Datta S, Spoley E E, Mavanji V K, Patterson E H
Sleep Research Laboratory, Department of Psychiatry and Program in Behavioral Neuroscience, Boston University School of Medicine, M-913, 715 Albany Street, Boston, MA 02118, USA.
Neuroscience. 2002;114(1):157-64. doi: 10.1016/s0306-4522(02)00250-6.
Considerable evidence suggests that pedunculopontine tegmental cholinergic cells are critically involved in normal regulation of rapid eye movement sleep. The major excitatory input to the cholinergic cell compartment of the pedunculopontine tegmentum arises from glutamatergic neurons in the pontine reticular formation. Immunohistochemical studies reveal that both ionotropic and metabotropic receptors are expressed in pedunculopontine tegmental cells. This study aimed to identify the role of endogenous glutamate and its specific receptors in the pedunculopontine tegmentum in the regulation of physiological rapid eye movement sleep. To identify this physiological rapid eye movement sleep-inducing glutamate receptor(s) in the pedunculopontine tegmental cholinergic cell compartment, specific receptors were blocked differentially by local microinjection of selective glutamate receptor antagonists into the pedunculopontine tegmental cholinergic cell compartment while quantifying the effects on rapid eye movement sleep in freely moving chronically instrumented rats. By comparing the alterations in the patterns of rapid eye movement sleep following injections of control vehicle and selective glutamate receptor antagonists, contributions made by each receptor subtype in rapid eye movement sleep were evaluated. The results demonstrate that when kainate receptors were blocked by local microinjection of a kainate receptor selective antagonist, spontaneous rapid eye movement sleep was completely absent for the first 2 h, and for the next 2 h the total percentage of rapid eye movement sleep was significantly less compared to the control values. In contrast, when N-methyl-D-aspartate, alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid, groups I, II, and III metabotropic receptors were blocked, total percentages of rapid eye movement sleep did not change compared to the control values. These findings suggest, for the first time, that the activation of kainate receptors within the cholinergic cell compartment of the pedunculopontine tegmentum is a critical step for the regulation of normal rapid eye movement sleep in the freely moving rat. The results also suggest that the different types of glutamate receptors within a small part of the brainstem may be involved in different types of physiological functions.
大量证据表明,脚桥被盖胆碱能细胞在快速眼动睡眠的正常调节中起关键作用。脚桥被盖胆碱能细胞区的主要兴奋性输入来自脑桥网状结构中的谷氨酸能神经元。免疫组织化学研究表明,离子型和代谢型受体均在脚桥被盖细胞中表达。本研究旨在确定内源性谷氨酸及其特异性受体在脚桥被盖中对生理性快速眼动睡眠调节的作用。为了确定脚桥被盖胆碱能细胞区中这种生理性快速眼动睡眠诱导性谷氨酸受体,通过向脚桥被盖胆碱能细胞区局部微量注射选择性谷氨酸受体拮抗剂来差异性地阻断特异性受体,同时在自由活动的慢性植入仪器的大鼠中量化其对快速眼动睡眠的影响。通过比较注射对照载体和选择性谷氨酸受体拮抗剂后快速眼动睡眠模式的变化,评估每种受体亚型在快速眼动睡眠中的作用。结果表明,当通过局部微量注射海人酸受体选择性拮抗剂阻断海人酸受体时,最初2小时完全没有自发快速眼动睡眠,在接下来的2小时内,快速眼动睡眠的总百分比与对照值相比显著降低。相比之下,当N-甲基-D-天冬氨酸、α-氨基-3-羟基-5-甲基-4-异恶唑丙酸、I、II和III组代谢型受体被阻断时,快速眼动睡眠的总百分比与对照值相比没有变化。这些发现首次表明,脚桥被盖胆碱能细胞区内海人酸受体的激活是自由活动大鼠正常快速眼动睡眠调节的关键步骤。结果还表明,脑干一小部分内不同类型的谷氨酸受体可能参与不同类型的生理功能。