Mishra A, Joy K P
Department of Zoology, Banaras Hindu University, Varanasi 221005, India.
Gen Comp Endocrinol. 2006 Jun;147(2):141-9. doi: 10.1016/j.ygcen.2005.12.016. Epub 2006 Feb 7.
In vitro effects of estradiol-17beta (E(2)), the catecholestrogens 2-hydroxyE(2) (2-OHE(2)) and 2-methoxyE(2), and the nonsteroidal antiestrogen clomiphene citrate (clomid) on oocyte maturation were investigated in the catfish Heteropneustes fossilis. Incubation of postvitellogenic follicles with 2-OHE(2) induced germinal vesicle breakdown (GVBD; 86% at 5 microM for 30 h) and progression of meiosis up to metaphase II, as evident from the presence of Hoechst stained metaphase chromosomes and anti-alpha-tubulin-positive bipolar spindles. The response was both concentration (1, 2.5, 5, 10, and 20 microM)- and duration (0, 3, 6, 12, 24, and 30 h)-dependent. The diameter of the follicles increased and about 20% follicles elicited ovulation. Incubation of the follicles with clomid (20 microM) induced only about 29-35% GVBD at 30 h. This might be due to the dual properties of clomid with estrogenic (cis-isomer) and antiestrogenic (trans-isomer) actions or due to estrogen receptor binding dynamics. Incubations of the follicles with E(2) or 2-methoxyE(2) did not induce oocyte maturation. The higher concentrations of 2-methoxyE(2) caused degenerative changes in the follicles. In competition studies, E(2) inhibited the GVBD response of 2-OHE(2) (5 microM) significantly in a concentration (1, 5, 10, and 20 microM) or duration (2, 4, and 6 h)-dependent manner after pre-incubation with 20 microM E(2) (P<0.001, one-way ANOVA, P<0.05, Newman-Keuls' test). The results show that 2-OHE(2) induces maturational activity while the parent estrogen is a strong inhibitor, alone or in combination with 2-OHE(2).
在鲶鱼(Heteropneustes fossilis)中研究了17β-雌二醇(E₂)、儿茶酚雌激素2-羟基E₂(2-OHE₂)和2-甲氧基E₂以及非甾体抗雌激素克罗米芬柠檬酸盐(克罗米酚)对卵母细胞成熟的体外作用。用2-OHE₂孵育卵黄生成后期卵泡可诱导生发泡破裂(GVBD;5μM处理30小时时为86%)并使减数分裂进展至中期II,从Hoechst染色的中期染色体和抗α-微管蛋白阳性双极纺锤体的存在可明显看出。该反应呈浓度(1、2.5、5、10和20μM)和时间(0、3、6、12、24和30小时)依赖性。卵泡直径增大,约20%的卵泡引发排卵。用克罗米酚(20μM)孵育卵泡在30小时时仅诱导约29 - 35%的GVBD。这可能是由于克罗米酚具有雌激素(顺式异构体)和抗雌激素(反式异构体)双重作用,或者是由于雌激素受体结合动力学。用E₂或2-甲氧基E₂孵育卵泡未诱导卵母细胞成熟。较高浓度的2-甲氧基E₂导致卵泡出现退行性变化。在竞争性研究中,用20μM E₂预孵育后,E₂以浓度(1、5、10和20μM)或时间(2、4和6小时)依赖性方式显著抑制2-OHE₂(5μM)的GVBD反应(P<0.001,单因素方差分析,P<0.05,Newman-Keuls检验)。结果表明,2-OHE₂诱导成熟活性,而母体雌激素单独或与2-OHE₂联合时是一种强抑制剂。