Murray Nicholas M, Buchanan Gordon F, Richerson George B
Department of Neurology, University of Iowa Carver College of Medicine, Iowa City, IA.
Department of Neurology, Yale School of Medicine, New Haven, CT.
Sleep. 2015 Dec 1;38(12):1985-93. doi: 10.5665/sleep.5256.
Serotonin (5-hydroxytryptamine, 5-HT) neurons are now thought to promote wakefulness. Early experiments using the tryptophan hydroxylase inhibitor para-chlorophenylalanine (PCPA) had led to the opposite conclusion, that 5-HT causes sleep, but those studies were subsequently contradicted by electrophysiological and behavioral data. Here we tested the hypothesis that the difference in conclusions was due to failure of early PCPA experiments to control for the recently recognized role of 5-HT in thermoregulation.
Adult male C57BL/6N mice were treated with PCPA (800 mg/kg intraperitoneally for 5 d; n = 15) or saline (n = 15), and housed at 20 °C (normal room temperature) or at 33 °C (thermoneutral for mice) for 24 h. In a separate set of experiments, mice were exposed to 4 °C for 4 h to characterize their ability to thermoregulate.
PCPA treatment reduced brain 5-HT to less than 12% of that of controls. PCPA-treated mice housed at 20 °C spent significantly more time awake than controls. However, core body temperature decreased from 36.5 °C to 35.1 °C. When housed at 33 °C, body temperature remained normal, and total sleep duration, sleep architecture, and time in each vigilance state were the same as controls. When challenged with 4 °C, PCPA-treated mice experienced a precipitous drop in body temperature, whereas control mice maintained a normal body temperature.
These results indicate that early experiments using para-chlorophenylalanine that led to the conclusion that 5-hydroxytryptamine (5-HT) causes sleep were likely confounded by hypothermia. Temperature controls should be considered in experiments using 5-HT depletion.
血清素(5-羟色胺,5-HT)神经元目前被认为可促进清醒。早期使用色氨酸羟化酶抑制剂对氯苯丙氨酸(PCPA)的实验得出了相反的结论,即5-HT会导致睡眠,但这些研究随后被电生理和行为数据所反驳。在此,我们检验了这样一个假设,即结论差异的原因是早期PCPA实验未能控制5-HT在体温调节中最近被认识到的作用。
成年雄性C57BL/6N小鼠接受PCPA(800mg/kg腹腔注射,持续5天;n = 15)或生理盐水(n = 15)处理,并在20°C(正常室温)或33°C(小鼠的热中性温度)饲养24小时。在另一组实验中,将小鼠暴露于4°C环境4小时以表征其体温调节能力。
PCPA处理使大脑5-HT水平降至对照组的12%以下。饲养在20°C的PCPA处理小鼠清醒时间显著多于对照组。然而,核心体温从36.5°C降至35.1°C。当饲养在33°C时,体温保持正常,总睡眠时间、睡眠结构以及各警觉状态下的时间与对照组相同。当受到4°C刺激时,PCPA处理小鼠体温急剧下降,而对照小鼠保持正常体温。
这些结果表明,早期使用对氯苯丙氨酸得出5-羟色胺(5-HT)导致睡眠这一结论的实验可能因体温过低而产生混淆。在使用5-HT耗竭的实验中应考虑温度控制。