- freely available
Metabolites 2013, 3(4), 881-911; doi:10.3390/metabo3040881
Published: 11 October 2013
Abstract: Calorie restriction (CR) has long been used to study lifespan effects and oppose the development of a broad array of age-related biological and pathological changes (increase healthspan). Yet, a comprehensive comparison of the metabolic phenotype across different genetic backgrounds to identify common metabolic markers affected by CR is still lacking. Using a system biology approach comprising metabonomics and liver transcriptomics we revealed the effect of CR across multiple mouse strains (129S1/SvlmJ, C57BL6/J, C3H/HeJ, CBA/J, DBA/2J, JC3F1/J). Oligonucleotide microarrays identified 76 genes as differentially expressed in all six strains confirmed. These genes were subjected to quantitative RT-PCR analysis in the C57BL/6J mouse strain, and a CR-induced change expression was confirmed for 14 genes. To fully depict the metabolic pathways affected by CR and complement the changes observed through differential gene expression, the metabolome of C57BL6/J was further characterized in liver tissues, urine and plasma levels using a combination or targeted mass spectrometry and proton nuclear magnetic resonance spectroscopy. Overall, our integrated approach commonly confirms that energy metabolism, stress response, lipids regulators and the insulin/IGF-1 are key determinants factors involved in CR regulation.
Managing the quality of life and delaying the onsets of aging related chronic disease is one of the quests to promote healthy aging. Within this aim, a significant proportion of research into this area is engaged in revealing the mechanisms underlying the aging and/or longevity processes and how such could be modulated. Aging is characterized by an increasing chronic, low-grade inflammatory status indicated as inflamm-aging [1,2] responsible for the major inflammation-driven age-related diseases, such as cardiovascular disease (CVD), diabetes mellitus (DM), Alzheimer disease (AD), and cancer [3,4]. Dietary caloric restriction (CR) is a robust but severe nutritional intervention with plausible effects on healthspan, body function and longevity . Unlike many interventions, life-long CR suggests alteration of fundamental biological processes that control aging , as observed in a diverse range of organisms [7,8], including nematodes, mice, rats, dogs [9,10] and/or humans . Both the duration and the time of CR initiation have been found to be crucial for developing an anti-aging strategy. Long-term CR initiated before mid-life has been reported to slow down the aging process and to increase life span in rodents  and dogs  whereas CR initiated late in life increases mortality in several rodent models . Humans are not likely to benefit from CR as much as these organism models for increased lifespan since they have evolved to minimize the effect of food shortage . However, CR may be a useful anti-aging (increase healthspan) strategy for humans to decrease or delay the onset of degenerative diseases as suggested by studies on non-human primates and human beings [16,17]. Studies of Okinawan centenarians support the view that a low-calorie diet can increase prospects for good health and longevity in humans [17,18]. Findings from the small group of volunteers confined to Biosphere 2 confirmed that a 30% dietary restriction could be imposed for two years and would produce many of the physiological, hormonal, and morphological effects expected . Therefore, identification of pathways and biomarkers activated by caloric restriction would highly contribute to the determination of nutritional strategies aiming to mimic the health benefits of CR. Indeed, CR mimetics provide a more realistic anti-aging strategy by modulating the energy metabolism towards the one observed in CR without the requirement for reduced food intake and to promote healthspan effects. CR mimetics at present include glycolytic inhibitors, stress response enhancers, sirtuin controllers, manipulation of the insulin/IGF-1, lipids and adipokines regulators, and autophagic enhancers .
Nowadays the diet-restricted rodent model is widely used to understand the mechanisms of the aging process .Yet the underlying the molecular mechanism of the extended life span by CR is still a matter of debate [22,23]. Moreover, despite CR resulting in similar benefits in various animal models, the impact on the physiology and metabolic adaptation to the new metabolic homeostasis varies greatly from one animal model/strain to another . It is therefore vital to delineate key regulatory processes and common metabolic pathways across species translating such knowledge into drug and/or nutritional targets for CR mimetics. Within this quest, metabolic phenotyping is a useful tool to establish gradual metabolic changes linked to dietary intervention and disease development. Recently, metabonomics had successfully been applied to study the modulation of the aging processes following nutritional interventions, including caloric restriction-induced metabolic changes in mouse  dogs [26,27], and non-human primates  as well as high fat induced weight gain and metabolic disorders . Yet, beyond the insight provided by these studies, a comprehensive and comparative capture of common metabolic functions across multiple animal species is missing. In the present study, liver tissue transcriptomics and blood plasma metabonomics were employed to capture the hepatic and systemic metabolic processes under the influence of CR initiated early in life across six mouse models. We herein report tissue-specific candidate biomarkers that were commonly affected by CR. To fully depict the metabolic pathways affected by CR and confirm the transcriptomics changes, the metabotypes of C57BL6/J mice were further characterized using nuclear magnetic resonance (1H-NMR) profiling approach in liver and urine. Among the selected strains of animals, the C57BL6/J mouse model is particularly interesting model due to its higher susceptibility to weight gain under specific dietary conditions due to its genetic background . Indeed C57BL6/J mice fed with a high fat diet develop obesity, mild to moderate glycemia and hyper-insulinemia and related disorders . Moreover, this strain of mice is a well-accepted system model to investigate the nutrition-metabolism paradigm and, therefore, well suited to investigate CR diet.
