Pharmacogenetic interaction between dexamethasone and Cd36-deficient segment of spontaneously hypertensive rat chromosome 4 affects triacylglycerol and cholesterol distribution into lipoprotein fractions

Dexamethasone (DEX) is known to induce diabetes and dyslipidemia. We have compared fasting triacylglycerol and cholesterol concentrations across 20 lipoprotein fractions and glucose tolerance in control (standard diet) and DEX-treated 7-month-old males of two rat strains, Brown Norway (BN) and congenic BN.SHR-(Il6-Cd36)/Cub (BN.SHR4). These two inbred strains differ in a defined segment of chromosome 4, originally transferred from the spontaneously hypertensive rat (SHR) including the mutant Cd36 gene, a known target of DEX. Compared to BN, the standard-diet-fed BN.SHR4 showed higher cholesterol and triacylglycerol concentrations across many lipoprotein fractions, particularly in small VLDL and LDL particles. Total cholesterol was decreased by DEX by more than 21% in BN.SHR4 contrasting with the tendency to increase in BN (strain*DEX interaction p = 0.0017). Similar pattern was observed for triacylglycerol concentrations in LDL. The LDL particle size was significantly reduced by DEX in both strains. Also, while control BN and BN.SHR4 displayed comparable glycaemic profiles during oral glucose tolerance test, we observed a markedly blunted DEX induction of glucose intolerance in BN.SHR4 compared to BN. In summary, we report a pharmacogenetic interaction between limited genomic segment with mutated Cd36 gene and dexamethasone-induced glucose intolerance and triacylglycerol and cholesterol redistribution into lipoprotein fractions.


Findings
Glucocorticoids (GC) have been utilized for decades in treatment of wide variety of inflammatory, allergic, hematological and other disorders. In spite of their demonstrated therapeutic value, glucocorticoid treatment is often accompanied with substantial side-effects, including dyslipidemia, diabetes, obesity, osteoporosis, muscle wasting, impaired wound healing or rheumatoid arthritis [1]. While the molecular mechanisms of the GC-induced metabolic disturbances have been subjected to intensive investigation [2], the genetic basis of the interindividual differences in response to GC received only limited attention so far. Several genes have been proposed to trans-duce or modulate the metabolic effects of glucocorticoids, including functional candidates like glucocorticoid receptor [3], 11β-hydroxysteroid dehydrogenases 1 and 2 (11β-HSD1, 2) [4] and corticosteroidbinding globulin (CBG) [5], and peroxisome proliferatoractivated receptor alpha (PPARα) [6]. We have previously reported a comprehensive set of quantitative trait loci related to genomic architecture of metabolic syndrome including its dynamics in response to dexamethasone (DEX)-induced derangements of lipid and carbohydrate metabolism [7].
In the current study, we tested the effect of deficiency of one of the DEX-target genes, fatty acid translocase Cd36 [8,9], on the DEX-induced metabolic changes. To that end, we have compared triacylglycerol and cholesterol concentrations across 20 lipoprotein fractions and glucose tolerance in control and DEX-treated adult males of two rat strains, Brown Norway (BN) and congenic BN.SHR-(Il6-Cd36)/Cub (BN.SHR4 hereafter; Rat Genome Database [10] (RGD) ID 728142). These two inbred strains differ in a defined segment of chromosome 4, originally transferred from the spontaneously hypertensive rat (SHR) including the mutant Cd36 gene into the genomic background of BN to create BN.SHR4 [11,12].
All experiments were performed in agreement with the Animal Protection Law of the Czech Republic (311/1997) which is in compliance with the European Community Council recommendations for the use of laboratory animals 86/609/ECC and were approved by the Ethical committee of the First Faculty of Medicine. Animals were held under temperature and humidity controlled conditions on 12 h/12 h light-dark cycle. At all times, the animals had free access to food and water. Male BN (n = 12) and BN.SHR4 (n = 13) rats were fed standard laboratory chow ad libitum. At the age of 7 months, the rats were randomly split into control (n = 6 and 7 for BN and BN.SHR4, respectively) and experimental groups (n = 6/ strain). Experimental groups were administered dexamethasone (Dexamed, Medochemie) in drinking water (2.6 μg/ml) for three days as described previously [7]. The OGTT was performed after overnight fasting. Blood for glycaemia determination (Ascensia Elite Blood Glucose Meter; Bayer HealthCare, Mishawaka, IN, validated by Institute of Clinical Biochemistry and Laboratory Diagnostics of the First Faculty of Medicine) was drawn from the tail at intervals of 0, 30, 60, 120 and 180 minutes after the intragastric glucose administration to conscious rats (3 g/kg body weight, 30% aqueous solution). Plasma lipoproteins were analyzed by an on-line dual enzymatic method for simultaneous quantification of cholesterol, triacylglycerol and free glycerol by HPLC at Skylight Bio-tech Inc. (Akita, Japan) according to the procedure described previously [13].
