Nutritional status modifies pregnane X receptor regulated transcriptome

• Published in: Scientific reports Vol. 9; no. 1; pp. 16728 - 13
• Main Authors: Hassani-Nezhad-Gashti, Fatemeh, Kummu, Outi, Karpale, Mikko, Rysä, Jaana, Hakkola, Jukka
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 13.11.2019; Nature Publishing Group
• Subjects: 38/39; 38/61; 38/77; 631/337/2019; 631/443/319/1557; 64/60; 692/4020/4021/288/2032; 82/58; Animals; Bile; Bile Acids and Salts - metabolism; Cells, Cultured; Cholesterol - metabolism; DNA microarrays; Energy balance; Gene expression; Gene Expression Profiling; Gene Expression Regulation - drug effects; Gene regulation; Genomes; Glucagon; Glucose; Glucose - pharmacology; Glucose metabolism; Hepatocytes; Hepatocytes - cytology; Hepatocytes - drug effects; Hepatocytes - metabolism; Homeostasis; Humanities and Social Sciences; Insulin; Lipid metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; multidisciplinary; Nutrition; Nutritional Status; Pregnane X Receptor - physiology; Pregnenolone; Science; Science (multidisciplinary); Sweetening Agents - pharmacology; Transcriptome - drug effects
• DOI: 10.1038/s41598-019-53101-9
• ISSN: 2045-2322

Pregnane X receptor (PXR) regulates glucose and lipid metabolism, but little is known of the nutritional regulation of PXR function. We investigated the genome wide effects of the nutritional status on the PXR mediated gene regulation in the liver. Mice were treated with a PXR ligand pregnenolone 16α-carbonitrile (PCN) for 4 days and subsequently either fasted for 5 hours or after 4-hour fast treated with intragastric glucose 1 hour before sample collection. Gene expression microarray study indicated that PCN both induced and repressed much higher number of genes in the glucose fed mice and the induction of multiple well-established PXR target genes was potentiated by glucose. A subset of genes, including bile acid synthesis gene Cyp8b1 , responded in an opposite direction during fasting and after glucose feeding. PXR knockout abolished these effects. In agreement with the Cyp8b1 regulation, PCN also modified the bile acid composition in the glucose fed mice. Contribution of glucose, insulin and glucagon on the observed nutritional effects was investigated in primary hepatocytes. However, only mild impact on PXR function was observed. These results show that nutritional status modifies the PXR regulated transcriptome both qualitatively and quantitatively and reveal a complex crosstalk between PXR and energy homeostasis.