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前列腺素E(EP)受体亚型与睡眠:EP4起促进作用,EP1/EP2起抑制作用。

Prostaglandin E (EP) receptor subtypes and sleep: promotion by EP4 and inhibition by EP1/EP2.

作者信息

Yoshida Y, Matsumura H, Nakajima T, Mandai M, Urakami T, Kuroda K, Yoneda H

机构信息

Department of Neuropsychiatry, Osaka Medical College, Takatsuki-City, Japan.

出版信息

Neuroreport. 2000 Jul 14;11(10):2127-31. doi: 10.1097/00001756-200007140-00014.

Abstract

Prostaglandin (PG) E2 reportedly augmented wakefulness when continuously infused into the third ventricle of the rat brain, whereas it promoted sleep when continuously infused into the subarachnoid space of the ventral surface zone of the rostral basal forebrain, which was designated previously as a PGD2-sensitive sleep-promoting zone (PGD2-SZ). In the present study, we investigated the effects of PGE (EP)-receptor agonists on sleep-wakefulness activities by infusing agonists into the third ventricle or into the subarachnoid space of the PGD2-SZ. Our results indicated that the waking effect is mediated by EP1 and EP2 receptors situating around the third ventricle, whereas the sleep-promoting effect is brought about mainly through activation of EP4 receptors located at or near the subarachnoid space of the PGD2-SZ.

摘要

据报道,当将前列腺素(PG)E2持续注入大鼠脑的第三脑室时会增强觉醒,而当将其持续注入喙状基底前脑腹侧表面区的蛛网膜下腔时则促进睡眠,该区域先前被指定为对PGD2敏感的促睡眠区(PGD2-SZ)。在本研究中,我们通过将激动剂注入第三脑室或PGD2-SZ的蛛网膜下腔来研究PGE(EP)受体激动剂对睡眠-觉醒活动的影响。我们的结果表明,觉醒效应由位于第三脑室周围的EP1和EP2受体介导,而促睡眠效应主要是通过激活位于PGD2-SZ蛛网膜下腔或其附近的EP4受体实现的。

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