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对狗岩螺(Nucella lapillus)性畸变诱导机制的新见解。

New insights into the mechanism of imposex induction in the dogwhelk Nucella lapillus.

作者信息

Santos M M, Castro L Filipe C, Vieira M N, Micael J, Morabito R, Massanisso P, Reis-Henriques M A

机构信息

Centre of Marine and Environmental Research, Rua dos Bragas 289, 4050-123 Porto, Portugal.

出版信息

Comp Biochem Physiol C Toxicol Pharmacol. 2005 May;141(1):101-9. doi: 10.1016/j.cca.2005.05.008.

Abstract

In an attempt to clarify the mechanism(s) of tributyltin-mediated imposex induction in females of the neogastropod Nucella lapillus, dogwhelks collected in an almost imposex free population were exposed to several treatments for a 3 month-period, and the effects on imposex induction and testosterone/estradiol levels were evaluated. As a positive control, tributyltin (50 ng TBT Sn/L) clearly induced imposex and led to a significant increase in the severity of the phenomenon. In contrast, although a selective P450 aromatase inhibitor (formestane at 0.3 mg/L) was capable of imposex induction, it failed to increase its severity. A vertebrate androgen receptor (AR) antagonist (cyproterone acetate at 1.25 mg/L) in combination with TBT completely blocked the imposex induction capacity of TBT. On the other hand, an estrogen receptor antagonist (tamoxifen at 0.3 mg/L) rendered no effect. The determination of steroid levels in female specimens revealed that TBT induces an elevation of free testosterone (but not the total amount, free+esterified), while the co-administration of the anti-androgen and TBT was able to rescue the increase of free testosterone levels. Despite a minor decrease in the amount of testosterone-fatty acid esters in the TBT group, significant differences in esterified testosterone were not found among treatments. On the contrary, free estradiol levels were elevated in the TBT, anti-androgens and TBT plus anti-androgens groups. These results indicate that free estradiol biosynthesis in TBT-exposed females does not seem to be affected. Overall, our results demonstrate that a selective aromatase inhibitor can induce imposex in N. lapillus but not to a similar extent of TBT, which may suggest the involvement of other mechanism in imposex induction, besides aromatase inhibition. Additionally, the study points to the involvement of AR receptors in imposex induction.

摘要

为了阐明三丁基锡介导的新腹足目动物滨螺雌性个体性畸变诱导机制,采集了来自几乎无性别畸变群体的滨螺,对其进行为期3个月的几种处理,并评估对性畸变诱导及睾酮/雌二醇水平的影响。作为阳性对照,三丁基锡(50纳克三丁基锡锡/升)明显诱导了性畸变,并导致该现象的严重程度显著增加。相比之下,尽管一种选择性细胞色素P450芳香化酶抑制剂(福美坦,浓度为0.3毫克/升)能够诱导性畸变,但其严重程度并未增加。一种脊椎动物雄激素受体(AR)拮抗剂(醋酸环丙孕酮,浓度为1.25毫克/升)与三丁基锡联合使用时,完全阻断了三丁基锡诱导性畸变的能力。另一方面,一种雌激素受体拮抗剂(他莫昔芬,浓度为0.3毫克/升)则没有效果。对雌性样本中类固醇水平的测定表明,三丁基锡会导致游离睾酮水平升高(但不是总量,即游离+酯化形式),而抗雄激素与三丁基锡共同给药能够挽救游离睾酮水平的升高。尽管三丁基锡组中睾酮脂肪酸酯的量略有下降,但各处理组之间酯化睾酮的差异并不显著。相反,三丁基锡组、抗雄激素组以及三丁基锡加抗雄激素组中的游离雌二醇水平均升高。这些结果表明,暴露于三丁基锡的雌性个体中游离雌二醇的生物合成似乎未受影响。总体而言,我们的结果表明,一种选择性芳香化酶抑制剂能够诱导滨螺出现性畸变,但程度不如三丁基锡,这可能表明除了芳香化酶抑制作用外,性畸变诱导还涉及其他机制。此外,该研究表明AR受体参与了性畸变诱导过程。

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