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促红细胞生成素的器官保护和免疫调节作用——近期临床试验的最新进展

Organ-protective and immunomodulatory effects of erythropoietin--an update on recent clinical trials.

作者信息

Sølling Christoffer

机构信息

Department of Anaesthesiology and Intensive Care Medicine, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Basic Clin Pharmacol Toxicol. 2012 Feb;110(2):113-21. doi: 10.1111/j.1742-7843.2011.00820.x. Epub 2011 Nov 9.

Abstract

Erythropoietin (EPO) belongs to a group of pharmacological agents with multifunctional effects. EPO was originally acknowledged as the main regulator of erythropoiesis, but it also exhibits several extra haematopoietic properties, such as promoting the maintenance of homeostasis of cells under stress. These pleiotropic effects have been extensively investigated in preclinical models including models of ischaemic-reperfusions injuries, inflammation, neuroprotection, neovascularisation and wound healing. Promising effects of EPO have especially been reported in models of ischaemic-reperfusions injuries. The mechanisms by which EPO exerts these organ-protective effects are not completely understood, although anti-apoptotic, anti-inflammatory and anti-oxidative properties have been described. Activation of the EPO receptor initiates several intracellular signalling systems, such as, phosphatidylinositol 3-kinase, STAT5, mitogen-activated protein kinase and nuclear factor-kappa B. These pathways are recognized as involved in the cellular response to stress and regulation of apoptosis. Although EPO has been demonstrated to be effective in animal models, the effect has not been clearly demonstrated in clinical trials. This MiniReview gives a brief introduction to the pleiotropic effects of EPO, the evidence of organ protection in animal models, and discusses the disappointing results obtained from recent clinical trials.

摘要

促红细胞生成素(EPO)属于一类具有多种功能效应的药物制剂。EPO最初被认为是红细胞生成的主要调节因子,但它也表现出多种造血外特性,比如在应激状态下促进维持细胞内环境稳定。这些多效性作用已在临床前模型中得到广泛研究,包括缺血再灌注损伤、炎症、神经保护、新生血管形成及伤口愈合等模型。尤其在缺血再灌注损伤模型中已报道了EPO的显著作用。尽管已经描述了EPO的抗凋亡、抗炎和抗氧化特性,但其发挥这些器官保护作用的机制尚未完全明确。EPO受体的激活启动了多个细胞内信号系统,如磷脂酰肌醇3激酶、信号转导子和转录激活子5、丝裂原活化蛋白激酶及核因子κB。这些信号通路被认为参与细胞对应激的反应及细胞凋亡的调控。尽管EPO已在动物模型中被证明有效,但其在临床试验中的效果尚未得到明确证实。本综述简要介绍了EPO的多效性作用、在动物模型中的器官保护证据,并讨论了近期临床试验中令人失望的结果。

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