» Articles » PMID: 30657992

Dose Effects of Ammonium Perfluorooctanoate on Lipoprotein Metabolism in APOE*3-Leiden.CETP Mice

Overview
Journal Toxicol Sci
Specialty Toxicology
Date 2019 Jan 19
PMID 30657992
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Epidemiological studies have reported positive associations between serum perfluorooctanoic acid (PFOA) and total and non-high-density lipoprotein cholesterol (non-HDL-C) although the magnitude of effect of PFOA on cholesterol lacks consistency. The objectives of this study were to evaluate the effect of PFOA on plasma cholesterol and triglyceride metabolism at various plasma PFOA concentrations relevant to humans, and to elucidate the mechanisms using APOE*3-Leiden.CETP mice, a model with a human-like lipoprotein metabolism. APOE*3-Leiden.CETP mice were fed a Western-type diet with PFOA (10, 300, 30 000 ng/g/d) for 4-6 weeks. PFOA exposure did not alter plasma lipids in the 10 and 300 ng/g/d dietary PFOA dose groups. At 30 000 ng/g/d, PFOA decreased plasma triglycerides (TG), total cholesterol (TC), and non-HDL-C, whereas HDL-C was increased. The plasma lipid alterations could be explained by decreased very low-density lipoprotein (VLDL) production and increased VLDL clearance by the liver through increased lipoprotein lipase activity. The concomitant increase in HDL-C was mediated by decreased cholesteryl ester transfer activity and changes in gene expression of proteins involved in HDL metabolism. Hepatic gene expression and pathway analysis confirmed the changes in lipoprotein metabolism that were mediated for a major part through activation of the peroxisome proliferator-activated receptor (PPAR)α. Our data confirmed the findings from a phase 1 clinical trial in humans that demonstrated high serum or plasma PFOA levels resulted in lower cholesterol levels. The study findings do not show an increase in cholesterol at environmental or occupational levels of PFOA exposure, thereby indicating these findings are associative rather than causal.

Citing Articles

Perfluorooctanoic acid increases serum cholesterol in a PPARα-dependent manner in female mice.

Nielsen G, Gondim D, Cave M, Heiger-Bernays W, Webster T, Schlezinger J Arch Toxicol. 2025; .

PMID: 40021516 DOI: 10.1007/s00204-025-03984-7.


Effects of PFAS on human liver transporters: implications for health outcomes.

Vujic E, Ferguson S, Brouwer K Toxicol Sci. 2024; 200(2):213-227.

PMID: 38724241 PMC: 11285162. DOI: 10.1093/toxsci/kfae061.


Perfluoroalkyl/Polyfluoroalkyl Substances: Links to Cardiovascular Disease Risk.

Schlezinger J, Gokce N Circ Res. 2024; 134(9):1136-1159.

PMID: 38662859 PMC: 11047059. DOI: 10.1161/CIRCRESAHA.124.323697.


PFAS Exposures and the Human Metabolome: A Systematic Review of Epidemiological Studies.

India-Aldana S, Yao M, Midya V, Colicino E, Chatzi L, Chu J Curr Pollut Rep. 2023; 9(3):510-568.

PMID: 37753190 PMC: 10520990. DOI: 10.1007/s40726-023-00269-4.


Exposure to low-dose perfluorooctanoic acid promotes hepatic steatosis and disrupts the hepatic transcriptome in mice.

Attema B, Janssen A, Rijkers D, van Schothorst E, Hooiveld G, Kersten S Mol Metab. 2022; 66:101602.

PMID: 36115532 PMC: 9526138. DOI: 10.1016/j.molmet.2022.101602.


References
1.
Post S, de Crom R, van Haperen R, Van Tol A, Princen H . Increased fecal bile acid excretion in transgenic mice with elevated expression of human phospholipid transfer protein. Arterioscler Thromb Vasc Biol. 2003; 23(5):892-7. DOI: 10.1161/01.ATV.0000067702.22390.20. View

2.
Wallace K, Cowie D, Konstantinou D, Hill S, Tjelle T, Axon A . The PXR is a drug target for chronic inflammatory liver disease. J Steroid Biochem Mol Biol. 2010; 120(2-3):137-48. PMC: 2937210. DOI: 10.1016/j.jsbmb.2010.04.012. View

3.
Kuhnast S, van der Hoorn J, Pieterman E, van den Hoek A, Sasiela W, Gusarova V . Alirocumab inhibits atherosclerosis, improves the plaque morphology, and enhances the effects of a statin. J Lipid Res. 2014; 55(10):2103-12. PMC: 4174003. DOI: 10.1194/jlr.M051326. View

4.
Haughom B, Spydevold O . The mechanism underlying the hypolipemic effect of perfluorooctanoic acid (PFOA), perfluorooctane sulphonic acid (PFOSA) and clofibric acid. Biochim Biophys Acta. 1992; 1128(1):65-72. DOI: 10.1016/0005-2760(92)90258-w. View

5.
Okochi E, Nishimaki-Mogami T, Suzuki K, Takahashi A . Perfluorooctanoic acid, a peroxisome-proliferating hypolipidemic agent, dissociates apolipoprotein B48 from lipoprotein particles and decreases secretion of very low density lipoproteins by cultured rat hepatocytes. Biochim Biophys Acta. 1999; 1437(3):393-401. DOI: 10.1016/s1388-1981(99)00024-4. View