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绵羊精液中20-羟基前列腺素E1和E2的分离与生物合成

Isolation and biosynthesis of 20-hydroxyprostaglandins E1 and E2 in ram seminal fluid.

作者信息

Oliw E H, Fahlstadius P, Hamberg M

出版信息

J Biol Chem. 1986 Jul 15;261(20):9216-21.

PMID:3087990
Abstract

Ram semen was found to contain 20-hydroxyprostaglandin E1 and 20-hydroxyprostaglandin E2. The relative amounts of the two compounds were almost equal, although ram semen contained at least 10 times more prostaglandin E1 than prostaglandin E2. The accessory genital glands of the ram were analyzed for their capacity to metabolize [14C]arachidonic acid to prostaglandins. Biosynthesis of prostaglandins was only found in microsomes of the mucosa of the ampulla of vas deferens and in microsomes of the vesicular glands. Ram vesicular glands and the ampulla of vas deferens were also found to contain the two 20-hydroxylated E prostaglandins. Microsomes of ram vesicular glands and NADPH metabolized exogenous prostaglandin E2 to 20-hydroxyprostaglandin E2 albeit in low yields. Prostaglandin E2 appeared to be a better substrate than prostaglandin E1. Microsomes of human seminal vesicles and NADPH metabolized exogenous prostaglandin E2 to 19-hydroxyprostaglandin E2. The results show that 19- and 20-hydroxylation of prostaglandins occurs in human and ram seminal vesicles, respectively, and possibly also in the ampulla of vas deferens of the ram. The ram and human enzymes specifically hydroxylated the terminal and the penultimate carbon of prostaglandin E2, respectively.

摘要

公羊精液中发现含有20-羟基前列腺素E1和20-羟基前列腺素E2。这两种化合物的相对含量几乎相等,尽管公羊精液中前列腺素E1的含量至少是前列腺素E2的10倍。分析了公羊附属生殖腺将[14C]花生四烯酸代谢为前列腺素的能力。仅在输精管壶腹黏膜的微粒体和精囊腺的微粒体中发现了前列腺素的生物合成。还发现公羊精囊腺和输精管壶腹中含有两种20-羟基化的E类前列腺素。公羊精囊腺微粒体和NADPH将外源性前列腺素E2代谢为20-羟基前列腺素E2,尽管产率较低。前列腺素E2似乎比前列腺素E1更适合作为底物。人精囊微粒体和NADPH将外源性前列腺素E2代谢为19-羟基前列腺素E2。结果表明,前列腺素的19-羟基化和20-羟基化分别发生在人和公羊的精囊中,公羊输精管壶腹可能也会发生。公羊和人的酶分别特异性地将前列腺素E2的末端碳和倒数第二个碳羟基化。

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Prostaglandin E2 20-hydroxylase in ampulla of vas deferens of sheep.绵羊输精管壶腹中的前列腺素E2 20-羟化酶
Acta Physiol Scand. 1987 Feb;129(2):259-62. doi: 10.1111/j.1748-1716.1987.tb08066.x.

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