| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
Papers In Press, published online ahead of print November 1, 2002
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Journal of Lipid Research, Vol. 43, 1809-1817, November 2002
Copyright © 2002 by Lipid Research, Inc.
agonist rosiglitazone
* Lipomics Technologies, Inc., 2545 Boatman Ave., West Sacramento, CA 95691
The Jackson Laboratory, 600 Main St., Bar Harbor, ME
Department of Food Science & Technology, University of California, Davis, CA
s The online version of this article (available at http://www.jlr.org) contains an additional 4 tables. 
Published, JLR Papers in Press, August 16, 2002. DOI 10.1194/jlr.M200169-JLR200
1 To whom correspondence should be addressed. e-mail: steve.watkins{at}lipomics.com
 |
ABSTRACT |
|---|
 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
(PPAR) agonist rosiglitazone on structural lipid metabolism in a new mouse model of Type 2 diabetes. Dietary supplementation with rosiglitazone (200 mg/kg diet) suppressed Type 2 diabetes in obese (NZO x NON)F1 male mice, but chronic treatment markedly exacerbated hepatic steatosis. The metabolomic data revealed that rosiglitazone i) induced hypolipidemia (by dysregulating liver–plasma lipid exchange), ii) induced de novo fatty acid synthesis, iii) decreased the biosynthesis of lipids within the peroxisome, iv) substantially altered free fatty acid and cardiolipin metabolism in heart, and v) elicited an unusual accumulation of polyunsaturated fatty acids within adipose tissue. These observations suggest that the phenotypes induced by rosiglitazone are mediated by multiple tissue-specific metabolic variables. Because many of the effects of rosiglitazone on tissue metabolism were reflected in the plasma lipid metabolome, metabolomics has excellent potential for developing clinical assessments of metabolic response to drug therapy.
Abbreviations: PPAR, peroxisome proliferator-activated receptor ; TZD, thiazolidinedione
Supplementary key words diabetes • lipid metabolism • metabolomics • steatosis • peroxisome proliferator-activated receptor • mouse
|
INTRODUCTION |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
Thiazolidinediones (TZDs) are potent therapeutic agents that have proven successful in the treatment of Type 2 diabetes in rodent models and in humans (1). These compounds, including troglitazone, rosiglitazone, and pioglitazone, are believed to exert their benefit as high affinity agonists of peroxisome proliferator-activated receptor (PPAR), whose subsequent activation of multiple nuclear genes reduces hyperlipidemia and hyperglycemia and improves insulin sensitivity (2). Included among the many actions of TZDs are shifts in systemic lipid profiles, with decreases in serum lipid concentrations. However, these actions of TZDs are accompanied by increased adipogenesis and lipid accumulation in tissues. A major question associated with these drugs and their mechanism of action is whether the benefits to circulating lipid concentrations can be disassociated from metabolic side effects, including hepatic lipid accumulation. Troglitazone- and rosiglitazone-associated hepatotoxicity (steatosis) was recently reported in KK-Ay mice in the absence of increased hepatic triacylglycerides concentrations (3). In addition, a small number of human patients treated with troglitazone developed severe hepatotoxicity (4). Assessing the variable metabolic response to TZDs is therefore necessary to evaluate the safety or efficacy of TZDs in individuals.
In mice, diabesity genes are defined as obesity-predisposing genes capable of interacting deleteriously with other susceptibility loci, as well as with environmental factors, to elicit a state of impaired glucose tolerance and insulin resistance sufficiently severe to precipitate development of Type 2 diabetes (5, 6). A new mouse diabesity model that potentially reflects the more common polygenic forms of Type 2 diabetes prevalent in humans is the F1 male generated by crossing mice from the New Zealand Obese (NZO/HlLt) and Nonobese Nondiabetic (NON/Lt) strains. F1 males of these two mouse strains develop early-onset obesity leading to a progressively more severe hyperinsulinemia and development of maturity-onset hyperglycemia in 90–100% of the males maintained on a standard rodent chow containing only 6% fat (5). Because preliminary studies showed that chronic feeding of troglitazone (2 g/kg diet) produced marked hepatic steatosis in these animals, they may provide an appropriate model for testing the potentially deleterious effects of TZD treatment on liver metabolism. These preliminary studies showed that rosiglitazone was a more potent anti-diabetic TZD than troglitazone. In this study, an assessment of the lipid metabolome (the concentration of each lipid class and each of its constituent fatty acids) was applied to evaluate the effect of chronic feeding of a low dose (0.2 g/kg diet) of rosiglitazone on the lipid metabolism of diabetic F1 males. Analysis of the results of the study revealed key targets of the actions of rosiglitazone, and putatively PPAR, on lipid metabolism.
