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系统评价和使用质量标准评估阿斯巴甜致癌性生物检测。

Systematic review and evaluation of aspartame carcinogenicity bioassays using quality criteria.

机构信息

Intertek Regulatory & Scientific Consultancy, 2233 Argentia Rd., Suite 201, Mississauga, ON, L5N 2X7, Canada.

Intertek Regulatory & Scientific Consultancy, 2233 Argentia Rd., Suite 201, Mississauga, ON, L5N 2X7, Canada.

出版信息

Regul Toxicol Pharmacol. 2019 Apr;103:332-344. doi: 10.1016/j.yrtph.2018.01.009. Epub 2018 Jan 12.

Abstract

The current review assessed cancer studies of aspartame based on a quality appraisal using the Klimisch grading system. Nine studies having complete histopathology were included: three 2-year studies by Searle; three transgenic mice studies by the NTP; three lifetime studies by the Ramazzini Institute. A tenth study limited to brain tumors was not rated. None were determined as Klimisch Code 1 (reliable without restrictions). The Searle studies predated GLP standards but their methodology was comparable; transgenic mouse models are not validated, but are accepted as supporting data. These studies were rated Klimisch Code 2 (reliable with restrictions). The Ramazzini Institute used a lifetime model of their own design that has been questioned due to high rates of spontaneous tumors, issues with tumor type diagnosis and concerns about the impact of chronic infections. As many of these problems could be attributed to using animals that died or were terminated near end of life, along with the other problems noted, these studies were rated Klimisch Code 3 (not reliable). As the Klimisch Code 2 studies demonstrated a lack of carcinogenic potential, and as aspartame is hydrolyzed to common components and lacks genotoxic activity, a conclusion that aspartame is not carcinogenic is supported.

摘要

本综述评估了基于 Klimisch 分级系统的质量评估的阿斯巴甜致癌研究。共有 9 项具有完整组织病理学的研究被纳入:Searle 的三项为期 2 年的研究;NTP 的三项转基因小鼠研究;Ramazzini 研究所的三项终生研究。第十项仅限于脑肿瘤的研究未被评级。没有一项被确定为 Klimisch 代码 1(可靠,无限制)。Searle 的研究早于 GLP 标准,但它们的方法学是可比的;转基因小鼠模型未经验证,但被认为是支持数据。这些研究被评为 Klimisch 代码 2(可靠,但有限制)。Ramazzini 研究所使用了他们自己设计的终生模型,由于自发肿瘤的高发生率、肿瘤类型诊断的问题以及对慢性感染影响的担忧,该模型受到了质疑。由于这些问题中的许多可以归因于使用接近生命末期死亡或终止的动物,以及其他注意到的问题,这些研究被评为 Klimisch 代码 3(不可靠)。由于 Klimisch 代码 2 研究表明缺乏致癌潜力,并且阿斯巴甜被水解为常见成分,缺乏遗传毒性活性,因此阿斯巴甜没有致癌性的结论得到了支持。

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