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首页> 外文期刊>Fish Physiology and Biochemistry >Estradiol and triiodothyronine differentially modulate reproductive and thyroidal genes in male goldfish.
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Estradiol and triiodothyronine differentially modulate reproductive and thyroidal genes in male goldfish.

机译:雌二醇和三碘甲腺氨酸差异调节雄性金鱼的生殖和甲状腺基因。

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摘要

While the reproductive and thyroidal systems are extensively studied in fish, they are largely studied in isolation from one another, but there is evidence supporting cross-regulation between these two systems. To better understand hormone action and the potential cross-regulation between estrogen and thyroid hormones, we examined gene expression changes in estrogen receptor (ER) and thyroid receptor (TR) subtypes and key enzymes responsible for the local synthesis and availability of estrogen and thyroid hormones (aromatase B and deiodinase, respectively) in sexually regressed, adult, male goldfish in response to 3 days waterborne exposures to 17 beta -estradiol (E2; 1 nM), triiodothyronine (T3; 20 and 100 nM), and co-treatments thereof. Treatments with E2 alone did not effect ER subtype transcripts in the liver, telencephalon, or testis; however, in the testis, 1 nM T3 decreased ER alpha and ER beta 1 and co-treatments of T3 and E2 decreased ER beta 1 levels. TR alpha -1 and TR beta transcripts were not auto-regulated by T3 or cross-regulated by E2. Although deiodinase type I levels were also unaffected, deiodinase type II decreased in response to T3 treatments. Liver deiodinase type III transcripts increased in response to T3 treatments, while E2 exhibited antagonistic effects on this T3-mediated induction. These results provide novel evidence of cross-talk between the reproductive and thyroid endocrine axes in a model teleost.
机译:尽管对鱼类的生殖和甲状腺系统进行了广泛的研究,但在很大程度上彼此隔离地研究了它们,但是有证据支持这两种系统之间的交叉调控。为了更好地了解激素的作用以及雌激素和甲状腺激素之间潜在的交叉调节,我们研究了雌激素受体(ER)和甲状腺受体(TR)亚型以及负责局部合成和利用雌激素和甲状腺激素的关键酶的基因表达变化分别对17天的雌二醇(E2; 1 nM),三碘甲腺嘌呤(T3; 20和100 nM)进行水暴露3天后,在性退化的成年雄性金鱼中(分别是芳香酶B和去碘化酶) 。单独使用E2的治疗不会影响肝脏,端脑或睾丸中的ER亚型;然而,在睾丸中,1 nM T3降低了ER alpha和ER beta 1,而T3和E2的联合治疗降低了ER beta 1水平。 TR alpha -1和TR beta转录本不是由T3自动调节或由E2交叉调节的。尽管I型脱碘酶水平也未受影响,但II型脱碘酶响应于T3处理而降低。肝脏脱碘酶III型转录物响应T3处理而增加,而E2对此T3介导的诱导显示拮抗作用。这些结果提供了模型硬骨鱼的生殖和甲状腺内分泌轴之间串扰的新证据。

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