The control groups of both strains showed similar morphometric profile, BN.SHR4 had slightly lower relative heart and testes weights compared to BN. DEX-treated BN.SHR4 displayed greater body weight loss while maintaining food intake comparable to BN ( Table 1). Despite that, the reduction of retroperitoneal fat mass was more pronounced in BN (Table 1).
Although total serum triacylglycerols (TG) were not significantly different between the control groups of the two strains, in-depth analysis revealed TG elevation in BN.SHR4 in small very low-density lipoprotein (VLDL), large, medium and small low-density lipoprotein (LDL) and small and very small high-density lipoprotein (HDL) subfractions ( Figure 1A). DEX induced substantially more robust decreases of TG in BN.SHR4 except for small HDL. Therefore, DEX-treated BN had higher concentrations of TG in large, medium and small LDL (Figure 1B). There were no strain-or DEX-related differences in fasting glycerol levels (data not shown).
Standard diet-fed BN.SHR4 showed in comparison to BN higher cholesterol content in most lipoprotein fractions except chylomicrons ( Figure 1C). Total cholesterol was decreased by DEX by more than 21% in BN.SHR4 contrasting with the tendency to increase in BN (strain*DEX interaction p = 0.0017, Table 2). When analyzed in detail, DEX-treated BN displayed higher cholesterol concentrations in very small LDL and across HDL spectrum ( Figure 1D). Concomitantly, the HDL particle size increased only in BN (Table 3).
While there was no strain difference in response to glucose bolus administration in the control groups, we observed a markedly diminished DEX induction of glucose intolerance in BN.SHR4 compared to BN (Figure 2, reflected by strain*DEX interaction in two-way ANOVA, p = 0.005). Actually, the incremental area under the glycaemic curve failed to increase significantly in BN.SHR4 (244 ± 34 vs. 418 ± 66 mmol/l/180 min in control vs. DEX-treated animals, respectively, p = 0.23), while we observed more than threefold, significant increase in BN rats (222 ± 30 vs. 817 ± 110 mmol/l/180 min in control vs. DEX-treated animals, respectively, p = 0.0002).
Our study presents a pharmacogenetic interaction between limited genomic segment with mutated Cd36 gene and dexamethasone-induced glucose intolerance and triacylglycerol and cholesterol redistribution into lipoprotein fractions. Genetic variation in fatty acid translocase CD36 has been previously linked with dyslipidemia and insulin resistance both in experimental models [14,15] and in human subjects [16,17]. Moreover, we have established Cd36 as key determinant of the metabolic effects of insulin-sensitizer drugs -thiazolidinediones by demonstrating their blunted action both in SHR [18] and BN.SHR4 [12,19]. The BN.SHR4 displays several derangements of lipid and carbohydrate metabolism compared to BN while fed standard or high-sucrose diet [11]. In this study, the Cd36-deficient congenic showed reduced susceptibility to diabetogenic action of DEX and even partial improvement of its lipid profile, contrasting with its BN progenitor. Dexamethasone is known to induce whole body insulin resistance and affect lipid metabolism after both short and long-term administration [20,1,21] while CD36 is one of its target genes [8,9]. We have previously shown DEX to concomitantly induce both muscle-specific insulin resistance and dyslipidemia in experimental models of metabolic syndrome including spontaneously hypertensive rat-derived congenic strain [22], polydactylous rat as well as BN [7]. The distinct pattern reported in the current study, i.e. induction of glucose intolerance by DEX combined with tendency to reduce concentrations of triacylglycerol and cholesterol in certain lipoprotein fractions may be attributed to short term administration of one-tenth of the dose used in our prior studies [7,22]. One of the limita-    tions of the current study is the possibility that other genes apart from mutated Cd36 present in the differential segment might be involved in the underlying mechanism of distinct metabolic response of the two strains, this issue will be addressed in future studies by e.g. generating Cd36 knockout rats [23]. Although it is premature to speculate on the detailed mechanism of the observed interaction, which might involve enhanced glucose utilization in peripheral tissues due to ineffective fatty-acid uptake [18], we may hypothesize that Cd36 and/or some other gene(s) present in the chromosome 4 differential segment may represent pharmacogenetic hubs [24] of particular importance for metabolic actions of glucocorticoids.