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内过氧化物类似物、前列腺素和花生四烯酸对肾血管的作用。

Renal vascular effects of endoperoxide analogs, prostaglandins, and arachidonic acid.

作者信息

Feigen L P, Chapnick B M, Flemming J E, Flemming J M, Kadowitz P J

出版信息

Am J Physiol. 1977 Nov;233(5):H573-9. doi: 10.1152/ajpheart.1977.233.5.H573.

Abstract

Renal vascular responses to analogs of prostaglandin H2(PGH2) were investigated in anesthetized dogs. The analogs were potent renal vasoconstrictors whose actions were not affected either by indomethacin or by alpha-adrenergic or angiotensin antagonists. The constrictor activity of the analogs approximated that of norepinephrine. Responses to PGD2 were also obtained. This prostaglandin, previously thought to be inactive, was found to cause renal vasodilation similar to that caused by PGA2. Responses to the prostaglandin precursor, arachidonic acid, were of two types. In some animals, the response was marked vasodilation, whereas in others transient vasoconstriction preceded the vasodilation. These studies demonstrate that PGH2 analogs are potent renal vasoconstrictors and that PGD2 possesses renal vasodilating properties. In addition, it is suggested that the rapid vasoconstrictor portion of the arachidonate response may represent effects of endogneously produced PGH2.

摘要

在麻醉犬中研究了前列腺素H2(PGH2)类似物对肾血管的反应。这些类似物是强效的肾血管收缩剂,其作用不受吲哚美辛、α-肾上腺素能拮抗剂或血管紧张素拮抗剂的影响。类似物的收缩活性与去甲肾上腺素相近。还获得了对PGD2的反应。这种以前被认为无活性的前列腺素被发现可引起与PGA2相似的肾血管舒张。对前列腺素前体花生四烯酸的反应有两种类型。在一些动物中,反应是明显的血管舒张,而在另一些动物中,短暂的血管收缩先于血管舒张。这些研究表明,PGH2类似物是强效的肾血管收缩剂,PGD2具有肾血管舒张特性。此外,提示花生四烯酸反应中快速的血管收缩部分可能代表内源性产生的PGH2的作用。

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