Johnson Stephen A, Young Chainllie, Olney John W
Department of Psychiatry, Washington University School of Medicine, St Louis, MO 63110, USA.
J Neurosurg Anesthesiol. 2008 Jan;20(1):21-8. doi: 10.1097/ANA.0b013e3181271850.
Drugs that suppress neuronal activity, including general anesthetics used in pediatric and obstetric medicine, trigger neuroapoptosis in the developing rodent brain. Exposure of infant rats for 6 hours to a combination of anesthetic drugs (midazolam, nitrous oxide, isoflurane) reportedly causes widespread apoptotic neurodegeneration, followed by lifelong cognitive deficits. Isoflurane, the dominant ingredient in this triple cocktail, has not been evaluated individually for apoptogenic potential. It was recently reported that (1) the minimum alveolar concentration (MAC) for anesthetizing infant mice with isoflurane is 2.26%, and; (2) that infant mice, without assisted respiration, maintain normal arterial oxygen values but become hypoglycemic when exposed to isoflurane 3% for 30 minutes, then 1.8% for 1 hour (1.46 MAC-hours). In the present experiments, infant mice were exposed to isoflurane at various sub-MAC concentrations and durations, and the brains were evaluated quantitatively 5 hours after initiation of anesthesia exposure to determine the number of neuronal profiles undergoing apoptosis. Blood glucose values were also determined under each of these conditions. All conditions tested (isoflurane at 0.75% for 4 h, 1.5% for 2 h, 2.0% for 1 h) triggered a statistically significant increase in neuroapoptosis compared with the rate of spontaneous apoptosis in littermate controls. Blood glucose determinations ruled out hypoglycemia as a potential cause of the brain damage. It is concluded that exposure to sub-MAC concentrations of isoflurane for one or more hours triggers neuroapoptosis in the infant mouse brain. These findings are consistent with other recent evidence demonstrating that brief exposure to ethanol, ketamine, or midazolam triggers neuroapoptosis in the developing mouse brain.
抑制神经元活动的药物,包括儿科和产科医学中使用的全身麻醉剂,会引发发育中的啮齿动物大脑中的神经细胞凋亡。据报道,将幼鼠暴露于麻醉药物(咪达唑仑、一氧化二氮、异氟烷)的组合中6小时会导致广泛的凋亡性神经退行性变,随后出现终身认知缺陷。异氟烷是这种三联麻醉剂中的主要成分,尚未单独评估其诱导凋亡的潜力。最近有报道称:(1)用异氟烷麻醉幼鼠的最低肺泡浓度(MAC)为2.26%;(2)在无辅助呼吸的情况下,幼鼠暴露于3%异氟烷30分钟,然后1.8%异氟烷1小时(1.46 MAC小时)时,动脉血氧值保持正常,但会出现低血糖。在本实验中,将幼鼠暴露于不同的亚MAC浓度和持续时间的异氟烷中,并在麻醉暴露开始5小时后对大脑进行定量评估,以确定发生凋亡的神经元轮廓数量。在每种情况下还测定了血糖值。与同窝对照的自发凋亡率相比,所有测试条件(0.75%异氟烷4小时、1.5%异氟烷2小时、2.0%异氟烷1小时)均引发了神经细胞凋亡的统计学显著增加。血糖测定排除了低血糖是脑损伤潜在原因的可能性。得出的结论是,暴露于亚MAC浓度的异氟烷1小时或更长时间会引发幼鼠大脑中的神经细胞凋亡。这些发现与最近的其他证据一致,这些证据表明,短暂暴露于乙醇、氯胺酮或咪达唑仑会引发发育中小鼠大脑中的神经细胞凋亡。