Exploring the adverse effects of 1,3,6,8-tetrabromo-9H-carbazole in atherosclerotic model mice by metabolomic profiling integrated with mechanism studies in vitro

• Published in: Chemosphere (Oxford) 2024-02, Vol.349, p.140767-140767, Article 140767
• Main Authors: Xu, Tong, Jiang, Yu, Fu, Hualing, Yang, Guanglei, Hu, Xiaoxu, Chen, Yangsheng, Zhang, Qian, Wang, Yuxi, Wang, Yilan, Xie, Heidi Qunhui, Han, Fang, Xu, Li, Zhao, Bin
• Format: Article
• Language: English
• Subjects: 1,3,6,8-Tetrabromo-9H-carbazole; Atherosclerosis; Atherosclerotic model mice; Energy metabolism; Metabolomics; Reactive oxygen species
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2023.140767

Given its wide distribution in the environment and latent toxic effects, 1,3,6,8-tetrabromo-9H-carbazole (1368-BCZ) is an emerging concern that has gained increasing attention globally. 1368-BCZ exposure is reported to have potential cardiovascular toxicity. Although atherosclerosis is a cardiovascular disease and remains a primary cause of mortality worldwide, no evidence has been found regarding the impact of 1368-BCZ on atherosclerosis. Therefore, we aimed to explore the deleterious effects of 1368-BCZ on atherosclerosis and the underlying mechanisms. Serum samples from 1368-BCZ-treated atherosclerotic model mice were subjected to metabolomic profiling to investigate the adverse influence of the pollutant. Subsequently, the molecular mechanism associated with the metabolic pathway of atherosclerotic mice that was identified following 1368-BCZ exposure was validated in vitro. Serum metabolomics analysis revealed that 1368-BCZ significantly altered the tricarboxylic acid cycle, causing a disturbance in energy metabolism. In vitro, we further validated general markers of energy metabolism based on metabolome data: 1368-BCZ dampened adenosine triphosphate (ATP) synthesis and increased reactive oxygen species (ROS) production. Furthermore, blocking the aryl hydrocarbon receptor (AhR) reversed the high production of ROS induced by 1368-BCZ. It is concluded that 1368-BCZ decreased the ATP synthesis by disturbing the energy metabolism, thereby stimulating the AhR-mediated ROS production and presumably causing aggravated atherosclerosis. This is the first comprehensive study on the cardiovascular toxicity and mechanism of 1368-BCZ based on rodent models of atherosclerosis and integrated with in vitro models. [Display omitted] •1368-BCZ presumably aggravates atherosclerosis in HFD-fed ApoE−/− mice.•1368-BCZ partially aggravates atherosclerosis by disturbing energy metabolism.•1368-BCZ contributes to the energy metabolism-correlated ROS generation.•1368-BCZ induces ROS generation mediated by AhR.