Long-Term Exposure to Polystyrene Microspheres and High-Fat Diet-Induced Obesity in Mice: Evaluating a Role for Microbiota Dysbiosis.

IF 10.1 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Environmental Health Perspectives Pub Date : 2024-09-01 Epub Date: 2024-09-03 DOI:10.1289/EHP13913
Zhian Zhai, Ying Yang, Sheng Chen, Zhenlong Wu
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引用次数: 0

Abstract

Background: Microplastics (MPs) have become a global environmental problem, emerging as contaminants with potentially alarming consequences. However, long-term exposure to polystyrene microspheres (PS-MS) and its effects on diet-induced obesity are not yet fully understood.

Objectives: We aimed to investigate the effect of PS-MS exposure on high-fat diet (HFD)-induced obesity and underlying mechanisms.

Methods: In the present study, C57BL/6J mice were fed a normal diet (ND) or a HFD in the absence or presence of PS-MS via oral administration for 8 wk. Antibiotic depletion of the microbiota and fecal microbiota transplantation (FMT) were performed to assess the influence of PS-MS on intestinal microbial ecology. We performed 16S rRNA sequencing to dissect microbial discrepancies and investigated the dysbiosis-associated intestinal integrity and inflammation in serum.

Results: Compared with HFD mice, mice fed the HFD with PS-MS exhibited higher body weight, liver weight, metabolic dysfunction-associated steatotic liver disease (MASLD) activity scores, and mass of white adipose tissue, as well as higher blood glucose and serum lipid concentrations. Furthermore, 16S rRNA sequencing of the fecal microbiota revealed that mice fed the HFD with PS-MS had greater α-diversity and greater relative abundances of Lachnospiraceae, Oscillospiraceae, Bacteroidaceae, Akkermansiaceae, Marinifilaceae, Deferribacteres, and Desulfovibrio, but lower relative abundances of Atopobiaceae, Bifidobacterium, and Parabacteroides. Mice fed the HFD with PS-MS exhibited lower expression of MUC2 mucin and higher levels of lipopolysaccharide and inflammatory cytokines [tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), IL-1β, and IL-17A] in serum. Correlation analyses revealed that differences in the microbial flora of mice exposed to PS-MS were associated with obesity. Interestingly, microbiota-depleted mice did not show the same PS-MS-associated differences in Muc2 and Tjp1 expression in the distal colon, expression of inflammatory cytokines in serum, or obesity outcomes between HFD and HFD + PS-MS. Importantly, transplantation of feces from HFD + PS-MS mice to microbiota-depleted HFD-fed mice resulted in a lower expression of mucus proteins, higher expression of inflammatory cytokines, and obesity outcomes, similar to the findings in HFD + PS-MS mice.

Conclusions: Our findings provide a new gut microbiota-driven mechanism for PS-MS-induced obesity in HFD-fed mice, suggesting the need to reevaluate the adverse health effects of MPs commonly found in daily life, particularly in susceptible populations. https://doi.org/10.1289/EHP13913.

长期暴露于聚苯乙烯微球和高脂饮食诱发小鼠肥胖:评估微生物群失调的作用。
背景:微塑料(MPs)已成为一个全球性的环境问题,它作为污染物的出现可能会带来令人担忧的后果。然而,长期暴露于聚苯乙烯微球(PS-MS)及其对饮食诱发肥胖的影响尚未得到充分了解:目的:我们旨在研究接触聚苯乙烯微球对高脂饮食(HFD)诱发肥胖的影响及其潜在机制:在本研究中,C57BL/6J 小鼠在没有或有 PS-MS 的情况下口服正常饮食(ND)或高脂饮食 8 周。为了评估 PS-MS 对肠道微生物生态的影响,对微生物群进行了抗生素耗竭和粪便微生物群移植(FMT)。我们进行了 16S rRNA 测序以剖析微生物差异,并研究了与菌群失调相关的肠道完整性和血清中的炎症:结果:与高脂饮食小鼠相比,以 PS-MS 喂养的高脂饮食小鼠的体重、肝脏重量、代谢功能障碍相关性脂肪性肝病(MASLD)活动评分和白色脂肪组织的质量均较高,血糖和血清脂质浓度也较高。此外,粪便微生物群的 16S rRNA 测序显示,用 PS-MS 喂养高脂饮食的小鼠,其粪便微生物群的α-多样性更高,Lachnospiraceae、Oscillospiraceae、Bacteroidaceae、Akkermansiaceae、Marinifilaceae、Deferribacteres 和 Desulfovibrio 的相对丰度更高,但 Atopobiaceae、Bifidobacterium 和 Parabacteroides 的相对丰度较低。以 PS-MS 喂养高氟日粮的小鼠血清中 MUC2 粘蛋白的表达量较低,脂多糖和炎症细胞因子[肿瘤坏死因子-α (TNF-α)、白细胞介素-6 (IL-6)、IL-1β 和 IL-17A] 的水平较高。相关分析表明,接触 PS-MS 的小鼠微生物菌群的差异与肥胖有关。有趣的是,缺失微生物群的小鼠在远端结肠中 Muc2 和 Tjp1 的表达、血清中炎症细胞因子的表达或高脂饮食与高脂饮食 + PS-MS 之间的肥胖结果方面并没有表现出与 PS-MS 相关的差异。重要的是,将 HFD + PS-MS 小鼠的粪便移植到微生物群缺失的 HFD 喂养小鼠体内会导致粘液蛋白表达降低、炎症细胞因子表达升高以及肥胖结果,这与 HFD + PS-MS 小鼠的研究结果类似:我们的发现为PS-MS诱导HFD喂养小鼠肥胖提供了一种新的肠道微生物群驱动机制,表明有必要重新评估日常生活中常见的MPs对健康的不利影响,尤其是在易感人群中。https://doi.org/10.1289/EHP13913。
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
Environmental Health Perspectives
Environmental Health Perspectives 环境科学-公共卫生、环境卫生与职业卫生
CiteScore
14.40
自引率
2.90%
发文量
388
审稿时长
6 months
期刊介绍: Environmental Health Perspectives (EHP) is a monthly peer-reviewed journal supported by the National Institute of Environmental Health Sciences, part of the National Institutes of Health under the U.S. Department of Health and Human Services. Its mission is to facilitate discussions on the connections between the environment and human health by publishing top-notch research and news. EHP ranks third in Public, Environmental, and Occupational Health, fourth in Toxicology, and fifth in Environmental Sciences.
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