|
MATERIALS AND METHODS |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
Phenotypes
Body weight was measured immediately pre-treatment and at 2 and 4 weeks during dietary treatment. Plasma glucose concentrations were measured immediately pre-treatment and after 4 weeks of treatment (Beckman Glucose 2 analyzer, Beckman Instruments, Fullerton, CA). Plasma insulin and leptin concentrations were measured at termination by rat insulin or mouse leptin radioimmune assay kits (Linco, St. Charles, MO). A Synchron 5 chemistry analyzer (Beckman Instruments) was used for clinical chemistry. Plasma alanine aminotransfease was assessed as an indicator of liver damage. Total serum cholesterol and triacylglycerides were also measured.
Gene expression
Total RNA was isolated from slices of frozen livers and inguinal adipose tissue from five mice per group using Trizol and following the protocol supplied by the manufacturer (Gibco-BRL, Gaithersburg, MD). Details regarding cDNA preparation, primer pair sequences for the transcripts shown in Table 2 and 3, and the conditions used for specific gene amplification in an ABI Prism® 7700 Sequence Detection System (PE Applied Biosystems, Foster City, CA) can be found at http://www.jax.org/research/leiter/documents/databases.html.
|
|
CT is the difference between the target gene and the internal reference (18S RNA). CT is the difference for the CT for the target gene as a function of treatment. Fold-differences are expressed as 2-CT.
Lipid metabolome data
The lipids from plasma and tissues were extracted in the presence of authentic internal standards by the method of Folch et al. (7) using chloroform-methanol (2:1, v/v). Heart or liver tissue (25 mg), 200 µl plasma, or 10 mg inguinal adipose tissue was used for each analysis. Individual lipid classes within each extract were separated by preparative thin-layer chromatography as described previously (8). Authentic lipid class standard compounds were spotted on the two outside lanes of the thin-layer chromatography plate to enable localization of the sample lipid classes. Each lipid fraction was scraped from the plate and trans-esterified in 3 N methanolic-HCl in a sealed vial under a nitrogen atmosphere at 100°C for 45 min. The resulting fatty acid methyl esters were extracted from the mixture with hexane containing 0.05% butylated hydroxytoluene and prepared for gas chromatography by sealing the hexane extracts under nitrogen.
Fatty acid methyl esters were separated and quantified by capillary gas chromatography using a gas chromatograph (Hewlett-Packard model 6890, Wilmington, DE) equipped with a 30 m DB-225MS capillary column (J&W Scientific, Folsom, CA) and a flame-ionization detector as described previously (8).
Data processing and statistics
Significance of differences in phenotypic parameters between rosiglitazone treated and control mice as well as treatment effects on tissue lipid metabolite concentrations were assessed by unpaired Student's t-tests, with significance assumed at P 
0.05. For the quantitative PCR comparisons of transcript levels in liver and inguinal fat, a paired Student's t-test assuming unequal variance was performed and a Bonferroni correction was made for multiple comparisons (
, 0.0042).
Quantitative (nmol/g) data were visualized using the Lipomics SurveyorTM software system, which creates a "heat-map" graph of the difference between the data for treated and control mice. The SurveyorTM data (see Results) are read as follows: the column headers display the fatty acid and the family of fatty acids present in each lipid class, which are in turn described in the row headers. The lipid classes are grouped by tissue. The heat map displays an increase in each metabolite in rosiglitazone-treated mice relative to control mice as a green square and a decrease in a metabolite as a red square. The brightness of the square indicates the magnitude of the difference, as detailed in the figure legends.
