Fukada Sachiko, Sakai Noriyoshi, Adachi Shinji, Nagahama Yoshitaka
Laboratory of Reproductive Biology, Department of Developmental Biology, National Institute for Basic Biology, Okazaki 444, Japan.
Department of Marine Bioscience, Fukui Prefecture University, Obama 917, Japan.
Dev Growth Differ. 1994 Feb;36(1):81-88. doi: 10.1111/j.1440-169X.1994.00081.x.
The metabolism of C-labeled steroid precursors by cell-free homogenates of medaka (Oryzias latipes, a daily spawner) ovarian follicles at 12 different developmental stages was examined using thin layer chromatography (TLC). The radioactive metabolites produced were identified and tested for their ability to induce germinal vesicle breakdown (GVBD) in oocytes in an in vitro homologous bioassay. When homogenates of follicles isolated during oocyte maturation were incubated with C-labeled 17α-hydroxyprogesterone, 13 metabolites were detected in TLC. Among these metabolites, one metabolite exhibited very high maturation inducing activity by the in vitro bioassay. This metabolite was identified as 17α,20β-dihydroxy-4-pregnen-3-one (17α,20β-DP) by its chromatographic mobility in TLC and recrystallization to constant specific activity. 17α,20β-DP production was high in follicles collected between 10 and 6 hr before spawning. A much less biologically active metabolite, 17α,20β-dihydroxy-5β-pregnane-3-one appeared in follicles immediately after the formation of 17α,20β-DP. A similar pattern of steroidogenesis was observed when the follicles were incubated with C-labeled pregnenolone and progesterone. The timely synthesis of 17α,20β-DP in medaka at the onset of oocyte maturation, together with the demonstration that this progestogen is the most potent inducer of oocyte maturation in vitro, provides further evidence that 17α,20β-DP is the naturally occurring maturation-inducing hormone in the medaka. The results also suggest that the conversion of 17α,20β-DP to its 5β-reduced metabolite may be an inactivation process.
利用薄层色谱法(TLC)检测了处于12个不同发育阶段的青鳉(Oryzias latipes,一种每日产卵的鱼类)卵巢卵泡的无细胞匀浆对碳标记类固醇前体的代谢情况。对产生的放射性代谢产物进行了鉴定,并在体外同源生物测定中测试了它们诱导卵母细胞生发泡破裂(GVBD)的能力。当将在卵母细胞成熟过程中分离出的卵泡匀浆与碳标记的17α-羟基孕酮一起孵育时,在TLC中检测到了13种代谢产物。在这些代谢产物中,有一种代谢产物通过体外生物测定显示出非常高的成熟诱导活性。通过其在TLC中的色谱迁移率和重结晶至恒定比活性,将该代谢产物鉴定为17α,20β-二羟基-4-孕烯-3-酮(17α,20β-DP)。在产卵前10至6小时收集的卵泡中,17α,20β-DP的产量很高。一种生物活性低得多的代谢产物,17α,20β-二羟基-5β-孕烷-3-酮在17α,20β-DP形成后立即出现在卵泡中。当卵泡与碳标记的孕烯醇酮和孕酮一起孵育时,观察到了类似的类固醇生成模式。青鳉在卵母细胞成熟开始时及时合成17α,20β-DP,以及证明这种孕激素是体外卵母细胞成熟最有效的诱导剂,进一步证明17α,20β-DP是青鳉中天然存在的成熟诱导激素。结果还表明,17α,20β-DP向其5β-还原代谢产物的转化可能是一个失活过程。