• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Qualitative and quantitative comparability of human and animal developmental neurotoxicants: a workshop summary.

作者信息

Rees D C, Francis E Z, Kimmel C A

机构信息

Health and Environmental Review Division, United States Environmental Protection Agency, Washington, DC 20460.

出版信息

Neurotoxicology. 1990 Summer;11(2):257-69.

PMID:1978270
Abstract

A Workshop on the Qualitative and Quantitative Comparability of Human and Animal Developmental Neurotoxicity was held in Williamsburg, Va. on April 11-13, 1989. Based upon data presented at the Workshop, the degree of qualitative and quantitative comparability between data obtained from humans and experimental animals is reviewed for several developmental neurotoxicants (lead, agents of abuse, alcohol, PCBs, phenytoin, methylmercury, and ionizing radiation). Qualitative comparability was considered for the following functional categories: motor development and function, cognitive function, sensory function, motivation/arousal behavior, and social behavior. Quantitative comparability was assessed by comparing administered dose as well as measures of internal dose (e.g., blood levels) for selected agents. Comparability of qualitative changes between humans and rodents was most apparent when comparisons were made on the basis of general categories of behavioral function. These data support the use of animal models in assessing risk for developmental neurotoxicants and provide guidance on the types of functional end points that can be incorporated into a developmental neurotoxicity testing battery. Evidence of quantitative comparability was most apparent when an internal measure of dose (e.g., blood level) was used.

摘要

相似文献

1
Qualitative and quantitative comparability of human and animal developmental neurotoxicants: a workshop summary.
Neurotoxicology. 1990 Summer;11(2):257-69.
2
Workshop on the qualitative and quantitative comparability of human and animal developmental neurotoxicity, Work Group I report: comparability of measures of developmental neurotoxicity in humans and laboratory animals.人类与动物发育神经毒性的定性和定量可比性研讨会,第一工作组报告:人类和实验动物发育神经毒性测量方法的可比性
Neurotoxicol Teratol. 1990 May-Jun;12(3):261-7. doi: 10.1016/0892-0362(90)90097-v.
3
Workshop on the qualitative and quantitative comparability of human and animal developmental neurotoxicity: summary and implications.
Neurotoxicol Teratol. 1990 May-Jun;12(3):285-92. doi: 10.1016/0892-0362(90)90101-h.
4
Scientific and regulatory issues relevant to assessing risk for developmental neurotoxicity: an overview.
Neurotoxicol Teratol. 1990 May-Jun;12(3):175-81. doi: 10.1016/0892-0362(90)90089-u.
5
Methylmercury developmental neurotoxicity: a comparison of effects in humans and animals.甲基汞对发育中的神经系统的毒性:人类与动物效应的比较。
Neurotoxicol Teratol. 1990 May-Jun;12(3):191-202. doi: 10.1016/0892-0362(90)90091-p.
6
Workshop on the qualitative and quantitative comparability of human and animal developmental neurotoxicity, Work Group II report: testing methods in developmental neurotoxicity for use in human risk assessment.
Neurotoxicol Teratol. 1990 May-Jun;12(3):269-74. doi: 10.1016/0892-0362(90)90098-w.
7
Workshop on the qualitative and quantitative comparability of human and animal developmental neurotoxicity, Work Group III report: weight of evidence and quantitative evaluation of developmental neurotoxicity data.
Neurotoxicol Teratol. 1990 May-Jun;12(3):275-80. doi: 10.1016/0892-0362(90)90099-x.
8
Workshop on the qualitative and quantitative comparability of human and animal developmental neurotoxicity, Work Group IV report: triggers for developmental neurotoxicity testing.
Neurotoxicol Teratol. 1990 May-Jun;12(3):281-4. doi: 10.1016/0892-0362(90)90100-q.
9
The comparative developmental neurotoxicity of lead in humans and animals.铅在人类和动物中的比较发育神经毒性。
Neurotoxicol Teratol. 1990 May-Jun;12(3):215-29. doi: 10.1016/0892-0362(90)90093-r.
10
Developmental neurotoxicity of anticonvulsants: human and animal evidence on phenytoin.抗惊厥药的发育神经毒性:关于苯妥英钠的人体及动物证据。
Neurotoxicol Teratol. 1990 May-Jun;12(3):203-14. doi: 10.1016/0892-0362(90)90092-q.

引用本文的文献

1
Non-disclosure of developmental neurotoxicity studies obstructs the safety assessment of pesticides in the European Union.未披露发育神经毒性研究阻碍了欧盟中农药的安全性评估。
Environ Health. 2023 Jun 1;22(1):44. doi: 10.1186/s12940-023-00994-9.
2
Roadbumps at the Crossroads of Integrating Behavioral and Approaches for Neurotoxicity Assessment.整合行为学与神经毒性评估方法交叉路口的障碍
Front Toxicol. 2022 Feb 25;4:812863. doi: 10.3389/ftox.2022.812863. eCollection 2022.
3
International STakeholder NETwork (ISTNET): creating a developmental neurotoxicity (DNT) testing road map for regulatory purposes.
国际利益相关者网络(ISTNET):为监管目的制定发育神经毒性(DNT)测试路线图。
Arch Toxicol. 2015 Feb;89(2):269-87. doi: 10.1007/s00204-015-1464-2. Epub 2015 Jan 25.
4
Evolution of our understanding of methylmercury as a health threat.我们对甲基汞作为一种健康威胁的认识的演变。
Environ Health Perspect. 1996 Apr;104 Suppl 2(Suppl 2):367-79. doi: 10.1289/ehp.96104s2367.