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雌二醇和三碘甲状腺原氨酸在雄性金鱼中差异调节生殖和甲状腺基因。

Estradiol and triiodothyronine differentially modulate reproductive and thyroidal genes in male goldfish.

机构信息

Department of Biology, Centre for Advanced Research in Environmental Genomics, University of Ottawa, Ottawa, ON, Canada.

出版信息

Fish Physiol Biochem. 2012 Apr;38(2):283-96. doi: 10.1007/s10695-011-9506-z. Epub 2011 May 17.

Abstract

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 17β-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 ERα and ERβ1 and co-treatments of T3 and E2 decreased ERβ1 levels. TRα-1 and TRβ 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.

摘要

虽然鱼类的生殖和甲状腺系统得到了广泛的研究,但这些系统通常是彼此孤立地进行研究的,但有证据表明这两个系统之间存在交叉调节。为了更好地理解激素作用以及雌激素和甲状腺激素之间的潜在交叉调节,我们研究了在性逆转的成年雄性金鱼中,雌激素受体 (ER) 和甲状腺受体 (TR) 亚型以及负责雌激素和甲状腺激素局部合成和可用性的关键酶(芳香酶 B 和脱碘酶)的基因表达变化,这些金鱼在 3 天的时间内通过水暴露于 17β-雌二醇 (E2;1 nM)、三碘甲状腺原氨酸 (T3;20 和 100 nM) 以及这些激素的混合物中。单独用 E2 处理不会影响肝脏、端脑或睾丸中 ER 亚型的转录物;然而,在睾丸中,1 nM T3 降低了 ERα 和 ERβ1,而 T3 和 E2 的共同处理降低了 ERβ1 水平。TRα-1 和 TRβ 转录物不受 T3 自身调节或受 E2 交叉调节。尽管碘酶 I 型水平也不受影响,但碘酶 II 型对 T3 处理有反应性下降。T3 处理后肝脏脱碘酶 III 转录物增加,而 E2 对这种 T3 介导的诱导表现出拮抗作用。这些结果为模型硬骨鱼生殖和甲状腺内分泌轴之间的交叉对话提供了新的证据。

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