鼻烟和无烟尼古丁袋提取物的多终点体外毒理学评估

IF 2.3 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation research. Genetic toxicology and environmental mutagenesis Pub Date : 2024-02-20 DOI:10.1016/j.mrgentox.2024.503738
Fan Yu, Emma Bishop, Fabio Miazzi, Rhian Evans, David Smart, Damien Breheny, David Thorne
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引用次数: 0

摘要

现代 "口服无烟草尼古丁袋(NPs)是一种含有尼古丁的产品,其外观和概念与瑞典的鼻烟(snus)相似。我们采用三步法对 NPs 和鼻烟提取物的生物效应进行了体外分析。使用 ToxTracker 筛选氧化应激、细胞应激、蛋白质损伤和 DNA 损伤的生物标志物。细胞毒性、诱变性和遗传毒性分别通过以下检测方法进行评估:中性红吸收试验(NRU)、艾姆斯试验和小鼠淋巴瘤试验(MLA)。对无毒条件下的磷酸化信号和炎症标志物进行了靶向分析,以研究任何潜在的信号通路或炎症反应。对一种参考鼻烟(CRP1.1)和四种具有不同口味和尼古丁强度的 NPs 进行了评估。将一个小袋放入 20 毫升培养基(针对每种检测方法)中培养,并加入小袋材料,即可产生检测物品提取物。NP 提取物未诱导任何细胞毒性或诱变反应,基因毒性反应极小,诱导的信号或炎症标志物有限。相比之下,在没有 S9 的情况下,CRP1.1 在四个毒理学终点中诱导出阳性反应:Srxn1(氧化应激)、Btg2(细胞应激)、Ddit3(蛋白质损伤)和 Rtkn(DNA 损伤);在有 S9 的情况下,在三个终点中诱导出阳性反应:Srxn1、Ddit3 和 Rtkn。在 MLA 中进行评估时,CRP1.1 具有基因毒性,它激活了涉及增殖和细胞应激的信号通路,并以剂量依赖的方式特异性地诱导了 c-JUN、CREB1、p53、p38 MAPK 的磷酸化,其次是 AKT1S1、GSK3α/β、ERK1/2 和 RSK1 的磷酸化。CRP 1.1 提取物会导致多种炎症介质的释放,包括细胞因子 IL-1α、IL5、IL6、IL8、IL-1RA、MIF 和 TNF-β,受体 IL-2RA,以及生长因子 FGF-basic、VEGF 和 M-CSF。总之,这些检测有助于对 NPs 和鼻烟的潜在健康风险进行证据权重评估。
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Multi-endpoint in vitro toxicological assessment of snus and tobacco-free nicotine pouch extracts

‘Modern’ oral tobacco-free nicotine pouches (NPs) are a nicotine containing product similar in appearance and concept to Swedish snus. A three-step approach was taken to analyse the biological effects of NPs and snus extracts in vitro. ToxTracker was used to screen for biomarkers for oxidative stress, cell stress, protein damage and DNA damage. Cytotoxicity, mutagenicity, and genotoxicity were assessed in the following respective assays: Neutral Red Uptake (NRU), Ames and Mouse Lymphoma Assay (MLA). Targeted analysis of phosphorylation signalling and inflammatory markers under non-toxic conditions was used to investigate any potential signalling pathways or inflammatory response. A reference snus (CRP1.1) and four NPs with various flavours and nicotine strengths were assessed. Test article extracts was generated by incubating one pouch in 20 mL of media (specific to each assay) with the inclusion of the pouch material. NP extracts did not induce any cytotoxicity or mutagenic response, genotoxic response was minimal and limited signalling or inflammatory markers were induced. In contrast, CRP1.1 induced a positive response in four toxicological endpoints in the absence of S9: Srxn1 (oxidative stress), Btg2 (cell stress), Ddit3 (protein damage) and Rtkn (DNA damage), and three endpoints in presence of S9: Srxn1, Ddit3 and Rtkn. CRP1.1 was genotoxic when assessed in MLA and activated signalling pathways involved in proliferation and cellular stress and specifically induced phosphorylation of c-JUN, CREB1, p53, p38 MAPK and to a lesser extent AKT1S1, GSK3α/β, ERK1/2 and RSK1 in a dose-dependent manner. CRP 1.1 extracts resulted in the release of several inflammatory mediators including cytokines IL-1α, IL5, IL6, IL8, IL-1RA, MIF and TNF-β, receptor IL-2RA, and growth factors FGF-basic, VEGF and M-CSF. In conclusion these assays contribute to the weight of evidence assessment of the potential comparative health risks of NPs and snus.

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来源期刊
CiteScore
3.80
自引率
5.30%
发文量
84
审稿时长
105 days
期刊介绍: Mutation Research - Genetic Toxicology and Environmental Mutagenesis (MRGTEM) publishes papers advancing knowledge in the field of genetic toxicology. Papers are welcomed in the following areas: New developments in genotoxicity testing of chemical agents (e.g. improvements in methodology of assay systems and interpretation of results). Alternatives to and refinement of the use of animals in genotoxicity testing. Nano-genotoxicology, the study of genotoxicity hazards and risks related to novel man-made nanomaterials. Studies of epigenetic changes in relation to genotoxic effects. The use of structure-activity relationships in predicting genotoxic effects. The isolation and chemical characterization of novel environmental mutagens. The measurement of genotoxic effects in human populations, when accompanied by quantitative measurements of environmental or occupational exposures. The application of novel technologies for assessing the hazard and risks associated with genotoxic substances (e.g. OMICS or other high-throughput approaches to genotoxicity testing). MRGTEM is now accepting submissions for a new section of the journal: Current Topics in Genotoxicity Testing, that will be dedicated to the discussion of current issues relating to design, interpretation and strategic use of genotoxicity tests. This section is envisaged to include discussions relating to the development of new international testing guidelines, but also to wider topics in the field. The evaluation of contrasting or opposing viewpoints is welcomed as long as the presentation is in accordance with the journal''s aims, scope, and policies.
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