AUTHOR=Hari Archana , AbdulHameed Mohamed Diwan M. , Balik-Meisner Michele R. , Mav Deepak , Phadke Dhiral P. , Scholl Elizabeth H. , Shah Ruchir R. , Casey Warren , Auerbach Scott S. , Wallqvist Anders , Pannala Venkat R. 

TITLE=Exposure to PFAS chemicals induces sex-dependent alterations in key rate-limiting steps of lipid metabolism in liver steatosis

JOURNAL=Frontiers in Toxicology

VOLUME=6

YEAR=2024

URL=https://www.frontiersin.org/journals/toxicology/articles/10.3389/ftox.2024.1390196

DOI=10.3389/ftox.2024.1390196

ISSN=2673-3080

ABSTRACT=<p>Toxicants with the potential to bioaccumulate in humans and animals have long been a cause for concern, particularly due to their association with multiple diseases and organ injuries. Per- and polyfluoro alkyl substances (PFAS) and polycyclic aromatic hydrocarbons (PAH) are two such classes of chemicals that bioaccumulate and have been associated with steatosis in the liver. Although PFAS and PAH are classified as chemicals of concern, their molecular mechanisms of toxicity remain to be explored in detail. In this study, we aimed to identify potential mechanisms by which an acute exposure to PFAS and PAH chemicals can induce lipid accumulation and whether the responses depend on chemical class, dose, and sex. To this end, we analyzed mechanisms beginning with the binding of the chemical to a molecular initiating event (MIE) and the consequent transcriptomic alterations. We collated potential MIEs using predictions from our previously developed ToxProfiler tool and from published steatosis adverse outcome pathways. Most of the MIEs are transcription factors, and we collected their target genes by mining the TRRUST database. To analyze the effects of PFAS and PAH on the steatosis mechanisms, we performed a computational MIE-target gene analysis on high-throughput transcriptomic measurements of liver tissue from male and female rats exposed to either a PFAS or PAH. The results showed peroxisome proliferator-activated receptor (PPAR)-α targets to be the most dysregulated, with most of the genes being upregulated. Furthermore, PFAS exposure disrupted several lipid metabolism genes, including upregulation of fatty acid oxidation genes (<italic>Acadm</italic>, <italic>Acox1</italic>, <italic>Cpt2</italic>, <italic>Cyp4a1</italic>-<italic>3</italic>) and downregulation of lipid transport genes (<italic>Apoa1</italic>, <italic>Apoa5</italic>, <italic>Pltp</italic>). We also identified multiple genes with sex-specific behavior. Notably, the rate-limiting genes of gluconeogenesis (<italic>Pck1</italic>) and bile acid synthesis (<italic>Cyp7a1</italic>) were specifically downregulated in male rats compared to female rats, while the rate-limiting gene of lipid synthesis (<italic>Scd</italic>) showed a PFAS-specific upregulation. The results suggest that the PPAR signaling pathway plays a major role in PFAS-induced lipid accumulation in rats. Together, these results show that PFAS exposure induces a sex-specific multi-factorial mechanism involving rate-limiting genes of gluconeogenesis and bile acid synthesis that could lead to activation of an adverse outcome pathway for steatosis.</p>