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缓激肽在通过花生四烯酸级联反应进行的前列腺素合成中,对环氧化酶步骤的作用。

Action of bradykinin at the cyclooxygenase step in prostanoid synthesis through the arachidonic acid cascade.

作者信息

Zhang H, Gaginella T S, Chen X, Cornwell D G

机构信息

University Hospital, Vancouver, B.C., Canada.

出版信息

Agents Actions. 1991 Nov;34(3-4):397-404. doi: 10.1007/BF01988735.

Abstract

Bradykinin enhances prostanoid synthesis in aorta smooth muscle cells. Free arachidonic acid also enhances prostanoid synthesis and bradykinin, unlike fatty acid releasing agents, has a synergistic effect with free arachidonic acid. Bradykinin promotes metabolite release from cells prelabeled with [14C]-arachidonic acid and this effect is blocked completely by indomethacin. High performance liquid chromatography shows increase amounts of labeled 6-keto-prostaglandin F1 alpha, prostaglandin E2 and three additional cyclooxygenase-dependent metabolites but no increase in free arachidonic acid or other metabolites either in the absence or presence of indomethacin. Fatty acid releasing agents such as A23187 and cyclosporine A have very different effects on cells. These agents enhance levels of prostanoids, a number of other cyclooxygenase-independent metabolites, and free arachidonic acid which is even more elevated with added indomethacin. Bradykinin behaves in all respects like another agent, bacterial lipopolysaccharide, and the action of both agents is consistent with a mechanism involving cyclooxygenase rather than fatty release in the arachidonic acid cascade.

摘要

缓激肽可增强主动脉平滑肌细胞中前列腺素的合成。游离花生四烯酸也可增强前列腺素的合成,并且与脂肪酸释放剂不同,缓激肽与游离花生四烯酸具有协同作用。缓激肽可促进用[14C] - 花生四烯酸预标记的细胞释放代谢产物,而吲哚美辛可完全阻断这种作用。高效液相色谱显示,无论是在不存在还是存在吲哚美辛的情况下,标记的6 - 酮 - 前列腺素F1α、前列腺素E2以及另外三种环氧化酶依赖性代谢产物的量均增加,但游离花生四烯酸或其他代谢产物没有增加。脂肪酸释放剂如A23187和环孢素A对细胞有非常不同的作用。这些试剂可提高前列腺素、许多其他非环氧化酶依赖性代谢产物以及游离花生四烯酸的水平,添加吲哚美辛后游离花生四烯酸水平升高得更多。缓激肽在所有方面的表现都与另一种物质细菌脂多糖相似,并且这两种物质的作用都与一种涉及环氧化酶而非花生四烯酸级联反应中脂肪酸释放的机制一致。

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