Ju Xianshu, Ryu Min Jeong, Cui Jianchen, Lee Yulim, Park Sangil, Hong Boohwi, Yoo Sungho, Lee Won Hyung, Shin Yong Sup, Yoon Seok-Hwa, Kweon Gi Ryang, Kim Yoon Hee, Ko Youngkwon, Heo Jun Young, Chung Woosuk
Department of Biochemistry, Chungnam National University School of Medicine, Daejeon, South Korea.
Department of Medical Science, Chungnam National University School of Medicine, Daejeon, South Korea.
Front Cell Neurosci. 2020 Jan 28;14:4. doi: 10.3389/fncel.2020.00004. eCollection 2020.
Preclinical animal studies have continuously reported the possibility of long-lasting neurotoxic effects after general anesthesia in young animals. Such studies also show that the neurological changes induced by anesthesia in young animals differ by their neurodevelopmental stage. Exposure to anesthetic agents increase dendritic spines and induce sex-dependent changes of excitatory/inhibitory synaptic transmission in late postnatal mice, a critical synaptogenic period. However, the mechanisms underlying these changes remain unclear. Abnormal activation of the mammalian target of rapamycin (mTOR) signaling pathway, an important regulator of neurodevelopment, has also been shown to induce similar changes during neurodevelopment. Interestingly, previous studies show that exposure to general anesthetics during neurodevelopment can activate the mTOR signaling pathway. This study, therefore, evaluated the role of mTOR signaling after exposing postnatal day (PND) 16/17 mice to sevoflurane, a widely used inhalation agent in pediatric patients. We first confirmed that a 2-h exposure of 2.5% sevoflurane could induce widespread mTOR phosphorylation in both male and female mice. Pretreatment with the mTOR inhibitor rapamycin not only prevented anesthesia-induced mTOR phosphorylation, but also the increase in mitochondrial respiration and male-dependent enhancement of excitatory synaptic transmission. However, the changes in inhibitory synaptic transmission that appear after anesthesia in female mice were not affected by rapamycin pretreatment. Our results suggest that mTOR inhibitors may act as potential therapeutic agents for anesthesia-induced changes in the developing brain.
临床前动物研究不断报道幼龄动物全身麻醉后可能产生持久的神经毒性作用。此类研究还表明,幼龄动物麻醉诱导的神经学变化因其神经发育阶段而异。在出生后晚期小鼠(关键的突触发生期),接触麻醉剂会增加树突棘,并诱导兴奋性/抑制性突触传递的性别依赖性变化。然而,这些变化背后的机制仍不清楚。雷帕霉素哺乳动物靶点(mTOR)信号通路作为神经发育的重要调节因子,其异常激活也已被证明在神经发育过程中会诱导类似变化。有趣的是,先前的研究表明,神经发育期间接触全身麻醉剂可激活mTOR信号通路。因此,本研究评估了出生后第16/17天的小鼠暴露于七氟醚(儿科患者中广泛使用的吸入剂)后mTOR信号通路的作用。我们首先证实,2.5%七氟醚暴露2小时可诱导雄性和雌性小鼠广泛的mTOR磷酸化。用mTOR抑制剂雷帕霉素预处理不仅可防止麻醉诱导的mTOR磷酸化,还可防止线粒体呼吸增加以及雄性依赖性兴奋性突触传递增强。然而,雌性小鼠麻醉后出现的抑制性突触传递变化不受雷帕霉素预处理的影响。我们的结果表明,mTOR抑制剂可能作为麻醉诱导发育中大脑变化的潜在治疗药物。