Yamuy J, Sampogna S, Morales F R, Chase M H
Department of Physiology and the Brain Research Institute, UCLA School of Medicine, Los Angeles, CA 90095, USA.
Sleep Res Online. 1998;1(1):28-40.
The interaction of cholinergic and catecholaminergic mechanisms in the mesopontine region has been hypothesized as being critical for the generation and maintenance of active (REM) sleep. To further examine this hypothesis, we sought to determine the pattern of neuronal activation (via c-fos expression) of catecholaminergic and cholinergic neurons in this region during active sleep induced by the pontine microapplication of carbachol (designated as active sleep-carbachol). Accordingly, we used two sets of double-labeling techniques; the first to identify tyrosine hydroxylase-containing neurons (putative catecholaminergic cells) which also express the c-fos protein product Fos, and the second to reveal choline acetyltransferase-containing neurons (putative cholinergic cells) which also express Fos. Compared to control cats, active sleep-carbachol cats exhibited a significantly greater number of Fos-expressing neurons in the dorsolateral region of the pons, which encompasses the locus coeruleus, the lateral pontine reticular formation, the peribrachial nuclei and the latero-dorsal and pedunculo-pontine tegmental nuclei. However, both control and active sleep-carbachol cats exhibited a similar number of catecholaminergic and cholinergic neurons in those regions that expressed Fos (i.e., double-labeled cells). A large number of c-fos-expressing neurons in the active sleep-carbachol cats whose neurotransmitter phenotype was not identified suggests that non-catecholaminergic, non-cholinergic neuronal populations in mesopontine regions are involved in the generation and maintenance of active sleep. The lack of increased c-fos expression in catecholaminergic neurons during active sleep-carbachol confirms and extends previous data that indicate that these cells are silent during active sleep-carbachol and naturally-occurring active sleep. The finding that cholinergic neurons of the dorsolateral pons were not activated either during wakefulness or active sleep-carbachol raises questions regarding the synaptic mechanisms of activation of these cells during these behavioral states.
中脑桥脑区域胆碱能和儿茶酚胺能机制的相互作用被认为对快速眼动(REM)睡眠的产生和维持至关重要。为了进一步检验这一假设,我们试图确定在脑桥微量注射卡巴胆碱诱导的快速眼动睡眠(称为快速眼动睡眠-卡巴胆碱)期间,该区域儿茶酚胺能和胆碱能神经元的神经元激活模式(通过c-fos表达)。因此,我们使用了两组双重标记技术;第一组用于识别也表达c-fos蛋白产物Fos的含酪氨酸羟化酶的神经元(假定的儿茶酚胺能细胞),第二组用于揭示也表达Fos的含胆碱乙酰转移酶的神经元(假定的胆碱能细胞)。与对照猫相比,快速眼动睡眠-卡巴胆碱猫在脑桥背外侧区域表现出显著更多的表达Fos的神经元,该区域包括蓝斑、脑桥外侧网状结构、臂旁核以及背外侧和脚桥被盖核。然而,对照猫和快速眼动睡眠-卡巴胆碱猫在那些表达Fos的区域(即双重标记细胞)中表现出相似数量的儿茶酚胺能和胆碱能神经元。快速眼动睡眠-卡巴胆碱猫中有大量表达c-fos的神经元,其神经递质表型未被识别,这表明中脑桥脑区域的非儿茶酚胺能、非胆碱能神经元群体参与了快速眼动睡眠的产生和维持。在快速眼动睡眠-卡巴胆碱期间儿茶酚胺能神经元中c-fos表达没有增加,这证实并扩展了先前的数据,表明这些细胞在快速眼动睡眠-卡巴胆碱和自然发生的快速眼动睡眠期间是沉默的。脑桥背外侧胆碱能神经元在清醒或快速眼动睡眠-卡巴胆碱期间均未被激活这一发现,引发了关于这些细胞在这些行为状态下激活的突触机制的问题。