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PET microplastics induce lipotoxicity in the porcine pancreas
Summary
Researchers exposed pigs to PET microplastics for four weeks and found dose-dependent changes in pancreatic protein profiles, with the higher dose altering 17 proteins involved in fatty acid synthesis, lipid peroxidation, and digestive enzyme production. Free fatty acid levels increased significantly at the higher dose, indicating lipotoxic stress in pancreatic tissue. The study suggests a novel pathway through which microplastics may contribute to metabolic disturbances by impairing pancreatic function.
UNLABELLED: Microplastics are a relatively new discovered environmental hazard that can contribute to the disruption of many physiological processes in the organism. There is evidence that they affect the physiology of the pancreas, but research in this area remains limited. Therefore, the aim of the study was to determine the effects of PET microplastics on the global proteomic profile of the pancreas using LC–MS/MS analysis, with the pig as a model organism. The pigs were treated either with a low (0.1 g/day) or a high dose (1 g/day) of PET microplastics for four weeks. The analysis revealed that PET microplastics affected protein abundance in a dose-dependent manner – the low dose altered the abundance of 7 proteins, while the high dose – 17. The differentially regulated proteins were involved in fatty acid biosynthesis (FASN, KAS), lipid peroxidation (CBR1) and digestive enzyme production (trypsinogen). Complementary colorimetric assays confirmed a significant increase in free fatty acids under the influence of a high dose of PET microplastics. Taken together, these results indicate that PET microplastics may affect oxidative status, induce lipotoxic stress and impair pancreatic exocrine function, suggesting a novel pathway through which microplastics may cause metabolic disturbances. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-025-12507-8.
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