|
RESULTS |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
|
|
, PPAR1, and PPAR2), acetyl-CoA carboxylase (ACC), acetyl-CoA oxidase (ACO), cytochrome P450 4A1 (CYP4a1), and carnitine palmitoyl transferase 1 (CPT1a) between treated and untreated mice were determined as described in the Materials and Methods. In confirmation of the morphology showing increased lipid accumulation in livers of rosiglitazone treated males, ADN, aP2, FAS, and LPL transcripts were quantitatively greater in treated mice relative to untreated controls (Table 2). The expression of PPAR1, PPAR2, and PPAR did not differ significantly between the groups (Table 2). The greater expression of FAS is consistent with the greater concentrations of 16:1n7 and 18:1n7 observed in treated mice relative to untreated mice, and together these observations demonstrate a clear upregulation of de novo fatty acid synthesis with rosiglitazone treatment. Increases in ADN and aP2 transcripts, both associated with adipogenesis, are consistent with the lipid metabolome profiles showing rosiglitazone-induced increases in hepatic lipid accumulation.
Table 3 shows rosiglitazone-mediated differences in gene expression in inguinal fat. In addition to the transcript panel described in Table 2, additional adipocyte-expressed transcripts analyzed included those of the family of uncoupling proteins (UCP1, UCP2, and UCP3), leptin, and tumor necrosis factor (TNF). The most striking difference was a 192-fold upregulation of UCP1 transcription. Adipsin, a marker of adipogenesis, was significantly decreased. A rosiglitazone-induced 6.7-fold increase in FAS, although not statistically significant after correction for multiple comparisons, correlated with the observed increase in UCP1 as well as the lipid metabolome profile showing increased 16:1n7 and 18:1n7 concentrations in inguinal adipose tissue (Fig. 2)
.
|
|
Heart lipid class metabolism
The results of the quantitative assessment of the heart lipid metabolome in rosiglitazone-treated and untreated mice are shown in Table 6 of the Supplemental Data and in Figs. 2 and 3. Free fatty acids are the primary source of energy for the heart. The average concentration of total free fatty acid in the heart was 5,100 nmol/gm untreated mice and 2,500 nmol/g in rosiglitazone-treated mice (Fig. 2). This difference was largely independent of the type of free fatty acid, as the saturated n-3, n-6, and n-9 families of fatty acids were all approximately 50% lower in treated mice than in untreated mice (Fig. 2). The free n-7 fatty acids were not depleted as substantially from heart, likely due to the increased biosynthesis of n-7 fatty acids and corresponding increased concentration of n-7 fatty acids within the triacylglycerides and free fatty acids of plasma.
The hearts of rosiglitazone-treated mice were significantly enriched with cardiolipin, the primary structural lipid of the inner mitochondrial membrane. The mean cardiolipin content of hearts from rosiglitazone-treated mice was 3,000 nmol/g as compared with 2,500 nmol/g in untreated mice. Unlike free fatty acids, the fatty acid components of cardiolipin were differentially modulated by rosiglitazone treatment. The primary fatty acid of cardiolipin, linoleic acid (18:2n6), was 4,550 nmol/g in control heart cardiolipin and 8,850 nmol/g in heart cardiolipin of rosiglitazone-treated mice. Docosahexaenoic acid (22:6n3) was depleted from cardiolipin in the hearts of treated mice (950 nmol/g) relative to hearts of control mice (2,200 nmol/g).
The plasmalogen lipids, those lipids that contain 1-enyl-ether-linked alkyl chains, are derived from the dihydroxyacetone phosphate pathway and are partially synthesized within the peroxisome (9). The concentration of plasmalogens was lower in the heart phospholipids of mice treated with rosiglitazone than of controls (Fig. 3). These data are consistent with a decreased peroxisomal synthesis of lipids within the hearts of treated mice.
Adipose lipid class metabolism
The results of the quantitative assessment of the inguinal adipose lipid metabolome in rosiglitazone-treated and untreated mice are shown in Table 7 of the Supplemental Data and in Figs. 2 and 3. Inguinal fat tissue from rosiglitazone-treated mice displayed a 5.7% lower triacylglyceride content (9,628 µmol/g) than inguinal adipose from controls (1,019 µmol/g), and 35% more free fatty acids (13,370 nmol/g in treated mice and 9,900 nmol/g in controls). No significant differences in total phospholipid or cholesterol ester concentrations were observed (Fig. 2).
