课题基金 / 基金详情

Environmental toxicants and reproductive health

Environmental toxicants and reproductive health
环境毒物与生殖健康
批准号:
6653002
负责人:
MOZHGAN SAVABIEASFAHANI
金额:
$3.26万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-01-01 至 2004-09-30

项目摘要

项目成果

相关文献

中文摘要
翻译
描述(申请人提供):目前,环境污染物通过影响内分泌功能,导致包括人类在内的各种物种的生殖和发育异常的可能性受到相当大的关注和辩论,而且越来越清楚的是,由内源性激素介导的细胞信号可以完全被内分泌干扰化合物(EDCs)的存在所掩盖或触发,内分泌干扰化合物(EDCs)作为雌激素模拟物或雌激素拮抗剂。在胎儿发育的关键阶段,这种扰动可能导致发育中器官的异常和不可逆转的编程,最终导致成人器官功能障碍或疾病。然而,迄今为止进行的大多数研究未能:1)利用与环境有关的低剂量内分泌碳化物和/或适当的对照;2)将选定的剂量与人体暴露水平联系起来;3)深入研究胎儿暴露及其对成年后生殖能力的影响。本研究的目的是在绵羊胚胎生殖神经内分泌系统分化的关键阶段暴露于环境相关的低浓度常见异种雌激素(双酚和甲氧氯胺),并确定这些污染物对生殖周期和卵泡纵向分布模式的影响。这项研究将利用一种具有良好特性的动物模型进行生殖研究,并明确确定发育关键期,以针对EDC治疗。
英文摘要
DESCRIPTION (provided by applicant): At present, there is considerable concern and debate about the possibility that environmental pollutants, through their effect on endocrine function, are responsible for reproductive and developmental abnormalities in various species including humans, it is also becoming increasingly clear that cellular signals mediated by endogenous hormones can be completely obscured or triggered by the presence of endocrine disrupting compounds (EDCs) which act as estrogen mimics or estrogen antagonists. Such perturbations during critical stages of fetal development can lead to abnormal and irreversible programming of developing organs and finally culminate in adult organ dysfunction or diseases. However, majority of the studies conducted thus far have failed to 1) utilize environmentally relevant low doses of EDCs and/or appropriate controls; 2) relate the selected doses to human exposure levels; and 3) take an indepth took at fetal exposures and its impact on reproductive competence as adult. The goal of this study is to expose sheep fetuses to environmentally relevant low concentrations of common xenoestrogens (bisphenol and methoxychlor) during critical stages of reproductive neuroendocrine system differentiation and to determine the impact of these pollutants on reproductive cyclicity and patterns of ovarian follicular distribution longitudinally. This study will utilize a well-characterized animal model for reproductive research with clearly identified developmental critical periods to target EDC treatment.
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