2.1. CR Led in a Significant Modulation of Body Weight Gain across the Animal Strains
Body weight gain was significantly lowered in all the animal strains by CR (Figure 1, Table A1). Differences of body weight gain were statistically significant between CR and the control group across the different mouse strains, except for 129S1/SvlmJ (only at Weeks 20 and 22) and C57BL6/J strains (from Week 12 to Week 22 only) as tested by ANOVA and Bonferroni post-tests. In particular, body weight was significantly lower in C57BL6/J starting at 20 weeks, which suggests a late response to CR that may be related to the specific genetic susceptibility of this animal strain to gain weight (31). This observation highlights the existence of a strong phenotypic variability within the different mice models and suggests the existence of specific metabolic signatures associated to these CR phenotypes.
2.2. Identification of Transcriptional Biomarkers of CR in Mouse Liver
Microarray analysis revealed that of the <20,000 transcripts represented, 76 genes were significantly changed in expression in all six mouse strains (Table A2). We selected 14 genes from this list to be confirmed by reverse transcriptase quantitative PCR (qPCR) in the C57BL6/J strain; selection criteria for qPCR confirmation included a robust fold change in expression (>2-fold change in expression) and a large relative signal intensity from the microarray data. All 14 genes tested by qPCR were confirmed to be significantly modulated by CR (Figure 2).
2.3. Identification of Common Pathways Affected by CR in Liver of Multiple Mice Strains
Pathway analysis of the microarray data revealed 24 Gene Ontology (p < 0.01 and FDR < 0.15) terms that were significantly modulated in at least five of the six mouse strains (Figure 3). A robust observation was a common induction for multiple strains of genes involved in tricarboxylic cycle (GO:0006099, GO:0072350), mitochondrial (GO:0005743, GO:0005746, GO:00031966, GO:00044429, GO:0044455, GO:0005740), and respiratory chain (GO:0070469, GO:0045271, GO:0022904) metabolism, as well as in specific glucose (GO:0006007), glutamine (GO:0009065, GO:0009084, GO:0009064), glutathione (GO:0004364), cholesterol (GO:0006695) and sterol (GO:0016126), metabolism.
2.4. 1H NMR Spectroscopy of Blood Plasma on the Six Strains Highlighted a Very Heterogeneous Response in Circulating Lipids Following CR
To characterize the differences in the metabolic profile between Control and CR mice from each of the six strains (10 mice per group), pairwise multivariate models were calculated using OPLS-DA (see Table A3 for model descriptors). Differences (Table 1) in metabolites under CR were mainly driven by changes in high density lipoprotein (HDL), low density lipoprotein (LDL), very low density lipoprotein (VLDL), and poly-unsaturated lipid (PUFA/UFA). Commonly, CR induced lower concentrations of LDL and UFA in 129S1/SvlmJ, C57BL6/J, C3H/HeJ, and JC3F1/J mouse strains. In addition, a lower concentration of HDL was noted in 129S1/SvlmJ and C57BL6/J strains. On the contrary, C3H/HeJ and DBA/2J mice displayed higher concentrations of HDL and, LDL, and both C3H/HeJ and CBA/J strains showed a lower concentration of VLDL under CR. The complexity of the biofluid matrix, which captures the contribution from all the biological compartments, did not enable the identification of robust metabolic signatures of CR across species, but highlighted alterations of lipid handling which is genetic-dependent.
|Table 1. Summary of metabolites affected by CR (CR vs. controls). Differences in peak intensityare listed by order of chemical shift.|
|1||Methyl signal of fatty acids in HDL||0.83 (m)||−0.60||−0.64||0.51||0.09||0.52||−0.37|
|2||Methyl signal of fatty acids in LDL||0.85 (m)||−0.64||−0.92||0.68||−0.30||0.79||−0.84|
|3||Methyl signal of fatty acids in VLDL||0.87 (m)||−0.15||−0.49||−0.69||−0.85||0.46||−0.62|
(NAG) associated resonances
|6||Lipids (FA chain)||2.23 (m)||−0.64||−0.57||−0.68||−0.85||0.37||−0.47|
|7||Lipids (Polyunsaturated FAs)||2.75 (m)||−0.85||−0.85||−0.63||−0.81||0.51||−0.91|
|9||Lipids (Unsaturated FAs)||5.30 (m)||−0.88||−0.88||−0.85||0.82||0.71||−0.96|
Key: Importance of metabolic changes is indicated by their correlation coefficients in the respective pairwise OPLS-DA multivariate analyses between controls and CR group for each mouse strain. The report values correspond to the p (corr) variables. Threshold for significant metabolites was calculated based on two-tailed probability of a Pearson correlation coefficient (r = 0.68, p < 0.001, n = 20), (s = singlets, m = multiplets).
