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前列腺素E2、类似物、脂肪酸和吲哚美辛对纤维蛋白原水平的影响。

Effects of prostaglandin E2, analogs, fatty acids, and indomethacin on fibrinogen level.

作者信息

Carlson T H, Wentland S H, Leonard B D, Ruder M A, Reeve E B

出版信息

Am J Physiol. 1978 Aug;235(2):H223-30. doi: 10.1152/ajpheart.1978.235.2.H223.

Abstract

Dose-response relations in rabbits for 3-h intravenous infusion of prostaglandin E2 (PGE2) and (15S)-15-methyl-1-prostaglandin E2 methyl ester (MePGE2) on plasma fibrinogen and systolic blood pressure were determined and described by regression equations. MePGE2 was 20 times more active than PGE2. Fibrinogen synthetic rate responses to PGE2 and MePGE2 were estimated. Infusion of the PGE2 precursor, arachidonic acid, elevated plasma fibrinogen, but fibrinogen response to 0.5-9 mg/kg arachidonic acid was unrelated to dose and half that given by 3 mg/kg PGE2. Slow infusion of several other fatty acids raised plasma fibrinogen as effectively as arachidonic acid, but prostaglandins D2 and F2alpha had only a slight effect. Infusion of 30 times the indomethacin dose that blocks platelet prostaglandin synthetase did not alter the plasma fibrinogen response to arachidonic acid. Indomethacin did not inhibit plasma fibrinogen elevations following ACTH or endotoxin infusion, or subcutaneous turpentine injection. Intravenous infusion of two cyclic ether prostaglandin endoperoxide analogs, (15S)-hydroxy-9alpha, 11alpha-(epoxymethano) prosta-5Z, 13E-dienoic acid, and (15S)-hydroxy-11alpha, 9alpha(epoxymethano) prosta-5Z, 13E-dienoic acid, failed to increase plasma fibrinogen.

摘要

通过回归方程确定并描述了兔子在静脉输注前列腺素E2(PGE2)和(15S)-15-甲基-1-前列腺素E2甲酯(MePGE2)3小时后,血浆纤维蛋白原和收缩压的剂量反应关系。MePGE2的活性比PGE2高20倍。估算了纤维蛋白原合成率对PGE2和MePGE2的反应。输注PGE2前体花生四烯酸可使血浆纤维蛋白原升高,但对0.5 - 9mg/kg花生四烯酸的纤维蛋白原反应与剂量无关,且仅为3mg/kg PGE2所致反应的一半。缓慢输注其他几种脂肪酸升高血浆纤维蛋白原的效果与花生四烯酸相同,但前列腺素D2和F2α的作用轻微。输注能阻断血小板前列腺素合成酶的吲哚美辛剂量的30倍,并未改变血浆纤维蛋白原对花生四烯酸的反应。吲哚美辛不抑制促肾上腺皮质激素或内毒素输注后或皮下注射松节油后血浆纤维蛋白原的升高。静脉输注两种环醚前列腺素内过氧化物类似物,(15S)-羟基-9α,11α-(环氧亚甲基)前列腺-5Z,13E-二烯酸和(15S)-羟基-11α,9α-(环氧亚甲基)前列腺-5Z,13E-二烯酸,未能增加血浆纤维蛋白原。

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