Document Detail

Unsaturated fatty acid regulation of cytochrome P450 expression via a CAR-dependent pathway.
Jump to Full Text
MedLine Citation:
PMID:  18778245     Owner:  NLM     Status:  MEDLINE    
The liver is responsible for key metabolic functions, including control of normal homoeostasis in response to diet and xenobiotic metabolism/detoxification. We have shown previously that inactivation of the hepatic cytochrome P450 system through conditional deletion of POR (P450 oxidoreductase) induces hepatic steatosis, liver growth and P450 expression. We have exploited a new conditional model of POR deletion to investigate the mechanism underlying these changes. We demonstrate that P450 induction, liver growth and hepatic triacylglycerol (triglyceride) homoeostasis are intimately linked and provide evidence that the observed phenotypes result from hepatic accumulation of unsaturated fatty acids, which mediate these phenotypes by activation of the nuclear receptor CAR (constitutive androstane receptor) and, to a lesser degree, PXR (pregnane X receptor). To our knowledge this is the first direct evidence that P450s play a major role in controlling unsaturated fatty acid homoeostasis via CAR. The regulation of P450s involved in xenobiotic metabolism by this mechanism has potentially significant implications for individual responses to drugs and environmental chemicals.
Robert D Finn; Colin J Henderson; Claire L Scott; C Roland Wolf
Related Documents :
2693005 - Ontogeny and regulation of drug metabolism in humans. phase i: monooxygenases.
16269465 - Saturated fatty acids promote endoplasmic reticulum stress and liver injury in rats wit...
8177225 - Methionine transamination--metabolic function and subcellular compartmentation.
17680645 - Palmitic acid induces production of proinflammatory cytokine interleukin-8 from hepatoc...
8827105 - Gamma-aminobutyric acid concentrations in the cerebrospinal fluid of newborn infants de...
5497895 - Inhibition of poxvirus replication by streptovaricin.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Biochemical journal     Volume:  417     ISSN:  1470-8728     ISO Abbreviation:  Biochem. J.     Publication Date:  2009 Jan 
Date Detail:
Created Date:  2008-12-08     Completed Date:  2009-01-16     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  2984726R     Medline TA:  Biochem J     Country:  England    
Other Details:
Languages:  eng     Pagination:  43-54     Citation Subset:  IM    
Cancer Research UK Molecular Pharmacology Unit, Biomedical Research Centre, Level 5, Ninewells Hospital and Medical School, Dundee DD19SY, UK.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Cell Line, Tumor
Cytochrome P-450 CYP1A1 / genetics,  metabolism
Cytochrome P-450 Enzyme System / genetics,  metabolism*
Fatty Acids, Unsaturated / administration & dosage,  pharmacology*
Gene Expression / drug effects
Linoleic Acid / pharmacology
Lipid Metabolism / drug effects
Liver / cytology,  drug effects,  metabolism
Methylcholanthrene / pharmacology
Mice, Transgenic
NADPH-Ferrihemoprotein Reductase / genetics,  metabolism*
Receptors, Cytoplasmic and Nuclear / genetics,  metabolism,  physiology*
Receptors, Steroid / genetics,  metabolism,  physiology
Reverse Transcriptase Polymerase Chain Reaction
Transcription Factors / genetics,  metabolism,  physiology*
Triglycerides / metabolism
Grant Support
C463/A5661//Cancer Research UK
Reg. No./Substance:
0/Fatty Acids, Unsaturated; 0/Receptors, Cytoplasmic and Nuclear; 0/Receptors, Steroid; 0/Transcription Factors; 0/Triglycerides; 0/constitutive androstane receptor; 0/pregnane X receptor; 2197-37-7/Linoleic Acid; 56-49-5/Methylcholanthrene; 9035-51-2/Cytochrome P-450 Enzyme System; EC P-450 CYP1A1; EC Reductase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Full Text
Journal Information
Journal ID (nlm-ta): Biochem J
Journal ID (pmc): bic
Journal ID (publisher-id): BJ
ISSN: 0264-6021
ISSN: 1470-8728
Publisher: Portland Press Ltd.
Article Information
Download PDF
? 2009 The Author(s) The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Non-Commercial Licence ( which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited.
open-access: This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Received Day: 11 Month: 4 Year: 2008
Revision Received Day: 1 Month: 9 Year: 2008
Accepted Day: 9 Month: 9 Year: 2008
epreprint publication date: Day: 9 Month: 9 Year: 2008
Electronic publication date: Day: 12 Month: 12 Year: 2008
Print publication date: Day: 1 Month: 1 Year: 2009
Volume: 417 Issue: Pt 1
First Page: 43 Last Page: 54
ID: 2605957
Publisher Id: bj4170043
DOI: 10.1042/BJ20080740
PubMed Id: 18778245

Unsaturated fatty acid regulation of cytochrome P450 expression via a CAR-dependent pathway Title for RRH:CAR-dependent fatty acid regulation of cytochromes P450 Alternate Title:R. D. Finn and others
Robert?D. FinnA1
Colin?J. HendersonA1
Claire?L. ScottA1
C.?Roland WolfA11
Cancer Research UK Molecular Pharmacology Unit, Biomedical Research Centre, Level 5, Ninewells Hospital and Medical School, Dundee DD1 9SY, U.K.
Correspondence: 1To whom correspondence should be addressed (email


Cytochrome P450 enzymes (P450s) play a major role in the metabolism and disposition of chemicals and their activities are critical in determining the efficacy or side effects of drugs. These enzymes also have additional functions in adrenal steroid hormone biosynthesis and the hepatic synthesis of cholesterol and its degradation to bile acids [1]. The P450s involved in these different pathways are distinct and their regulation has conventionally been considered to be by different mechanisms. This is manifest in that many of the hepatic enzymes involved in foreign compound metabolism are expressed constitutively at low levels, but become highly induced on exogenous chemical exposure, resulting in an increased rate of excretion of the compound(s). Significant advances have been made in our understanding of this adaptive response through the identification of transcription factors, such as AhR (aryl hydrocarbon receptor), PXR (pregnane X receptor) and CAR (constitutive androstane receptor), which have the capacity to bind drugs and exogenous chemicals, resulting in transcriptional activation of genes that mediate their detoxification [2?5]. Although distinct classes of compounds bind to each receptor, owing to the diversity of these compounds' chemical structures, promiscuity exists in their specificity, particularly in the case of PXR and CAR [6,7].

We, and the group of Ding, have reported a mouse model where hepatic P450 activity has been reduced by >95% by the conditional deletion of the Por (P450 oxidoreductase) gene [8,9]. This was achieved by crossing mice carrying the Por gene flanked by loxP sites with mice expressing Cre recombinase under the control of the rat albumin promoter. This resulted in the specific hepatic deletion of POR neonatally with a concomitant reduction in P450 activity [8,9]. Although HRN (hepatic reductase-null) mice developed normally and were fertile, there were a number of intriguing phenotypic changes, including an enlarged liver and hepatic steatosis. Also, there was a profound increase in the expression of a range of P450s, with the most marked changes being in the expression of CYP2B10 (CYP is cytochrome P450) and CYP3A11 [10]. These enzymes, which are expressed at low levels in untreated animals, are highly inducible by exogenous chemicals such as barbiturates and synthetic glucocorticoids [11,12]. These data show that the P450 system is a key regulator of hepatic lipid homoeostasis and liver growth and that this metabolic homoeostasis can have a profound effect on the control of P450 gene expression and, as a consequence, on the metabolism/deposition of drugs. The HRN mouse therefore provides a model for investigating the endogenous factors involved in regulating P450 genes and the role of the P450 system in controlling hepatic steatosis and liver growth.

Studies of the temporal events that lead to the hepatic phenotype are, however, not possible in the HRN mice because the deletion of the Por gene occurs neonatally. To overcome this, we have created a model where the HRN genotype is regulated conditionally and in an inducible manner. This was achieved by crossing Por-floxed mice with mice where Cre recombinase is conditionally regulated by the rat Cyp1a1 promoter. This promoter is activated through the AhR, and administration of a single dose of 3MC (3-methlycholanthrene) at 40?mg/kg results in a specific, time-dependent, hepatic deletion of POR and a phenotype identical with that observed in HRN mice [13].

In the present study, we have used the new model to study the temporal biochemical changes that control lipid accumulation and P450 overexpression. We provide evidence that dietary unsaturated fatty acids play a key role in both lipid accumulation and P450 induction. Also, using nuclear receptor/HRN double- and triple-knockout mice, we show that P450 overexpression occurs predominantly through the activation of CAR.


