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17,20β,21-三羟基-4-孕烯-3-酮的生物合成和 20β-羟甾脱氢酶在雌雄同体黄鳍鲷终末卵母细胞成熟过程中的表达。

17,20β,21-Trihydroxy-4-pregnen-3-one biosynthesis and 20β-hydroxysteroid dehydrogenase expression during final oocyte maturation in the protandrous yellowfin porgy, Acanthopagrus latus.

机构信息

Department of Aquaculture, National Kaohsiung Marine University, Kaohsiung 811, Taiwan.

出版信息

Gen Comp Endocrinol. 2012 Apr 1;176(2):192-200. doi: 10.1016/j.ygcen.2012.01.010. Epub 2012 Feb 2.

Abstract

The purpose of this study was to investigate the physiological maturation-inducing steroid (MIS) in the marine protandrous yellowfin porgy (Acanthopagrus latus). Female fish were injected with 2 doses of LHRH analog (10 and 40 μg per kg). Ovarian tissue was obtained at 6 h intervals for in vitro analysis of oocyte maturation. The most effective steroids for inducing in vitro maturation (germinal vesicle breakdown and GVBD) in cultured oocytes were 17,20β-dihydroxy-4-pregnen-3-one (17,20βP) and 17,20β,21-trihydroxy-4-pregnen-3-one (20β-S). 17,20βP was less potent than 20βS in inducing oocyte maturation. At higher concentrations, 11-deoxycortisol, 17α-hydroxy-progesterone, and 20β-21-dihydroxy-4-pregnen-3-one also significantly induced oocyte maturation. A tritiated precursor [(3)H]-pregnenolone, was cultured in vitro together with the maturing ovarian tissue. The tritiated metabolites were purified and identified by solvent extraction, HPLC, TLC, acetylation reaction and recrystallization. HPLC, TLC and recrystallization analysis showed that significant levels of tritiated 11-deoxycortisol (a precursor of 20β-S) and 20β-S, but not 17,20βP, were biosynthesized from [(3)H]-pregnenolone. Similar TLC profiles were obtained from the tritiated products that were isolated from the HPLC/TLC 20β-S fraction and standard 20β-S after the acetylation reaction. Constant specific radioactivity of tritiated 11-deoxycortisol and 20β-S but not 17,20βP by recrystallization was obtained in the tritiated metabolites isolated from HPLC and TLC fractions. The expression of 20β-hydroxysteroid dehydrogenase (20β-HSD) mRNA (a key enzyme that converts 11-deoxycortisol to 20β-S) was significantly increased in maturing ovarian tissue. This study provides the first evidence that 20β-S is converted from 11-deoxycortisol and is the possible MIS in yellowfin porgy.

摘要

本研究旨在探讨海洋过渡性黄鳍鲷(Acanthopagrus latus)的生理成熟诱导类固醇(MIS)。对雌性鱼注射 2 剂 LHRH 类似物(每公斤 10 和 40 μg)。每隔 6 小时从卵巢组织中取出体外分析卵母细胞成熟。在培养的卵母细胞中,最有效的诱导体外成熟(卵母细胞核破裂和 GVBD)的类固醇是 17,20β-二羟基-4-孕烯-3-酮(17,20βP)和 17,20β,21-三羟基-4-孕烯-3-酮(20β-S)。17,20βP 诱导卵母细胞成熟的作用不及 20β-S。在较高浓度下,11-脱氧皮质醇、17α-羟孕酮和 20β-21-二羟基-4-孕烯-3-酮也能显著诱导卵母细胞成熟。放射性前体 [(3)H]-孕烯醇酮在体外与成熟的卵巢组织一起培养。放射性代谢物通过溶剂萃取、HPLC、TLC、乙酰化反应和重结晶进行纯化和鉴定。HPLC、TLC 和重结晶分析表明,从 [(3)H]-孕烯醇酮生物合成了大量放射性 11-脱氧皮质醇(20β-S 的前体)和 20β-S,但未检测到 17,20βP。从 HPLC/TLC 20β-S 级分和乙酰化反应后标准 20β-S 中分离出的放射性产物的 TLC 图谱相似。从 HPLC 和 TLC 级分中分离出的放射性代谢物经重结晶后,放射性 11-脱氧皮质醇和 20β-S 的比放射性保持不变,但 17,20βP 则不然。成熟卵巢组织中 20β-羟甾脱氢酶(20β-HSD)mRNA 的表达(将 11-脱氧皮质醇转化为 20β-S 的关键酶)显著增加。本研究首次提供证据表明,20β-S 是由 11-脱氧皮质醇转化而来,可能是黄鳍鲷的 MIS。

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