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脂氧素对大鼠肾脏血流动力学的作用:一项比较生理学研究。

Renal hemodynamic actions of lipoxins in rats: a comparative physiological study.

作者信息

Katoh T, Takahashi K, DeBoer D K, Serhan C N, Badr K F

机构信息

Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2372.

出版信息

Am J Physiol. 1992 Sep;263(3 Pt 2):F436-42. doi: 10.1152/ajprenal.1992.263.3.F436.

Abstract

Interactions between either the arachidonate 5-lipoxygenase (5-LO) and 15-LO or 5-LO and 12-LO can lead to the formation of lipoxins. Although the functional significance of lipoxygenase products of arachidonic acid has been recognized increasingly in glomerular inflammation, less is known regarding the specific effects of lipoxins on renal hemodynamics. Here, we examine the renal actions of lipoxin (LX) A4, LXB4, and, the recently identified 7-cis-11-trans-LXA4, which were administered into the renal artery of the euvolemic male Munich-Wistar rat. LXA4 caused increases in renal plasma flow (RPF) and glomerular filtration rate (GFR) in a dose-dependent manner. These effects were reversed during cyclooxygenase inhibition. LXB4 decreased both RPF and GFR, and its mode of action was independent of cyclooxygenase activity. 7-cis-11-trans-LXA4 decreased RPF and GFR, which effects were abolished during systemic infusion of the leukotriene D4 receptor antagonist SKF 104353. Results indicate that each of these lipoxins displays distinct hemodynamic effects via a specific mode of action on the renal vasculature of rats. Moreover, they suggest mechanisms whereby lipoxins may participate in the changes of renal hemodynamics that occur during glomerular inflammatory processes.

摘要

花生四烯酸5-脂氧合酶(5-LO)与15-脂氧合酶或5-LO与12-脂氧合酶之间的相互作用可导致脂氧素的形成。尽管花生四烯酸脂氧合酶产物在肾小球炎症中的功能意义已得到越来越多的认识,但关于脂氧素对肾血流动力学的具体影响却知之甚少。在此,我们研究了脂氧素(LX)A4、LXB4以及最近发现的7-顺式-11-反式-LXA4对正常血容量雄性慕尼黑-威斯塔大鼠肾动脉的作用。LXA4以剂量依赖性方式使肾血浆流量(RPF)和肾小球滤过率(GFR)增加。在环氧化酶抑制期间,这些作用被逆转。LXB4使RPF和GFR均降低,其作用方式与环氧化酶活性无关。7-顺式-11-反式-LXA4使RPF和GFR降低,在全身输注白三烯D4受体拮抗剂SKF 104353期间,这些作用被消除。结果表明,这些脂氧素中的每一种都通过对大鼠肾血管系统的特定作用方式表现出独特的血流动力学效应。此外,它们提示了脂氧素可能参与肾小球炎症过程中发生的肾血流动力学变化的机制。

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