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离体兔主动脉中超氧化物的产生以及四氧嘧啶、吲哚美辛和硝基血管扩张剂的作用。

Superoxide production in the isolated rabbit aorta and the effect of alloxan, indomethacin and nitrovasodilators.

作者信息

Heim K F, Thomas G, Ramwell P W

机构信息

Department of Physiology and Biophysics, Georgetown University Medical Center, Washington, District of Columbia.

出版信息

J Pharmacol Exp Ther. 1991 Feb;256(2):537-41.

PMID:1847199
Abstract

The purpose of this investigation was to develop a simple model to assess superoxide production from isolated vessels and to use this model to study the effects of various compounds on superoxide generation. The established method of cytochrome C reduction by superoxide was modified to measure superoxide production in vascular rings from rabbit aortae. The diabetogenic compound alloxan significantly increased superoxide production in a concentration-dependent manner. The nitrovasodilators nitroprusside and minoxidil exhibited contrasting effects. Nitroprusside inhibited alloxan-stimulated production of superoxide, but minoxidil had no effect, suggesting different mechanisms of action for these drugs. The cyclooxygenase inhibitor indomethacin had no effect on the production of superoxide stimulated by alloxan, demonstrating that superoxide production induced by this compound is not affected by mechanisms involving cyclooxygenase. These data demonstrate the use of a simple, rapid and inexpensive method for measuring superoxide produced by intact vessels. This may be useful in testing drugs exhibiting antioxidant and vasoactive properties. Finally, because superoxide is implicated in the destruction of endothelium-derived relaxing factor, and the presence of the vasodilator nitroprusside reduces superoxide production, it is concluded that some nitrovasodilators may have additional vascular effects through the suppression of superoxide formation.

摘要

本研究的目的是建立一个简单模型来评估分离血管中超氧化物的产生,并利用该模型研究各种化合物对超氧化物生成的影响。对通过超氧化物还原细胞色素C的既定方法进行了修改,以测量兔主动脉血管环中超氧化物的产生。致糖尿病化合物四氧嘧啶以浓度依赖的方式显著增加超氧化物的产生。硝基血管扩张剂硝普钠和米诺地尔表现出相反的作用。硝普钠抑制四氧嘧啶刺激的超氧化物产生,但米诺地尔没有作用,这表明这些药物的作用机制不同。环氧化酶抑制剂吲哚美辛对四氧嘧啶刺激的超氧化物产生没有影响,表明该化合物诱导的超氧化物产生不受涉及环氧化酶的机制影响。这些数据证明了使用一种简单、快速且廉价的方法来测量完整血管产生的超氧化物。这可能有助于测试具有抗氧化和血管活性特性的药物。最后,由于超氧化物与内皮源性舒张因子的破坏有关,并且血管扩张剂硝普钠的存在会减少超氧化物的产生,因此得出结论,一些硝基血管扩张剂可能通过抑制超氧化物的形成而具有额外的血管效应。

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