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丙泊酚麻醉诱导发育中大鼠脑内细胞死亡的潜在机制。

Potential mechanism of cell death in the developing rat brain induced by propofol anesthesia.

作者信息

Pesić Vesna, Milanović Desanka, Tanić Nikola, Popić Jelena, Kanazir Selma, Jevtović-Todorović Vesna, Ruzdijić Sabera

机构信息

Department of Neurobiology, Institute for Biological Research, University of Belgrade, Bulevar despota Stefana 142, 11060 Belgrade, Serbia.

出版信息

Int J Dev Neurosci. 2009 May;27(3):279-87. doi: 10.1016/j.ijdevneu.2008.12.005. Epub 2008 Dec 27.

Abstract

Commonly used general anesthetics can have adverse effects on the developing brain by triggering apoptotic neurodegeneration, as has been documented in the rat. The rational of our study was to examine the molecular mechanisms that contribute to the apoptotic action of propofol anesthesia in the brain of 7-day-old (P7) rats. The down-regulation of nerve growth factor (NGF) mRNA and protein expression in the cortex and thalamus at defined time points between 1 and 24h after the propofol treatment, as well as a decrease of phosphorylated Akt were observed. The extrinsic apoptotic pathway was induced by over-expression of tumor necrosis factor (TNF) which led to the activation of caspase-3 in both examined structures. Neurodegeneration was confirmed by Fluoro-Jade B staining. Our findings provide direct experimental evidence that the anesthetic dose (25mg/kg) of propofol induces complex changes that are accompanied by cell death in the cortex and thalamus of the developing rat brain.

摘要

常用的全身麻醉剂可通过引发凋亡性神经退行性变对发育中的大脑产生不良影响,这在大鼠中已有记载。我们研究的目的是探究导致丙泊酚麻醉对7日龄(P7)大鼠大脑产生凋亡作用的分子机制。在丙泊酚治疗后1至24小时的特定时间点,观察到皮质和丘脑神经生长因子(NGF)mRNA和蛋白表达下调,以及磷酸化Akt减少。肿瘤坏死因子(TNF)过表达诱导了外在凋亡途径,导致两个检测结构中的半胱天冬酶-3激活。通过Fluoro-Jade B染色证实了神经退行性变。我们的研究结果提供了直接的实验证据,表明麻醉剂量(25mg/kg)的丙泊酚会在发育中的大鼠大脑皮质和丘脑中引起复杂变化并伴有细胞死亡。

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