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用于神经系统神经毒性体外评估的新模型及“分层测试”模型的初步验证阶段

New models for the In vitro assessment of neurotoxicity in the nervous system and the preliminary validation stages of a 'tiered-test' model.

作者信息

Atterwill C K, Davenport-Jones J, Goonetilleke S, Johnston H, Purcell W, Thomas S M, West M, Williams S

机构信息

The CellTox Centre, Division of Biosciences, University of Hertfordshire, College Lane, Hatfield, Herts. AL10 9AB, UK.

出版信息

Toxicol In Vitro. 1993 Sep;7(5):569-80. doi: 10.1016/0887-2333(93)90090-r.

Abstract

Many cell culture models are available for the in vitro assessment of neurotoxicity. The use of three culture types has been investigated: neuroblastoma cell lines, primary cultures of rat and chick midbrain, and organotypic whole brain reaggregate cultures. A tiered system has been proposed involving hierarchical testing through three layers of different neural complexities. This scheme is currently undergoing validation under the auspices of FRAME/EC using 40 test chemicals. To determine the performance and suitability of these culture models studies on selected neurotoxins have been performed: ethylcholine mustard aziridinium, vincristine, aluminium, glutamate, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine and T(3)-deprivation. Aspects of this work are described, including mechanistic investigations in rat brain reaggregate cultures. In vitro exposure of xenobiotics through a tiered testing system (ranging from simple cell-based assays measuring cytotoxicological parameters to more complex markers in organotypic cultures) may permit detection of central nervous system neurotoxicity in the contexts of both 'screening' and mechanistics. The degree of simplicity, automaticity and transportability of the tests requires consideration as will the possibility of endpoints for specific classes of chemicals, for example cholinesterase for organophosphorus insecticides. Factors such as extrapolation from the central nervous system to the peripheral nervous system, metabolic activation, the blood-brain barrier, degree of neural cell activation, repair mechanisms, and developing versus adult nervous systems are considered.

摘要

有许多细胞培养模型可用于体外神经毒性评估。人们已经研究了三种培养类型的用途:神经母细胞瘤细胞系、大鼠和鸡中脑的原代培养物以及器官型全脑重聚培养物。有人提出了一种分层系统,涉及通过三层具有不同神经复杂性的层次测试。该方案目前正在FRAME/EC的支持下,使用40种测试化学品进行验证。为了确定这些培养模型的性能和适用性,已经对选定的神经毒素进行了研究:乙基胆碱氮芥吖丙啶、长春新碱、铝、谷氨酸、1-甲基-4-苯基-1,2,3,6-四氢吡啶和T(3)剥夺。本文描述了这项工作的各个方面,包括对大鼠脑重聚培养物的机制研究。通过分层测试系统(从测量细胞毒理学参数的简单基于细胞的试验到器官型培养物中更复杂的标志物)对异生物素进行体外暴露,可能允许在“筛选”和机制研究的背景下检测中枢神经系统神经毒性。测试的简单程度、自动化程度和可运输性需要考虑,特定类化学品的终点可能性也需要考虑,例如有机磷杀虫剂的胆碱酯酶。还考虑了从中枢神经系统向外周神经系统的外推、代谢活化、血脑屏障、神经细胞活化程度、修复机制以及发育中的与成年神经系统等因素。

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