2.5. Metabolic Profiling of Urine and Liver Tissues in C57BL6/J Mice
Liver tissue extracts as well as urine samples from C57BL6/J mice were further analyzed using 1H-NMR spectroscopy, and CR effect was assessed using chemometric approaches, including pairwise O-PLSA (See Table A4 for model descriptors). Initial analysis of the metabolic signatures (Table 2) ascribed to hydrophilic and lipophilic extracts from liver described a significant alteration of branched chain amino acid, as noted as per accumulation of valine and isoleucine, and a decreased level of the aromatic amino acid phenylalanine. Moreover, increased levels of glutathione were observed in CR. These changes were correlated with an increased level of dimethylglycine, a key metabolic intermediate in the betaine/homcysteine pathway, as well as nicotinurate, and carnosine. CR animals exhibited higher liver concentrations of free and esterified cholesterol, and phospholipids, including phosphatidylcholine and sphyngomyelines, and decreased triacylglycerides. These changes were associated with a remodeling of fatty acid composition, including increased n-3 and n-6 fatty acids C20:3, C20:4, C20:5, and C22:6, retinyl-conjgates, and a decrease in saturated fatty acids. The urine showed changes in several gut microbial metabolites, including an increase in several compounds related to bacterial protein fermentation, (e.g., phenylacetylglycine). This signature of protein digestion was associated with a deep remodelling of host protein/amino acid metabolism, as marked by different excretions of intermediate in the tricarboxylic acid cycle and urea cycle (e.g., α-ketoglutarate and allantoin). A concomitant modulation of the NADP metabolic pathway was also noted with increased concentration of 1-methylnicotinamide, suggesting a differential contribution of TCA and urea cycle for energy production. In addition, some metabolites putatively related to protein synthesis/breakdown were also found in higher urine concentrations of CR animals, including deoxycytidine, taurine, uracil, and pseudouridine.
|Table 2. Peak integrals (as a.u. = area under) for significantly regulated metabolites in liver tissues, urine from C57BL6/J strain (control vs. CR) as detected by 1H-NMR.|
Mean ± SD
Mean ± SD
|OPLS-DA correlation coefficients (p corr)||p-Value|
|Liver hydrophilic fraction||Valine||1.04 (d)||4.54 ± 1.26||7.11 ± 2.12||0.68||<0.001|
|Isoleucine||1.02 (d)||1.22 ± 2.90||1.84 ± 5.75||0.74||0.001|
|GSH||2.55(m)||3.55 ± 1.04||6.60 ± 1.94||0.87||<0.001|
|Carnosine||4.46(m)||2.86 ± 0.68||4.38 ± 1.09||0.73||<0.001|
|Uridine||5.9 (d)||2.11 ± 0.5||2.03 ± 0.72||−0.79||0.01|
|Phenylalanine||7.36 (m)||1.26 ± 0.26||1.02 ± 0.34||−0.73||<0.01|
|Nicotinurate||8.93 (d)||1.34 ± 0.37||2.44 ± 0.52||0.77||<0.001|
|N,N-dimethylglycine||2.92 (s)||3.91 ± 1.1||6.14 ± 1.37||0.81||<0.001|
|Liver Organic Phase||Cholesterol (free)||0.93, 1.01, 1.04 (m)||1.26 ± 0.92||3.14 ± 0.33||0.84||<0.001|
|Cholesterol (total)||0.69 (s), 0.86–0.88 (dd)||1.54 ± 0.31||3.67 ± 0.31||0.68||<0.001|
|Sphingomyeline||5.61 (m), 5.35 (m)3.29 (s)||5.98 ± 3.26||18.7 ± 3.36||0.97||<0.001|
|-3 FA||0.97 (t)||3.50 ± 0.16||5.61 ± 0.13||0.68||<0.001|
|UFA||5.31 (m),||2.63 ± 0.28||2.05 ± 0.24||−0.69||<0.001|
|Retyl-Conjugate||6.18 (d)||2.57 ± 1.07||9.37 ± 1.11||0.87||<0.001|
|Fatty acyl chain||2.34 (m)||4.05 ± 0.23||3.25 ± 0.15||−0.97||<0.001|
|Triacylglycerides (TAG)||5.09 (m)||5.14 ± 0.56||2.19 ± 0.53||−0.68||<0.001|
|Urine||L-Fucose||4.56 (d)||2.90 ± 0.21||3.87 ± 0.42||0.83||<0.001|
|Allantoin||5.41 (s)||5.10 ± 1.35||9.28 ± 2.30||0.84||<0.001|
|alpha-ketogluterate||3.01 (t)||1.16 ± 0.11||1.74 ± 0.22||0.88||0.01|
|Taurine||3.26 (t)||4.63 ± 0.59||7.06± 2.14||0.84||0.001|
|Uracil||7.54 (d)||5.96 ± 1.15||8.25 ± 1.25||0.72||0.001|
|Pseudouridine||7.69 (s)||5.01 ± 0.51||6.75 ± 0.96||0.88||0.001|
|N-Methylnicotinamide||9.28 (s)||2.22 ± 0.49||3.45 ± 0.52||0.76||0.001|
|Phenylacetylglycine||7.43 (m)||1.47 ± 0.33||2.00 ± 0.24||0.77||0.001|
|Deoxycytidine||7.83 (d), 6.28 (t), 6.06 (d)||3.95 ± 0.56||6.67 ± 1.72||0.77||<0.001|
Key: Importance of metabolic changes is indicated by their correlation coefficients in the respective pairwise OPLS-DA multivariate analyses between controls and CR group for each mouse strain. The report values correspond to the p (corr) variables. Threshold for significant metabolites was calculated based on two-tailed probability of a Pearson correlation coefficient (r = 0.68, p < 0.001, n = 20), (s = singlet, d = doublets, t = triplets, m = multiplet, dd = dublet of dublet, blue: decrease, orange: increase).