All chemicals were purchased from Sigma?Aldrich, except where indicated.

Production of transgenic mice

Porlox/lox/CreAlb (HRN) and Porlox/lox/CreCYP1A1 mice on a C57/BL6 genetic background were generated as described previously [9,13]. Littermates with the Porlox/lox genotype were used as controls. PXR-null (Pxr?/?) and CAR-null (Car?/?) mice on a C57/BL6 genetic background were crossed on to the HRN line to generate Pxr?/?/Porlox/loxCreAlb (Pxr?/?/HRN) and Car?/?/Porlox/loxCreAlb (Car?/?/HRN) double-knockout mice respectively. Pxr?/?/HRN and Car?/?/HRN were crossed to generate Car?/?/Pxr?/?/Porlox/loxCreAlb (Car?/?/Pxr?/?/HRN) triple-knockout mice. Pxr?/?/Porlox/lox, Car?/?/Porlox/lox and Car?/?/Pxr?/?/Porlox/lox littermates were used as controls. Pxr?/? and Car?/? mice were identified by PCR as described previously [14,15].

All mice were maintained under standard animal house conditions with a 12?h light/12?h dark cycle and free access to water and RM1 (control) diet (Special Diets Services). All studies were carried out on 12-week-old male mice, except where indicated, in accordance with the Animal Scientific Procedures Act (1986) and after local ethical review.

Drug treatments

3MC in corn oil was administered to Porlox/lox/CreCYP1A1 and Porlox/lox mice by i.p. (intraperitoneal) injection at 40?mg/kg of body weight, and animals were killed at the indicated times.

Dietary restrictions

Porlox/lox/CreCYP1A1 and Porlox/lox mice were weaned and maintained on a control diet until 8?weeks of age before being transferred to either a fat-deficient diet (Special Diets Services, 821459) or a fatty-acid-supplemented fat-deficient diet (Supplementary Table S1 at, for an additional 6?weeks. As controls, both Porlox/lox/CreCYP1A1 and Porlox/lox mice were weaned and maintained on the control diet for the duration of the experiment. All diets were isocaloric and free from cholesterol. At 12?weeks of age, mice were administered either a single i.p. dose of 3MC (40?mg/kg of body weight) or corn oil, and killed 14?days later.

For linoleic acid treatment, Porlox/lox/CreCYP1A1 mice were maintained on the fat-deficient diet as described above. At 12?weeks of age, mice were administered a single i.p. dose of 3MC (40?mg/kg of body weight), followed by an oral dose of linoleic acid of 65?mg/day from day 5 after 3MC administration until being killed 9?days later.

Immunoblotting and biochemical analysis

Microsomal fractions were prepared by differential centrifugation [12], and protein concentrations were determined using the Bio-Rad Protein Assay Reagent. Western blot analysis was carried out as described previously [16] using 5??g of microsomal protein per lane and polyclonal antisera raised against human POR [17], murine CYP7A1 [13] or rat P450s [16]. Purified human POR, rat CYP4A1 and the following murine P450s, CYP2B10, His6?CYP3A11 and His6?CYP7A1, were used as standards. Immunoreactive proteins were detected using horseradish-peroxidase-conjugated donkey anti-(rabbit IgG) as a secondary antibody (Dako) and visualized by ECL? Plus (enhanced chemiluminescence (GE Healthcare). The relative protein content of individual P450s in microsomal fractions was determined by direct scanning of ECL? membranes with Bio-Rad Quantity One densitometry software. POR activity was determined by NADPH-dependent reduction of cytochrome c as described previously [17].

RNA isolation and real-time quantitative PCR analysis

Total RNA was isolated from snap-frozen liver samples using TRIzol? (Invitrogen). Genomic DNA was removed using RQ1 DNase (Promega), and RNA (600?ng) was reverse-transcribed using random hexamers and Superscript II RNase H reverse transcriptase polymerase (Invitrogen). Real-time quantitative PCR analysis was carried out with gene-specific primers for CYP2B10, CYP3A11 and CAR as described previously [10] and CD36 (Mm01135198_m1), FAS (fatty acid synthase) (Mm01253292_m1) and Cpt1a (carnitine palmitoyltransferase 1a) (Mm00550438_m1) were supplied by Applied Biosystems. Reactions were carried out in triplicate and monitored by measuring fluorescence at 518?nm with excitation at 494?nm. mRNA levels were quantified using the Prism 7700 associated software and GAPDH (glyceraldehyde-3-phosphate dehydrogenase) as an internal standard.

Blood chemistry

Blood was collected by cardiac puncture into heparinized tubes, and plasma was analysed for non-fasting total cholesterol and non-fasting triacylglycerols (triglycerides) using assay kits (Thermo Trace) on a Cobas Fara II centrifugal analyser (Roche).


Tissue samples were snap-frozen in Cryo-M-Bed (Bright Instrument Co.), cryo-sectioned (10??m) and stained with Oil Red O (lipid content) or haematoxylin and eosin (morphological analysis).

Lipid isolation and analysis

A small piece of liver was homogenized in PBS containing 0.1% Triton X-100, and hepatic triacylglycerol and cholesterol levels were determined using assay kits on a Cobas Fara II centrifugal analyser [18].

Detailed fatty acid analysis of the various diets was carried out by Special Diet Services (Supplementary Tables S2 and S3 at

Plasmid construction

The plasmids pCMX Gal4-hPXR-LBD and p4*4xGal4-UAS-luciferase were a gift from Luisella Vignati (Department of Pharmacokinetics, Dynamics and Metabolism, Gruppo Pfizer Inc., Italy) [19] and the former was used as a source of the pCMX Gal4 vector to facilitate the generation of further reporter constructs. The mouse CAR ligand-binding domain from amino acids 118?358 (mCAR-LBD) was amplified using 5?-GCGGAATTCGGTACTAAAGCATCTTTGCAACTGAA-3? and 5?-GCGGATCCTCAACTGCAAATCTCCCCGAGC-3? as forward and reverse primers respectively, incorporating 5? EcoRI and 3? BamHI sites to facilitate cloning. The resulting 738?bp PCR product was cloned as an EcoRI/BamHI fragment into pCMX Gal4-hPXR-LBD replacing the hPXR-LDB section and generating the vector pCMX Gal4-mCAR-LBD.

Cell culture, transient transfection and cell treatments

All cell culture media and supplements were supplied by Invitrogen. HepG2 cells were cultured in DMEM (Dulbecco's modified Eagle's medium) containing 10%(v/v) heat-inactivated foetal bovine serum, 1? non-essential amino acids, 100?units/ml penicillin, 100??g/ml streptomycin and 2?mM L-glutamine at 37??C and 5% CO2.

HepG2 cells were transiently transfected with pCMX Gal4-mCAR-LBD/p4*4xGal4-UAS-luciferase using the method of Vignati et al. [19], with the following modifications: FuGENE? 6 (Roche) was used instead of Lipofectamine? Plus (Invitrogen), assays were carried out in serum-containing medium and 0.2??g of the plasmid pRL-TK was included to allow normalization of luciferase reporter gene activity. Cells were treated with 0.25?0.5??M TCPOBOP {1,4-bis-[2-(3,5-dichloropyridyloxy)]benzene} and 1?mM PB (phenobarbital) as positive controls and DMSO as a further control. Linoleic acid, complexed to fatty-acid-free BSA at a molar ratio of 2:1, was tested at various concentrations ranging from 0 to 12.5??M, with the addition of 20??M ?-tocopheryl succinate to prevent lipid peroxidation. Luciferase reporter activity was determined using the Dual-Luciferase Reporter Assay System (Promega).

Temporal analysis of the phenotypic changes observed in the HRN mice

Porlox/lox/CreCYP1A1 mice, in the absence of a chemical inducer, were phenotypically normal and indistinguishable from wild-type animals. Treatment with a single dose of 3MC (40?mg/kg) led to a time-dependent complete deletion of the hepatic POR and the development of a phenotype that was identical with that of the original HRN model [13]. We therefore used this model to study the sequential development of the HRN phenotypic traits over a 28?day period following 3MC treatment.

