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血清素和去甲肾上腺素摄取阻滞剂对猫的清醒和睡眠的影响。

Effects of serotonin and noradrenaline uptake blockers on wakefulness and sleep in cats.

作者信息

Hilakivi I, Kovala T, Leppävuori A, Shvaloff A

出版信息

Pharmacol Toxicol. 1987 Mar;60(3):161-6. doi: 10.1111/j.1600-0773.1987.tb01725.x.

DOI:10.1111/j.1600-0773.1987.tb01725.x
PMID:3473457
Abstract

The aim of the study was to examine the role of serotonergic (5-HT) and noradrenergic mechanisms in the regulation of wakefulness and sleep. For this purpose, adult cats with implanted electrodes for EEG, EOG and EMG were exposed to the 5-HT uptake blocker citalopram (0.1, 0.5 and 5.0 mg/kg intraperitoneally) and the noradrenaline uptake blocker prindamine (5 mg/kg intraperitoneally) at the start of continuous 16-hour sleep-wake recordings. Citalopram increased deep slow wave sleep and decreased REMS. Also prindamine decreased REMS but initially increased the proportion of time spent in the state of active wakefulness. Furthermore, to examine the interactions between 5-HT-nergic and noradrenergic mechanisms in the regulation of sleep, the administration of citalopram was preceded by intraperitoneal injections of phentolamine (10 mg/kg), an alpha-antagonist, and propranolol (5 mg/kg), a beta-antagonist. Phentolamine was totally ineffective against citalopram whereas propranolol partially counteracted the effects of citalopram on sleep. Prindamine was combined with the alpha-antagonists yohimbine (1 mg/kg), phentolamine (10 mg/kg) and prazosin (1 mg/kg) or with the beta-antagonist propranolol (5 mg/kg). Yohimbine was without any effect on REMS, phentolamine partly antagonized prindamine-induced decrease in the percentage of REMS, and prazosin only prolonged REMS latency and reduced deep SWS as well. Propranolol partially antagonized the prindamine-induced initial increase in active wakefulness time.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

该研究的目的是考察血清素能(5-羟色胺,5-HT)和去甲肾上腺素能机制在清醒和睡眠调节中的作用。为此,在连续16小时的睡眠-清醒记录开始时,对植入脑电图(EEG)、眼电图(EOG)和肌电图(EMG)电极的成年猫腹腔注射5-HT摄取阻滞剂西酞普兰(0.1、0.5和5.0毫克/千克)和去甲肾上腺素摄取阻滞剂丙咪嗪(5毫克/千克)。西酞普兰增加了深度慢波睡眠并减少了快速眼动睡眠(REMS)。丙咪嗪也减少了快速眼动睡眠,但最初增加了主动清醒状态下所花费的时间比例。此外,为了考察5-羟色胺能和去甲肾上腺素能机制在睡眠调节中的相互作用,在注射西酞普兰之前腹腔注射α拮抗剂酚妥拉明(10毫克/千克)和β拮抗剂普萘洛尔(5毫克/千克)。酚妥拉明对西酞普兰完全无效,而普萘洛尔部分抵消了西酞普兰对睡眠的影响。丙咪嗪与α拮抗剂育亨宾(1毫克/千克)、酚妥拉明(10毫克/千克)和哌唑嗪(1毫克/千克)或β拮抗剂普萘洛尔(5毫克/千克)联合使用。育亨宾对快速眼动睡眠没有任何影响,酚妥拉明部分拮抗丙咪嗪引起的快速眼动睡眠百分比下降,哌唑嗪仅延长了快速眼动睡眠潜伏期并减少了深度慢波睡眠。普萘洛尔部分拮抗丙咪嗪引起的主动清醒时间的最初增加。(摘要截选至250字)

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