对紫卟啉的遗传毒性和大鼠 90 天重复剂量口服毒性的评估。

IF 2.7 4区 医学 Q3 TOXICOLOGY
Timothy S. Murbach, Róbert Glávits, John R. Endres, Gábor Hirka, Adél Vértesi, Erzsébet Béres, Ilona Pasics Szakonyiné
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引用次数: 0

摘要

随着全球人口的不断增长以及与气候相关的农业问题的增多,人们对可持续和具有成本效益的食品选择的需求也在不断增长,因此人们对用于食品的微藻产品的兴趣也在不断增加。目前已对一些微藻品种进行了毒理学评估,但关于口服红色微藻紫卟啉的数据很少,也没有关于遗传毒性的数据。本文阐述了根据经合组织准则进行的遗传毒性评估和大鼠 90 天重复剂量口服毒性研究。在实验条件下,测试物在细菌反向突变测试中没有诱发基因突变,在菌株基因组中没有出现碱基对变化或框架转换。同样,在 V79 仓鼠肺细胞中,受试物也没有诱发染色体结构畸变。在哺乳动物微核试验中,受试物也没有对小鼠骨髓造成染色体损伤。大鼠 90 天重复剂量口服毒性研究的无观测不良效应水平(NOAEL)被确定为测试的最高剂量,即 3000 毫克/千克体重/天。这些数据为紫锥菊供人类食用的安全性提供了更多证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An evaluation of the genotoxicity and 90-day repeated dose oral toxicity in rats of Porphyridium purpureum

Interest in microalgae products for use in food is increasing, as demands for sustainable and cost-effective food choices grow due to the escalating global population and increase in climate-related struggles with agriculture. Toxicological assessments of some species of microalgae have been conducted, but there were little data available for the oral consumption of the red microalgae Porphyridium purpureum and no data on genotoxicity. This article articulates a genotoxicity assessment and a 90-day repeated dose oral toxicity study in rats performed according to OECD guidelines. Under the experimental conditions applied, the test item did not induce gene mutations by base pair changes or frameshifts in the genome of the strains used in the bacterial reverse mutation test. Similarly, the test item did not induce structural chromosomal aberrations in V79 hamster lung cells. The test item also did not cause chromosomal damage in bone marrow of mice in the mammalian micronucleus test. The no observed adverse effect level (NOAEL) of the 90-day repeated dose oral toxicity study in rats was determined to be the highest dose tested, 3000 mg/kg bw/day. These data add to the body of evidence regarding the safety of P. purpureum for human consumption.

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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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