The fatty acid composition of inguinal fat triacylglycerides was substantially altered by rosiglitazone treatment, with inguinal fat from treated mice accumulating fatty acids from the saturated, n-7, and n-3 families of fatty acids while being depleted of the n-9 family of fatty acids (Fig. 2). In particular, an unusual accumulation of n-3 fatty acids was observed in inguinal fat from rosiglitazone-treated animals. The concentration of total n-3 fatty acids in the inguinal fat triacylglycerides of treated mice was 71,260 nmol/g, representing a 120% greater concentration than that in untreated mice (Fig. 2). The most notable increases within the n-3 family of fatty acids were a 522% greater concentration (4,100 nmol/g) of eicosapentaenoic acid, a 612% greater concentration (7,000 nmol/g) of docosahexaenoic acid, and 84% (24,300 nmol/g) more -linolenic acid in inguinal fat triacylglycerides in treated as compared with control mice (Fig. 3). The concentration of n-7 fatty acids in inguinal fat triacylglycerides was 303 µmol/g in treated mice and 204 µmol/g in untreated controls (Fig. 2). In contrast, the total concentration of n-6 fatty acids was less than 3% higher. However, the accumulation or depletion of individual fatty acids within the n-6 family varied substantially. Whereas linoleic acid (18:2n6), by far the most prominent n-6 fatty acid in inguinal fat, was not significantly altered by treatment, the concentrations of -linolenic, dihomo--linolenic, and arachidonic acids in inguinal fat were respectively, 1,225 nmol/g (78%), 1,300 nmol/g (64%), and 3,800 nmol/g (276%) greater in treated mice than in untreated controls (Fig. 3).
The concentration of plasmalogen lipids in inguinal fat phospholipids was depleted by rosiglitazone treatment (Fig. 2). The concentration of total plasmalogen fatty acids from the phospholipids of inguinal fat was 130 nmol/g (60%) less in treated mice than untreated controls.
|
DISCUSSION |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
Because rosiglitazone decreased the concentrations of plasma lipids as classes of molecules (i.e., triacylglycerides, cholesterol esters, etc.), standard clinical markers of lipid metabolism (Table 1) did not reflect the increased hepatic de novo lipogenesis in response to rosiglitazone treatment. In contrast, the metabolomic assessment of plasma lipids identified several markers of increased liver lipogenesis, including an increased absolute concentration of 16:1n7 and 18:1n7 in plasma cholesteryl esters, phosphatidylcholine, and triacylglycerides, despite the decrease in the concentration of total plasma lipid classes. The metabolomic analysis of the plasma alone was therefore capable of making the important discrimination between hypolipidemia caused by decreased lipid synthesis compared with hypolipidemia caused by impaired export of lipid by the liver. These data suggest that metabolomic analyses of human plasma may have strong potential as clinical diagnostics. Further demonstrating the strong relations between the plasma lipid metabolome and tissue metabolism were the decreased concentration of plasmalogen lipids in plasma and the similarity between the composition of the plasma lipid metabolome and liver and adipose metabolomes.
Heart lipid metabolism was strongly influenced by rosiglitazone treatment. In particular, heart free fatty acids, cardiolipin, plasmalogen lipids, and the important polyunsaturated fatty acids 22:6n3 and 18:2n6 were significantly modulated by treatment. Some of these changes, particularly those involving the concentration and composition of cardiolipin and free fatty acids, may in part represent the alterations in muscle metabolism that improve insulin sensitivity. Cardiolipin is an essential phospholipid for energy metabolism and the primary phospholipid of the inner mitochondrial membrane (16–18). The content and composition of cardiolipin are important to the efficiency of electron transport. Rosiglitazone caused an increase in heart cardiolipin concentration and a substantial remodeling of cardiolipin toward an elevated 18:2n6 content and a diminished 22:6n3 content. Interestingly, this is precisely the change in cardiolipin content and composition that would increase electron transport efficiency (17, 19–21) and decrease electron leakage (22), according to the existing in vitro data. Rosiglitazone-induced remission from hyperglycemia in combination with reduced plasma insulin concentrations indicated that glucose oxidation by tissues was increased by this insulin-sensitizing agent. Thus, it is possible that increased energy metabolism as well as decreased plasma lipids may have caused the decreased heart free fatty acid concentrations.
