Sone Kiyoaki, Hinago Megumi, Kitayama Atsushi, Morokuma Junji, Ueno Naoto, Watanabe Hajime, Iguchi Taisen
Okazaki Institute for Integrative Bioscience, National Institute for Basic Biology, National Institutes of Natural Science, 5-1 Higashiyama, Myodaiji, Okazaki 444-8787, Japan.
Gen Comp Endocrinol. 2004 Sep 15;138(3):228-36. doi: 10.1016/j.ygcen.2004.06.011.
Many chemicals released into the environment have the capacity to disrupt the normal development of aquatic animals. We investigated the influence of nonylphenol (NP), bisphenol-A (BPA), and 17beta-estradiol (E2) on developing Xenopus laevis embryos, as a model animal in the aquatic environment. Embryos were exposed to eight different concentrations of NP, BPA or E2 between 3 and 96 h post-fertilization (p.f.). Short body length, microcephaly, flexure, edema, and abnormal gut coiling were induced by 20 microM NP, BPA or 10 microM E2 by 96 h p.f. To clarify sensitive stages to these compounds, embryos were exposed to chemicals for 45 or 48 h starting at different developmental stages and experiments were terminated 96 h p.f. BPA and NP induced abnormalities in developing X. laevis, though the sensitive stages of embryos to these chemicals are different, BPA affecting earlier stages and NP affecting at later stages. To analyze the functional mechanisms of BPA and NP in induction of morphological changes, we adapted a DNA array technology and identified 6 X. laevis genes, XIRG, alpha skeletal tropomyosin, cyclin G1, HGF, troponin C2, and ribosomal protein L9. These findings may provide important clues to elucidate common mechanisms underlying teratogenic effects of these chemicals.
许多释放到环境中的化学物质有能力干扰水生动物的正常发育。我们研究了壬基酚(NP)、双酚A(BPA)和17β-雌二醇(E2)对非洲爪蟾胚胎发育的影响,非洲爪蟾作为水生环境中的一种模式动物。在受精后3至96小时(p.f.),将胚胎暴露于八种不同浓度的NP、BPA或E2中。到受精后96小时,20微摩尔的NP、BPA或10微摩尔的E2会诱导出短体长、小头畸形、弯曲、水肿和肠道异常卷曲。为了明确胚胎对这些化合物的敏感阶段,从不同发育阶段开始将胚胎暴露于化学物质中45或48小时,并在受精后96小时终止实验。BPA和NP会诱导非洲爪蟾发育异常,尽管胚胎对这些化学物质的敏感阶段不同,BPA影响早期阶段,NP影响后期阶段。为了分析BPA和NP诱导形态变化的功能机制,我们采用了DNA阵列技术并鉴定出6个非洲爪蟾基因,即XIRG、α-骨骼肌原肌球蛋白、细胞周期蛋白G1、肝细胞生长因子、肌钙蛋白C2和核糖体蛋白L9。这些发现可能为阐明这些化学物质致畸作用的共同机制提供重要线索。