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白三烯缺陷小鼠的炎症反应改变。

Altered inflammatory responses in leukotriene-deficient mice.

作者信息

Goulet J L, Snouwaert J N, Latour A M, Coffman T M, Koller B H

机构信息

Department of Medicine, University of North Carolina, Chapel Hill 27599-7020.

出版信息

Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12852-6. doi: 10.1073/pnas.91.26.12852.

Abstract

Leukotrienes have been implicated in the regulation of immune responses, including inflammation and immediate hypersensitivity reactions. Here, we describe the phenotypic analysis of leukotriene-deficient mice generated by inactivation of the 5-lipoxygenase (5LO) gene. These 5LO(-/-) mice were unable to synthesize detectable levels of leukotrienes and were more resistant to lethal anaphylaxis induced by platelet-activating factor. The intensity of an acute inflammatory response induced by arachidonic acid was similar in 5LO(-/-) mice and controls. However, the response in 5LO(-/-) mice, but not in controls, could be virtually eliminated by a cyclooxygenase inhibitor. These data suggest that inflammatory responses are modulated by arachidonic acid metabolites through a variety of interconnected mechanisms. This has important implications for understanding the early events of an inflammatory response and for designing drugs for use in therapeutic intervention.

摘要

白三烯与免疫反应的调节有关,包括炎症和速发型超敏反应。在此,我们描述了通过灭活5-脂氧合酶(5LO)基因产生的白三烯缺陷小鼠的表型分析。这些5LO(-/-)小鼠无法合成可检测水平的白三烯,并且对血小板活化因子诱导的致死性过敏反应更具抵抗力。花生四烯酸诱导的急性炎症反应强度在5LO(-/-)小鼠和对照组中相似。然而,5LO(-/-)小鼠而非对照组中的反应几乎可被环氧化酶抑制剂消除。这些数据表明,炎症反应通过多种相互关联的机制受到花生四烯酸代谢产物的调节。这对于理解炎症反应的早期事件以及设计用于治疗干预的药物具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c29/45538/d8569d96f379/pnas01477-0508-a.jpg

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