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尾加压素II通过激活脑干胆碱能神经元来调节快速眼动睡眠。

Urotensin II modulates rapid eye movement sleep through activation of brainstem cholinergic neurons.

作者信息

Huitron-Resendiz Salvador, Kristensen Morten P, Sánchez-Alavez Manuel, Clark Stewart D, Grupke Stephen L, Tyler Christopher, Suzuki Chisa, Nothacker Hans-Peter, Civelli Olivier, Criado Jose R, Henriksen Steven J, Leonard Christopher S, de Lecea Luis

机构信息

Department of Neuropharmacology, The Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

J Neurosci. 2005 Jun 8;25(23):5465-74. doi: 10.1523/JNEUROSCI.4501-04.2005.

Abstract

Urotensin II (UII) is a cyclic neuropeptide with strong vasoconstrictive activity in the peripheral vasculature. UII receptor mRNA is also expressed in the CNS, in particular in cholinergic neurons located in the mesopontine tegmental area, including the pedunculopontine tegmental (PPT) and lateral dorsal tegmental nuclei. This distribution suggests that the UII system is involved in functions regulated by acetylcholine, such as the sleep-wake cycle. Here, we tested the hypothesis that UII influences cholinergic PPT neuron activity and alters rapid eye movement (REM) sleep patterns in rats. Local administration of UII into the PPT nucleus increases REM sleep without inducing changes in the cortical blood flow. Intracerebroventricular injection of UII enhances both REM sleep and wakefulness and reduces slow-wave sleep 2. Intracerebroventricular, but not local, administration of UII increases cortical blood flow. Moreover, whole-cell recordings from rat-brain slices show that UII selectively excites cholinergic PPT neurons via an inward current and membrane depolarization that were accompanied by membrane conductance decreases. This effect does not depend on action potential generation or fast synaptic transmission because it persisted in the presence of TTX and antagonists of ionotropic glutamate, GABA, and glycine receptors. Collectively, these results suggest that UII plays a role in the regulation of REM sleep independently of its cerebrovascular actions by directly activating cholinergic brainstem neurons.

摘要

尾加压素 II(UII)是一种环状神经肽,在外周血管系统中具有强大的血管收缩活性。UII 受体 mRNA 也在中枢神经系统中表达,特别是在位于中脑桥被盖区的胆碱能神经元中,包括脚桥被盖核(PPT)和背外侧被盖核。这种分布表明 UII 系统参与了由乙酰胆碱调节的功能,如睡眠 - 觉醒周期。在此,我们检验了 UII 影响胆碱能 PPT 神经元活动并改变大鼠快速眼动(REM)睡眠模式的假说。向 PPT 核局部注射 UII 可增加 REM 睡眠,而不引起皮质血流变化。脑室内注射 UII 可增强 REM 睡眠和觉醒,并减少慢波睡眠 2。脑室内(而非局部)注射 UII 可增加皮质血流。此外,大鼠脑片的全细胞记录显示,UII 通过内向电流和膜去极化选择性地兴奋胆碱能 PPT 神经元,同时伴有膜电导降低。这种效应不依赖于动作电位的产生或快速突触传递,因为在存在河豚毒素以及离子型谷氨酸、γ-氨基丁酸和甘氨酸受体拮抗剂的情况下该效应仍然持续。总体而言,这些结果表明 UII 通过直接激活脑干胆碱能神经元,在 REM 睡眠调节中发挥作用,而与其脑血管作用无关。

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