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兔内毒素休克:给予前列腺素和花生四烯酸的影响。

Endotoxic shock in the rabbit: the effects of prostaglandin and arachidonic acid administration.

作者信息

Flynn J T

出版信息

J Pharmacol Exp Ther. 1978 Sep;206(3):555-66.

PMID:359777
Abstract

A rabbit model was used to determine the effects of prostaglandins and arachidonic acid on cellular integrity and survival during endotoxic shock. Prostaglandins A2, E1 and F2alpha were infused intravenously at a rate of 1.0 microgram/kg/min for 105 min beginning 15 min after the administration of an LD60 dose of Escherichia coli endotoxin. While each of the prostaglandins tested significantly attenuated the accumulation of lactic acid dehydrogenase in the plasma of shocked animals, none were able to protect against the increase in the plasma activities of glutamic pyruvic transaminase or cathepsin D during the shock state. Prostaglandins A2, E1 and F2alpha did not significantly enhance the survival of the treated animals as compared to vehicle-treated controls. In contrast, arachidonic acid 15 microgram/kg/min i.v.) significantly prevented the accumulation of lactic acid dehydrogenase and glutamic-pyruvic transaminase activities in the plasma of shocked animals, and also significantly increased the number of survivors in this group 48 hours after the endotoxin administration. In summary, while the treatment of endotoxic rabbits with prostaglandins of the A, E and F series was of no survival value, the treatment of these animals with a substrate of the prostaglandin synthetase complex resulted in a dramatic increase in the survival rate. The mechanism of action of arachidonic acid in this regard is not clear.

摘要

采用兔模型来确定前列腺素和花生四烯酸对内毒素休克期间细胞完整性和存活的影响。在给予致死剂量60%的大肠杆菌内毒素15分钟后,以1.0微克/千克/分钟的速率静脉输注前列腺素A2、E1和F2α,持续105分钟。虽然所测试的每种前列腺素均显著减轻了休克动物血浆中乳酸脱氢酶的积累,但在休克状态下,没有一种能够防止血浆中谷丙转氨酶或组织蛋白酶D活性的增加。与赋形剂处理的对照组相比,前列腺素A2、E1和F2α并未显著提高治疗动物的存活率。相比之下,花生四烯酸(15微克/千克/分钟,静脉注射)显著防止了休克动物血浆中乳酸脱氢酶和谷丙转氨酶活性的积累,并且在内毒素给药48小时后,该组的存活动物数量也显著增加。总之,虽然用A、E和F系列前列腺素治疗内毒素血症兔没有生存价值,但用前列腺素合成酶复合物的一种底物治疗这些动物可显著提高存活率。花生四烯酸在这方面的作用机制尚不清楚。

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