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Antidepressants and REM sleep in Wistar-Kyoto and Sprague-Dawley rats.

机译:Wistar-Kyoto和Sprague-Dawley大鼠的抗抑郁药和REM睡眠。

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Compared to other rat strains, the Wistar-Kyoto rats show increased amount of REM sleep, one of the characteristic sleep changes observed in depressed patients. The aims of this study were firstly to validate a simple sleep stage discriminator and then compare the effect of antidepressants on suppression of rapid eye movement (REM) sleep in Wistar-Kyoto rats and an outbred rat strain (Sprague-Dawley). Rats were implanted with telemetry transmitters with electroencephalogram/electromyogram electrodes. Following recovery, the animals were orally dosed at light onset with either desipramine (20 mg/kg), fluoxetine (10 mg/kg), citalopram (10 or 40 mg/kg) or vehicle in a cross-over design. Every 12-s epoch was automatically scored as WAKE, NREM or REM sleep. Results confirm that Wistar-Kyoto rats show increased amount of REM sleep and decreased REM latency compared with Sprague-Dawley rats. All antidepressants significantly suppressed REM sleep in Sprague-Dawley rats, but only the high dose of citalopram suppressed REM sleep in Wistar-Kyoto rats. These findings suggest that the enhanced REM activity in Wistar-Kyoto rats is less sensitive to the effect of antidepressants and therefore does not provide any additional predictive validity for assessing antidepressant efficacy.
机译:与其他大鼠品系相比,Wistar-Kyoto大鼠的REM睡眠量增加,这是在抑郁症患者中观察到的特征性睡眠变化之一。这项研究的目的是首先验证一个简单的睡眠阶段鉴别器,然后比较抗抑郁药对Wistar-Kyoto大鼠和近交大鼠品系(Sprague-Dawley)抑制快速眼动(REM)睡眠的作用。大鼠被植入带有脑电图/肌电图电极的遥测发射机。恢复后,以交叉设计向动物口服地昔帕明(20 mg / kg),氟西汀(10 mg / kg),西酞普兰(10或40 mg / kg)或赋形剂。每12秒钟就会自动计为WAKE,NREM或REM睡眠。结果证实,与Sprague-Dawley大鼠相比,Wistar-Kyoto大鼠的REM睡眠量增加,REM潜伏期缩短。所有抗抑郁药均能显着抑制Sprague-Dawley大鼠的REM睡眠,但只有高剂量的西酞普兰能抑制Wistar-Kyoto大鼠的REM睡眠。这些发现表明,Wistar-Kyoto大鼠中增强的REM活性对抗抑郁药的作用较不敏感,因此不能为评估抗抑郁药的疗效提供任何其他预测效度。

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