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动物外推法与人类异质性的挑战。

Animal extrapolation and the challenge of human heterogeneity.

作者信息

Calabrese E J

出版信息

J Pharm Sci. 1986 Nov;75(11):1041-6. doi: 10.1002/jps.2600751105.

DOI:10.1002/jps.2600751105
PMID:3820097
Abstract

The capacity of animal models to predict the responses of humans to carcinogenic agents in light of the occurrence of human heterogeneity is assessed in this paper. It is widely accepted that human susceptibility to toxic substances, including carcinogens, is highly variable. At the same time, it is believed that the conventional rodent models, which are usually highly inbred and reared in standard ways, display a very homogeneous response to toxic agents, including carcinogens. The question then becomes, To which narrow band of the broad spectrum of human responses can specific animal models likely be extrapolated? First, the occurrence of human heterogeneity is examined with respect to a broad range of biological characteristics (e.g., aryl hydrocarbon hydroxylase activity, epoxide hydrase activity, glutathione S-transferase activity, beta-glucuronidase activity, debrisoquine hydroxylation, and DNA adduct formation), with particular emphasis on those which affect responses to carcinogens. Second, the occurrence of heterogeneity for selected animal models for these characteristics is assessed and the outcomes are related to the spectrum of human responses noted above.

摘要

本文评估了动物模型根据人类异质性的存在来预测人类对致癌剂反应的能力。人们普遍认为,人类对包括致癌物在内的有毒物质的易感性差异很大。同时,人们认为传统的啮齿动物模型通常高度近亲繁殖且以标准方式饲养,对包括致癌物在内的有毒物质表现出非常一致的反应。那么问题就变成了,特定的动物模型可能会外推到人类广泛反应的哪一个狭窄范围呢?首先,研究了人类在广泛的生物学特征(如芳烃羟化酶活性、环氧化物水解酶活性、谷胱甘肽S-转移酶活性、β-葡萄糖醛酸酶活性、异喹胍羟化以及DNA加合物形成)方面的异质性存在情况,特别强调那些影响对致癌物反应的特征。其次,评估了针对这些特征的选定动物模型的异质性存在情况,并将结果与上述人类反应范围相关联。

相似文献

1
Animal extrapolation and the challenge of human heterogeneity.动物外推法与人类异质性的挑战。
J Pharm Sci. 1986 Nov;75(11):1041-6. doi: 10.1002/jps.2600751105.
2
Comparative biology of test species.受试物种的比较生物学
Environ Health Perspect. 1988 Apr;77:55-62. doi: 10.1289/ehp.887755.
3
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4
Genetic susceptibility to toxic substances and its relationship to carcinogenesis.
IARC Sci Publ. 1984(59):99-106.
5
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6
Interstrain comparison of hepatic and renal microsomal carcinogen metabolism and liver S9-mediated mutagenicity in DA and Lewis rats phenotyped as poor and extensive metabolizers of debrisoquine.作为异喹胍代谢能力差和代谢能力强的表型的DA大鼠和Lewis大鼠肝和肾微粒体致癌物代谢及肝S9介导的致突变性的品系间比较。
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7
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8
[Biotransformation enzymes : their role in carcinogenesis].[生物转化酶:它们在致癌作用中的角色]
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9
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10
Extrapolating carcinogenesis data from animals to humans.将动物致癌数据外推至人类。
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