Akanmu Moses A, Ukponmwan Otas E, Katayama Yoshifumi, Honda Kazuki
Department of Biosystem Regulation, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Tokyo 101-0062, Japan.
Neurosci Res. 2006 Mar;54(3):165-70. doi: 10.1016/j.neures.2005.11.006. Epub 2005 Dec 27.
PYY3-36 is a major component of the gut-brain axis and peripheral administration has been reported to exert significant effects on feeding, brain function and is more selective for neuropeptide Y2 receptor. Therefore, we investigated the effects of nocturnal intraperitoneal administration of single doses of PYY3-36 (30 and 100 microg/kg i.p.) on food intake, water intake and the sleep-wake cycle in rats. Sleep recordings were carried out in male Sprague-Dawley rats implanted with cortical electroencephalogram (EEG) and neck electromyogram (EMG) electrodes. The EEG, EMG, food intake and water intake were assessed. The electrographic recordings obtained were scored visually as rapid eye movement (REM) sleep, non-REM (NREM) sleep and wakefulness. PYY3-36 administration 15 min prior to dark onset significantly (p<0.05) increased non-rapid eye movement (NREM) sleep and decreased wakefulness. Analysis of the dark-period at 4-h time intervals showed that nocturnal administration of PYY3-36 (30 and 100 microg/kg) significantly suppressed wakefulness and increased non-REM sleep during the first 4-h time interval. Time spent in wakefulness was significantly decreased after administration of PYY3-36 (30 and 100 microg/kg) when compared with administration of vehicle. In addition, PYY3-36 (30 and 100 microg/kg i.p.) induced an increase in the time spent in NREM sleep. The nocturnal intraperitoneal administration of the lower dose of PYY3-36 (30 microg/kg) also significantly decreased food intake [F (2,23)=4.90, p<0.05] but had no effect on water intake. These findings suggest that PYY3-36 may play an important role in the enhancement of NREM sleep and feeding behavior.
PYY3-36是肠-脑轴的主要组成部分,据报道,外周给药对进食、脑功能有显著影响,且对神经肽Y2受体更具选择性。因此,我们研究了夜间腹腔注射单剂量PYY3-36(30和100微克/千克腹腔注射)对大鼠食物摄入、水摄入和睡眠-觉醒周期的影响。在植入皮质脑电图(EEG)和颈部肌电图(EMG)电极的雄性Sprague-Dawley大鼠中进行睡眠记录。评估脑电图、肌电图、食物摄入和水摄入情况。对获得的电图记录进行视觉评分,分为快速眼动(REM)睡眠、非快速眼动(NREM)睡眠和清醒状态。在黑暗开始前15分钟给予PYY3-36显著(p<0.05)增加了非快速眼动(NREM)睡眠并减少了清醒时间。以4小时时间间隔对黑暗期进行分析表明,夜间给予PYY3-36(30和100微克/千克)在第一个4小时时间间隔内显著抑制了清醒并增加了非快速眼动睡眠。与给予赋形剂相比,给予PYY3-36(30和100微克/千克)后清醒时间显著减少。此外,PYY3-36(30和100微克/千克腹腔注射)使非快速眼动睡眠的时间增加。夜间腹腔注射较低剂量的PYY3-36(30微克/千克)也显著减少了食物摄入量[F(2,23)=4.90,p<0.05],但对水摄入量没有影响。这些发现表明,PYY3-36可能在增强非快速眼动睡眠和进食行为中起重要作用。