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20-羟基二十碳四烯酸在大鼠肾小动脉中的形成与作用

Formation and actions of 20-hydroxyeicosatetraenoic acid in rat renal arterioles.

作者信息

Imig J D, Zou A P, Stec D E, Harder D R, Falck J R, Roman R J

机构信息

Department of Physiology, Medical college of Wisconsin, Milwaukee 53226, USA.

出版信息

Am J Physiol. 1996 Jan;270(1 Pt 2):R217-27. doi: 10.1152/ajpregu.1996.270.1.R217.

Abstract

The present study examined whether preglomerular arterioles of the rat produce 20-hydroxyeicosatetraenoic acid (20-HETE) and whether 20-HETE is vasoactive on these vessels. Raf preglomerular arterioles produced 20-HETE (4.8 +/- 1.0 pmol.min-1.mg-1, n = 7) and, to a lesser extent, 14-, 15-, 11-, and 12-dihydroxyeicosatetraenoic acid, 6-ketoprostaglandin F/alpha and prostaglandin E2 when incubated with [14C]larachidonic acid. The results of immunoblotting and reverse-transcription polymerase chain reaction experiments indicate that these vessels express mRNA and protein for a P-450 4A2 enzyme. With the use of a rat juxtamedullary nephron microvascular preparation perfused in vitro with a cell-free media, addition of 20-HETE (1 nM-1 microM) to the bath reduced the diameter of proximal and distal portions of the efferent arterioles. At a concentration of 1 microM, the diameter of the proximal and distal portions of the afferent arteriole fell by 14 +/- 1 and 16 +/- 3% after 20-HETE. The response to 20-HETE (1 microM) was not altered by blockade of cyclooxygenase, lipoxygenase, and p-450 pathways. Blockade of the large-conductance Ca(2+)-activated K+ channel with tetraethylammonium (1 mM) reduced the diameter of afferent arterioles by 10% and blocked the vasoconstrictor response to 20-HETE (1 microM). These results indicate that 20-HETE is an endogenous constrictor of preglomerular arterioles and suggest a role for the P-450 4A2 enzyme in the regulation of renal vascular tone.

摘要

本研究检测了大鼠球前小动脉是否产生20-羟基二十碳四烯酸(20-HETE),以及20-HETE对这些血管是否具有血管活性。用[14C]花生四烯酸孵育时,Raf球前小动脉产生20-HETE(4.8±1.0 pmol·min-1·mg-1,n = 7),并在较小程度上产生14-、15-、11-和12-二羟基二十碳四烯酸、6-酮前列腺素F/α和前列腺素E2。免疫印迹和逆转录聚合酶链反应实验结果表明,这些血管表达P-450 4A2酶的mRNA和蛋白质。使用体外无细胞培养基灌注的大鼠近髓肾单位微血管制备物,向浴槽中添加20-HETE(1 nM - 1 μM)可减小出球小动脉近端和远端的直径。在1 μM浓度下,添加20-HETE后,入球小动脉近端和远端的直径分别下降14±1%和16±3%。环氧化酶、脂氧化酶和p-450途径的阻断并未改变对20-HETE(1 μM)的反应。用四乙铵(1 mM)阻断大电导钙激活钾通道可使入球小动脉直径减小10%,并阻断对20-HETE(1 μM)的血管收缩反应。这些结果表明,20-HETE是球前小动脉的内源性收缩剂,并提示P-450 4A2酶在肾血管张力调节中起作用。

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