Raeside J I, Renaud R L
J Endocrinol. 1985 Dec;107(3):415-9. doi: 10.1677/joe.0.1070415.
Isolation of 3 beta-hydroxy-5,7-androstadien-17-one, as a major component of steroids extracted from vein blood of the fetal gonads of the horse, supports the proposed role for the compound as a precursor for equilin formation in the placenta of the mare. The 5,7-diene was extracted from blood collected from gonadal veins of fetal ovaries and testes in situ, and from a fetal testis connected to an artery in the neck region of the mare. Perfusion of fetal gonads in the laboratory was carried out to allow longer periods of collection. In addition, isolated cell preparations from a fetal testis were incubated for 4-8 h in tissue culture to investigate steroid secretion in vitro. Final purification of neutral steroids in the extracts was carried out by high performance liquid chromatography, and identification was made by u.v. and mass spectrometry. The presence of 3 beta-hydroxy-5,7-androstadien-17-one in extracts from all sources provided evidence for its secretion in vivo and in vitro. Other 5,7-dienes, which were less polar than the C19 compound, were noted in extracts of media but not identified. These data support the view that a 5,7-diene pathway is involved in the biosynthesis of 3 beta-hydroxy-5,7-androstadien-17-one in the fetal horse gonad.
从马胎儿性腺静脉血中提取的类固醇的主要成分3β-羟基-5,7-雄甾二烯-17-酮的分离,支持了该化合物作为母马胎盘内马萘雌酮形成前体的推测作用。5,7-二烯是从原位采集的胎儿卵巢和睾丸性腺静脉血以及与母马颈部动脉相连的胎儿睾丸中提取的。在实验室中对胎儿性腺进行灌注,以便进行更长时间的采集。此外,将从胎儿睾丸分离的细胞制剂在组织培养中孵育4 - 8小时,以研究体外类固醇分泌情况。提取物中中性类固醇的最终纯化通过高效液相色谱法进行,鉴定则通过紫外光谱和质谱法进行。所有来源提取物中均存在3β-羟基-5,7-雄甾二烯-17-酮,这为其在体内和体外的分泌提供了证据。在培养基提取物中还发现了其他比C19化合物极性小的5,7-二烯,但未进行鉴定。这些数据支持了5,7-二烯途径参与胎儿马性腺中3β-羟基-5,7-雄甾二烯-17-酮生物合成的观点。