At 6?days after 3MC administration a >85% reduction in the expression of POR protein, determined both by immunoblotting and cytochrome c activity, had occurred (Figures 1A and 1B, i), increasing to approx. 96% by day 14. These data were confirmed by immunohistochemistry where staining was reduced in all hepatocytes by day 3 and undetectable on day 14 and remained absent for at least 28?days (results not shown). Treatment with 3MC resulted in the anticipated induction of CYP1A1 as a consequence of the activation of the AhR. By days 7?9, CYP1A1 levels, presumably due to the metabolism and elimination of 3MC, were undetectable, indicating that the level of CYP1A1 was not induced by the POR deletion (Figure 1A). The transient changes observed in CYP1A1 expression imply that Cre recombinase expression would follow the same pattern and suggest that the deletion of POR is reversible. Cre recombinase is indeed expressed transiently, similarly to CYP1A1; however, return of POR is dependent on cell turnover, which, in the case of hepatocytes, takes several weeks. In Porlox/lox/CreCYP1A1 mice, no return of POR was observed for 60?days after 3MC treatment (results not shown). In contrast, very marked increases in the expression of other P450s were detected (Figure 1A). CYP2B, CYP2C, CYP3A and CYP7A1 levels increased profoundly as a function of time and in association with the decrease in POR expression. Particularly marked changes were obtained in P450s identified as CYP2B10 (corresponding to the upper band and CYP2B9 to the lower band according to the findings of Li-Masters and Morgan [20]) and CYP3A11. Interestingly, a stepwise increase in the level of CYP2B proteins occurred between days 9 and 11, whereas the increase in CYP2C and CYP3A proteins appeared to occur more gradually. An induction of CYP7A1 occurred on day 7 and continued to increase until day 21 (Figure 1A). CYP4A levels decreased from day 11 in both control (Porlox/lox) as well as HRN mice, after which time they remained slightly higher in HRN mice (results not shown). No changes were observed in the expression levels of CYP2D proteins in any samples. In control Porlox/lox animals, 3MC treatment had no effect on any of the P450s measured other than on the induction of CYP1A1 (results not shown).

Associated with the time-dependent reduction in POR were changes in liver size and non-fasting plasma total cholesterol and triacylglycerols levels (Figure 1B, ii, iii and iv). Significant consistent changes in liver/body weight ratio were observed from day 11, suggesting that other phenotypic changes must precede this effect (Figure 1B, ii). A significant decrease in non-fasting plasma triacylglycerol levels also occurred at this time (Figure 1B, iv). A reduction in non-fasting total plasma cholesterol levels was also observed which reduced steadily from day 3, in parallel with POR reduction (Figure 1B, iii), indicating that the reduction in triacylglycerols occurs independently of the changes in cholesterol, but in parallel with liver enlargement.

Loss of POR also led to a profound increase in hepatic lipids (Figure 1C). This accumulation occurred rapidly after 3MC administration and paralleled the loss of POR. At early time points, increases in lipid appeared to be localized to the perivenous region, the major site of POR and P450 expression, and not to the periportal region [21,22]. At later time points, this zonal localization was lost, leading to lipid accumulation throughout the liver. Quantification of hepatic lipid content demonstrated that the hepatic steatosis was due to increases in hepatic triacylglycerols by day 11 (Figure 2A). No significant changes in hepatic cholesterol levels were observed over the entire time course of the experiment (Figure 2B). The changes in hepatic triacylglycerol content were closely correlated with changes in both liver/body weight ratio and the reduction in plasma triacylglycerols (Figures 2C and 2D). This suggests that the level of hepatic triacylglycerols determines the circulating triacylglycerol levels and that they are related to liver enlargement.

Changes in hepatic lipid homoeostasis mediate P450 induction

Hepatic deletion of POR led to a profound time-dependent induction of several P450s, including members of the CYP2B and CYP3A families. This appeared to occur at both the protein and the mRNA level [9,10]. Changes in CYP2B10 expression were first seen on day 3, with a very marked increase between days 9 and 11 (Figure 1A). The increases in CYP2B10 protein and mRNA were not correlated with the decrease in POR activity (Supplementary Figure S1A, i and ii, at and therefore did not appear to be due to changes in the metabolism of an endogenous inducing agent. However, CYP2B10 protein and mRNA levels were correlated with each other, indicating that the induction of the Cyp2b10 gene occurs mainly at a transcriptional level (Supplementary Figure S1A, iii). In addition, Cyp2b10 mRNA levels were correlated with hepatic triacylglycerol concentration (Supplementary Figure S1A, iv). Similar analysis for CYP3A11 indicated that the increased protein expression occurred more rapidly than for CYP2B10, steadily increasing from day 2, reaching a maximum by day 21, but also did not directly correlate with changes in POR activity (Figure S1B). Although Cyp3a11 mRNA levels were increased in POR mice, this did not correlate with the level of CYP3A11 protein, indicating a more complex mechanism of regulation of this gene (Supplementary Figure S1B, iii), possibly involving both transcriptional and post-translational mechanisms. Unlike Cyp2b10, only a weak correlation between the increases in Cyp3a11 mRNA levels and hepatic triacylglycerol levels was observed (Supplementary Figure S1B, iv). Thus differences observed in the induction kinetics of CYP2B10 and CYP3A11, at both the protein and the mRNA level, suggests that the mechanisms regulating their overexpression are, at least in part, distinguishable.

To determine the contributions of lipid uptake, oxidation and synthesis to the development of the fatty liver phenotype and the induction of P450s, changes in the expression levels of CD36, FAS and Cpt1a were determined in 3MC-treated Porlox/lox/CreCYP1A1 mice compared with Porlox/lox mice (Supplementary Figure S2 at No significant changes in the expression levels of these genes were observed, except for in Cpt1a on day 28 which showed a minor, but significant, increase and may possibly be an attempt to reverse lipid accumulation by increasing ?-oxidation. Increased expression of CD36 was observed on days 21 and 28 in Porlox/lox/CreCYP1A1 mice, which may contribute to the increase in hepatic lipid at these time points; however, no correlation could be made before day 21. There was no correlation between the expression levels of these genes and the increases in P450 expression. They therefore do not appear to contribute to the lipid accumulation.

Dietary fatty acids mediate P450 induction in HRN mice

In view of the finding that changes in hepatic fatty acid homoeostasis correlated with the increases in P450 expression, detailed fatty acid analysis was carried out on livers from HRN and Porlox/lox (control) mice (Supplementary Tables S4 and S5 at Changes in all fatty acid classes occurred; however, the most significant changes were in mono-unsaturated and polyunsaturated fatty acids (Supplementary Table S5), with C16:1, C18:1 and C20:3 increasing 6.78-, 14.06- and 6.19-fold respectively (Supplementary Table S4). These data are in close agreement with the report of Weng et al. [23], who, for their HRN model, reported additional fold changes of 7.3 and 14.9 for C18:3 and C20:1 unsaturated fatty acids respectively. Together, these findings suggest that the accumulated hepatic triacylglycerols preferentially contain unsaturated fatty acid chains and that these fatty acid classes may mediate the P450 induction.

In the light of this possibility, Porlox/lox/CreCYP1A1 mice were placed on a fat-deficient diet for 4?weeks before 3MC administration. This treatment completely prevented the increases in P450 protein and mRNA expression as a consequence of POR deletion (Figure 3A). Maintenance of control Porlox/lox mice on a fat-deficient diet caused slight reductions in the constitutive expression of CYP7A and CYP2C protein, and did not affect the levels of the other P450s (results not shown). In addition to the changes in hepatic P450 expression, maintenance of Porlox/lox/CreCYP1A1 mice on a fat-deficient diet prevented the accumulation of lipid in the livers of these animals (Figure 3C), resulting in an Oil Red O staining pattern that was indistinguishable from that of Porlox/lox mice on a control diet. Also no significant changes in total plasma cholesterol or triacylglycerol levels were measured on deletion of POR in Porlox/lox/CreCYP1A1 mice fed a fat-deficient diet (Supplementary Figure S3). These data indicate that hepatic triacylglycerol accumulation in POR mice originates from the diet and that as a consequence of the inactivation of the P450 system an inability to maintain hepatic lipid homoeostasis occurs which triggers increased P450 expression (possibly in an attempt to restore normal hepatic lipid levels). It is worth noting that the fat-deficient diet also prevented the liver enlargement seen on POR deletion, thus providing a metabolic link to all three phenomena.

