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尼古丁在体外微核试验中诱导作用的作用机制分析。

Mode-of-action analysis of the effects induced by nicotine in the in vitro micronucleus assay.

机构信息

PMI R&D, Philip Morris Products S.A., Neuchâtel, Switzerland.

出版信息

Environ Mol Mutagen. 2019 Dec;60(9):778-791. doi: 10.1002/em.22314. Epub 2019 Aug 30.

Abstract

Nicotine's genotoxic potential has been extensively studied in vitro. While the results of mammalian cell-based studies have inferred that it can potentially damage chromosomes, in general and with few exceptions, adverse DNA effects have been observed primarily at supraphysiological concentrations in nonregulatory assays that provide little information on its mode-of-action (MoA). In this study, a modern-day regulatory genotoxicity assessment was conducted using a flow cytometry-based in vitro micronucleus (MN) assay, Good Laboratory Practice study conditions, Chinese hamster ovary cells of known provenance, and acceptance/evaluation criteria from the current OECD Test Guideline 487. Nicotine concentrations up to 3.95 mM had no effect on background levels of DNA damage; however, concentrations above the point-of-departure range of 3.94-4.54 mM induced increases in MN and hypodiploid nuclei, indicating a possible aneugenicity hazard. Follow-up experiments designed to elucidate nicotine's MoA revealed cellular vacuolization, accompanying distortions in microtubules, inhibition of tubulin polymerization, centromere-positive DNA, and multinucleate cells at MN-inducing concentrations. Vacuoles likely originated from acidic cellular compartments (e.g., lysosomes). Remarkably, genotoxicity was suppressed by chemicals that raised the luminal pH of these organelles. Other endpoints (e.g., changes in phosphorylated histones) measured in the study cast doubt on the biological relevance of this apparent genotoxicity. In addition, three major nicotine metabolites, including cotinine, had no MN effects but nornicotine induced a nicotine-like profile. It is possible that nicotine's lysosomotropic properties drive the genotoxicity observed in vitro; however, the potency and mechanistic insights revealed here indicate that it is likely of minimal physiological relevance for nicotine consumers. Environ. Mol. Mutagen. 2019. © 2019 The Authors. Environmental and Molecular Mutagenesis published by Wiley Periodicals, Inc. on behalf of Environmental Mutagen Society.

摘要

尼古丁的遗传毒性潜力已在体外得到广泛研究。虽然哺乳动物细胞研究的结果推断它可能潜在地损伤染色体,但一般来说,除了少数例外,在非监管性测定中,在超生理浓度下观察到的不良 DNA 效应主要提供了关于其作用模式(MoA)的信息很少。在这项研究中,使用基于流式细胞术的体外微核(MN)测定、良好实验室规范研究条件、已知来源的中国仓鼠卵巢细胞以及当前 OECD 测试指南 487 的接受/评估标准,进行了现代监管遗传毒性评估。尼古丁浓度高达 3.95mM 对 DNA 损伤的背景水平没有影响;然而,浓度超过 3.94-4.54mM 的起始点范围会导致 MN 和亚二倍体核的增加,表明可能存在着变向遗传毒性危险。为阐明尼古丁的 MoA 而设计的后续实验揭示了细胞空泡化,伴随着微管扭曲、微管蛋白聚合抑制、着丝粒阳性 DNA 和 MN 诱导浓度下的多核细胞。空泡可能起源于酸性细胞区室(例如溶酶体)。值得注意的是,在这些细胞器中提高腔室 pH 的化学物质抑制了遗传毒性。该研究中测量的其他终点(例如,磷酸化组蛋白的变化)对这种明显遗传毒性的生物学相关性提出了质疑。此外,三种主要的尼古丁代谢物,包括可替宁,没有 MN 效应,但去甲烟碱诱导了类似于尼古丁的表型。尼古丁的溶酶体趋向性特性可能导致了体外观察到的遗传毒性;然而,这里揭示的效力和机制见解表明,对于尼古丁消费者来说,它可能具有最小的生理相关性。环境分子突变 2019。©2019 作者。环境与分子诱变由 Wiley 期刊出版,代表环境诱变剂协会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99e/6900147/4023f1437eca/EM-60-778-g001.jpg

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