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细胞色素P - 450介导的花生四烯酸对大鼠肾脏的血管舒张作用。

Cytochrome P-450-dependent vasodilation of rat kidney by arachidonic acid.

作者信息

Oyekan A O, McGiff J C, Quilley J

机构信息

Department of Pharmacology, New York Medical College, Valhalla 10595.

出版信息

Am J Physiol. 1991 Sep;261(3 Pt 2):H714-9. doi: 10.1152/ajpheart.1991.261.3.H714.

Abstract

Our previous studies indicated a role for cytochrome P-450-dependent enzymes in generating the mediators of the vasodilator effect of arachidonic acid (AA) in the preconstricted indomethacin-treated perfused kidney of the rat. We report that in vivo induction of cytochrome P-450 enzymes with 3-methylcholanthrene-beta-naphthoflavone or dexamethasone enhanced the renal vasodilator effect of AA in this experimental preparation. Conversely, depletion of cytochrome P-450 enzymes with stannous chloride or cobalt chloride diminished the vasodilator response to AA. Injection of AA resulted in the release of relaxant material into the renal effluent detected by superfusion of rabbit aortic rings. Inhibition of cytochrome P-450 with 7-ethoxyresorufin reduced the release of vasorelaxant material. Metabolism of labeled AA by the kidney revealed four peaks of radioactivity that were recovered from the renal effluent. The heights of these peaks were reduced by 7-ethoxyresorufin. These results provide further evidence for cytochrome P-450-dependent metabolism of AA to one or more vasodilator products by the rat kidney.

摘要

我们之前的研究表明,细胞色素P - 450依赖性酶在生成花生四烯酸(AA)对预先收缩的经消炎痛处理的大鼠灌注肾血管舒张作用的介质中发挥作用。我们报告,在该实验制剂中,用3 - 甲基胆蒽 - β - 萘黄酮或地塞米松对细胞色素P - 450酶进行体内诱导可增强AA的肾血管舒张作用。相反,用氯化亚锡或氯化钴消耗细胞色素P - 450酶会减弱对AA的血管舒张反应。注射AA导致通过兔主动脉环灌流检测到肾流出液中释放出舒张物质。用7 - 乙氧基试卤灵抑制细胞色素P - 450可减少血管舒张物质的释放。肾脏对标记AA的代谢显示从肾流出液中回收了四个放射性峰。这些峰的高度被7 - 乙氧基试卤灵降低。这些结果为大鼠肾脏将AA通过细胞色素P - 450依赖性代谢为一种或多种血管舒张产物提供了进一步的证据。

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