Acute Intake of Plant Stanol Esters Induces Changes in Lipid and Lipoprotein Metabolism‐Related Gene Expression in the Liver and Intestines of Mice. Issue 6 (1st May 2015)

• Record Type: Journal Article
• Authors: De Smet, Els; Mensink, Ronald P.; Konings, Maurice; Brufau, Gemma; Groen, Albert K.; Havinga, Rick; Schonewille, Marleen; Kerksiek, Anja; Lütjohann, Dieter; Plat, Jogchum
• Is Part Of: Lipids. Volume 50:Issue 6(2015)
• Page Start: 529
• Page End: 541
• Publication Date: 2015-05-01
• Subjects: Cholesterol -- Gene expression -- Lipids -- Lipoproteins -- Lymph canulation -- Plant stanols -- Intestines; Lipids -- Periodicals; Lipids -- Periodicals; Lipiden; Lipides -- Périodiques; 547.77
• DOI: 10.1007/s11745-015-4020-1
• Languages: English
• ISSNs: 0024-4201

Abstract

Abstract: The kinetics of plant stanol uptake and routing in 8‐week‐old C57BL/6J mice were determined after a plant stanol ester gavage. In addition, acute changes in intestinal and hepatic gene expression were investigated. Mice were fed a plant sterol/stanol poor diet from weaning. At the age of 8 weeks, they received an oral gavage consisting of 0.25 mg cholesterol + 50 mg plant stanol esters dissolved in olive oil. Animals were euthanized at different time points. In a second comparable set‐up, mesenteric lymph‐cannulated versus sham‐operated mice received the same oral gavage, which was now deuterium labeled. Intestinal and hepatic sitostanol concentrations increased within 15 min post‐gavage. This rapid hepatic appearance was absent in lymph‐cannulated mice, suggesting a very fast lymph‐mediated uptake. Hepatic mRNA expression of SREBP2 and its target genes rapidly decreased, whereas expression of LXR target genes increased. The intestinal SREBP2 pathway was increased, whereas the expression of LXR target genes hardly changed. The fivefold and sixfold increased expression of intestinal LDLr and PCSK9 is suggestive of TICE activation. We conclude that in C57BL/6J mice plant stanol kinetics are fast, and affect intestinal and hepatic gene expression within 15 min postprandial after lymph‐mediated uptake.