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腺苷 A(1)受体在大鼠睡眠-觉醒调节中穹窿周-外侧下丘脑区的作用。

Role of adenosine A(1) receptor in the perifornical-lateral hypothalamic area in sleep-wake regulation in rats.

机构信息

Research Service (151A3), Veterans Affairs Greater Los Angeles Healthcare System, 16111 Plummer Street, Sepulveda, CA 91343, USA.

出版信息

Brain Res. 2009 Dec 22;1304:96-104. doi: 10.1016/j.brainres.2009.09.066. Epub 2009 Sep 23.

DOI:10.1016/j.brainres.2009.09.066
PMID:19781535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2783843/
Abstract

The perifornical-lateral hypothalamic area (PF-LHA) has been implicated in the regulation of arousal. The PF-LHA contains wake-active neurons that are quiescent during non-REM sleep and in the case of neurons expressing the peptide hypocretin (HCRT), quiescent during both non-REM and REM sleep. Adenosine is an endogenous sleep factor and recent evidence suggests that adenosine via A(1) receptors may act on PF-LHA neurons to promote sleep. We examined the effects of bilateral activation as well as blockade of A(1) receptors in the PF-LHA on sleep-wakefulness in freely behaving rats. The sleep-wake profiles of male Wistar rats were recorded during reverse microdialysis perfusion of artificial cerebrospinal fluid (aCSF) and two doses of adenosine A(1) receptor antagonist, 1,3-dipropyl-8-phenylxanthine (CPDX; 5 microM and 50 microM) or A(1) receptor agonist, N(6)-cyclopentyladenosine (CPA; 5 microM and 50 microM) into the PF-LHA for 2 h followed by 4 h of aCSF perfusion. CPDX perfused into the PF-LHA during lights-on phase produced arousal (F=7.035, p<0.001) and concomitantly decreased both non-REM (F=7.295, p<0.001) and REM sleep (F=3.456, p<0.004). In contrast, CPA perfused into the PF-LHA during lights-off phase significantly suppressed arousal (F=7.891, p<0.001) and increased non-REM (F=8.18, p <0.001) and REM sleep (F=30.036, p<0.001). These results suggest that PF-LHA is one of the sites where adenosine, acting via A(1) receptors, inhibits PF-LHA neurons to promote sleep.

摘要

外侧下丘脑peri-fornical 区(PF-LHA)被认为在觉醒调节中起作用。PF-LHA 包含在非快速眼动睡眠期间静止的觉醒活性神经元,并且在表达肽下丘脑泌素(HCRT)的神经元的情况下,在非快速眼动和快速眼动睡眠期间都静止。腺苷是一种内源性睡眠因子,最近的证据表明,腺苷通过 A1 受体可能作用于 PF-LHA 神经元以促进睡眠。我们检查了在自由行为大鼠中双侧激活以及 PF-LHA 中的 A1 受体阻断对睡眠觉醒的影响。在逆行微透析灌流人工脑脊液(aCSF)和两种剂量的腺苷 A1 受体拮抗剂 1,3-二丙基-8-苯基黄嘌呤(CPDX;5μM 和 50μM)或 A1 受体激动剂 N6-环戊基腺苷(CPA;5μM 和 50μM)时,雄性 Wistar 大鼠的睡眠觉醒谱在 PF-LHA 中记录 2 小时,然后用 aCSF 灌流 4 小时。CPDX 在光照期间灌流到 PF-LHA 中会产生觉醒(F=7.035,p<0.001),并同时减少非快速眼动(F=7.295,p<0.001)和快速眼动睡眠(F=3.456,p<0.004)。相比之下,CPA 在熄灯期间灌流到 PF-LHA 中会显著抑制觉醒(F=7.891,p<0.001)并增加非快速眼动(F=8.18,p<0.001)和快速眼动睡眠(F=30.036,p<0.001)。这些结果表明,PF-LHA 是腺苷通过 A1 受体作用以抑制 PF-LHA 神经元从而促进睡眠的部位之一。

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