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本文引用的文献

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Effects of acrylamide given during gestation on dopamine receptor binding in rat pups.孕期给予丙烯酰胺对大鼠幼崽多巴胺受体结合的影响。
Toxicol Lett. 1981 Jan;7(3):233-8. doi: 10.1016/0378-4274(81)90074-6.
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The effects of postpartum exposure to triethyl tin on the neurobehavioral functioning of rats.
Neurotoxicology. 1981 Oct;2(2):283-96.
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Postpartum exposure to triethyl tin produces long-term alterations in responsiveness to apomorphine.
Neurotoxicology. 1982 Jul;3(1):64-71.
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A review of acrylamide neurotoxicity. Part I. Properties, uses and human exposure.丙烯酰胺神经毒性综述。第一部分。性质、用途及人体暴露情况。
Can J Neurol Sci. 1974 May;1(2):143-50. doi: 10.1017/s0317167100019739.
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Measuring early pregnancy loss: laboratory and field methods.测量早期妊娠丢失:实验室及现场方法
Fertil Steril. 1985 Sep;44(3):366-74.
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Human teratogenicity.人类致畸性。
Adv Pediatr. 1986;33:225-68.
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Current status of behavioral teratology: science and regulation.行为致畸学的现状:科学与监管
Crit Rev Toxicol. 1988;19(1):1-10. doi: 10.3109/10408448809040814.
8
Potential human developmental toxicants and the role of animal testing in their identification and characterization.潜在的人类发育毒物以及动物试验在其识别和特征描述中的作用。
Crit Rev Toxicol. 1989;19(3):251-339. doi: 10.3109/10408448909037473.
9
Delayed neurotoxicity in monkeys exposed developmentally to methylmercury.发育过程中接触甲基汞的猴子出现迟发性神经毒性。
Neurotoxicology. 1989 Winter;10(4):645-50.
10
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.

对发育神经毒理学的关注:是否合理,以及针对此采取了哪些措施?

The concern for developmental neurotoxicology: is it justified and what is being done about it?

作者信息

Tilson H A

机构信息

Neurotoxicology Division (MD-74B), HERL/EPA, Research Triangle Park, NC 27711, USA.

出版信息

Environ Health Perspect. 1995 Sep;103 Suppl 6(Suppl 6):147-51. doi: 10.1289/ehp.95103s6147.

DOI:10.1289/ehp.95103s6147
PMID:8549464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1518918/
Abstract

In general, it is believed that the possibility of an adverse developmental outcome following conception is relatively high. In most cases, the cause of the defect is not clear, although exposure to chemical agents at a critical period during development has been proposed to play a significant role. Consequently, regulatory agencies such as the U.S. Environmental Protection Agency (U.S. EPA) have promulgated testing guidelines for assessing developmental neurotoxicity of chemicals in animal testing protocols. Concerns have been expressed about the use of behavioral tests to evaluate chemicals for developmental neurotoxicity, since some investigators believe that they lack predictive validity for human developmental neurotoxicity. Other investigators have indicated that results from such studies are difficult to interpret because of a lack of standardization and sensitivity of the tests. Furthermore, it has been argued that the developing organism is not especially sensitive to chemicals or, if effects are observed, the developing organism is capable of compensating for the deficit. Recent research, however, has adequately demonstrated that developing organisms are especially vulnerable to chemical agents if the exposure occurs at a critical period during development, while other studies have supported the assumption that functional or behavioral effects observed in animal models can be extrapolated to humans. These findings support the routine assessment of chemicals for developmental neurotoxicity using functional end points and suggest that currently available methods could be used to determine more precisely the mechanism of chemical-induced developmental defects.

摘要

一般来说,人们认为受孕后出现不良发育结果的可能性相对较高。在大多数情况下,缺陷的原因尚不清楚,尽管有人提出在发育的关键时期接触化学物质起到了重要作用。因此,像美国环境保护局(U.S. EPA)这样的监管机构已经颁布了在动物试验方案中评估化学物质发育神经毒性的测试指南。有人对使用行为测试来评估化学物质的发育神经毒性表示担忧,因为一些研究人员认为这些测试对人类发育神经毒性缺乏预测效度。其他研究人员指出,由于这些测试缺乏标准化和敏感性,此类研究的结果难以解释。此外,有人认为发育中的生物体对化学物质不是特别敏感,或者即使观察到了影响,发育中的生物体也能够弥补缺陷。然而,最近的研究充分证明,如果在发育的关键时期发生接触,发育中的生物体对化学物质特别敏感,而其他研究支持这样一种假设,即在动物模型中观察到的功能或行为影响可以外推到人类。这些发现支持使用功能终点对化学物质进行发育神经毒性的常规评估,并表明目前可用的方法可用于更精确地确定化学物质诱导发育缺陷的机制。