2.6. Targeted MS Profiles of Blood Plasma from C57BL6/J Mice
We monitored changes in C57BL6/J mouse blood plasma in the 10 CR and 10 control animals. O-PLS-DA was performed for quantitative information for 163 metabolites, including amino acids, sugars, acyl-carnitines, sphingolipids, and glycerophospholipids, to maximize the separation among CR and control animals. The model descriptors are characterized by high and positive R2X, R2Y and Q2 parameters (Table S3). Based on a variable importance in projection (VIP) threshold (VIP < 1.5) from the seven-fold cross-validated OPLS-DA model together with the V-plot (plot constructed with the VIP value vs. p (corr) value of each metabolite), the 10 most influential metabolites responsible for class separation among CR and control are computed  (Table 3). Supporting the changes noted in NMR metabolic profiles, CR induced a reduction in circulating levels of polyunsaturated phospholipids, including diacyl and acyl ether phosphocholines. In addition, the concentration of long chain acyl-carnitines (C14:1, C18:1) suggested a modification of long chain fatty acid β-oxidation in mitochondria, whilst decreased concentration of sugars (mainly hexose) further illustrate the depth of the modulation of gluconeogenesis.
|Table 3. Top 10 most discriminating metabolites in blood serum (mean values ± SD) from the targeted MS on the C57BL6/J strain. Significant differences were assessed by Mann-Whitney U test.|
|Control Mean ± SD||CR Mean ± SD||p-Value||OPLS-DA correlation coefficients (p corr)|
|PC-O 34:1||188.5 ± 11.05||62.6 ± 10.5||<0.001||−0.81|
|C18:1||0.44 ± 0.07||0.22 ± 0.06||<0.001||−0.90|
|PC 36:1||24.73 ± 3.65||16.4 ± 1.58||<0.001||−0.86|
|PC 34:3||6.73 ± 1.13||3.49 ± 1.15||0.0001||−0.88|
|C14:1||0.22 ± 0.04||0.14 ± 0.03||0.0002||−0.82|
|PC-O 38:0||3.91 ± 0.92||2.31 ± 0.57||0.0002||−0.89|
|PC-O 40:5||3.48 ± 1.04||2.90 ± 0.53||0.01||−0.80|
|PC 40:4||1.61 ± 0.30||1.24 ± 0.24||0.007||−0.75|
|PC 36:5||3.51 ± 0.92||2.08 ± 0.61||<0.001||−0.83|
|Sugars-Hexose||5996 ± 1.303||3534 ± 1397||0.001||−0.68|
Key: Importance of metabolic changes ais indicated by their correlation coefficients in the respective pairwise OPLS-DA multivariate analyses between controls and CR group for each mouse strain. The report values correspond to the p (corr) variables. Threshold for significant metabolites was calculated based on two-tailed probability of a Pearson correlation coefficient (r = 0.68, p < 0.001, n = 20).
In this study, we report metabolic readouts which are common across mouse strains in response to early CR. Transcriptomic results from the six mouse strains commonly revealed a CR-induced enhancement of mitochondrial metabolic pathways (including fatty acid β-oxidation, modulation of Krebs cycle and overall energy metabolism), a decreased intracellular insulin signaling metabolism, and complementary resistance against oxidative damage. Using complementary metabolic profiling on biofluids and liver, we further describe the metabolic changes in C57BL6/J mice, which support further some of these metabolic adaptive processes to CR.
3.1. Complementary Transcriptomics and Metabonomics Reveal CR Effects on Fatty Acid Oxidation, Gluconeogenesis and Cholesterol Metabolism
Our study reveal changes in genes related to acetyl CoA metabolic and catabolic processes (GO: 0006084 and GO: 0046356) in the liver, which illustrates how metabolic response to CR involves mobilization and metabolism of fatty acids. Although fatty acids are metabolized in the mitochondrial matrix, they cannot bypass the mitochondrial membrane without appropriate biochemical processing. Accordingly, the first enzymes involved in processing fatty acids for transport into the mitochondria are a family of acyl CoA synthetases which ligate a molecule of CoA to each fatty acid .
Moreover, in the liver of mice subjected to CR, the expression of Acss2 (acyl-CoA synthetase short-chain family member 2) was increased 6.9-fold (p < 0.0001). The increased expression of this gene describes an enhanced ability for hepatocytes to process fatty acids for mitochondrial β-oxidation. Interestingly, these physiological changes are mirrored by human studies, as it was hypothesised that inefficient muscle long chain fatty acid (LCFA) β-oxidation is associated with insulin resistance and increased blood plasma fatty acylcarnitines (AC) was reported as a feature specific to type 2 diabetes subjects . AC species are found as a consequence of incompletely oxidized fatty acids with higher rates of substrate use than energy demand, with accumulated acyl-CoA converted to AC that then exits cells and tissues . Our data might suggest reduced entry in and flux through the mitochondrial fatty acid oxidation (FAO) pathway causing a reduced pool of acylcarnitines back into the plasma compartments. Moreover, studies using microarrays have shown that short-term fasting  and long-term CR  induce a metabolic shift in liver favoring gluconeogenesis over glycolysis, and a very similar pattern was also observed in the current study. In addition, two significant metabolic features associated with hepatic response to CR are representative of differences in mediating the influx of amino acids into the gluconeogenic pathway. The first gene Got1 encodes a cytosolic protein, namely glutamate oxaloacetate transaminase 1 or cytosolic aspartate aminotransferase, which catalyzes the conversion of glutamate into α-ketoglutarate (α-KG). However, the shuttling of α-KG into the mitochondria requires a transport protein located in the mitochondrial inner membrane, namely malate-α-ketoglutarate transporter. The gene coding for this protein (Slc25a11) was as also highlighted as having a significantly up-regulated gene expression in the liver of mice under CR. Therefore, the net effect of these two genes would be an increase in the influx of carbon skeletons into the Krebs cycle which can then be used for gluconeogenesis. The difference in gluconeogenetic metabolic pathways was further illustrated through the observed changes in specific gluconeogenic amino acids and a decreased level of glucose in liver tissues as evidenced by metabonomics. In response to