Two major types of lipids quantified in this study are synthesized at least in part within the peroxisome. These are the fatty acids with three double bonds on the carboxylic acid side of an n9 double bond (22:5n6 and 22:6n3) (23–25), and the plasmalogen lipids, which are synthesized by the dihydroxyacetone phosphate biosynthetic pathway (9). Heart tissue from rosiglitazone-treated mice contained significantly less 22:6n3 in phosphatidylcholine, phosphatidylethanolamine, cardiolipin, phosphatidylserine/inositol, free fatty acids, and cholesterol esters than did heart from untreated control mice. Additionally, there was a significant depletion of plasmalogen lipids from the heart phospholipids of treated mice relative to untreated controls. These observations suggest that rosiglitazone, a known PPAR agonist, has an inhibitory effect on lipid biosynthesis in the peroxisome. The decreased production of 22:6n3 and plasmalogen lipid may have important physiologic consequences. Dietary 22:6n3 has well-documented positive effects on cardiac function (26–31), and plasmalogen lipids have recently been shown to be essential to membrane trafficking and the structure of caveolae, clathrin-coated pits, endoplasmic reticulum, and Golgi cisternae (32).
A curious finding in this study was the inguinal fat tissue accumulation of polyunsaturated fatty acids in response to rosiglitazone. The accumulation of 22:6n3 and other long-chain polyunsaturated fatty acids likely occurs via a pathway independent of their biosynthesis de novo from precursors. The conversion of polyunsaturated-rich phospholipids to triacylglycerides via a phospholipase C pathway also does not appear to be the primary metabolic basis for the enrichment with polyunsaturates, as phospholipids were also enriched with polyunsaturated fatty acids. This unusual response may be an important clue to understanding the physiology of adipose tissue activated by PPAR agonists, and should be investigated further.
The present study utilized a diabetic mouse model in which the anti-diabetic action of a TZD was accompanied by excessive weight gain and major alterations in the lipid metabolome. Its major findings were that rosiglitazone i) induced hypolipidemia by disrupting the mobilization of liver lipids into plasma, ii) induced de novo fatty acid synthesis, iii) diminished the biosynthesis of lipid synthesized within the peroxisome, iv) had substantial effects on heart cardiolipin and free fatty acid metabolism, and v) exerted tissue-specific effects on lipid metabolism. The unusually high sensitivity of the diabetic (NZO x NON)F1 male to thiazolidinedione-induced lipid accumulation in liver may be related to the observation that a moderate level of hepatic steatosis had already initiated in the diabetic control group fed a chow diet containing only 6% fat. We hypothesize that these F1 mice have underlying defects in hepatic lipid metabolism that render them particularly sensitive to the steatosis-inducing effects of TZDs. Elucidation of the metabolic and pharmacogenetic bases for the metabolic responses to rosiglitazone described in this study will be valuable in determining markers of efficacy and safety for TZD treatment in humans and for defining species and individual-specific responses to TZDs. However, it should be noted that lipid metabolism in mice is distinct in many ways from that in humans, and that the direct applicability of these data to human subjects remains to be tested.
|
ACKNOWLEDGMENTS |
|---|
Manuscript received April 19, 2002 and in revised form July 26, 2002.
|
REFERENCES |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
-linolenic acids. Lipids. 36: 247–254.[Medline]
) and PPAR-gamma messenger ribonucleic acid expression in the liver in murine obesity: troglitazone induces expression of PPAR-gamma-responsive adipose tissue-specific genes in the liver of obese diabetic mice. Endocrinology. 141: 4021–4031.
CiteULike 
Complore 
Connotea 
Del.icio.us 
Digg 
Reddit 
Technorati What's this?
