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前列腺素合成抑制剂对西氯他宁诱导的离体人胃上动脉舒张的不同作用。

Differential effects of prostanoid synthesis inhibitors on cicletanine-induced relaxation of isolated human epigastric arteries.

作者信息

Ebeigbe A B, Oguogho A, Ighoroje A D, Aloamaka C P

机构信息

Department of Physiology, College of Health Sciences, University of Benin, Nigeria.

出版信息

Clin Auton Res. 1994 Jun;4(3):137-9. doi: 10.1007/BF01845778.

Abstract

We have examined the influence of prostanoid synthesis inhibitors on the relaxation responses induced by cicletanine in ring preparations of isolated human epigastric arteries following precontraction induced by 10(-7) M noradrenaline. Cicletanine caused concentration-dependent relaxations, uninfluenced by the cyclooxygenase inhibitors, meclofenamate (1, 10 microM) and indomethacin (1, 10 microM) but significantly (p < 0.05) attenuated by the specific prostacyclin synthesis inhibitor, tranylcypromine (0.1-10 microM) (n > 6 in each). In contrast, cromakalim-induced relaxations were significantly attenuated by indomethacin, meclofenamate and tranylcypromine. The tranylcypromine-sensitive cicletanine-induced relaxation suggests, at least in part, the involvement of prostacyclin in the vasodilator action of cicletanine.

摘要

我们研究了前列腺素合成抑制剂对环戊噻嗪在由10(-7)M去甲肾上腺素预收缩后的离体人胃上动脉环制备物中诱导的舒张反应的影响。环戊噻嗪引起浓度依赖性舒张,不受环氧化酶抑制剂甲氯芬那酸(1、10 microM)和吲哚美辛(1、10 microM)的影响,但被特异性前列环素合成抑制剂反苯环丙胺(0.1 - 10 microM)显著(p < 0.05)减弱(每组n > 6)。相比之下,克罗卡林诱导的舒张被吲哚美辛、甲氯芬那酸和反苯环丙胺显著减弱。反苯环丙胺敏感的环戊噻嗪诱导的舒张至少部分表明前列环素参与了环戊噻嗪的血管舒张作用。

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