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一种前列腺素内过氧化物类似物对犬胃酸和黏液分泌的影响。

The effects of a prostaglandin endoperoxide analogue on canine gastric acid and mucus secretion.

作者信息

Tao P, Scruggs W, Wilson D E

出版信息

Dig Dis Sci. 1979 Jun;24(6):449-54. doi: 10.1007/BF01299826.

Abstract

The effects of U-46619, a stable analogue of the prostaglandin endoperoxide PGH2, were studied on canine gastric acid secretion, gastric mucosal blood flow, and secretion of mucus into gastric juice and compared to those of PGE2. U-46619 was approximately four and three times as potent as PGE2 in inhibiting acid secretion and stimulating mucus secretion, respectively. When infused at a low dose, U-46619 inhibited acid secretion directly without causing a decrease in the ratio of mucosal blood flow to volume rate of secretion (R), this effect being similar to that observed for PGE2. However, unlike PGE2, U-46619 when administered in a higher dose caused a decline in R while decreasing acid secretion and mucosal blood flow, suggesting a primary restriction of blood flow. The antisecretory effects of arachidonic acid may be due in part to the endogenous formation of prostaglandin endoperoxides as opposed solely to prostaglandin formation. Considering the antisecretory and mucogenic actions of U-46619, nontoxic analogues of prostaglandin endoperoxides may be of value as antiulcer agents.

摘要

研究了前列腺素内过氧化物PGH2的稳定类似物U - 46619对犬胃酸分泌、胃黏膜血流量以及胃液中黏液分泌的影响,并与PGE2的影响进行了比较。U - 46619在抑制胃酸分泌和刺激黏液分泌方面的效力分别约为PGE2的四倍和三倍。低剂量输注时,U - 46619直接抑制胃酸分泌,而不会导致黏膜血流量与分泌量体积比(R)降低,这种效应与PGE2观察到的相似。然而,与PGE2不同,高剂量给药时,U - 46619在降低胃酸分泌和黏膜血流量的同时导致R下降,提示存在血流的原发性受限。花生四烯酸的抗分泌作用可能部分归因于前列腺素内过氧化物的内源性形成,而非仅仅是前列腺素的形成。考虑到U - 46619的抗分泌和促黏液生成作用,前列腺素内过氧化物的无毒类似物可能作为抗溃疡药物具有价值。

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