Choi Kyung-Chul, Jeung Eui-Bae
Department of Obstetrics and Gynecology, British Columbia Children's and Women's Hospital, University of British Columbia, Vancouver, BC, V6H 3V5 Canada.
J Reprod Dev. 2003 Oct;49(5):337-45. doi: 10.1262/jrd.49.337.
The compounds that bind steroid hormone receptors including estrogen receptors (ERs), progesterone receptor (PR) or androgen receptor (AR), and induce or modulate a steroid hormone receptor-mediated response could be defined as endocrine disruptors (EDs). Currently, there are no standard methods to determine whether a chemical is an endocrine disruptor or not. Most results of in vitro and in vivo data are derived from assays that measure estrogenic activity, thus fewer data are available from assays that measure androgenic and progestogenic activities. In this review, we introduce a novel in vivo model to detect EDs using immature rats in the induction of Calbindin-D(9k) (CaBP-9k) mRNA and protein by estrogenic compounds. In addition, we summarize other biomarkers and screening methods for EDs in mammals to describe the usefulness of indicated biomarkers, although mammalian models are very few based on experimental findings.
能够结合类固醇激素受体(包括雌激素受体(ERs)、孕激素受体(PR)或雄激素受体(AR))并诱导或调节类固醇激素受体介导反应的化合物可被定义为内分泌干扰物(EDs)。目前,尚无确定一种化学物质是否为内分泌干扰物的标准方法。大多数体外和体内数据结果来自测量雌激素活性的试验,因此来自测量雄激素活性和孕激素活性试验的数据较少。在本综述中,我们介绍了一种新型体内模型,该模型利用未成熟大鼠通过雌激素化合物诱导钙结合蛋白-D(9k)(CaBP-9k)mRNA和蛋白质来检测内分泌干扰物。此外,我们总结了哺乳动物内分泌干扰物的其他生物标志物和筛选方法,以描述所指出生物标志物的有用性,尽管基于实验结果的哺乳动物模型非常少。