人肿瘤坏死因子输注后白三烯和前列腺素的产生。

Eicosanoids Pub Date : 1991-01-01
K P Moore, N Sheron, P Ward, G W Taylor, G J Alexander, R Williams
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引用次数: 0

摘要

肿瘤坏死因子- α被认为是内毒素血症和脓毒性休克的重要介质,其作用被认为是通过产生半胱氨酸-白三烯、血栓素A2和其他前列腺素介导的。我们研究了4例慢性乙型肝炎病毒感染患者输注肿瘤坏死因子- α后体内这些类二十烷酸和前列环素的产生。这导致血浆TNF水平明显高于感染性休克。在TNF输注后8小时,所有受试者白三烯E4尿排泄率增加2 - 3倍。然而,3/4的受试者尿液中血栓素B2和6-氧-前列腺素F1 α的排泄量在前4小时增加了2 - 40倍,并在8小时后恢复到基线水平。所有受试者的肝脏代谢物2,3-二或6-氧-前列腺素F1 α的排泄量都增加了(4小时时增加了2 - 4倍)。我们的结论是,肿瘤坏死因子输注人体内后,半胱氨酸白三烯、血栓素A2和前列环素的产生增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leukotriene and prostaglandin production after infusion of tumour necrosis factor in man.

Tumor necrosis factor-alpha is believed to be an important mediator of endotoxaemia and septic shock, the effects of which are thought to be mediated through the generation of cysteinyl-leukotrienes, thromboxane A2 and other prostanoids. We have investigated the production of these eicosanoids and also that of prostacyclin in vivo after infusion of tumor necrosis factor-alpha into 4 subjects with a chronic hepatitis B virus infection. This resulted in plasma TNF levels considerably greater than those observed in septic shock. Urinary excretion rate of leukotriene E4 increased by 2 to 3-fold in all subjects by 8 h following TNF infusion. Urinary excretion of thromboxane B2 and 6-oxo-prostaglandin F1 alpha, however, increased in the first 4 h in 3/4 subjects by 2 to 40-fold and returned towards baseline by 8 h. Excretion of the hepatic metabolite, 2,3-dinor 6-oxo-prostaglandin F1 alpha, increased in all subjects (2 to 4-fold at 4h). We conclude that there is increased production of cysteinyl leukotrienes, thromboxane A2 and prostacyclin after infusion of tumour necrosis factor into man.

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