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从动物到胚胎干细胞的发育毒性测试。

Developmental toxicity testing from animal towards embryonic stem cells.

作者信息

Pellizzer Cristian, Bremer Susanne, Hartung Thomas

机构信息

European Centre for the Validation of Alternative Methods, Institute for Health and Consumer Protection, Joint Research Centre, Ispra, Italy.

出版信息

ALTEX. 2005;22(2):47-57.

Abstract

Developmental toxicology is the study of undesirable effects on the development of the organism, which may result from exposure before conception, from the period of prenatal development, or postnatally during the time of sexual maturation. The principal manifestations of developmental toxicity include: embryolethality, malformations, growth retardation, and functional impairment. In 2001, the European Commission published the future chemicals policy entitled "White Paper: Strategy for a Future Chemicals Policy". The new regulation requires a toxicological evaluation with strong emphasis on reproductive toxicity, by using in vitro methods, especially for those chemicals marketed at more than 1 ton per year. For this reason, the establishment of in vitro models capable of detecting major undesirable manifestations in the fetus, are urgently required. The aim of the present review is to explore the capacity of existing in vitro systems, based on embryonic stem (ES) cells, to identify embryotoxicity with a focus on specific effects such as teratogenicity and growth retardation. In addition, we discuss the possibility to adapt the mouse ES cells based tests to human ES cells, avoiding inter-species variations in developmental toxicity studies and address related ethical issues. Considering the different manifestations of developmental toxicity, only a battery of in vitro tests will provide the necessary information for regulatory developmental toxicity assessment.

摘要

发育毒理学是研究生物体发育过程中受到的不良影响,这些影响可能源于受孕前、产前发育期间或性成熟后的暴露。发育毒性的主要表现包括:胚胎致死、畸形、生长迟缓以及功能损害。2001年,欧盟委员会发布了题为《白皮书:未来化学品政策战略》的未来化学品政策。新法规要求进行毒理学评估,特别强调生殖毒性,采用体外方法,尤其是针对每年销售量超过1吨的化学品。因此,迫切需要建立能够检测胎儿主要不良表现的体外模型。本综述的目的是探讨基于胚胎干细胞(ES细胞)的现有体外系统识别胚胎毒性的能力,重点关注致畸性和生长迟缓等特定效应。此外,我们讨论了将基于小鼠ES细胞的试验适用于人类ES细胞的可能性,避免发育毒性研究中的种间差异,并探讨相关伦理问题。考虑到发育毒性的不同表现,只有一系列体外试验才能为监管发育毒性评估提供必要信息。

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