a putative increase in mitochondrial α-KG (above), enzymes within the Krebs cycle and downstream of α-KG entry would be predicted to be up-regulated as well. Our study reveals indeed an up-regulation of set of genes related to TCA metabolic processes (GO: 0072350) and TCA cycle (GO: 0006099). In detail, genes encoding succinate dehydrogenase D (Sdhd) and fumarate hydratase 1 (Fh1) were increased in expression in response to CR (1.6- and 4.2-fold; p = 0.0307 and 0.0148, respectively). The net result of increases in the activity of these two enzymes would be an increased production of malate which would then be returned to the cytosol via the malate-α-ketoglutarate transporter Slc25a11  and was identified as a transcriptional biomarker of CR. In response to CR, the pyruvate dehydrogenase complex is inhibited in multiple tissues by activating the family of pyruvate dehydrogenase kinase (Pdk) enzymes  the resulting phosphorylation inactivates the pyruvate dehydrogenase complex and inhibits glycolytic glucose metabolism. The gene encoding the mitochondrial isoform of malate dehydrogenase (Mdh2) was increased in expression 1.7-fold in response to CR (p = 0.0189), and mitochondrial malate can be subsequently transported to the cytoplasm for gluconeogenesis via Slc25a11. If cytosolic concentrations of malate are indeed increased, as suggested by the regulation of biomarkers of CR, and if malate were converted to phosphoenolpyruvate (PEP) via two known biochemical conversions, this would drive the glycolysis in reverse from PEP through several metabolic conversions to fructose-6-phosphate. Two enzymes in this pathway are phophoglycerate mutase and aldolase, and the genes encoding these proteins were increased in expression in response to CR (Pgam1 = 1.6-fold, p = 0.0057; Aldoc = 2.7-fold, p = 0.0008). The final transcriptional marker of CR is Pfkfb1 which encodes a single bifunctional protein that responds to circulating hormone levels to shift glycolysis pathways towards glucose catabolism or gluconeogenesis . Circulating glucagon predominates over insulin levels during fasting and CR, and glucagon initiates a signaling cascade that phosphorylates the protein encoded by Pfkfb1 resulting in both a depletion of fructose-2,6-bisphosphate (an allosteric activator of glycolysis) and an accumulation of fructose-6-phosphate which together stimulate gluconeogenic pathways at the hepatic level. Thus, the increased expression of Pfkfb1 (1.7-fold, p = 0.0312) combined with relative abundance of glucagon (over insulin) serves to promote hepatic gluconeogenesis during CR. In our study, CR also induced an 8.6-fold increase (p < 0.0001) in Pmvk expression, a gene encoding the enzyme phosphomevalonate kinase involved in cholesterol synthesis. Therefore, it is likely that the role of increased Pmvk in response to CR relates to an alternative function of the mevalonate pathway, including synthesis of other sterols and isoprenoids . Transcriptomics data also released that CR has an impact on Hsp90aa1 as well across the six mouse strains. Hsp90aa1 encodes the cytosolic heat shock protein 90 alpha, a molecular chaperone that has specificity for proteins involved in signal transduction. Hsp90aa1 is particularly noted for binding and activating members of the steroid hormone receptor family. In CR mice, Hsp90aa1 expression was changed 1.6-fold (p = 0.0067), suggesting a decreased demand for activation of steroid hormone receptors. This possibility is reinforced by the observation of decreased expression of enzymes involved in steroid hormones in response to CR. Moreover, the set of genes related to cholesterol and sterol metabolism were up-regulated (GO: 0006695 and GO: 0016126). Indeed we observed a 5.9-fold change (p = 0.0067) in the expression of Hsd3b5 in liver of CR mice, pointing out their role in the response to decreased food intake. It has been suggested that decreased activity of this family of proteins maintains high circulating levels of dehydroepiandrosterone (DHEAS) which has been associated with rhesus monkeys subjected to CR and with longevity in humans. Although the relationship between DHEA and longevity remains controversial, an alternative consequence of decreased Hsd3b5 expression is a decrease in the levels of steroid hormones.
Furthermore, plasma metabotype analysis revealed impact of CR on lipoprotein/lipid metabolism in C57BL6/J mice, as noted with reduced levels of high density lipoproteins (HDL), low density lipoproteins (LDL), and poly-unsaturated fatty acids (PUFA). Here, CR intervention displayed capabilities to modulate the typical lipoprotein atherogenic profile (e.g., high TG/HDL ratio and/or increased LDL concentration), common to metabolic syndrome and/or diabetes, but also in previous studies on CR in lifelong studies in dog . In addition, targeted MS analysis of blood plasma lipids further described a decrease in several polyunsaturated phospholipids, including the following lipid species: PC 34:3, PC 36:1, PC 36:5, PC 40:4. We previously observed similar changes in non-human primates in response to CR, whilst older humans tend to generally show higher PUFAs compared to young, and in obese compared to lean males . Thus, the observation in the current study may be explained in part by the lower fat mass of CR animals. Moreover, increased concentrations of plasma polyunsaturated fatty acids have been implicated in the pathogenesis of chronic diseases , with previous reports on higher unsaturated lipids in plasma from obese subjects compared to lean males . Our results showed also an overall decrease on the levels of TAGs in liver from C57BL6/J under CR. The CR-induced decrease in hepatic triglycerides suggests a decreased lipogenesis (reduced FAS expression) and reduced incorporation of triacylglycerols into nascent lipoprotein particles. Despite that no significant changes in circulating levels of VLDL was noted by NMR spectroscopy, the profound remodeling of HDL and LDL levels with CR highlight a different dynamics in lipid exchange from peripherical tissues and the hepatic compartment, which may be involved in greater variations in hepatic lipid metabolism and recycling.
