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芳香化酶抑制剂和17α-甲基睾酮可使日本牙鲆(Paralichthys olivaceus)的遗传雌性发生性逆转,转变为表型雄性,并抑制P450芳香化酶基因的表达。

Aromatase inhibitor and 17alpha-methyltestosterone cause sex-reversal from genetical females to phenotypic males and suppression of P450 aromatase gene expression in Japanese flounder (Paralichthys olivaceus).

作者信息

Kitano T, Takamune K, Nagahama Y, Abe S I

机构信息

Kumamoto Prefectural Fisheries Research Center, Ohyano, Amakusa, Kumamoto, Japan.

出版信息

Mol Reprod Dev. 2000 May;56(1):1-5. doi: 10.1002/(SICI)1098-2795(200005)56:1<1::AID-MRD1>3.0.CO;2-3.

Abstract

The sex of Japanese flounder (Paralichthys olivaceus) is easily altered by water temperature or sex steroid hormone treatment during the period of sex determination. We have previously shown that rearing the genetically female larvae at high water temperature caused the suppression of P450 aromatase (P450arom) gene expression in the gonad and phenotypic sex-reversal of the individuals to males (Kitano et al. 1999. J Mol Endocrinol 23:167-176). In the present study, we show that treatment of genetically female larvae with fadrozole (aromatase inhibitor) or 17alpha-methyltestosterone induces sex-reversal as well as suppression of P450arom gene expression. The effect of fadrozole was counteracted by co-administration of estradiol-17beta. Effective periods for fadrozole treatment to induce sex-reversal were similar to those for high water temperature treatment. RT-PCR did not detect P450arom mRNA in gonad of the sex-reversed, phenotypic males. These results indicate that sex-reversal of the genetically female larvae by aromatase inhibitor (or 17alpha-methyltestosterone) may be due to the suppression of P450arom gene expression and the resultant decrease in the amount of estrogen.

摘要

在性别决定期间,牙鲆(Paralichthys olivaceus)的性别很容易受到水温或性类固醇激素处理的影响而发生改变。我们之前已经表明,在高水温下饲养遗传雌性幼体,会导致性腺中P450芳香化酶(P450arom)基因表达受到抑制,个体的表型性逆转成为雄性(Kitano等人,1999年。《分子内分泌学杂志》23:167 - 176)。在本研究中,我们发现用法倔唑(芳香化酶抑制剂)或17α - 甲基睾酮处理遗传雌性幼体,会诱导性逆转以及抑制P450arom基因表达。法倔唑的作用可通过共同给予17β - 雌二醇来抵消。法倔唑处理诱导性逆转的有效时期与高水温处理的相似。逆转录 - 聚合酶链反应(RT - PCR)未在性逆转的表型雄性性腺中检测到P450arom mRNA。这些结果表明,芳香化酶抑制剂(或17α - 甲基睾酮)使遗传雌性幼体发生性逆转,可能是由于P450arom基因表达受到抑制以及由此导致的雌激素量减少。

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