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全身麻醉会抑制小鼠大脑缺氧条件下促红细胞生成素的诱导。

General anesthetics inhibit erythropoietin induction under hypoxic conditions in the mouse brain.

机构信息

Department of Anesthesia, Kyoto University Hospital, Kyoto, Japan.

出版信息

PLoS One. 2011;6(12):e29378. doi: 10.1371/journal.pone.0029378. Epub 2011 Dec 27.

Abstract

BACKGROUND

Erythropoietin (EPO), originally identified as a hematopoietic growth factor produced in the kidney and fetal liver, is also endogenously expressed in the central nervous system (CNS). EPO in the CNS, mainly produced in astrocytes, is induced under hypoxic conditions in a hypoxia-inducible factor (HIF)-dependent manner and plays a dominant role in neuroprotection and neurogenesis. We investigated the effect of general anesthetics on EPO expression in the mouse brain and primary cultured astrocytes.

METHODOLOGY/PRINCIPAL FINDINGS: BALB/c mice were exposed to 10% oxygen with isoflurane at various concentrations (0.10-1.0%). Expression of EPO mRNA in the brain was studied, and the effects of sevoflurane, halothane, nitrous oxide, pentobarbital, ketamine, and propofol were investigated. In addition, expression of HIF-2α protein was studied by immunoblotting. Hypoxia-induced EPO mRNA expression in the brain was significantly suppressed by isoflurane in a concentration-dependent manner. A similar effect was confirmed for all other general anesthetics. Hypoxia-inducible expression of HIF-2α protein was also significantly suppressed with isoflurane. In the experiments using primary cultured astrocytes, isoflurane, pentobarbital, and ketamine suppressed hypoxia-inducible expression of HIF-2α protein and EPO mRNA.

CONCLUSIONS/SIGNIFICANCE: Taken together, our results indicate that general anesthetics suppress activation of HIF-2 and inhibit hypoxia-induced EPO upregulation in the mouse brain through a direct effect on astrocytes.

摘要

背景

促红细胞生成素(EPO)最初被鉴定为一种在肾脏和胎肝中产生的造血生长因子,也在内源性表达于中枢神经系统(CNS)中。CNS 中的 EPO 主要由星形胶质细胞产生,在缺氧诱导因子(HIF)依赖性方式下,在缺氧条件下诱导产生,并在神经保护和神经发生中发挥主导作用。我们研究了全身麻醉药对小鼠大脑和原代培养星形胶质细胞中 EPO 表达的影响。

方法/主要发现:BALB/c 小鼠暴露于不同浓度(0.10-1.0%)的异氟烷 10%氧气中。研究了大脑中 EPO mRNA 的表达,并研究了七氟醚、氟烷、一氧化二氮、戊巴比妥、氯胺酮和丙泊酚的作用。此外,通过免疫印迹研究了 HIF-2α 蛋白的表达。异氟烷以浓度依赖性方式显著抑制了脑内缺氧诱导的 EPO mRNA 表达。所有其他全身麻醉药也证实了类似的效果。缺氧诱导的 HIF-2α 蛋白表达也被异氟烷显著抑制。在使用原代培养星形胶质细胞的实验中,异氟烷、戊巴比妥和氯胺酮抑制了缺氧诱导的 HIF-2α 蛋白和 EPO mRNA 的表达。

结论/意义:总之,我们的结果表明,全身麻醉药通过直接作用于星形胶质细胞,抑制 HIF-2 的激活,并抑制小鼠大脑中缺氧诱导的 EPO 上调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff1/3246473/f8457edefdf7/pone.0029378.g001.jpg

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