3.2. Complementary Transcriptomics and Metabonomics Reveal Impact of CR on Insulin Signaling and Stress Response
There is increasing awareness that the insulin pathway IIS is one of the most potent regulators of aging, by modulating glycolytic processes, lipid metabolism, and the metabolic response to oxidative stress. Indeed, there is a large body of evidence in diverse species showing that longevity is associated with decreased insulin-like signaling . Pathway analysis of the microarray data shows increased liver glucose metabolism with up regulation of set of genes related to glucose catabolic processes (GO:0006007) as well as insulin-like growth factor binding protein 1 (Igfbp1). The latter was significantly increased in five of six strains of mice (not changed in the 129S1/SvImJ, p = 0.17) and qPCR analysis indicated that this gene was increased in expression 7.6-fold (p < 0.0001) by CR in the C57BL6/J strain (data not shown). An increase in the level of this protein would be predicted to sequester insulin-like growth factor (IGF), thereby decreasing IGF signaling. Interestingly, the expression of several IGF binding proteins was increased in the heart of mice subjected to a similar duration of CR as in this study  and in the liver of mice subjected to a 48-hour fast . Thus, IGF binding proteins appear be important transcriptional regulators in response to CR. These changes were further supported by an overall decrease in the concentration of blood and hepatic glucose in C57BL6/J mice under CR, suggesting increased insulin sensitivity and glucose uptake. Another specific signature associated with changes in insulin signaling pathway was also noted via changes in hepatic branched chain amino acids  which highlight a change in central energy metabolic and exchanges with peripheral tissues, through BCAA dependent gluconeogenic pathway. Insulin resistance in muscle and fat cells reduces glucose uptake (and also local storage of glucose as glycogen and triglycerides, respectively), whereas insulin resistance in liver cells results in reduced glycogen synthesis and storage and a failure to suppress glucose production and release into the blood.
Following CR intervention, our data also suggest a differential metabolic response to oxidative stress. Here, the set of genes related to glutathione metabolism is up-regulated (GO: 0004364). Specifically, Gstm6 encodes the protein glutathione transferase 6, a member of a family of proteins important in drug metabolism and for defense against oxidative damage. Gstm6 was found to be decreased in expression in liver of diabetic mice , whereas Gstm6 was increased in expression 2.6-fold (p < 0.0001) by CR. Moreover, increased levels of glutathione and its precursor in the gamma-glutamyl cycle, glutamine, also suggest a different oxidative response induced by CR. In particular, GSH is important in the regulation of the redox state, and a decline in its tissue level has often been considered to be indicative of increased oxidative stress . Further carnosine, found generally in any tissue, is considered to be an anti-aging substance, capable of counteracting oxidative damage and protein glycation . In addition, NMR profiling of liver organic phase revealed increase production of retinly conjugates suggesting an increased protecting role. The liver is the major vitamin A reservoir in mammals, storing up to 80% of the total body vitamin A, and plays therefore a central role in the metabolism, storage and the distribution of retinol to peripheral tissues . The identification of redox homeostasis and its core glutathione as affected pathways in our liver metabonomic analysis, suggesting that reactive oxygen species play a role in the initiation or progression of the CR phenotype. In agreement with these findings, C57BL6/J strain displayed reduction, under CR, in concentration of several acyl-ether (PC-O 34:1, PC-O 38:0, PC-O 40:5), namely plasmalogens. Plasmalogens containing a vinyl ether bond link to the sn-1 aliphatic chain of the glycerol backbone are endogenous antioxidant. Plasmalogens have been implicated in protection of cellular functions against oxidative damage  and recent studies displayed that VLDL, LDL and HDL particles are characterized by class-specific ether lipid species composition [53,54].
4. Experimental Section
4.1. Animals and Dietary Manipulation
All procedures were approved by the Animal Care Committee at the William S. Middleton Memorial Veterans Hospital. Six strains (129S1/SvImJ, C57BL6/J, C3H/HeJ, CBA/J, DBA/2J and /F1) of male mice were purchased at six weeks of age from Jackson Laboratories (Bar Harbor, Maine) and were individually housed in a specific pathogen free facility. Upon arrival, mice were provided with 12.7 kcal (53.1 kJ)·day−1 of a pelleted ration of AIN93M diet (Bio-Serv; Frenchtown, New Jersey). At eight weeks of age, half of the mice from each strain were randomly assigned to a control or 25% calorie restricted (CR, 9.44 kcal/39.5kJ·day−1) treatment group such that there were 10 mice of each strain in the control or CR group. Details on the feeding regiment and diets used in this study are described elsewhere . Body weight was measured every other week for all mice. For two strains of mice (129S1/SvImJ and C57BL6/J), food intake of the CR group was subsequently decreased to 7.34 kcal (30.7 kJ)·day−1 at 16 weeks of age.
4.2. Sample Collection
At 20 weeks of age, C57BL6/J mice were individually maintained in Tecniplast metabolic cages for two days to collect urine. At 22 weeks of age, all mice strains were euthanized by cervical dislocation and blood was collected from the body cavity into two heparinized tubes. Tissues from the mice were rapidly dissected, flash-frozen in liquid nitrogen and were stored at −80 °C.