In order to identify the fatty acids that mediated P450 induction, various fatty acids were added back to the fat-deficient diet as outlined in Supplementary Table S1. Porlox/lox/CreCYP1A1 and Porlox/lox were maintained on the supplemented diets and analysed 14?days after 3MC administration. In diets containing unsaturated fatty acids, the loss of P450 gene expression observed with the fat-deficient diet was reversed. This was particularly the case for diets containing sunflower oil (which is composed of approx. 88% unsaturated fatty acids) (Figure 3B, Supplementary Table S2). The inclusion of saturated fatty acids in the diet was essentially without effect. None of the treatments had effects on POR or P450 gene expression in the control Porlox/lox animals, with the exception of CYP4A which was induced by all three unsaturated fatty acid diets (results not shown). Analysis of Cyp2b10 and Cyp3a11 mRNA levels confirmed that the changes in protein expression were at least in part a result of transcriptional activation, the highest increases in mRNA being found in mice on the sunflower-oil-supplemented diet (Figure 3B, ii and iii). Analysis of plasma lipid levels revealed some minor decreases in both total cholesterol and triacylglycerol levels between Porlox/lox/CreCYP1A1 and Porlox/lox for all dietary treatments; however, these were only significant for the sunflower-oil-supplemented diet where a 1.5- (P=0.036) and 1.8- (P=0.013) fold decrease was observed respectively (Supplementary Figures S3A and S3B at Hepatic lipid accumulation was observed for all diets, except for the fat-deficient diet, indicating that lipid accumulation alone is not sufficient to cause P450 induction (Figure 3C). In addition, no significant increases in liver/body weight ratio were observed for the diets used, except that containing sunflower oils (Supplementary Figure S3C). These data indicate that lipid accumulation alone was not the cause of liver enlargement, but that unsaturated fatty acids had the capacity to induce the effect. Comparison of the fatty acid composition of the diets (Supplementary Tables S2 and S3), identified C18:2 (linoleic acid), an n?6 PUFA (polyunsaturated fatty acid), as a candidate fatty acid mediator of both P450 induction and liver growth as it was the only fatty acid present in the diets that correlated with the effects observed. This hypothesis suggests that the addition of linoleic acid as the sole dietary fatty acid should be sufficient to induce P450 expression in Porlox/lox/CreCYP1A1 mice maintained on a fat-deficient diet. This was indeed found to be the case, with oral administration of linoleic acid (65?mg/day for 9?days) to Porlox/lox/CreCYP1A1 mice on a fat-deficient diet, resulting in induction of CYP2B10, CYP3A11 and CYP2C proteins (Figure 4A). Analysis of Cyp2b10 and Cyp3a11 mRNA levels showed this induction to occur at the transcription level (Figure 4B). In addition, administration of linoleic acid was found to promote hepatic lipid accumulation (Figure 4C). This lipid accumulation was reduced compared with Porlox/lox/CreCYP1A1 mice maintained on a control diet and appeared to be concentrated around the blood vessels, a pattern similar to that observed at early time points following 3MC administration (Figure 1C); however, in this case, it is probably due to differences in the amount of fat intake. These results therefore indicate that linoleic acid, an n?6 dietary essential fatty acid, is a key regulator of P450 expression in HRN models and that members of the CYP2B, CYP3A and CYP2C, in a normal physiological situation, are involved in its metabolism.

Role of nuclear receptors in P450 induction in HRN mice

Nuclear receptors that have been shown to mediate the regulation of many P450 genes in response to exogenous chemicals [24,25] have also been shown to play an important role in controlling liver growth [26,27]. Of particular interest with regards to this study were CAR and PXR, which have been intimately linked to the regulation of CYP2B and CYP3A proteins in response to both exogenous and endogenous inducing agents [28?30], and PXR has been linked to triacylglycerol homoeostasis [27]. In order to investigate whether these nuclear receptors mediate the P450 overexpression in the HRN mice, we crossed the HRN animals with mice nulled at either the Car or Pxr locus alone or in combination to generate Car?/?/HRN, Pxr?/?/HRN and Pxr?/?/Car?/?/HRN genotypes.

Loss of PXR did not affect POR deletion or the induction of P450 proteins observed in HRN mice (Figure 5A). In agreement with previous findings, Pxr?/? mice exhibited slight increases in CYP3A11 protein [14], and also CYP2B and CYP2C proteins (Figure 5A, i); Cyp3a11 mRNA was also elevated relative to levels in control Porlox/lox mice (Figure 5A, ii). Basal expression of Cyp2b10 mRNA was also very slightly increased (Figure 5A, ii), although this was not reflected in detectable protein expression (Figure 5A, i). The deletion of PXR did not affect the increases in both CYP2B10 and CYP3A11 protein in HRN animals; however, a reduction in both Cyp2b10 and Cyp3a11 mRNA levels was observed, but this was not significant compared with HRN mice (Figure 5A, ii). No changes in plasma and hepatic lipid levels were observed in Pxr?/?/HRN mice compared with HRN mice (Supplementary Table S6 at and Figure 5D); however, in Pxr?/? mice, non-fasting plasma total cholesterol and triacylglycerol levels were reduced, the former significantly, in comparison with wild-type mice (Supplementary Table S6).

In relation to HRN mice nulled for CAR, profound changes in the HRN phenotype were observed. The elevated expression of CYP2B, CYP7A and CYP2C was markedly attenuated; however, CYP3A11 expression appeared to be unaffected (Figure 5B). Analysis of mRNA levels also showed that no induction of Cyp2b10 mRNA occurred in Car?/?/HRN mice, indicating that the increase in the expression of this P450 observed in HRN mice was a consequence of CAR activation (Figure 5B, ii). Interestingly, deletion of CAR in both control and HRN mice further increased Cyp3a11 mRNA levels (Figure 5B, ii). The reduction in non-fasting plasma total cholesterol and triacylglycerol levels observed in the HRN mice were, however, not reversed on the Car?/? background (Supplementary Table S6); however, a significant reduction in hepatic lipid content for Car?/?/HRN mice compared with HRN mice was observed (Figure 5D). These data suggest that, in addition to mediating P450 induction in HRN mice, CAR plays a role in hepatic lipid accumulation.

Finally, owing to the cross-talk between PXR and CAR [31], the effect of deleting both receptors on the development of the HRN phenotype was analysed. In Pxr?/?/Car?/?/HRN mice, consistent with the Car?/? mice, the expression of CYP2B and CYP2C proteins was profoundly reduced, whereas, in contrast, CYP7A expression levels were only slightly affected (Figure 5C). In mice nulled at both the Car and Pxr gene loci, a marked decrease in CYP3A11 protein was also observed (Figure 5C, i). The change in CYP2B protein expression was also reflected in a reduction in Cyp2b10 mRNA levels (Figure 5C, ii). A slight decrease in Cyp3a11 mRNA was observed in Pxr?/?/Car?/?/HRN mice, although this was not significantly different from that of HRN or Pxr?/?/Car?/? mice (Figure 5C, ii). Deletion of both CAR and PXR on an HRN background resulted in an increase in non-fasting plasma total cholesterol level that was not significantly different from control (Porlox/lox) mice. Although an increase in plasma triacylglycerols was also observed, this was not significantly different from the HRN value (Supplementary Table S6). Hepatic lipid content was reduced in Pxr?/?/Car?/?/HRN mice compared with HRN mice, similar to levels observed in Car?/?/HRN mice, but still elevated compared with controls (Figure 5D); however, this reduction did result in a change in liver size (Supplementary Table S6).

Direct activation of CAR by linoleic acid in HRN mice

In order to establish whether PUFAs could activate CAR directly, we carried out transactivation assays using a Gal4-CAR-LBD reporter assay in HepG2 cells [32]. In these experiments, both TCPOBOP and linoleic acid could activate CAR directly (Figure 6). PB, which is known to activate CAR by an indirect mechanism, was not active in this assay. In view of reports that the fatty-acid-sensitive transcription factor, PPAR? (peroxisome-proliferator-activated receptor ?) can effect CAR expression [33,34] and that the effects in the POR mice may be indirect, we measured Car mRNA expression in Porlox/lox/CreCYP1A1 mice. Expression levels of CAR were found to be unchanged (Supplementary Figure S2D).


The liver is the major organ controlling metabolic homoeostasis due to dietary change. It is also the major tissue responsible for drug and dietary chemical detoxification through the actions of phase I and phase II drug metabolism in which the P450 system plays a pivotal role. Although it has been known for some time that alterations in diet and disease states such as diabetes affect the P450 system, there has been little evidence that P450s can play a direct role in metabolic control [35?37]. However, there is a growing body of evidence, as demonstrated in the present paper, that these pathways are intimately linked. This has a wide range of implications not only for how alterations in P450 function may influence the pathogenesis of disease, but also for how diet and disease states may influence the metabolism and disposition of drugs and environmental agents; for example, obesity in rats has been shown to reduce expression levels of CAR and impaired CYP2B induction by PB [38].

