Isoflurane preconditioning induced genomic changes in mouse cortex

Umeshkumar Athiraman , Tusar Giri
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引用次数: 0

Abstract

Background

Altered patterns of genetic expression induced by isoflurane preconditioning in mouse brain have not yet been investigated. The aim of our pilot study is to examine the temporal sequence of changes in the transcriptome of mouse brain cortex produced by isoflurane preconditioning.

Methods

Twelve-wk-old wild-type (C57BL/6J) male mice were randomly assigned for the experiments. Mice were exposed to isoflurane 2% in air for 1 h and brains were harvested at the following time points—immediately (0 h), and at 6, 12, 24, 36, 48, and 72 h after isoflurane exposure. A separate cohort of mice were exposed to three doses of isoflurane on days 1, 2, and 3 and brains were harvested after the third exposure. The NanoString mouse neuropathology panel was used to analyse isoflurane-induced gene expression in the cortex. The neuropathology panel included 760 genes covering pathways involved in neurodegeneration and other nervous system diseases, and 10 internal reference genes for data normalisation.

Results

Genes involving several pathways were upregulated and downregulated by isoflurane preconditioning. Interestingly, a biphasic response was noted, meaning, an early expression of genes (until 6 h), followed by a transient pause (until 24 h), and a second wave of genomic response beginning at 36 h of isoflurane exposure was noted.

Conclusions

Isoflurane preconditioning induces significant alterations in the genes involved in neurodegeneration and other nervous system disorders in a temporal sequence. These data could aid in the identification of molecular mechanisms behind isoflurane preconditioning-induced neuroprotection in various central nervous system diseases.

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异氟烷预处理诱导小鼠皮层基因组变化
背景尚未研究过异氟烷预处理诱导的小鼠大脑基因表达模式的改变。我们的试验性研究旨在研究异氟醚预处理引起的小鼠大脑皮层转录组变化的时间顺序。小鼠在空气中暴露于 2% 的异氟烷 1 小时,并在以下时间点收获大脑:立即(0 小时)、暴露于异氟烷后 6、12、24、36、48 和 72 小时。另一组小鼠在第 1、2 和 3 天暴露于三种剂量的异氟烷,在第三次暴露后收获大脑。NanoString 小鼠神经病理学面板用于分析异氟醚诱导的皮层基因表达。神经病理学面板包括 760 个基因,涵盖神经变性和其他神经系统疾病的相关通路,以及 10 个用于数据归一化的内部参考基因。有趣的是,研究人员注意到了一种双相反应,即基因的早期表达(直到 6 小时),随后是短暂的停顿(直到 24 小时),而第二波基因组反应则从异氟烷暴露 36 小时开始。这些数据有助于确定异氟醚预处理诱导神经保护作用在各种中枢神经系统疾病中的分子机制。
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来源期刊
BJA open
BJA open Anesthesiology and Pain Medicine
CiteScore
0.60
自引率
0.00%
发文量
0
审稿时长
83 days
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