4.3. Transcriptomic Analyses
Affymetrix Mouse Genome 430 2.0 microarrays representing 20,341 known genes were used for gene expression profiling; detailed procedures for the microarray analysis are published elsewhere . Briefly, the list of 45,101 probe sets represented on this array was filtered to a list of unique transcripts with an Entrez Gene ID (i.e., a gene was only represented once) probe sets representing more than one Entrez Gene ID were removed from the original dataset, and if a gene was represented by more than one probe set, we only retained that probe set having the largest signal intensity when averaged across all Control and CR samples within a strain. For each strain, a gene was considered to be differentially expressed when Two-tailed t-tests p < 0.01 using a two tailed t test and when the false discovery rate was < 0.15  were used to identify genes that were differentially expressed in response to CR (p < 0.01). Using an Eppendorf realplex2 instrument, the same RNA samples from C57BL6/J mice used for microarray analysis were analyzed by qPCR as described previously . qPCR primers for all genes were purchased from Applied Biosystems. The TATA box binding protein (Tbp) gene was found to be unchanged by CR in all strains according to the microarray data and was therefore used as a housekeeping gene. Of the 19 genes examined by qPCR, only two genes (Foxa3 and Ugt2b35) were not confirmed as being changed by CR. To identify functional classes of genes changed by treatment, we performed parametric analysis of gene set enrichment (PAGE) . PAGE allows for the detection of gene classes that are modulated by an intervention even when there are modest (not statistically significant) but consistent changes in the expression of genes within that functional category (relative to all genes represented on the array. In addition, PAGE generates a z-score indicating if a gene class was activated (z-score < 0) or repressed (z-score < 0) by treatment. We grouped genes into functional classes using the Gene Ontology (GO) hierarchy and only considered those GO terms that were annotated with at least 10 but not more than 1,000 genes per term. Gene functional classes were considered to be significantly altered by treatment at p < 0.01. Microarray data have been uploaded to NCBI-GEO .
4.4. Targeted LC-MS/MS Metabolite Profiling
A targeted LC-MS/MS global metabonomic approach on plasma was used by combining the Biocrates Life Sciences AbsoluteIDQTM kit for plasma samples as previously published .
4.5. Annotation of Lipid Species
C, acyl-carnitine; LPC, Lysophosphatidylcholines; PC, Phosphatidylcholines; PC-O, 1-O-alkyl-2-acylglycerophosphocholines. Individual lipid species were annotated as follows: [lipid class] [total number of carbon atoms]:[total number of double bonds]. For example, PC 34:4 reflects a phosphatidylcholine species comprising 34 carbon atoms and four double bonds.
4.6. Metabolite Profiling-Sample Preparation and 1H NMR Spectroscopic Analysis
Around 5–10 mg of freeze dried and ground tissue was used to extract hydrophilic and lipophilic metabolites applying an adapted Folch procedure  as below. Samples were extracted three times with 0.5 mL of a chloroform-methanol solution (2:1, v:v). Combined extracts were washed first with 0.5 mL of water and second with 0.5 mL of water-methanol (1:1, v:v). The upper hydrophilic phases were collected each time and combined together. Lipophilic and hydrophilic fractions were afterwards evaporated to dryness under nitrogen flow and freeze dried, respectively. Hydrophilic fractions were dissolved in 60 μL of a deuterated phosphate buffer (pH 7.4) containing 1 mM of 3-trimethylsilyl-1-[2,2,3,3,-2H4]-propionate (TSP) as a standard reference (δ = 0.0) and transferred into 1.7 mm NMR tubes. The lipophilic phases were reconstituted in 60 μL of a deuteriated chloroform-methanol solution (2:1, v:v) and transferred into 1.7 mm NMR tubes using octamethylcyclotetrasiloxane (OMS) as standard reference (δ = 0.092). All samples were analyzed at ambient temperature (300 K) by 1H NMR spectroscopy at 600.13 MHz using a Bruker Avance II NMR spectrometer. For statistical analysis, all NMR spectra were converted into 22 K data points over the range of δ 0.2–10.0 and imported into the MATLAB software (version 7.0; The MathWorks Inc., Natick, MA, USA). The spectra were normalized to a constant total sum of all intensities within the specified range and auto scaled.
Statistical analysis was performed by Multivariate Data Analysis (MVA) carried out with the Simca-P+ software (version 12.0; Umetrics AB, Umeå, Sweden) and the MATLAB software package (version 7.0; The Mathworks Inc., Natwick, MA). Data import and pre-processing steps for both 1H NMR and targeted MS data from C57BL6/J mice groups were done using “in-house” routines written in MATLAB (version 7.11.0, The Mathworks Inc., Natick, MA, USA). Full resolution 1H-NMR spectra incorporating data points within the δ 0.4–9.5 region were used for statistical multivariate analysis excluding the water residue signal between δ 4.5–6.5 (urine, plasma, tissue water extract dataset), ethanol δ 1.18 and δ 3.66 (plasma, ethanol residues from antiseptic swabbing contaminated plasma samples during collection), solvent signals (methanol δ = 3.24–3.27 and δ = 4.25–4.60; chloroform δ = 7.35–7.45 for liver tissues organic phase). The supervised Orthogonal PLS discriminant analyses (O-PLS-DA) was applied to the examined biofluids and tissue NMR profiling, and targeted LC-MS/MS metabolite profiling in plasma to maximize the separation between control and CR animals. The validity of the model against overfitting was monitored by computing the cross-validation parameter Q2 which represents the predictability of the models and relates to the statistical significance. For the NMR data, differences between samples in the scores’ plot were extracted by using the variable coefficients according to a previously published method .Variables correlating with the group separation in the MS data were identified by using the S-plot. It visualizes the variable importance (VIP) score, representing the impact of a single metabolite to the group discrimination of the model . Metabolomics data (C57BL6/J LC-MS/MS μM data concentration of plasma, and C57BL6/J area intensities (a.u.) of urine and tissues 1H-NMR data) of representative metabolite signals responsible for class separation is uploaded as a supplemental file (MS Excel).
