J Comp Neurol. 2006 Dec 1;499(4):645-61. doi: 10.1002/cne.21131.
Orexin/hypocretin (Orx) neurons are critical for the maintenance of waking in association with behavioral arousal and postural muscle tone, since with their loss narcolepsy with cataplexy occurs. Given that basal forebrain (BF) neurons project to the hypothalamus and play important diverse roles in sleep/wake states, we sought to determine whether acetylcholine (ACh), glutamate (Glu), and/or GABA-releasing BF neurons innervate and could thereby differentially regulate the Orx neurons. From discrete injections of biotinylated dextran amine (BDA, 10,000 MW) into the magnocellular preoptic nucleus (MCPO) and substantia innominata (SI) in the rat, BDA-labeled fibers projected to the lateral hypothalamus (LH), perifornical area (PF), and dorsomedial hypothalamus (DMH), where approximately 41%, approximately 11%, and 9% of Orx-positive (+) neurons were respectively contacted in each region. Employing triple fluorescent staining for Orx, BDA, and presynaptic vesicular (V) transporters (T), we found that only 4% of the innervated Orx+ neurons in the LH were contacted by BDA+[VAChT+] terminals, whereas approximately 31% and approximately 67% were respectively contacted by BDA+[VGluT2+] and BDA+[VGAT+] terminals. In 3D-rendered and rotated confocal images, we confirmed the latter contacts and examined staining for postsynaptic proteins PSD-95, a marker for glutamatergic synapses, and gephyrin, a marker for GABAergic synapses, that were located on Orx+ neurons facing BDA-labeled terminals in approximately 20% and approximately 50% of contacts, respectively. With such synaptic input, BF glutamatergic neurons can excite Orx neurons and thus act to maintain behavioral arousal with muscle tone, whereas GABAergic neurons can inhibit Orx neurons and thus promote behavioral quiescence and sleep along with muscle atonia.
食欲素/下丘脑泌素(Orexin/hypocretin,Orx)神经元对于维持清醒并伴有行为觉醒和姿势肌张力至关重要,因为其丧失会导致发作性睡病伴猝倒。鉴于基底前脑(BF)神经元投射至下丘脑并在睡眠/觉醒状态中发挥多种重要作用,我们试图确定释放乙酰胆碱(ACh)、谷氨酸(Glu)和/或γ-氨基丁酸(GABA)的BF神经元是否支配并由此差异性地调节Orx神经元。通过向大鼠的大细胞视前核(MCPO)和无名质(SI)分别注射生物素化葡聚糖胺(BDA,分子量10,000),BDA标记的纤维投射至下丘脑外侧区(LH)、穹窿周区(PF)和下丘脑背内侧核(DMH),在每个区域分别有大约41%、大约11%和9%的Orx阳性(+)神经元与之接触。利用对Orx、BDA和突触前囊泡(V)转运体(T)进行三重荧光染色,我们发现LH中仅4%的受支配Orx+神经元被BDA+[囊泡乙酰胆碱转运体(VAChT)+]终末接触,而大约31%和大约67%分别被BDA+[囊泡谷氨酸转运体2(VGluT2)+]和BDA+[囊泡GABA转运体(VGAT)+]终末接触。在三维渲染和旋转的共聚焦图像中,我们证实了后者的接触,并检查了突触后蛋白PSD-95(一种谷氨酸能突触标记物)和gephyrin(一种GABA能突触标记物)的染色情况,它们分别在大约20%和大约50%的接触中位于面对BDA标记终末的Orx+神经元上。有了这样的突触输入,BF谷氨酸能神经元可兴奋Orx神经元,从而起到维持伴有肌张力的行为觉醒的作用,而GABA能神经元可抑制Orx神经元,从而促进行为静止和睡眠以及肌肉弛缓。