Touitou Yvan, Mauvieux Benoit, Reinberg Alain, Dispersyn Garance
a Unité de Chronobiologie, Fondation A. de Rothschild , Paris , France.
b INSERM UMR U1075, Université de Caen , Caen , France.
Chronobiol Int. 2016;33(9):1247-1254. doi: 10.1080/07420528.2016.1208664. Epub 2016 Jul 27.
The circadian time structure of an organism can be desynchronized in a large number of instances, including the intake of specific drugs. We have previously found that propofol, which is a general anesthetic, induces a desynchronization of the circadian time structure in rats, with a 60-80 min significant phase advance of body temperature circadian rhythm. We thus deemed it worthwhile to examine whether this phase shift of body temperature was related to a modification of the circadian period Tau. Propofol was administered at three different Zeitgeber Times (ZTs): ZT6 (middle of the rest period), ZT10 (2 h prior to the beginning of activity period), ZT16 (4 h after the beginning of the activity period), with ZT0 being the beginning of the rest period (light onset) and ZT12 being the beginning of the activity period (light offset). Control rats (n = 20) were injected at the same ZTs with 10% intralipid, which is a control lipidic solution. Whereas no modification of the circadian period of body temperature was observed in the control rats, propofol administration resulted in a significant shortening of the period by 96 and 180 min at ZT6 and ZT10, respectively. By contrast, the period was significantly lengthened by 90 min at ZT16. We also found differences in the time it took for the rats to readjust their body temperature to the original 24-h rhythm. At ZT16, the speed of readjustment was more rapid than at the two other ZTs that we investigated. This study hence shows (i) the disruptive effects of the anesthetic propofol on the body temperature circadian rhythm, and it points out that (ii) the period Tau for body temperature responds to this anesthetic drug according to a Tau-response curve. By sustaining postoperative sleep-wake disorders, the disruptive effects of propofol on circadian time structure might have important implications for the use of this drug in humans.
生物体的昼夜节律时间结构在很多情况下会被打乱,包括摄入特定药物。我们之前发现,作为一种全身麻醉剂的丙泊酚会导致大鼠昼夜节律时间结构失调,体温昼夜节律会显著提前60 - 80分钟。因此,我们认为有必要研究体温的这种相位变化是否与昼夜节律周期Tau的改变有关。在三个不同的授时时间(ZT)给予丙泊酚:ZT6(休息期中期)、ZT10(活动期开始前2小时)、ZT16(活动期开始后4小时),其中ZT0为休息期开始(光照开始),ZT12为活动期开始(光照结束)。对照组大鼠(n = 20)在相同的ZT时间注射10%的脂质乳剂,这是一种对照脂质溶液。虽然在对照组大鼠中未观察到体温昼夜节律周期的改变,但在ZT6和ZT10给予丙泊酚分别导致周期显著缩短96分钟和180分钟。相比之下,在ZT16时周期显著延长90分钟。我们还发现大鼠将体温重新调整到原来的24小时节律所需的时间存在差异。在ZT16时,重新调整的速度比我们研究的其他两个ZT时间更快。因此,本研究表明:(i)麻醉剂丙泊酚对体温昼夜节律有破坏作用,并且指出(ii)体温的周期Tau根据Tau反应曲线对这种麻醉药物作出反应。由于丙泊酚对昼夜节律时间结构的破坏作用会持续术后睡眠 - 觉醒障碍,这可能对该药物在人类中的使用具有重要意义。