The metabolic dialogue between the pathways of detoxification and metabolic homoeostasis are manifest in the findings that, when the P450 system is inactivated, profound changes in lipid homoeostasis and liver size occur which are paralleled by the marked induction of P450s associated with drug metabolism in the absence of an exogenous inducing agent. We have demonstrated that P450s from a range of gene families are induced and that this induction parallels the accumulation of hepatic triacylglycerols. We have also shown that the regulation of different P450s is, in part, distinguishable, as exemplified by CYP2B10 and CYP3A11. CYP2B10 induction is almost entirely controlled at the transcriptional level and occurs at a time point when there is a stepwise increase in triacylglycerol accumulation, whereas, in the case of CYP3A11, there is only a poor correlation between mRNA induction and protein levels, indicating that both transcriptional and post-translational mechanisms are involved. The latter mechanism could possibly occur via phosphorylation or ubiquitination [39?41]. This may also be the case for CYP2C proteins. Evidence for distinct pathways of regulation is also reflected in the finding that the overexpression of these proteins is, at least in part, mediated by different transcription factors (see below). We have also demonstrated that hepatic steatosis is not sufficient to induce the hepatic P450 expression, but this effect is mediated by dietary unsaturated fatty acids such as linoleic acid, which we have found is sufficient on its own to reverse the fat-deficient phenotype.

P450s of the CYP2B family are the major enzymes induced in the liver by barbiturate drugs such as PB [42] and have the capacity to metabolize fatty acids such as arachidonic acid [43]. Interestingly, Fulco and co-workers demonstrated over 20?years ago that a fatty acid mono-oxygenase involved in fatty acid oxidation in Bacillus megaterium is highly inducible by PB [44,45]. In fact, studies on this pathway have demonstrated that its induction provides an adaptive response against unsaturated fatty acid toxicity [46]. Whether the induction of enzymes such as CYP2B10 and CYP3A11 in mammals are part of a similar detoxification pathway against dietary unsaturated fatty acids which are not produced endogenously, such as linoleic acid, remains to be determined. However the data in the present study do raise the possibility that, under certain circumstances, diets containing unsaturated fatty acids may influence hepatic detoxification systems.

A wide range of transcription factors have now been discovered which control fatty acid homoeostasis and liver growth, including PPAR?, CAR, PXR, LXR (liver X receptor) and HNF4? (hepatocyte nuclear factor 4?) [26,27,47?49]. For example, it has been demonstrated that PPAR? mediates liver growth induced by perturbations in fatty acid homoeostasis as a consequence of peroxisome proliferation and that PXR plays a role in controlling hepatic triacylglycerol homoeostasis [27,50,51]. It was therefore intriguing that the majority of the phenotypes resulting from inactivation of the hepatic P450 system and the downstream effects on fatty acid homoeostasis were mediated by the transcription factor CAR. It has been postulated for some time that CAR function is regulated by both endogenous and exogenous inducing agents including metabolic control through AMPK (AMP-activated protein kinase) [52], interaction with the forkhead transcription factor FoxO1 (forkhead box O1) [53] and activation during fasting [54]. It has also been postulated that CAR function can be modulated by the fatty-acid-sensitive transcription factor PPAR? [33,34]. However, this mechanism of CAR activation would not appear to explain the hepatic phenotype, as no changes in CAR expression were found and also linoleic acid activated CAR directly. However, to our knowledge, the finding that CAR may play a role in linking the control of hepatic lipid homoeostasis and endogenous P450 expression has not been reported previously. We provide additional evidence that, for one group of enzymes in the Cyp3a gene family, PXR may also play a role in defining the response to unsaturated fatty acids. The finding that feeding conditional HRN mice a fat-deficient diet prevents the induction of CYP3A11 suggests that fatty acids, as well as bile acids [14], can influence PXR function.

A possible pathway linking P450 function to the findings observed in the present study is shown in Figure 7. As described in this model, dietary unsaturated fatty acids enter the liver via fatty acid transporters, where, in wild-type mice, they are oxidized for energy purposes or detoxified by P450s. Inactivation of the P450 system as a result of Por deletion leads to hepatic accumulation of unsaturated fatty acids initially via increase import due to the induction of lipid transporters such as CD36 [23] and a reduction of plasma lipid levels. Hepatic lipid accumulation triggers the activation of the nuclear receptor CAR (and possibly PXR), leading to P450 induction and liver growth through the activation of other downstream growth/transcription factors [26,27]. The overexpression of P450s is aimed at re-establishing hepatic lipid homoeostasis and the prevention of toxicity via increased metabolism of unsaturated fatty acids. Inactivation of POR prevents this increased metabolism and ultimately leads to hepatic steatosis, which establishes a cyclical process that promotes further hepatic lipid accumulation and growth. The ability to control the hepatic deletion of POR conditionally using the CYP1A1?Cre system has allowed us to provide evidence in support of this pathway. Activation of Cre through the administration of 3MC resulted in the rapid deletion of POR, in that over 85% of hepatocytes did not express the protein after 6?days. Although accumulation of lipid was already occurring at this time point, there appears to be a threshold at which point the CAR pathway becomes activated. This hypothesis is supported by the finding that it was only after 9?11?days that a marked change in triacylglycerol accumulation occurred which was linked directly to changes in plasma lipids, liver growth and P450 induction. Loss of P450 activity itself was not responsible for its auto-induction (although the corresponding accumulation of a metabolite produced, e.g. a bile acid precursor, which binds to CYP3A11 could explain the stabilization of this protein). Whether the inactivation of the P450 system causes the triacylglycerol accumulation and liver growth and whether their induction is to attenuate the phenotypic changes produced remains uncertain; however, it is quite clear that the accumulation of hepatic triacylglycerols activates CAR. The demonstration of cross-talk between drugs and lipids on CAR implies that there will be drug?lipid interactions associated with effects on this receptor and evidence for this is provided by the work of Li et al. [55], who showed that PUFAs could influence the induction of P450 genes by PB. Why the HRN phenotype results in the reduction in circulating triacylglycerols and cholesterol remains to be established. It is interesting to note, however, that the cholesterol 7?-hydroxylase enzyme (CYP7A1) involved in bile acid homoeostasis also appears to be affected by unsaturated fatty acid levels in a CAR-dependent manner and possibly a PXR-dependent manner, as suggested by the opposing effects on this protein's expression observed in Car?/? and Pxr?/?/Car?/?/HRN mice. The effect observed here on this enzyme's expression is intriguing as a previous report suggested that CAR activation represses CYP7A1 expression [56]. The contrasting results may be a consequence of the fact that fasted, as opposed to non-fasted, animals were used in the study of Miao et al. [56]. Despite this, these data suggest the existence of a new pathway for the dietary regulation of CYP7A1 by unsaturated fatty acids.

In summary, we have used a novel conditional HRN model to investigate the sequential development of the phenotypic changes observed in mice on deletion of POR. POR deletion and the associated inactivation of hepatic P450 function leads to accumulation of dietary fatty acids in the liver, in the form of triacylglycerols of unsaturated fatty acids, leading to organ enlargement and increased P450 expression, in the case of CYP2B, CYP2C and CYP7A1 via a CAR-dependent signalling pathway. The molecular mechanism underlying CYP3A11 expression appears to involve CAR, PXR and protein stabilization. Induction of the P450 system appears to be mediated by the accumulation of PUFAs, such as linoleic acid (C18:2,n?6) and suggests that this may be part of an adaptive response to prevent the deleterious effects of PUFA accumulation. The finding that the major P450s that are inducible by exogenous chemicals are also regulated by changes in fatty acid homoeostasis has potentially significant implications for the variability observed in drug responses in humans.

We thank Dr Steven Kliewer for his gift of Pxr?/? and Car?/? mice and Dr Alexander Hill for carrying out the hepatic fatty acid analysis. Dianne Carrie and Catherine Hughes are thanked for excellent technical assistance with the animal work.


This work was funded by Cancer Research UK [grant number C463/A5661] (to C.R.W.).

