Journal: Toxicological Sciences
Article Title: Dioxin-like PCB 126 Increases Systemic Inflammation and Accelerates Atherosclerosis in Lean LDL Receptor-Deficient Mice
doi: 10.1093/toxsci/kfx275
Figure Lengend Snippet: Exposure to PCB 126 modulates hepatic lipid accumulation at 14 weeks in mice fed a high cholesterol diet. Male Ldlr–/– mice were fed a low fat, 0.15% cholesterol diet and exposed to 1 µmol/kg PCB 126 at weeks 2 and 4. All mRNA values were determined using the relative quantification method (ΔΔCt) and normalized to control. Hprt1 was used as the housekeeping gene for all mRNA quantifications. A, PCB 126 increased hepatic mRNA levels of fatty acid translocase (CD36), INSIG-1, IL-1β, LPL, Phospholipase A2 Group IVA, and downregulated Fads1, Scd1, Gyk, Solute Carrier Family 16 Member 6, and leukotriene A4 hydrolase. Data are presented as mean ± SEM (n = 5 per group; Student’s t-test). B, Shown are representative H&E stained hepatic sections which illustrate the observed PCB-induced significant microvesicular fatty change in centrilobular regions.
Article Snippet: Lipid profiles Plasma total cholesterol (Infinity Cholesterol, ThermoScientific, USA), triglyceride (TRIGS, Randox, UK), phospholipid (Phospholipids C, Wako Pure Chemical Industries, Japan), and free fatty acid (Reagent A/B, Wako, Pure Chemical Industries, Japan) concentrations were determined via colorimetric kits, as per the manufacturer’s instructions.
Techniques: Quantitative Proteomics, Control, Staining