Long-Term Exposure to Microplastics Promotes Early-Stage Hepatocarcinogenesis Induced by Diethylnitrosamine in Rats by Modulation of Their Gut Microbiota.

IF 3.9 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
Toxics Pub Date : 2025-04-29 DOI:10.3390/toxics13050353
Huina Guo, Jianan Wang, Shaowen Huang, Suren Rao Sooranna, Fangyi Shu, Genliang Li
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Abstract

Hepatocarcinogenesis is linked to environmental factors, with microplastics (MPs) emerging as a global environmental concern that may contribute to liver injury. However, the impact of MPs on the early stages of hepatocarcinogenesis has been largely ignored. Here we investigated the impact of long-term MP exposure on the formation of preneoplastic lesions during hepatocarcinogenesis induced by diethylnitrosamine (DEN) in rats. Rats were injected with DEN to induce preneoplastic lesions, and then they were orally administered with 1 µm MPs 0.5 mg/kg body weight per day for 20 weeks. The results revealed that long-term exposure to MPs did not induce the formation of glutathione S-transferase placental form (GST-P)-positive foci as preneoplastic lesions during hepatocarcinogenesis in these animals, thereby indicating non-carcinogenicity. However, MP exposure resulted in a 1-fold increase in both the number and size of GST-P-positive foci in rats initiated with DEN compared to those treated with DEN alone. Accordingly, MP exposure led to a 0.61-fold increase in the index of proliferating cell nuclear antigen (PCNA)-positive cells in DEN-initiated rats when compared to DEN treatment alone. In addition, the composition of the gut microbiota was significantly altered, accompanied by various levels of short-chain fatty acids. Our results suggest that long-term MP exposure can promote pre-neoplastic lesion formation in DEN-induced rats by increased cell proliferation as well as alterations in the gut microbiota and short-chain fatty acid levels. This highlights the potential health risks associated with hepatocarcinogenesis linked to long-term exposure to MPs.

长期接触微塑料可通过调节大鼠肠道微生物群促进二乙基亚硝胺诱导的早期肝癌的发生。
肝癌的发生与环境因素有关,微塑料(MPs)正在成为全球关注的环境问题,可能导致肝损伤。然而,MPs对早期肝癌发生的影响在很大程度上被忽视了。本研究研究了长期暴露于MP对二乙基亚硝胺(DEN)诱导大鼠肝癌形成过程中瘤前病变形成的影响。先给大鼠注射DEN诱导肿瘤前病变,然后每天口服1µm MPs 0.5 mg/kg体重,连续20周。结果显示,在这些动物的肝癌发生过程中,长期暴露于MPs不会诱导谷胱甘肽s -转移酶胎盘形式(GST-P)阳性灶的形成,从而表明非致癌性。然而,与单独使用DEN治疗的大鼠相比,MP暴露导致DEN初始大鼠gst -p阳性灶的数量和大小增加1倍。因此,与单独DEN处理相比,MP暴露导致DEN启动大鼠增殖细胞核抗原(PCNA)阳性细胞指数增加了0.61倍。此外,肠道菌群的组成也发生了显著变化,并伴有不同水平的短链脂肪酸。我们的研究结果表明,长期MP暴露可以通过增加细胞增殖以及肠道微生物群和短链脂肪酸水平的改变,促进den诱导的大鼠肿瘤前病变的形成。这突出了与长期接触多磺酸粘多糖相关的肝癌发生相关的潜在健康风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Toxics
Toxics Chemical Engineering-Chemical Health and Safety
CiteScore
4.50
自引率
10.90%
发文量
681
审稿时长
6 weeks
期刊介绍: Toxics (ISSN 2305-6304) is an international, peer-reviewed, open access journal which provides an advanced forum for studies related to all aspects of toxic chemicals and materials. It publishes reviews, regular research papers, and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in detail. There is, therefore, no restriction on the maximum length of the papers, although authors should write their papers in a clear and concise way. The full experimental details must be provided so that the results can be reproduced. Electronic files or software regarding the full details of calculations and experimental procedure can be deposited as supplementary material, if it is not possible to publish them along with the text.
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