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异氟烷麻醉会导致持续且逐渐加重的记忆损伤,使年轻而非成年啮齿动物的神经干细胞丢失,并减少神经发生。

Isoflurane anesthesia induced persistent, progressive memory impairment, caused a loss of neural stem cells, and reduced neurogenesis in young, but not adult, rodents.

机构信息

Center for Brain Repair and Rehabilitation, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

出版信息

J Cereb Blood Flow Metab. 2010 May;30(5):1017-30. doi: 10.1038/jcbfm.2009.274. Epub 2010 Jan 13.

Abstract

Isoflurane and related anesthetics are widely used to anesthetize children, ranging from premature babies to adolescents. Concerns have been raised about the safety of these anesthetics in pediatric patients, particularly regarding possible negative effects on cognition. The purpose of this study was to investigate the effects of repeated isoflurane exposure of juvenile and mature animals on cognition and neurogenesis. Postnatal day 14 (P14) rats and mice, as well as adult (P60) rats, were anesthetized with isoflurane for 35 mins daily for four successive days. Object recognition, place learning and reversal learning as well as cell death and cytogenesis were evaluated. Object recognition and reversal learning were significantly impaired in isoflurane-treated young rats and mice, whereas adult animals were unaffected, and these deficits became more pronounced as the animals grew older. The memory deficit was paralleled by a decrease in the hippocampal stem cell pool and persistently reduced neurogenesis, subsequently causing a reduction in the number of dentate gyrus granule cell neurons in isoflurane-treated rats. There were no signs of increased cell death of progenitors or neurons in the hippocampus. These findings show a previously unknown mechanism of neurotoxicity, causing cognitive deficits in a clearly age-dependent manner.

摘要

异氟醚和相关的麻醉剂被广泛用于麻醉儿童,范围从早产儿到青少年。人们对这些麻醉剂在儿科患者中的安全性表示担忧,特别是对其对认知可能产生的负面影响。本研究旨在研究幼年和成年动物反复暴露于异氟醚对认知和神经发生的影响。在出生后第 14 天(P14),用异氟醚麻醉大鼠和小鼠,每天 35 分钟,连续 4 天。评估了物体识别、位置学习和反转学习以及细胞死亡和细胞发生。异氟醚处理的幼鼠和幼鼠的物体识别和反转学习显著受损,而成年动物不受影响,随着动物年龄的增长,这些缺陷变得更加明显。记忆缺陷与海马干细胞池减少和持续减少的神经发生平行,随后导致异氟醚处理的大鼠齿状回颗粒细胞神经元数量减少。海马中没有祖细胞或神经元死亡增加的迹象。这些发现显示了一种以前未知的神经毒性机制,以明显的年龄依赖性方式导致认知缺陷。

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