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前列腺素H2和血栓素A2是自发性高血压大鼠肾内动脉的收缩因子。

Prostaglandin H2 and thromboxane A2 are contractile factors in intrarenal arteries of spontaneously hypertensive rats.

作者信息

Dai F X, Skopec J, Diederich A, Diederich D

机构信息

Department of Medicine, University of Kansas Medical Center, Kansas City 66103.

出版信息

Hypertension. 1992 Jun;19(6 Pt 2):795-8. doi: 10.1161/01.hyp.19.6.795.

Abstract

Vascular resistance is increased in the kidneys of spontaneously hypertensive rats (SHR). Previous studies have demonstrated impaired vascular relaxations of mesenteric resistance arteries of SHR because of increased production of a cyclooxygenase-dependent endothelium-derived contracting factor. To test the hypothesis that altered endothelial function contributes to the enhanced constriction in kidneys of SHR, endothelium-mediated relaxations of renal resistance arteries from 5-6-week-old prehypertensive SHR and Wistar-Kyoto rats were compared in arteriographs. Acetylcholine induced endothelium-dependent contractions in SHR arteries, while potent endothelium-dependent relaxations were noted in renal arteries from Wistar-Kyoto rats. Inhibition of cyclooxygenase (indomethacin) or blockade of prostaglandin H2-thromboxane A2 receptors (SQ 29,548) blocked acetylcholine-induced contractions in SHR renal arteries; relaxations in SHR renal arteries after either treatment were similar to those observed in renal arteries from Wistar-Kyoto rats. NG-Nitro-L-arginine inhibited acetylcholine-mediated relaxations in both SHR and Wistar-Kyoto arteries. Endothelium-independent relaxations induced by verapamil were comparable in SHR and Wistar-Kyoto arteries. Thus, the impaired response to acetylcholine in SHR renal resistance arteries may result from the release of endothelium-derived cyclooxygenase products (prostaglandin H2 or thromboxane A2), which oppose endothelium-derived nitric oxide-mediated relaxation.

摘要

自发性高血压大鼠(SHR)肾脏的血管阻力增加。先前的研究表明,由于环氧化酶依赖性内皮衍生收缩因子的产生增加,SHR肠系膜阻力动脉的血管舒张功能受损。为了验证内皮功能改变导致SHR肾脏血管收缩增强这一假说,在血管造影仪中比较了5至6周龄高血压前期SHR和Wistar-Kyoto大鼠肾阻力动脉的内皮介导舒张功能。乙酰胆碱在SHR动脉中诱导内皮依赖性收缩,而在Wistar-Kyoto大鼠的肾动脉中则观察到强效的内皮依赖性舒张。抑制环氧化酶(吲哚美辛)或阻断前列腺素H2-血栓素A2受体(SQ 29,548)可阻断乙酰胆碱诱导的SHR肾动脉收缩;两种处理后SHR肾动脉的舒张与Wistar-Kyoto大鼠肾动脉中观察到的相似。NG-硝基-L-精氨酸抑制SHR和Wistar-Kyoto动脉中乙酰胆碱介导的舒张。维拉帕米诱导的非内皮依赖性舒张在SHR和Wistar-Kyoto动脉中相当。因此,SHR肾阻力动脉对乙酰胆碱的反应受损可能是由于内皮衍生的环氧化酶产物(前列腺素H2或血栓素A2)的释放,其对抗内皮衍生的一氧化氮介导的舒张。

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