This article has been cited by other articles:
|
|
 |
|
  P. Dallaire, K. Bellmann, M. Laplante, S. Gelinas, C. Centeno-Baez, P. Penfornis, M.-L. Peyot, M. G. Latour, J. Lamontagne, M. E. Trujillo, et al. Obese Mice Lacking Inducible Nitric Oxide Synthase Are Sensitized to the Metabolic Actions of Peroxisome Proliferator-Activated Receptor-{gamma} Agonism Diabetes, August 1, 2008; 57(8): 1999 - 2011. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. L. Griffin and A. Vidal-Puig Current challenges in metabolomics for diabetes research: a vital functional genomic tool or just a ploy for gaining funding? Physiol Genomics, June 10, 2008; 34(1): 1 - 5. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. R. Benton, G. P. Holloway, S. E. Campbell, Y. Yoshida, N. N. Tandon, J. F. C. Glatz, J. J. J. F. P. Luiken, L. L. Spriet, and A. Bonen Rosiglitazone increases fatty acid oxidation and fatty acid translocase (FAT/CD36) but not carnitine palmitoyltransferase I in rat muscle mitochondria J. Physiol., March 15, 2008; 586(6): 1755 - 1766. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. Astle, J. T. Ferguson, J. B. German, G. G. Harrigan, N. L. Kelleher, T. Kodadek, B. A. Parks, M. J. Roth, K. W. Singletary, C. D. Wenger, et al. Characterization of Proteomic and Metabolomic Responses to Dietary Factors and Supplements J. Nutr., December 1, 2007; 137(12): 2787 - 2793. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. R. Waites, M. A. Dominick, T. P. Sanderson, and B. E. Schilling Nonclinical Safety Evaluation of Muraglitazar, a Novel PPAR{alpha}/{gamma} Agonist Toxicol. Sci., November 1, 2007; 100(1): 248 - 258. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 R. L. Walzem, R. A. Baillie, M. Wiest, R. Davis, S. M. Watkins, T. E. Porter, J. Simon, and L. A. Cogburn Functional Annotation of Genomic Data with Metabolic Inference Poult. Sci., July 1, 2007; 86(7): 1510 - 1522. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 L. A. Morehouse, E. D. Sugarman, P.-A. Bourassa, T. M. Sand, F. Zimetti, F. Gao, G. H. Rothblat, and A. J. Milici Inhibition of CETP activity by torcetrapib reduces susceptibility to diet-induced atherosclerosis in New Zealand White rabbits J. Lipid Res., June 1, 2007; 48(6): 1263 - 1272. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
G. Rizki, L. Arnaboldi, B. Gabrielli, J. Yan, G. S. Lee, R. K. Ng, S. M. Turner, T. M. Badger, R. E. Pitas, and J. J. Maher Mice fed a lipogenic methionine-choline-deficient diet develop hypermetabolism coincident with hepatic suppression of SCD-1 J. Lipid Res., October 1, 2006; 47(10): 2280 - 2290. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 V. Shulaev Metabolomics technology and bioinformatics Brief Bioinform, June 1, 2006; 7(2): 128 - 139. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 E. H. Leiter, P. C. Reifsnyder, W. Zhang, H.-j. Pan, Q. Xiao, and J. Mistry Differential Endocrine Responses to Rosiglitazone Therapy in New Mouse Models of Type 2 Diabetes Endocrinology, February 1, 2006; 147(2): 919 - 926. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 G. S. Ginsburg, M. P. Donahue, and L. K. Newby Prospects for Personalized Cardiovascular Medicine: The Impact of Genomics J. Am. Coll. Cardiol., November 1, 2005; 46(9): 1615 - 1627. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 D. M. Mutch, W. Wahli, and G. Williamson Nutrigenomics and nutrigenetics: the emerging faces of nutrition FASEB J, October 1, 2005; 19(12): 1602 - 1616. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 M. J Gibney, M. Walsh, L. Brennan, H. M Roche, B. German, and B. van Ommen Metabolomics in human nutrition: opportunities and challenges Am. J. Clinical Nutrition, September 1, 2005; 82(3): 497 - 503. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
H.-J. Pan, P. Reifsnyder, D. E. Vance, Q. Xiao, and E. H. Leiter Pharmacogenetic Analysis of Rosiglitazone-Induced Hepatosteatosis in New Mouse Models of Type 2 Diabetes Diabetes, June 1, 2005; 54(6): 1854 - 1862. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 L. Makowski, K. C. Brittingham, J. M. Reynolds, J. Suttles, and G. S. Hotamisligil The Fatty Acid-binding Protein, aP2, Coordinates Macrophage Cholesterol Trafficking and Inflammatory Activity: MACROPHAGE EXPRESSION OF aP2 IMPACTS PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR {gamma} AND I{kappa}B KINASE ACTIVITIES J. Biol. Chem., April 1, 2005; 280(13): 12888 - 12895. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. K. Wu, H. Hyogo, S. K. Yadav, P. M. Novikoff, and D. E. Cohen Impaired response of biliary lipid secretion to a lithogenic diet in phosphatidylcholine transfer protein-deficient mice J. Lipid Res., March 1, 2005; 46(3): 422 - 431. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 E. D. Bruder |
