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挥发性麻醉剂和右旋糖酐铁对大鼠慢性炎症和抗氧化防御系统的影响

Effects of Volatile Anaesthetics and Iron Dextran on Chronic Inflammation and Antioxidant Defense System in Rats.

作者信息

Odeh Dyana, Oršolić Nada, Adrović Emanuela, Gaćina Lydia, Perić Petra, Odeh Sahar, Balta Vedran, Lesar Nikola, Kukolj Marina

机构信息

Division of Animal Physiology, Faculty of Science, University of Zagreb, Rooseveltov Trg 6, 10000 Zagreb, Croatia.

出版信息

Antioxidants (Basel). 2022 Apr 3;11(4):708. doi: 10.3390/antiox11040708.

DOI:10.3390/antiox11040708
PMID:35453393
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9025161/
Abstract

Iron, as an essential microelement, is involved in cell proliferation, metabolism, and differentiation. It also modulates the fate and function of macrophages in hematopoiesis and macrophage-mediated inflammatory responses. On the other hand, anesthetics can affect the inflammatory process by modulating the response to stress or the functions of immune cells. The aim of this paper is to understand how excessive iron intake alters physiological, functional characteristics of peripheral tissues and whether different anesthetics can alter cell metabolism regarding oxidative stress (OS) and inflammation through regulation of macrophage polarization. Y59 rats were injected intraperitoneally with iron dextran solution at a dose of 50 mg/kg or were exposed to inhaled anesthetics sevoflurane and isoflurane and their combination for 28 days every other day. The results show that the use of anesthetics reduces the rat's organ weight and increases OS in peripheral tissues, leading to M1 macrophage polarization. Excessive iron intake leads to increased OS, inflammation, and an increased ratio of IL-12/IL-10 cytokines to the M1 macrophage phenotype. Iron, in combination with sevoflurane, has a protective effect in tissues showing the M2 phenotype of macrophages. The combination of iron dextran and isoflurane in rats leads to an increase in the erythropoiesis process made possible through the induction of hypoxia.

摘要

铁作为一种必需的微量元素,参与细胞增殖、代谢和分化。它还在造血过程以及巨噬细胞介导的炎症反应中调节巨噬细胞的命运和功能。另一方面,麻醉剂可通过调节对应激的反应或免疫细胞的功能来影响炎症过程。本文的目的是了解过量摄入铁如何改变外周组织的生理和功能特性,以及不同的麻醉剂是否能通过调节巨噬细胞极化来改变与氧化应激(OS)和炎症相关的细胞代谢。对Y59大鼠每隔一天腹腔注射剂量为50 mg/kg的右旋糖酐铁溶液,或使其暴露于吸入麻醉剂七氟烷和异氟烷及其组合中,持续28天。结果表明,使用麻醉剂会降低大鼠的器官重量,并增加外周组织中的氧化应激,导致M1巨噬细胞极化。过量摄入铁会导致氧化应激增加、炎症加剧以及IL-12/IL-10细胞因子与M1巨噬细胞表型的比例增加。铁与七氟烷联合使用时,对呈现巨噬细胞M2表型的组织具有保护作用。大鼠体内右旋糖酐铁与异氟烷的组合通过诱导缺氧使红细胞生成过程增加。

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引用本文的文献

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本文引用的文献

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Macrophages and Iron: A Special Relationship.巨噬细胞与铁:一种特殊关系。
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Coaction of hepatic thioredoxin and glutathione systems in iron overload-induced oxidative stress.肝脏硫氧还蛋白和谷胱甘肽系统在铁过载诱导的氧化应激中的共同作用。
J Biochem Mol Toxicol. 2021 Apr;35(4):e22704. doi: 10.1002/jbt.22704. Epub 2021 Jan 3.
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The effects of heavy metals on human metabolism.重金属对人体代谢的影响。
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Sevoflurane Promotes Bactericidal Properties of Macrophages through Enhanced Inducible Nitric Oxide Synthase Expression in Male Mice.七氟醚通过增强雄性小鼠诱导型一氧化氮合酶表达促进巨噬细胞的杀菌特性。
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Pharmacogenomics of inhalational anesthetic agents.吸入性麻醉药的药物基因组学
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Cell iron status influences macrophage polarization.细胞铁状态影响巨噬细胞极化。
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