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用对氯苯丙氨酸预处理使大鼠失眠后,前列腺素D2对睡眠的促进作用。

Promotion of sleep by prostaglandin D2 in rats made insomniac by pretreatment with para-chlorophenylalanine.

作者信息

Satoh S, Matsumura H, Nakajima T, Onoe H, Sakai K, Nakajima T, Jouvet M, Hayaishi O

机构信息

Osaka Bioscience Institute, Japan.

出版信息

Neurosci Res. 1994 Nov;21(1):41-50. doi: 10.1016/0168-0102(94)90066-3.

Abstract

The correlation between the somnogenic effect of prostaglandin (PG) D2 and the serotoninergic system was examined in freely-moving rats (n = 64) by use of a continuous infusion method. Rats pretreated with para-chlorophenylalanine (PCPA: 450 mg/kg body weight, i.p.) or non-PCPA-pretreated rats received infusion of PGD2, serotonin, or its direct precursor, 5-hydroxytryptophan (5HTP), into their third cerebral ventricle at a rate of 100 pmol/0.2 microliter/min between 11:00 and 17:00 h. In the PCPA-pretreated insomniac rats, PGD2 infusion resulted in an immediate increase in slow-wave sleep (SWS) and an increase with a 2-h latency in paradoxical sleep (PS). The total amounts of SWS and PS during the PGD2-infusion period were 151% and 154% of the respective control values. These results indicate that inhibition of the biosynthesis of serotonin and 5HTP by PCPA marginally affects the sleep-promoting effect of PGD2. The transient sleep restoration produced by 5HTP infusion into PCPA-pretreated rats was hardly affected by the simultaneous infusion (200 pmol/0.2 microliter/min; 07:00-17:00 h) of diclofenac sodium, an inhibitor of cyclo-oxygenase, suggesting that PGD2 production is not critically involved in the sleep restoration by 5HTP. The sleep-promoting property of PGD2 is thus probably independent of the serotoninergic modulation of sleep-wake activity.

摘要

采用连续输注法,在自由活动的大鼠(n = 64)中研究了前列腺素(PG)D2的致眠作用与5-羟色胺能系统之间的相关性。用对氯苯丙氨酸(PCPA:450 mg/kg体重,腹腔注射)预处理的大鼠或未用PCPA预处理的大鼠,于11:00至17:00期间以100 pmol/0.2微升/分钟的速率向其第三脑室输注PGD2、5-羟色胺或其直接前体5-羟色氨酸(5HTP)。在PCPA预处理的失眠大鼠中,输注PGD2导致慢波睡眠(SWS)立即增加,异相睡眠(PS)在2小时潜伏期后增加。PGD2输注期间SWS和PS的总量分别为各自对照值的151%和154%。这些结果表明,PCPA对5-羟色胺和5HTP生物合成的抑制对PGD2的促睡眠作用影响很小。向PCPA预处理的大鼠输注5HTP所产生的短暂睡眠恢复几乎不受同时输注(200 pmol/0.2微升/分钟;07:00 - 17:00)环氧化酶抑制剂双氯芬酸钠的影响,这表明PGD2的产生与5HTP的睡眠恢复作用并无关键关联。因此,PGD2的促睡眠特性可能独立于睡眠 - 觉醒活动的5-羟色胺能调节。

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