1. Ortiz?de?Montellano P.. Cytochrome P450: structure, mechanism and biochemistry2005New York: Kluwer Academic/Plenum Publishers;
2. Okey A.?B.,Bondy G.?P.,Mason M.?E.,Kahl G.?F.,Eisen H.?J.,Guenthner T.?M.,Nebert D.?W.. Regulatory gene product of the Ah locus: characterization of the cytosolic inducer?receptor complex and evidence for its nuclear translocationJ. Biol. Chem. 1979;254:11636–11648. [pmid: 500663]
3. Kliewer S.?A.,Moore J.?T.,Wade L.,Staudinger J.?L.,Watson M.?A.,Jones S.?A.,McKee D.?D.,Oliver B.?B.,Willson T.?M.,Zetterstrom R.?H.,et al. An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathwayCell 1998;92:73–82. [pmid: 9489701]
4. Lehmann J.?M.,McKee D.?D.,Watson M.?A.,Willson T.?M.,Moore J.?T.,Kliewer S.?A.. The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactionsJ. Clin. Invest. 1998;102:1016–1023. [pmid: 9727070]
5. Choi H.?S.,Chung M.,Tzameli I.,Simha D.,Lee Y.?K.,Seol W.,Moore D.?D.. Differential transactivation by two isoforms of the orphan nuclear hormone receptor CARJ. Biol. Chem. 1997;272:23565–23571. [pmid: 9295294]
6. Jones S.?A.,Moore L.?B.,Shenk J.?L.,Wisely G.?B.,Hamilton G.?A.,McKee D.?D.,Tomkinson N.?C.,LeCluyse E.?L.,Lambert M.?H.,Willson T.?M.,et al. The pregnane X receptor: a promiscuous xenobiotic receptor that has diverged during evolutionMol. Endocrinol. 2000;14:27–39. [pmid: 10628745]
7. Maglich J.?M.,Stoltz C.?M.,Goodwin B.,Hawkins-Brown D.,Moore J.?T.,Kliewer S.?A.. Nuclear pregnane X receptor and constitutive androstane receptor regulate overlapping but distinct sets of genes involved in xenobiotic detoxificationMol. Pharmacol. 2002;62:638–646. [pmid: 12181440]
8. Gu J.,Weng Y.,Zhang Q.?Y.,Cui H.,Behr M.,Wu L.,Yang W.,Zhang L.,Ding X.. Liver-specific deletion of the NADPH?cytochrome P450 reductase gene: impact on plasma cholesterol homeostasis and the function and regulation of microsomal cytochrome P450 and heme oxygenaseJ. Biol. Chem. 2003;278:25895–25901. [pmid: 12697746]
9. Henderson C.?J.,Otto D.?M.,Carrie D.,Magnuson M.?A.,McLaren A.?W.,Rosewell I.,Wolf C.?R.. Inactivation of the hepatic cytochrome P450 system by conditional deletion of hepatic cytochrome P450 reductaseJ. Biol. Chem. 2003;278:13480–13486. [pmid: 12566435]
10. Wang X.?J.,Chamberlain M.,Vassieva O.,Henderson C.?J.,Wolf C.?R.. Relationship between hepatic phenotype and changes in gene expression in cytochrome P450 reductase (POR) null miceBiochem. J. 2005;388:857–867. [pmid: 15717863]
11. Simmons D.?L.,McQuiddy P.,Kasper C.?B.. Induction of the hepatic mixed-function oxidase system by synthetic glucocorticoids: transcriptional and post-transcriptional regulationJ. Biol. Chem. 1987;262:326–332. [pmid: 3098741]
12. Meehan R.?R.,Forrester L.?M.,Stevenson K.,Hastie N.?D.,Buchmann A.,Kunz H.?W.,Wolf C.?R.. Regulation of phenobarbital-inducible cytochrome P-450s in rat and mouse liver following dexamethasone administration and hypophysectomyBiochem. J. 1988;254:789–797. [pmid: 3058117]
13. Finn R.?D.,McLaren A.?W.,Carrie D.,Henderson C.?J.,Wolf C.?R.. Conditional deletion of cytochrome P450 oxidoreductase in the liver and gastrointestinal tract: a new model for studying the functions of the P450 systemJ. Pharmacol. Exp. Ther. 2007;322:40–47. [pmid: 17435107]
14. Staudinger J.?L.,Goodwin B.,Jones S.?A.,Hawkins-Brown D.,MacKenzie K.?I.,LaTour A.,Liu Y.,Klaassen C.?D.,Brown K.?K.,Reinhard J.,et al. The nuclear receptor PXR is a lithocholic acid sensor that protects against liver toxicityProc. Natl. Acad. Sci. U.S.A. 2001;98:3369–3374. [pmid: 11248085]
15. Wei P.,Zhang J.,Egan-Hafley M.,Liang S.,Moore D.?D.. The nuclear receptor CAR mediates specific xenobiotic induction of drug metabolismNature 2000;407:920–923. [pmid: 11057673]
16. Forrester L.?M.,Henderson C.?J.,Glancey M.?J.,Back D.?J.,Park B.?K.,Ball S.?E.,Kitteringham N.?R.,McLaren A.?W.,Miles J.?S.,Skett P.,et al. Relative expression of cytochrome P450 isoenzymes in human liver and association with the metabolism of drugs and xenobioticsBiochem. J. 1992;281:359–368. [pmid: 1736885]
17. Smith G.?C.,Tew D.?G.,Wolf C.?R.. Dissection of NADPH?cytochrome P450 oxidoreductase into distinct functional domainsProc. Natl. Acad. Sci. U.S.A. 1994;91:8710–8714. [pmid: 8078947]
18. Yoshinari K.,Takagi S.,Yoshimasa T.,Sugatani J.,Miwa M.. Hepatic CYP3A expression is attenuated in obese mice fed a high-fat dietPharm. Res. 2006;23:1188–1200. [pmid: 16715367]
19. Vignati L.?A.,Bogni A.,Grossi P.,Monshouwer M.. A human and mouse pregnane X receptor reporter gene assay in combination with cytotoxicity measurements as a tool to evaluate species-specific CYP3A inductionToxicology 2004;199:23–33. [pmid: 15125996]
20. Li-Masters T.,Morgan E.?T.. Effects of bacterial lipopolysaccharide on phenobarbital-induced CYP2B expression in miceDrug Metab. Dispos. 2001;29:252–257. [pmid: 11181491]
21. Wolf C.?R.,Moll E.,Friedberg T.,Oesch F.,Buchmann A.,Kuhlmann W.?D.,Kunz H.?W.. Characterization, localization and regulation of a novel phenobarbital-inducible form of cytochrome P450, compared with three further P450-isoenzymes, NADPH P450-reductase, glutathione transferases and microsomal epoxide hydrolaseCarcinogenesis 1984;5:993–1001. [pmid: 6430587]
22. Oinonen T.,Lindros K.?O.. Zonation of hepatic cytochrome P-450 expression and regulationBiochem. J. 1998;329:17–35. [pmid: 9405271]
23. Weng Y.,Dirusso C.?C.,Reilly A.?A.,Black P.?N.,Ding X.. Hepatic gene expression changes in mouse models with liver-specific deletion or global suppression of the NADPH?cytochrome P450 reductase gene: mechanistic implications for the regulation of microsomal cytochrome P450 and the fatty liver phenotypeJ. Biol. Chem. 2005;280:31686–31698. [pmid: 16006652]
24. Honkakoski P.,Negishi M.. Regulation of cytochrome P450 (CYP) genes by nuclear receptorsBiochem. J. 2000;347:321–337. [pmid: 10749660]
25. Xie W.,Barwick J.?L.,Simon C.?M.,Pierce A.?M.,Safe S.,Blumberg B.,Guzelian P.?S.,Evans R.?M.. Reciprocal activation of xenobiotic response genes by nuclear receptors SXR/PXR and CARGenes Dev. 2000;14:3014–3023. [pmid: 11114890]
26. Huang W.,Zhang J.,Washington M.,Liu J.,Parant J.?M.,Lozano G.,Moore D.?D.. Xenobiotic stress induces hepatomegaly and liver tumors via the nuclear receptor constitutive androstane receptorMol. Endocrinol. 2005;19:1646–1653. [pmid: 15831521]
27. Zhou J.,Zhai Y.,Mu Y.,Gong H.,Uppal H.,Toma D.,Ren S.,Evans R.?M.,Xie W.. A novel pregnane X receptor-mediated and sterol regulatory element-binding protein-independent lipogenic pathwayJ. Biol. Chem. 2006;281:15013–15020. [pmid: 16556603]
28. Honkakoski P.,Zelko I.,Sueyoshi T.,Negishi M.. The nuclear orphan receptor CAR-retinoid X receptor heterodimer activates the phenobarbital-responsive enhancer module of the CYP2B geneMol. Cell. Biol. 1998;18:5652–5658. [pmid: 9742082]
