Zipser R D, Martin K
Am J Physiol. 1982 Mar;242(3):E171-7. doi: 10.1152/ajpendo.1982.242.3.E171.
To determine the fraction of the arterial prostaglandin E2 (PGE2), 6-ketoprostaglandin F1 alpha (6-keto-PGF1 alpha), and thromboxane B2 (TXB2) that is excreted unmetabolized into human urine, the 3H-labeled compounds were separately infused into the renal artery or brachial vein of 23 subjects. Urine extracts were subjected to sequential chromatography on thin-layer plates, Sephadex LH-20, and reverse-phase high-pressure liquid chromatography to isolate the unmetabolized fraction. Dual isotope ratio techniques were used to identify peak fractions, to assess purity, and to calculate recovery. Following renal artery infusions, 32.2% of 6-keto-PGF1 alpha, 13.5% of TXB2, and 3.9% of PGE2 were excreted unmetabolized. Calculated fractional excretion of these compounds on a single transit through the kidney are approximately 30, 13, and 3.9%, respectively. Following brachial vein infusion of [3H]prostaglandin I2, 2.7% of the infusate was excreted as 6-keto-PGF1 alpha, suggesting that circulating prostaglandin I2 may contribute to urinary 6-keto-PGF1 alpha. When combined with published measurements of urinary PGE2, 6-keto-PGF1 alpha, and TXB2, these data can be used to calculate the maximum arterial blood concentration of these substances. The results indicate that arterial blood concentration of PGE2, TXB2, and 6-keto-PGF1 alpha in man are only a few picograms per milliliter or less.
为了确定动脉中前列腺素E2(PGE2)、6-酮-前列腺素F1α(6-酮-PGF1α)和血栓素B2(TXB2)未经代谢而排泄到人体尿液中的比例,将3H标记的这些化合物分别注入23名受试者的肾动脉或肱静脉。尿液提取物依次在薄层板、葡聚糖凝胶LH-20和反相高压液相色谱上进行层析,以分离出未代谢部分。采用双同位素比率技术来鉴定峰值部分、评估纯度并计算回收率。肾动脉注射后,6-酮-PGF1α的32.2%、TXB2的13.5%和PGE2的3.9%未经代谢而排泄。计算出这些化合物单次通过肾脏时的排泄分数分别约为30%、13%和3.9%。经肱静脉注入[3H]前列腺素I2后,2.7%的注入物以6-酮-PGF1α的形式排泄,这表明循环中的前列腺素I2可能是尿液中6-酮-PGF1α的来源之一。当与已发表的尿液中PGE2、6-酮-PGF1α和TXB2的测量值相结合时,这些数据可用于计算这些物质的最大动脉血浓度。结果表明,人体中PGE2、TXB2和6-酮-PGF1α的动脉血浓度仅为每毫升几皮克或更低。