Gascon E, Klauser P, Kiss J Z, Vutskits L
University of Geneva Medical School, Department of Anesthesiology, Pharmacology and Intensive Care, Geneva, Switzerland.
Eur J Anaesthesiol. 2007 Mar;24(3):213-24. doi: 10.1017/S0265021506002365. Epub 2007 Jan 30.
A growing body of experimental evidence suggests that anaesthetics, by influencing GABAergic and glutaminergic neural signalling, can have adverse effects on the developing central nervous system. The biological foundation for this is that gamma-aminobutyric acid and glutamate could act non-synaptically, in addition to their role in neurotransmission in the adult brain, in the regulation of neuronal development in the central nervous system. These neurotransmitters and their receptors are expressed from very early stages of central nervous system development and appear to influence neural progenitor proliferation, cell migration and neuronal differentiation. During the synaptogenetic period, pharmacological blockade of N-methyl-d-aspartate (NMDA)-type glutamate receptors as well as stimulation of GABAA receptors has been reported to be associated with increased apoptosis in the developing brain. Importantly, recent data suggest that even low, non-apoptogenic concentrations of anaesthetics can perturb neuronal dendritic development and thus could potentially lead to impairment of developing neuronal networks. The extrapolation of these experimental observations to clinical practice is of course very difficult and requires extreme caution as differences in drug concentrations and exposure times as well as interspecies variations are all important confounding variables. While clinicians should clearly not withhold anaesthesia based on current animal studies, these observations should urge more laboratory and clinical research to further elucidate this issue.
越来越多的实验证据表明,麻醉药通过影响γ-氨基丁酸(GABA)能和谷氨酸能神经信号传导,可能会对发育中的中枢神经系统产生不良影响。其生物学基础在于,γ-氨基丁酸和谷氨酸除了在成人大脑中发挥神经传递作用外,还可在中枢神经系统神经元发育的调节中发挥非突触作用。这些神经递质及其受体在中枢神经系统发育的早期阶段就开始表达,并且似乎会影响神经祖细胞的增殖、细胞迁移和神经元分化。在突触发生期,据报道,N-甲基-D-天冬氨酸(NMDA)型谷氨酸受体的药理学阻断以及GABAA受体的刺激与发育中大脑的细胞凋亡增加有关。重要的是,最近的数据表明,即使是低浓度、非致凋亡浓度的麻醉药也会干扰神经元树突的发育,从而可能导致发育中的神经网络受损。当然,将这些实验观察结果外推至临床实践非常困难,需要格外谨慎,因为药物浓度和暴露时间的差异以及种间差异都是重要的混杂变量。虽然临床医生显然不应基于当前的动物研究而拒绝给予麻醉,但这些观察结果应促使更多的实验室和临床研究进一步阐明这一问题。