29. Zhang J.,Huang W.,Qatanani M.,Evans R.?M.,Moore D.?D.. The constitutive androstane receptor and pregnane X receptor function coordinately to prevent bile acid-induced hepatotoxicityJ. Biol. Chem. 2004;279:49517–49522. [pmid: 15358766]
30. Xie W.,Yeuh M.?F.,Radominska-Pandya A.,Saini S.?P.,Negishi Y.,Bottroff B.?S.,Cabrera G.?Y.,Tukey R.?H.,Evans R.?M.. Control of steroid, heme, and carcinogen metabolism by nuclear pregnane X receptor and constitutive androstane receptorProc. Natl. Acad. Sci. U.S.A. 2003;100:4150–4155. [pmid: 12644700]
31. Pascussi J.?M.,Gerbal-Chaloin S.,Duret C.,Daujat-Chavanieu M.,Vilarem M.?J.,Maurel P.. The tangle of nuclear receptors that controls xenobiotic metabolism and transport: crosstalk and consequencesAnnu. Rev. Pharmacol. Toxicol. 2008;10:1–32. [pmid: 17608617]
32. Honkakoski P.,Jaaskelainen I.,Kortelahti M.,Urtti A.. A novel drug-regulated gene expression system based on the nuclear receptor constitutive androstane receptor (CAR)Pharm. Res. 2001;18:146–150. [pmid: 11405283]
33. Wieneke N.,Hirsch-Ernst K.?I.,Kuna M.,Kersten S.,Puschel G.?P.. PPAR?-dependent induction of the energy homeostasis-regulating nuclear receptor NR1i3 (CAR) in rat hepatocytes: potential role in starvation adaptationFEBS Lett. 2007;581:5617–5626. [pmid: 18023279]
34. Guo D.,Sarkar J.,Suino-Powell K.,Xu Y.,Matsumoto K.,Jia Y.,Yu S.,Khare S.,Haldar K.,Rao M.?S.,et al. Induction of nuclear translocation of constitutive androstane receptor by peroxisome proliferator-activated receptor ? synthetic ligands in mouse liverJ. Biol. Chem. 2007;282:36766–36776. [pmid: 17962186]
35. Kato J.,Ikemoto A.,Mizutani T.. The effect of dietary fatty acids on the expression levels and activities of hepatic drug metabolizing enzymesJ. Health Sci. 2003;49:105–114.
36. Yoshinari K.,Takagi S.,Sugatani J.,Miwa M.. Changes in the expression of cytochromes P450 and nuclear receptors in the liver of genetically diabetic db/db miceBiol. Pharm. Bull. 2006;29:1634–1638. [pmid: 16880618]
37. Khemawoot P.,Yokogawa K.,Shimada T.,Miyamoto K.. Obesity-induced increase of CYP2E1 activity and its effect on disposition kinetics of chlorzoxazone in Zucker ratsBiochem. Pharmacol. 2007;73:155–162. [pmid: 17049493]
38. Xiong H.,Yoshinari K.,Brouwer K.?L.,Negishi M.. Role of constitutive androstane receptor in the in vivo induction of Mrp3 and CYP2B1/2 by phenobarbitalDrug Metab. Dispos. 2002;30:918–923. [pmid: 12124310]
39. Posti K.,Leinonen S.,Tetri S.,Kottari S.,Viitala P.,Pelkonen O.,Raunio H.. Modulation of murine phenobarbital-inducible CYP2A5, CYP2B10 and CYP1A enzymes by inhibitors of protein kinases and phosphatasesEur. J. Biochem. 1999;264:19–26. [pmid: 10447669]
40. Oesch-Bartlomowicz B.,Oesch F.. Cytochrome-P450 phosphorylation as a functional switchArch. Biochem. Biophys. 2003;409:228–234. [pmid: 12464263]
41. Zangar R.?C.,Kimzey A.?L.,Okita J.?R.,Wunschel D.?S.,Edwards R.?J.,Kim H.,Okita R.?T.. Cytochrome P450 3A conjugation to ubiquitin in a process distinct from classical ubiquitination pathwayMol. Pharmacol. 2002;61:892–904. [pmid: 11901229]
42. Honkakoski P.,Negishi M.. Regulatory DNA elements of phenobarbital-responsive cytochrome P450 CYP2B genesJ. Biochem. Mol. Toxicol. 1998;12:3–9. [pmid: 9414482]
43. Keeney D.?S.,Skinner C.,Wei S.,Friedberg T.,Waterman M.?R.. A keratinocyte-specific epoxygenase, CYP2B12, metabolizes arachidonic acid with unusual selectivity, producing a single major epoxyeicosatrienoic acidJ. Biol. Chem. 1998;273:9279–9284. [pmid: 9535921]
44. Ruettinger R.?T.,Fulco A.?J.. Epoxidation of unsaturated fatty acids by a soluble cytochrome P-450-dependent system from Bacillus megateriumJ. Biol. Chem. 1981;256:5728–5734. [pmid: 6787044]
45. Narhi L.?O.,Fulco A.?J.. Phenobarbital induction of a soluble cytochrome P-450-dependent fatty acid monooxygenase in Bacillus megateriumJ. Biol. Chem. 1982;257:2147–2150. [pmid: 6801029]
46. Palmer C.?N.,Axen E.,Hughes V.,Wolf C.?R.. The repressor protein, Bm3R1, mediates an adaptive response to toxic fatty acids in Bacillus megateriumJ. Biol. Chem. 1998;273:18109–18116. [pmid: 9660768]
47. Li Y.,Nara T.?Y.,Nakamura M.?T.. Peroxisome proliferator-activated receptor ? is required for feedback regulation of highly unsaturated fatty acid synthesisJ. Lipid Res. 2005;46:2432–2440. [pmid: 16106047]
48. Hayhurst G.?P.,Lee Y.?H.,Lambert G.,Ward J.?M.,Gonzalez F.?J.. Hepatocyte nuclear factor 4? (nuclear receptor 2A1) is essential for maintenance of hepatic gene expression and lipid homeostasisMol. Cell. Biol. 2001;21:1393–1403. [pmid: 11158324]
49. Laffitte B.?A.,Chao L.?C.,Li J.,Walczak R.,Hummasti S.,Joseph S.?B.,Castrillo A.,Wilpitz D.?C.,Mangelsdorf D.?J.,Collins J.?L.,et al. Activation of liver X receptor improves glucose tolerance through coordinate regulation of glucose metabolism in liver and adipose tissueProc. Natl. Acad. Sci. U.S.A. 2003;100:5419–5424. [pmid: 12697904]
50. McCarthy T.?C.,Pollak P.?T.,Hanniman E.?A.,Sinal C.?J.. Disruption of hepatic lipid homeostasis in mice after amiodarone treatment is associated with peroxisome proliferator-activated receptor-? target gene activationJ. Pharmacol. Exp. Ther. 2004;311:864–873. [pmid: 15265979]
51. Yang Q.,Ito S.,Gonzalez F.?J.. Hepatocyte-restricted constitutive activation of PPAR? induces hepatoproliferation but not hepatocarcinogenesisCarcinogenesis 2007;28:1171–1177. [pmid: 17331954]
52. Rencurel F.,Stenhouse A.,Hawley S.?A.,Friedberg T.,Hardie D.?G.,Sutherland C.,Wolf C.?R.. AMP-activated protein kinase mediates phenobarbital induction of CYP2B gene expression in hepatocytes and a newly derived human hepatoma cell lineJ. Biol. Chem. 2005;280:4367–4373. [pmid: 15572372]
53. Kodama S.,Koike C.,Negishi M.,Yamamoto Y.. Nuclear receptors CAR and PXR cross talk with FOXO1 to regulate genes that encode drug-metabolizing and gluconeogenic enzymesMol. Cell. Biol. 2004;24:7931–7940. [pmid: 15340055]
54. Maglich J.?M.,Watson J.,McMillen P.?J.,Goodwin B.,Willson T.?M.,Moore J.?T.. The nuclear receptor CAR is a regulator of thyroid hormone metabolism during caloric restrictionJ. Biol. Chem. 2004;279:19832–19838. [pmid: 15004031]
55. Li C.?C.,Lii C.?K.,Liu K.?L.,Yang J.?J.,Chen H.?W.. n?6 and n?3 polyunsaturated fatty acids down-regulate cytochrome P-450 2B1 gene expression induced by phenobarbital in primary rat hepatocytesJ. Nutr. Biochem. 2006;17:707–715. [pmid: 16517146]
56. Miao J.,Fang S.,Bae Y.,Kemper J.?K.. Functional inhibitory cross-talk between constitutive androstane receptor and hepatic nuclear factor-4 in hepatic lipid/glucose metabolism is mediated by competition for binding to the DR1 motif and to the common coactivators, GRIP-1 and PGC-1?J. Biol. Chem. 2006;281:14537–14546. [pmid: 16492670]


