Nuclear receptors CAR and PXR as cardiometabolic regulators
The constitutive androstane receptor (CAR) and pregnane X receptor (PXR) were initially described as xenobiotic sensors, but an increasing number of studies have linked their activity to other important physiological processes including glucose and lipid metabolism, implying an expanded role as meta...
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Elsevier
2025-09-01
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| Series: | Pharmacological Research |
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| Online Access: | http://www.sciencedirect.com/science/article/pii/S1043661825003172 |
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| author | Janne Hukkanen Jenni Küblbeck Jukka Hakkola Jaana Rysä |
| author_facet | Janne Hukkanen Jenni Küblbeck Jukka Hakkola Jaana Rysä |
| author_sort | Janne Hukkanen |
| collection | DOAJ |
| description | The constitutive androstane receptor (CAR) and pregnane X receptor (PXR) were initially described as xenobiotic sensors, but an increasing number of studies have linked their activity to other important physiological processes including glucose and lipid metabolism, implying an expanded role as metabolic sensors. CAR and PXR are nuclear receptors, which share similarities in expression, ligand-specificity, and mechanism of transcriptional regulation but they have their distinct features as well. Together, they regulate a wide array of target genes, whose functions range from elimination of xenobiotics to energy metabolism. Both CAR and PXR have large ligand binding pockets, and especially the PXR pocket is flexible for structurally different chemicals. Consequently, CAR and PXR could have a role in mediating the harmful metabolic effects of drugs and environmental chemicals. Current knowledge supports a role for PXR in the regulation of lipid and cholesterol metabolism. The actions seem to be mostly unfavorable, since the activation of PXR has been shown to promote hepatic lipogenesis and hyperlipidemia, increase plasma cholesterol and impair hepatic LDL uptake. PXR and PXR-regulated circulating 4β-hydroxycholesterol may also influence blood pressure regulation. CAR, in contrast, tends to exert beneficial effects on lipid and glucose homeostasis, since CAR activation has been shown to reduce serum triglyceride and cholesterol levels and have anti-atherogenic properties. Here we review current knowledge on CAR and PXR as regulators of cardiometabolic functions, including glucose and lipid homeostasis, blood pressure regulation and atherosclerosis. |
| format | Article |
| id | doaj-art-5bfc9c18f89440889d891ccba5d5a7f8 |
| institution | Kabale University |
| issn | 1096-1186 |
| language | English |
| publishDate | 2025-09-01 |
| publisher | Elsevier |
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| series | Pharmacological Research |
| spelling | doaj-art-5bfc9c18f89440889d891ccba5d5a7f82025-08-20T03:42:34ZengElsevierPharmacological Research1096-11862025-09-0121910789210.1016/j.phrs.2025.107892Nuclear receptors CAR and PXR as cardiometabolic regulatorsJanne Hukkanen0Jenni Küblbeck1Jukka Hakkola2Jaana Rysä3Research Unit of Biomedicine and Internal Medicine, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, FinlandA.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio 70211, FinlandResearch Unit of Biomedicine and Internal Medicine, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, FinlandSchool of Pharmacy, University of Eastern Finland, P.O. Box 1627, Kuopio 70211, Finland; Corresponding author.The constitutive androstane receptor (CAR) and pregnane X receptor (PXR) were initially described as xenobiotic sensors, but an increasing number of studies have linked their activity to other important physiological processes including glucose and lipid metabolism, implying an expanded role as metabolic sensors. CAR and PXR are nuclear receptors, which share similarities in expression, ligand-specificity, and mechanism of transcriptional regulation but they have their distinct features as well. Together, they regulate a wide array of target genes, whose functions range from elimination of xenobiotics to energy metabolism. Both CAR and PXR have large ligand binding pockets, and especially the PXR pocket is flexible for structurally different chemicals. Consequently, CAR and PXR could have a role in mediating the harmful metabolic effects of drugs and environmental chemicals. Current knowledge supports a role for PXR in the regulation of lipid and cholesterol metabolism. The actions seem to be mostly unfavorable, since the activation of PXR has been shown to promote hepatic lipogenesis and hyperlipidemia, increase plasma cholesterol and impair hepatic LDL uptake. PXR and PXR-regulated circulating 4β-hydroxycholesterol may also influence blood pressure regulation. CAR, in contrast, tends to exert beneficial effects on lipid and glucose homeostasis, since CAR activation has been shown to reduce serum triglyceride and cholesterol levels and have anti-atherogenic properties. Here we review current knowledge on CAR and PXR as regulators of cardiometabolic functions, including glucose and lipid homeostasis, blood pressure regulation and atherosclerosis.http://www.sciencedirect.com/science/article/pii/S1043661825003172AtherosclerosisBlood pressureHypercholesterolemiaHypertensionMetabolismNuclear receptor |
| spellingShingle | Janne Hukkanen Jenni Küblbeck Jukka Hakkola Jaana Rysä Nuclear receptors CAR and PXR as cardiometabolic regulators Pharmacological Research Atherosclerosis Blood pressure Hypercholesterolemia Hypertension Metabolism Nuclear receptor |
| title | Nuclear receptors CAR and PXR as cardiometabolic regulators |
| title_full | Nuclear receptors CAR and PXR as cardiometabolic regulators |
| title_fullStr | Nuclear receptors CAR and PXR as cardiometabolic regulators |
| title_full_unstemmed | Nuclear receptors CAR and PXR as cardiometabolic regulators |
| title_short | Nuclear receptors CAR and PXR as cardiometabolic regulators |
| title_sort | nuclear receptors car and pxr as cardiometabolic regulators |
| topic | Atherosclerosis Blood pressure Hypercholesterolemia Hypertension Metabolism Nuclear receptor |
| url | http://www.sciencedirect.com/science/article/pii/S1043661825003172 |
| work_keys_str_mv | AT jannehukkanen nuclearreceptorscarandpxrascardiometabolicregulators AT jennikublbeck nuclearreceptorscarandpxrascardiometabolicregulators AT jukkahakkola nuclearreceptorscarandpxrascardiometabolicregulators AT jaanarysa nuclearreceptorscarandpxrascardiometabolicregulators |