Oliw E H
Acta Physiol Scand. 1987 Feb;129(2):259-62. doi: 10.1111/j.1748-1716.1987.tb08066.x.
Microsomes were prepared from the ampullary mucosa of ram ductus deferens. The microsomal fraction was supplemented with 1 mM NADPH and was found to metabolize PGE2 to 20-hydroxy-PGE2. The product was identified by gas chromatography-mass spectrometry (GC-MS). The biosynthesis of 20-hydroxy-PGE2 was assessed by reversed-phase high performance liquid chromatography (HPLC) using 19-hydroxy-PGE1 as an internal standard and 0.2 mM PGE2 was found to be metabolized to 20-hydroxy-PGE2 at a rate of 7.1 pmol min-1 mg-1 of protein. Like a prostaglandin 20-hydroxylase of sheep vesicular glands, the 20-hydroxylase of the ampulla was only partly inhibited by metyrapone. 20-Hydroxy E prostaglandins, which occur in ram semen, are likely to be formed by the vesicular glands and the ampulla of vas deferens in the sheep.
从公羊输精管壶腹黏膜制备微粒体。微粒体部分添加1 mM烟酰胺腺嘌呤二核苷酸磷酸(NADPH)后,发现其可将前列腺素E2(PGE2)代谢为20-羟基-PGE2。产物通过气相色谱-质谱联用仪(GC-MS)进行鉴定。以19-羟基-PGE1为内标,采用反相高效液相色谱法(HPLC)评估20-羟基-PGE2的生物合成,发现0.2 mM PGE2以7.1皮摩尔每分钟每毫克蛋白质的速率代谢为20-羟基-PGE2。与绵羊精囊的前列腺素20-羟化酶一样,壶腹的20-羟化酶仅被甲吡酮部分抑制。存在于公羊精液中的20-羟基E类前列腺素可能由绵羊的精囊和输精管壶腹形成。