[Figure ID: F1]
Figure 1  Time course of the phenotypic changes in conditional HRN mice

Porlox/lox/CreCYP1A1 and Porlox/lox mice were treated with a single dose of 3MC (40?mg/kg of body weight) before plasma and liver samples were collected at the time points shown. (A) POR and P450 protein expression. Samples represent a pool of three animals per time point and 5??g of hepatic microsomal protein per lane. Purified human POR and murine P450s were used as standards. (B) (i) Hepatic microsomal POR activity. (ii) Liver/body weight ratios. Black bars: Porlox/lox/CreCYP1A1. Grey bars: Porlox/lox. (iii) Non-fasting plasma total cholesterol. (iv) Non-fasting plasma triacylglycerol (triglyceride) levels. Results are means?S.E.M. for three animals per time point, and in (i), (iii) and (iv) are expressed as a percentage compared with Porlox/lox mice at the same time point. *P?0.05; **P?0.01; ***P?0.001 compared with Porlox/lox mice. (C) Hepatic lipid content was visualized by Oil Red O staining of snap-frozen sections. Photomicrographs were taken at 10? magnification, bright field, and are representative of the results from at least three mice per group.

[Figure ID: F2]
Figure 2  Hepatic lipid accumulation and its relationship with organ weight and plasma lipid levels in conditional HRN mice

Porlox/lox/CreCYP1A1 and Porlox/lox mice were treated with a single dose of 3MC (40?mg/kg of body weight), and killed on the indicated days. (A) Hepatic triacylglycerol (triglyceride) concentrations. (B) Hepatic cholesterol concentrations. Correlation of hepatic triacylglycerol concentration with (C) liver/body weight ratio and (D) non-fasting plasma triacylglycerol levels. Results are means?S.E.M. for three animals per time point. *P?0.05; **P?0.01 compared with lipid levels on day 1.

[Figure ID: F3]
Figure 3  Development of phenotypic changes in conditional HRN mice on restricted fatty acid diets

Porlox/lox/CreCYP1A1 mice were maintained on a control diet until 8?weeks of age, and then either placed on a fat-deficient or fatty-acid-supplemented diet, or continued on the control diet, for a further 6?weeks. At 12?weeks of age, they were treated with a single dose of 3MC (40?mg/kg of body weight) and killed 14?days later. (A) POR and P450 expression levels in Porlox/lox/CreCYP1A1 and Porlox/lox mice maintained on a control or fat-deficient diet treated with 3MC (+) or corn oil (CO) (?). (i) Protein expression determined by Western blotting. Hepatic Cyp2b10 (ii) and Cyp3a11 (iii) mRNA levels expressed as a fold change compared with Porlox/lox mice. (B) POR and P450 expression levels in Porlox/lox/CreCYP1A1 mice maintained on fatty-acid-supplemented diets and treated with 3MC. (i) Protein expression determined by Western blotting. Hepatic Cyp2b10 (ii) and Cyp3a11 (iii) mRNA levels expressed as a fold change compared with Porlox/lox mice. (C) Hepatic lipid content determined by Oil Red O staining of snap-frozen liver sections of Porlox/lox/CreCYP1A1 mice maintained on fatty-acid-supplemented diets and treated with 3MC. Photomicrographs were taken at 10? magnification, bright field, and are representative of the results from at least three mice per group. For mRNA analysis in (A) and (B), results are means?S.E.M. (n=3). *P?0.05; **P?0.01; ***P?0.001 compared with Porlox/lox mice. std, standard. Black bars: Porlox/lox/CreCYP1A1; grey bars: Porlox/lox. In all panels: SFA, saturated fatty acids; MUFA, mono-unsaturated fatty acids; PUFA, polyunsaturated fatty acids; SunFl, 1% sunflower oil.

[Figure ID: F4]
Figure 4  Induction of hepatic P450 expression in conditional HRN mice by linoleic acid

Porlox/lox/CreCYP1A1 mice were maintained on a control diet until 8?weeks of age, and then placed on a fat-deficient diet for a further 6?weeks. At 12?weeks of age, they were treated with a single dose of 3MC (40?mg/kg of body weight) and 5?days later administered linoleic acid (65?mg/day) for 9?days before being killed. (A) POR and P450 expression levels were determined by Western blotting. WT, wild-type; std, standard; Con, control; F.D., fat-deficient diet. (B) Hepatic Cyp2b10 (black bars) and Cyp3a11 (grey bars) mRNA levels expressed as a fold change compared with Porlox/lox/CreCYP1A1 mice maintained on a fat-deficient diet. Results are means?S.E.M. (n=3). *P?0.05 compared with Porlox/lox/CreCYP1A1 mice maintained on a fat-deficient diet. (C) Hepatic lipid content determined by Oil Red O staining of snap-frozen liver sections. Photomicrographs were taken at 10? magnification, bright field, and are representative of the results from at least three mice per group.

[Figure ID: F5]
Figure 5  Induction of hepatic P450 expression and other phenotypes in HRN mice on nuclear receptor-null backgrounds

(A) POR and P450 expression levels in Pxr?/?/HRN mice: (i) protein expression determined by Western blotting; and (ii) hepatic Cyp2b10 (black bars) and Cyp3a11 (grey bars) mRNA levels expressed as a fold change compared with Porlox/lox mice. (B) POR and P450 expression levels in Car?/?/HRN mice: (i) protein expression determined by Western blotting; and (ii) hepatic Cyp2b10 (black bars) and Cyp3a11 (grey bars) mRNA expressed as a fold change compared with Porlox/lox mice. (C) POR and P450 expression levels in Car?/?/Pxr?/?/HRN mice: (i) protein expression determined by Western blotting; and (ii) hepatic Cyp2b10 (black bars) and Cyp3a11 (grey bars) mRNA expressed as a fold change compared with Porlox/lox mice. (D) Hepatic lipid content determined by Oil Red O staining of snap-frozen liver sections. Photomicrographs were taken at 10? magnification, bright field, and are representative of the results from at least three mice per group. For mRNA analysis in (A), (B) and (C), results are means?S.E.M. (n=3). *P?0.05; **P?0.01; ***P?0.001 compared with Porlox/lox mice. WT, wild-type.

[Figure ID: F6]
Figure 6  Activation of CAR by linoleic acid

HepG2 cells were transfected with pCMX Gal4-mCAR-LBD and p4*4xGal4-UAS4-luciferase as outlined in the Experimental section. Transfected cells were subsequently treated with linoleic acid at a concentration ranging from 0 to 12.5??M, and luciferase activity was analysed 24?h later. Transfected cells were treated with 0.25?0.5??M TCPOBOP or 1?mM PB as positive and negative controls respectively. Results are means?S.E.M. (n=6 determinations) and are expressed as a fold change compared with cells treated with either DMSO in the case of TCPOBOP and PB or the 0??M sample in the case of linoleic acid. *P?0.05; ***P?0.001.

[Figure ID: F7]
Figure 7  Schematic representation of the phenotypic changes that occur in HRN mouse models

Dietary unsaturated fatty acids enter the liver via fatty acid transporters where they are oxidized for energy purposes or detoxified by P450s. Inactivation of the P450 system as a result of Por deletion leads to hepatic accumulation of unsaturated fatty acids and a reduction of plasma lipid levels. Hepatic lipid accumulation triggers the activation of the nuclear receptor CAR (and possibly PXR), leading to P450 induction and liver growth. The overexpression of P450s is aimed at re-establishing hepatic lipid homoeostasis and the prevention of toxicity via increased metabolism of unsaturated fatty acids. Inactivation of POR prevents this increased metabolism and ultimately leads to hepatic steatosis. The development of steatosis establishes a cyclical process that potentiates hepatic lipid accumulation and growth. The adverse effect of P450 induction is altered drug metabolism and environmental chemical detoxification, but, in addition, the increased production of oxidized lipids could result in development of oxidative stress.

Article Categories:
  • Research Article

Keywords: constitutive androstane receptor (CAR), cytochrome P450, linoleic acid, P450 oxidoreductase (POR), pregnane X receptor (PXR), steatosis.
Keywords: AhR, aryl hydrocarbon receptor, CAR, constitutive androstane receptor, Cpt1a, carnitine palmitoyltransferase 1a, CYP, cytochrome P450, FAS, fatty acid synthase, HRN, hepatic reductase-null, i.p., intraperitoneal, 3MC, 3-methylcholanthrene, P450, cytochrome P450, PB, phenobarbital, POR, P450 oxidoreductase, PPAR, peroxisome-proliferator-activated receptor, PUFA, polyunsaturated fatty acid, PXR, pregnane X receptor, TCPOBOP, 1,4-bis-[2-(3,5-dichloropyridyloxy)]benzene.

Previous Document:  Characterization of the activity and folding of the glutathione transferase from Escherichia coli an...
Next Document:  Glucose regulation of insulin gene expression in pancreatic beta-cells.