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微塑料通过破坏 PP2A/AMPK/HNF4A 介导的糖脂代谢和激活 Wnt/β-连环蛋白通路促进肝纤维化进而导致糖尿病小鼠产生肝毒性。

Microplastics cause hepatotoxicity in diabetic mice by disrupting glucolipid metabolism via PP2A/AMPK/HNF4A and promoting fibrosis via the Wnt/β-catenin pathway.

机构信息

Department of Urology, Wuhan Third Hospital, Medical School of Wuhan University, Wuhan, China.

Department of Urology, Wuhan Third Hospital, School of Medicine, Wuhan University of Science and Technology, Wuhan, China.

出版信息

Environ Toxicol. 2024 Feb;39(2):1018-1030. doi: 10.1002/tox.24034. Epub 2023 Dec 8.

Abstract

In recent years, microplastics (MPs) have gained significant attention as a persistent environmental pollutant resulting from the decomposition of plastics, leading to their accumulation in the human body. The liver, particularly of individuals with type 2 diabetes mellitus (T2DM), is known to be more susceptible to the adverse effects of environmental pollutants. Therefore, to investigate the potential impact of MPs on the liver of diabetic mice and elucidate the underlying toxicological mechanisms, we exposed db/db mice to 0.5 μm MPs for 3 months. Our results revealed that MPs exposure resulted in several harmful effects, including decreased body weight, disruption of liver structure and function, elevated blood glucose levels, impaired glucose tolerance, and increased glycogen accumulation in the hepatic tissue of the mice. Furthermore, MPs exposure was found to promote hepatic gluconeogenesis by perturbing the PP2A/AMPK/HNF4A signaling pathway. In addition, MPs disrupt redox balance, leading to oxidative damage in the liver. This exposure also disrupted hepatic lipid metabolism, stimulating lipid synthesis while inhibiting catabolism, ultimately resulting in the development of fatty liver. Moreover, MPs were found to induce liver fibrosis by activating the Wnt/β-catenin signaling pathway. Furthermore, MPs influenced adaptive thermogenesis in brown fat by modulating the expression of uncoupling protein 1 (UCP1) and genes associated with mitochondrial oxidative respiration thermogenesis in brown fat. In conclusion, our study demonstrates that MPs induce oxidative damage in the liver, disturb glucose and lipid metabolism, promote hepatic fibrosis, and influence adaptive thermogenesis in brown fat in diabetic mice. These findings underscore the potential adverse effects of MPs on liver health in individuals with T2DM and highlight the importance of further research in this area.

摘要

近年来,微塑料(MPs)作为塑料分解产生的持久性环境污染物引起了广泛关注,导致其在人体内积累。已知肝脏,特别是 2 型糖尿病(T2DM)患者的肝脏,更容易受到环境污染物的不良影响。因此,为了研究 MPs 对糖尿病小鼠肝脏的潜在影响并阐明其潜在的毒理学机制,我们将 db/db 小鼠暴露于 0.5μm MPs 中 3 个月。我们的结果表明,MPs 暴露会导致多种有害影响,包括体重下降、肝结构和功能紊乱、血糖水平升高、葡萄糖耐量受损以及肝组织中糖原积累增加。此外,MPs 暴露通过扰乱 PP2A/AMPK/HNF4A 信号通路促进肝糖异生。此外,MPs 破坏氧化还原平衡,导致肝脏氧化损伤。这种暴露还破坏了肝脂代谢,刺激脂质合成,同时抑制分解代谢,最终导致脂肪肝的发展。此外,MPs 通过激活 Wnt/β-catenin 信号通路诱导肝纤维化。此外,MPs 通过调节解偶联蛋白 1(UCP1)的表达和棕色脂肪中线粒体氧化呼吸产热相关基因来影响棕色脂肪的适应性产热。总之,我们的研究表明 MPs 可诱导糖尿病小鼠肝脏氧化损伤,扰乱葡萄糖和脂质代谢,促进肝纤维化,并影响棕色脂肪的适应性产热。这些发现强调了 MPs 对 T2DM 患者肝脏健康的潜在不良影响,并突出了该领域进一步研究的重要性。

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