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异前列腺素对去甲肾上腺素和血管紧张素II缩血管效应的影响。

Influence of isoprostanes on vasoconstrictor effects of noradrenaline and angiotensin II.

作者信息

Sametz W, Grobuschek T, Hammer-Kogler S, Juan H, Wintersteiger R

机构信息

Department of Biomedical Research, University of Graz, Austria.

出版信息

Eur J Pharmacol. 1999 Jul 28;378(1):47-55. doi: 10.1016/s0014-2999(99)00437-9.

Abstract

The isoprostanes, 8-iso-prostaglandin F2alpha and 8-iso-prostaglandin E2, which are released in vivo by free radical-catalyzed peroxidation of arachidonic acid, are potent vasoconstrictors. Increased formation of 8-iso-prostaglandin F2alpha has been detected in human cardiovascular diseases, in which enhanced plasma levels of noradrenaline and angiotensin II have harmful vasoconstrictor effects. Therefore, we investigated the influence of perfusions with the thromboxane A2 mimetic, U 46619, and with the isoprostanes, 8-iso-prostaglandin F2alpha, 8-iso-prostaglandin E2, 8-iso-prostaglandin E1 and 8-iso-prostaglandin F3alpha, on the vasoconstrictor effects of noradrenaline and angiotensin II in the isolated perfused rabbit ear. Our results demonstrate that perfusions with U 46619, 8-iso-prostaglandin E2 and 8-iso-prostaglandin F2alpha, at a subthreshold concentration (30 nM), amplified the vasoconstrictions induced by noradrenaline or angiotensin II significantly. In addition, the results show that U 46619, 8-iso-prostaglandin F2alpha, 8-iso-prostaglandin E2 and 8-iso-prostaglandin E1, which were applied as a bolus, induced much more pronounced vasoconstrictions than prostaglandin F2alpha, prostaglandin E2 and prostaglandin F3alpha. Prostaglandin E1 and 8-iso-prostaglandin F3alpha, showed no effects. In conclusion, it can be assumed that the powerful vasoconstrictions induced by 8-iso-prostaglandin E2 and 8-iso-prostaglandin F2alpha and their potentiating effects on vasoconstrictions induced by noradrenaline or angiotensin II might be of pathophysiological relevance in cardiovascular diseases.

摘要

异前列腺素,8-异前列腺素F2α和8-异前列腺素E2,由花生四烯酸的自由基催化过氧化反应在体内释放,是强效血管收缩剂。在人类心血管疾病中已检测到8-异前列腺素F2α的生成增加,其中去甲肾上腺素和血管紧张素II的血浆水平升高具有有害的血管收缩作用。因此,我们研究了用血栓素A2类似物U 46619以及异前列腺素8-异前列腺素F2α、8-异前列腺素E2、8-异前列腺素E1和8-异前列腺素F3α灌注对去甲肾上腺素和血管紧张素II在离体灌注兔耳中的血管收缩作用的影响。我们的结果表明,用阈下浓度(30 nM)的U 46619、8-异前列腺素E2和8-异前列腺素F2α灌注可显著增强去甲肾上腺素或血管紧张素II诱导的血管收缩。此外,结果表明,以推注方式应用的U 46619、8-异前列腺素F2α、8-异前列腺素E2和8-异前列腺素E1比前列腺素F2α、前列腺素E2和前列腺素F3α诱导的血管收缩更明显。前列腺素E1和8-异前列腺素F3α无作用。总之,可以认为8-异前列腺素E2和8-异前列腺素F2α诱导的强大血管收缩及其对去甲肾上腺素或血管紧张素II诱导的血管收缩的增强作用可能在心血管疾病中具有病理生理学意义。

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