Jevtovic-Todorovic Vesna, Hartman Richard E, Izumi Yukitoshi, Benshoff Nicholas D, Dikranian Krikor, Zorumski Charles F, Olney John W, Wozniak David F
Department of Anesthesiology, University of Virginia Health System, Charlottesville, Virginia 22908, USA.
J Neurosci. 2003 Feb 1;23(3):876-82. doi: 10.1523/JNEUROSCI.23-03-00876.2003.
Recently it was demonstrated that exposure of the developing brain during the period of synaptogenesis to drugs that block NMDA glutamate receptors or drugs that potentiate GABA(A) receptors can trigger widespread apoptotic neurodegeneration. All currently used general anesthetic agents have either NMDA receptor-blocking or GABA(A) receptor-enhancing properties. To induce or maintain a surgical plane of anesthesia, it is common practice in pediatric or obstetrical medicine to use agents from these two classes in combination. Therefore, the question arises whether this practice entails significant risk of inducing apoptotic neurodegeneration in the developing human brain. To begin to address this problem, we have administered to 7-d-old infant rats a combination of drugs commonly used in pediatric anesthesia (midazolam, nitrous oxide, and isoflurane) in doses sufficient to maintain a surgical plane of anesthesia for 6 hr, and have observed that this causes widespread apoptotic neurodegeneration in the developing brain, deficits in hippocampal synaptic function, and persistent memory/learning impairments.
最近有研究表明,在突触发生期,发育中的大脑暴露于阻断NMDA谷氨酸受体的药物或增强GABAA受体的药物下,可引发广泛的凋亡性神经退行性变。目前所有常用的全身麻醉剂都具有NMDA受体阻断或GABAA受体增强特性。为诱导或维持手术麻醉平面,儿科或产科医学中常用这两类药物联合使用。因此,问题就出现了,这种做法是否会给发育中的人类大脑带来引发凋亡性神经退行性变的重大风险。为了开始解决这个问题,我们给7日龄的幼鼠注射了儿科麻醉中常用的药物组合(咪达唑仑、一氧化二氮和异氟烷),剂量足以维持手术麻醉平面6小时,并且观察到这会在发育中的大脑中引发广泛的凋亡性神经退行性变、海马突触功能缺陷以及持续的记忆/学习障碍。