Liston T E, Roberts L J
Proc Natl Acad Sci U S A. 1985 Sep;82(18):6030-4. doi: 10.1073/pnas.82.18.6030.
In vitro studies examining the metabolic transformation of prostaglandin D2 (PGD2) by human liver were conducted. PGD2 was found to be converted by a NADPH-dependent enzyme in the 100,000 X g supernatant of human liver exclusively to a single more polar compound that had a mass spectrum essentially the same as that of prostaglandin F2 alpha (PGF2 alpha). However, this compound could be chromatographically separated from PGF2 alpha and failed to form a butylboronate derivative. The structure of this compound was established as 9 alpha, 11 beta-(15S)-trihydroxyprosta-(5Z, 13E)-dien-1-oic acid (9 alpha, 11 beta-PGF2) by comparison of its chromatographic and mass spectral characteristics with authentic 9 alpha, 11 beta-PGF2. This compound was found to be biologically active by demonstrating increases in blood pressure in rats in a dose-related fashion following intravenous administration. By using a mass spectrometric assay, levels of this compound in plasma and urine from a normal volunteer were 6 pg/ml and 982 ng/24 hr, respectively. In a patient with systemic mastocytosis associated with overproduction of PGD2, urinary excretion of 9 alpha, 11 beta-PGF 2 was 6634 ng/24 hr and a circulating plasma level as high as 490 ng/ml was found during a severe episode of systemic mast cell activation. 9 alpha, 11 beta-PGF2 is structurally a unique prostaglandin, is enzymatically formed, is produced in vivo in humans, and is biologically active.
开展了关于人肝脏对前列腺素D2(PGD2)进行代谢转化的体外研究。研究发现,PGD2在人肝脏100,000×g超速离心上清液中,通过一种依赖烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的酶,专一性地转化为一种单一的极性更强的化合物,该化合物的质谱与前列腺素F2α(PGF2α)基本相同。然而,这种化合物可以通过色谱法与PGF2α分离,并且不能形成硼酸丁酯衍生物。通过将其色谱和质谱特征与 authentic 9α, 11β-PGF2 进行比较,确定该化合物的结构为9α, 11β-(15S)-三羟基前列腺素-(5Z, 13E)-二烯-1-酸(9α, 11β-PGF2)。静脉注射后,该化合物在大鼠体内呈现剂量依赖性的血压升高,表明其具有生物活性。通过质谱分析法测定,一名正常志愿者血浆和尿液中该化合物的水平分别为6 pg/ml和982 ng/24小时。在一名与PGD2过度产生相关的系统性肥大细胞增多症患者中,9α, 11β-PGF2的尿排泄量为6634 ng/24小时,并且在一次严重的系统性肥大细胞激活发作期间,发现循环血浆水平高达490 ng/ml。9α, 11β-PGF2在结构上是一种独特的前列腺素,通过酶促形成,在人体内有内源性生成,并且具有生物活性。