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聚苯乙烯微塑料和纳米塑料混合物影响3T3-L1脂肪细胞和斑马鱼幼虫的脂肪与葡萄糖代谢。

Mixtures of polystyrene micro and nanoplastics affects fat and glucose metabolism in 3T3-L1 adipocytes and zebrafish larvae.

作者信息

Kim Jung Eun, Sonar Narayan Sah, Thakuri Laxmi Sen, Park Jin Woo, Kim Ki-Tae, Rhyu Dong Young

机构信息

Department of Nutraceutical Resources, Mokpo National University, Jeonnam 58554, Republic of Korea; ROK-Biotech, Hwasun-gun, Jeonnam 58112, Republic of Korea.

Department of Nutraceutical Resources, Mokpo National University, Jeonnam 58554, Republic of Korea; Department of Biomedicine, Health & Life Convergence Sciences, BK21 FOUR, Mokpo National University, Jeonnam 58554, Republic of Korea.

出版信息

NanoImpact. 2025 Jan;37:100549. doi: 10.1016/j.impact.2025.100549. Epub 2025 Feb 16.

Abstract

Microplastics (MPs) and nanoplastics (NPs) are pervasive pollutants that pose a hazard to human health. Although most previous studies have investigated the effects of MPs and NPs on digestion, oxidative stress, and inflammation in diverse models, the combined effect of plastic mixtures (PM) containing MPs and NPs on obesity and type 2 diabetes mellitus (T2DM) remains unknown. The hypothesis of our study is to verify the association between PM exposure and clinical features of metabolic diseases such as lipogenesis and insulin resistance. Therefore, we investigated the effects of PM on fat and glucose metabolism in 3T3-L1 cells and high-fat diet (HFD)-induced zebrafish larvae. PM exposure increased cell viability, differentiation, adipogenesis (PPARγ and C/EBPα), and lipogenesis (FAS and SREBP-1c), while it decreased glucose uptake and inhibited insulin signal (IRS1, PI3K, AKT, and GLUT4) expression 3T3-L1 cells. In zebrafish larvae, PM mainly bioaccumulated in the intestine and pancreatic tissue, reducing glucose uptake and increasing body weight and blood glucose compared to controls. Moreover, PM significantly increased adipogenic differentiation (PPARγ) and synthesis (FASN and FABP), proinflammatory cytokines (TNF-α and IL-6), and gluconeogenesis (PCK1 and G6Pase). Conversely, energy and fat metabolism (AMPKα and adiponectin), insulin production (INSα), signaling pathway (IRS1, AKT, and GLUT2), and anti-inflammatory cytokines (IL-10 and IL-4) were suppressed. Overall, this study sheds light on the mechanisms responsible for the detrimental effects of PM exposure on fat and glucose metabolism, providing insights into metabolic disorders, like type 2 diabetes, in both in vitro and in vivo models.

摘要

微塑料(MPs)和纳米塑料(NPs)是普遍存在的污染物,对人类健康构成危害。尽管此前大多数研究调查了微塑料和纳米塑料在不同模型中对消化、氧化应激和炎症的影响,但含有微塑料和纳米塑料的塑料混合物(PM)对肥胖和2型糖尿病(T2DM)的综合影响仍不清楚。我们研究的假设是验证塑料混合物暴露与脂肪生成和胰岛素抵抗等代谢疾病临床特征之间的关联。因此,我们研究了塑料混合物对3T3-L1细胞和高脂饮食(HFD)诱导的斑马鱼幼虫脂肪和葡萄糖代谢的影响。暴露于塑料混合物会增加3T3-L1细胞的活力、分化、脂肪生成(PPARγ和C/EBPα)和脂肪生成(FAS和SREBP-1c),同时降低葡萄糖摄取并抑制胰岛素信号(IRS1、PI3K、AKT和GLUT4)的表达。在斑马鱼幼虫中,塑料混合物主要在肠道和胰腺组织中生物蓄积,与对照组相比,降低了葡萄糖摄取,增加了体重和血糖。此外,塑料混合物显著增加了脂肪生成分化(PPARγ)和合成(FASN和FABP)、促炎细胞因子(TNF-α和IL-6)以及糖异生(PCK1和G6Pase)。相反,能量和脂肪代谢(AMPKα和脂联素)、胰岛素产生(INSα)、信号通路(IRS1、AKT和GLUT2)以及抗炎细胞因子(IL-10和IL-4)受到抑制。总体而言,本研究揭示了塑料混合物暴露对脂肪和葡萄糖代谢产生有害影响的机制,为体外和体内模型中的2型糖尿病等代谢紊乱提供了见解。

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