Department of Neurology, Shanghai Jiao Tong University, Affiliated Sixth People' s Hospital, NO. 222, Huanhuxisan Road, Shanghai, 201306, PR China.
Department of Anesthesiology, Shanghai Jiao Tong University, Affiliated Sixth People' s Hospital, NO. 222, Huanhuxisan Road, Shanghai, 201306, PR China.
Behav Brain Res. 2021 Aug 6;411:113380. doi: 10.1016/j.bbr.2021.113380. Epub 2021 May 24.
Previous studies have shown that the synchronization of electroencephalogram (EEG) signals is found during propofol-induced general anesthesia, which is similar to that of slow-wave sleep (SWS). However, a complete understanding is lacking in terms of the characteristics of EEG changes in rats after propofol administration and whether propofol acts through natural sleep circuits. Here, we examined the characteristics of EEG patterns induced by intraperitoneal injection of propofol in rats. We found that high (10 mg/kg) and medium (5 mg/kg) doses of propofol induced a cortical EEG of low-frequency, high-amplitude activity with rare electromyographic activity and markedly shortened sleep latency. The high dose of propofol increased deep slow-wave sleep (SWS2) to 4 h, as well as the number of large SWS2 bouts (>480 s), their mean duration and the peak of the power density curve in the delta range of 0.75-3.25 Hz. After the medium dose of propofol, the total number of wakefulness, light slow-wave sleep (SWS1) and SWS2 episodes increased, whereas the mean duration of wakefulness decreased. The high dose of propofol significantly increased c-fos expression in the ventrolateral preoptic nucleus (VLPO) sleep center and decreased the number of c-fos-immunoreactive neurons in wake-related systems including the tuberomammillary nucleus (TMN), perifornical nucleus (PeF), lateral hypothalamic nucleus (LH), ventrolateral periaqueductal gray (vPAG) and supramammillary region (SuM). These results indicated that the high dose of propofol produced high-quality sleep by increasing SWS2, whereas the medium dose produced fragmented and low-quality sleep by disrupting the continuity of wakefulness. Furthermore, sleep-promoting effects of propofol are correlated with activation of the VLPO cluster and inhibition of the TMN, PeF, LH, vPAG and SuM.
先前的研究表明,丙泊酚诱导的全身麻醉期间发现脑电图(EEG)信号同步,这与慢波睡眠(SWS)相似。然而,对于丙泊酚给药后大鼠 EEG 变化的特征以及丙泊酚是否通过自然睡眠回路起作用,尚缺乏全面的了解。在这里,我们检查了腹腔注射丙泊酚在大鼠中诱导的 EEG 模式的特征。我们发现,高(10mg/kg)和中(5mg/kg)剂量的丙泊酚诱导出低频、高振幅活动的皮质 EEG,肌电图活动很少,睡眠潜伏期明显缩短。高剂量的丙泊酚将深度慢波睡眠(SWS2)增加到 4 小时,并且大 SWS2 发作(>480s)的数量、它们的平均持续时间和 0.75-3.25Hz 的 delta 范围内的功率密度曲线的峰值增加。中剂量的丙泊酚后,觉醒、轻度慢波睡眠(SWS1)和 SWS2 发作的总次数增加,而觉醒的平均持续时间减少。高剂量的丙泊酚显著增加了腹外侧视前核(VLPO)睡眠中心的 c-fos 表达,并且减少了与觉醒相关的系统(包括结节乳头核(TMN)、peri 穹窿核(PeF)、外侧下丘脑核(LH)、腹外侧导水管周围灰质(vPAG)和穹窿上区(SuM)中的 c-fos-免疫反应性神经元的数量。这些结果表明,高剂量的丙泊酚通过增加 SWS2 产生高质量的睡眠,而中剂量的丙泊酚通过破坏觉醒的连续性产生碎片化和低质量的睡眠。此外,丙泊酚的促眠作用与 VLPO 簇的激活和 TMN、PeF、LH、vPAG 和 SuM 的抑制相关。