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背缝核中的 5-羟色胺能神经元介导孤啡肽在雄性大鼠异氟烷麻醉期间促觉醒的作用。

Serotonergic neurons in the dorsal raphe nucleus mediate the arousal-promoting effect of orexin during isoflurane anesthesia in male rats.

机构信息

Department of Anesthesiology and Perioperative Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, Shaanxi, China; Department of Anesthesiology, Shenzhen University General Hospital, Shenzhen University, Shenzhen, Guangdong Province 518055, China.

Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of stomatology, Xi'an Jiaotong University, Xi'an 710032, Shaanxi, China.

出版信息

Neuropeptides. 2019 Jun;75:25-33. doi: 10.1016/j.npep.2019.03.004. Epub 2019 Mar 20.

Abstract

Previous studies have demonstrated that the activation of orexinergic neurons facilitates the recovery of animals from general anesthesia. Moreover, serotonergic neurons that receive projections from orexin neurons have also been shown to participate in sleep-wakefulness regulation. In the present study, we aimed to explore whether orexinergic neurons facilitate emergence from isoflurane anesthesia in rats by activating serotonergic neurons. Orexin A (30 or 100 pmol), orexin B (30 or 100 pmol), and their respective antagonists SB-334867 and TCS-OX2-29 (5 or 20 μg) were microinjected into the dorsal raphe nucleus (DRN) of rats, and their effects on induction and emergence times were analyzed. Electroencephalogram (EEG) changes were also recorded and analyzed to illuminate the effect of orexin injection into the DRN on cortical excitability under isoflurane anesthesia. Activation of serotonergic neurons was detected via immunohistochemical analysis of c-Fos expression following orexin administration. Our results indicated that injection of neither orexins nor orexin antagonists into the rat DRN exerted an impact on induction time, whereas orexin-A injection (100 pmol) enhanced arousal when compared with the saline group. In contrast, administration of orexin receptor type 1 antagonist SB-334867 (20 μg) prolonged emergence time from isoflurane anesthesia. Microinjection of orexin-A induced an arousal pattern on EEG, and decreased the burst suppression ratio under isoflurane anesthesia. Isoflurane anesthesia inhibited the activity of serotonergic neurons, as shown by decrease in the number of c-Fos-immunoreactive serotonergic neurons when compared with the sham group. This inhibitory effect was partially reversed by administration of orexin-A. Taken together, our findings suggest that orexinergic signals facilitate emergence from isoflurane anesthesia, at least partially, by reversing the effects of isoflurane on serotonergic neurons of the DRN.

摘要

先前的研究表明,孤啡肽能神经元的激活有助于动物从全身麻醉中恢复。此外,接收孤啡肽神经元投射的 5-羟色胺能神经元也被证明参与了睡眠觉醒调节。在本研究中,我们旨在通过激活 5-羟色胺能神经元来探索孤啡肽能神经元是否有助于大鼠从异氟醚麻醉中苏醒。将孤啡肽 A(30 或 100 pmol)、孤啡肽 B(30 或 100 pmol)及其各自的拮抗剂 SB-334867 和 TCS-OX2-29(5 或 20 μg)微注射到大鼠中脑导水管周围灰质(DRN),并分析它们对诱导和苏醒时间的影响。还记录和分析脑电图(EEG)变化,以阐明孤啡肽注射到 DRN 对异氟醚麻醉下皮质兴奋性的影响。通过孤啡肽给药后 c-Fos 表达的免疫组织化学分析检测 5-羟色胺能神经元的激活。结果表明,孤啡肽或孤啡肽拮抗剂注射到大鼠 DRN 均不会影响诱导时间,而孤啡肽-A 注射(100 pmol)与生理盐水组相比增强了觉醒。相反,孤啡肽受体 1 拮抗剂 SB-334867(20 μg)给药延长了异氟醚麻醉的苏醒时间。孤啡肽-A 注射引起 EEG 上的觉醒模式,并降低异氟醚麻醉下的爆发抑制比。与假手术组相比,异氟醚麻醉抑制了 5-羟色胺能神经元的活性,表现为 c-Fos 免疫反应性 5-羟色胺能神经元数量减少。孤啡肽-A 的给药部分逆转了这种抑制作用。总之,我们的研究结果表明,孤啡肽能信号至少部分通过逆转异氟醚对 DRN 5-羟色胺能神经元的作用来促进异氟醚麻醉的苏醒。

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