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

Author:

Li Xinxin1,Feng Lixiang2,Kuang Qihui1ORCID,Wang Xiong3,Yang Jun1,Niu Xuan4,Gao Likun5,Huang Lizhi6,Luo Pengcheng1,Li Lili7ORCID

Affiliation:

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

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

3. Department of Pharmacy, Wuhan Third Hospital Medical School of Wuhan University Wuhan China

4. Department of Neurology Renmin Hospital of Wuhan University Wuhan China

5. Department of Pathology, Shenzhen People's Hospital The Second Clinical Medical College of Jinan University Shenzhen China

6. School of Civil Engineering Wuhan University Wuhan China

7. Central Laboratory Renmin Hospital of Wuhan University Wuhan China

Abstract

AbstractIn 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.

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Management, Monitoring, Policy and Law,Toxicology,General Medicine

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