The present study provided a comprehensive comparison of the metabolic phenotype at both transcriptomics and metabolomics levels across mice with different genetic backgrounds to identify common metabolic markers affected by CR. Using a system biology approach comprising phenotyping of liver tissue and biofluids, we described the effect of CR across multiple mouse strains (129S1/SvlmJ, C57BL6/J, C3H/HeJ, CBA/J, DBA/2J, JC3F1/J). Overall, our integrated approach commonly described that lipid metabolism between liver and peripheral tissues, oxidative stress response and insulin dependent metabolic pathways are conserved, and are determinant factors involved in CR regulation.
We thank Serge Rezzi for helpful discussions. The authors also thank Philippe Guy and Emilie Reginato for assistance in MS analysis.
Conflicts of Interest
The authors declare no conflict of interest.
- Sansoni, P.; Vescovini, R.; Fagnoni, F.; Biasini, C.; Zanni, F.; Zanlari, L.; Telera, A.; Lucchini, G.; Passeri, G.; Monti, D.; et al. The immune system in extreme longevity. Exp. Gerontol. 2008, 43, 61–65, doi:10.1016/j.exger.2007.06.008.
- Franceschi, C. Inflammaging as a major characteristic of old people: Can it be prevented or cured? Nutr. Rev. 2007, 65, 173–176, doi:10.1301/nr.2007.dec.S173-S176.
- Burkle, A.; Caselli, G.; Franceschi, C.; Mariani, E.; Sansoni, P.; Santoni, A.; Vecchio, G.; Witkowski, J.M.; Caruso, C. Pathophysiology of ageing, longevity and age related diseases. Immun. Ageing 2007, 4, 4–17, doi:10.1186/1742-4933-4-4.
- Franceschi, C.; Capri, M.; Monti, D.; Giunta, S.; Olivieri, F.; Sevini, F.; Panourgia, M.P.; Invidia, L.; Celani, L.; Scurti, M.; et al. Inflammaging and anti-inflammaging: A systemic perspective on aging and longevity emerged from studies in humans. Mech. Ageing Dev. 2007, 128, 92–105, doi:10.1016/j.mad.2006.11.016.
- Weindruch, R. Caloric restriction and aging. Sci. Am. 1996, 274, 46–52, doi:10.1038/scientificamerican0196-46.
- Roth, G.S.; Lane, M.A.; Ingram, D.K. Caloric restriction mimetics: The next phase. Ann. NY Acad. Sci. 2005, 1057, 365–371, doi:10.1196/annals.1356.027.
- Anderson, R.M.; Weindruch, R. Metabolic reprogramming, caloric restriction and aging. Trends Endocrin. Metab 2010, 21, 134–141.
- Weindruch, R.; Naylor, P.H.; Goldstein, A.L.; Walford, R.L. Influences of aging and dietary restriction on serum thymosin alpha 1 levels in mice. J. Gerontol. 1988, 43, B40–B42, doi:10.1093/geronj/43.2.B40.
- Selman, C.; Withers, D.J. Mammalian models of extended healthy lifespan. Philos. T. R. Soc. B. 2011, 366, 99–107, doi:10.1098/rstb.2010.0243.
- Fontana, L.; Partridge, L.; Longo, V.D. Extending healthy life span—from yeast to humans. Science 2010, 328, 321–326, doi:10.1126/science.1172539.
- Fontana, L.; Villareal, D.T.; Weiss, E P.; Racette, S.B.; Steger-May, K.; Klein, S.; Holloszy, J.O. Calorie restriction or exercise: Effects on coronary heart disease risk factors. A randomized, controlled trial. Am. J. Physiol—Endoc. M. 2007, 293, 197–202.
- Weindruch, R.; Walford, R.L.; Fligiel, S.; Guthrie, D. The retardation of aging in mice by dietary restriction: Longevity, cancer, immunity and lifetime energy intake. J. Nutr. 1986, 116, 641–654.
- Kealy, R.D.; Lawler, D.F.; Ballam, J.M.; Mantz, S.L.; Biery, D.N.; Greeley, E.H. Effects of diet restriction on life span and age-related changes in dogs. J. Am. Vet. Med. A. 2001, 220, 1315–1320.
- Forster, M.J.; Morris, P.; Sohal, R.S. Genotype and age influence the effect of caloric intake on mortality in mice. FASEB J. 2003, 17, 690–692.
- De Grey, A.D. The unfortunate influence of the weather on the rate of ageing: Why human caloric restriction or its emulation may only extend life expectancy by 2–3 years. Gerontology 2005, 51, 73–82, doi:10.1159/000082192.
- Heilbronn, L.K.; Ravussin, E. Calorie restriction and aging: Review of the literature and implications for studies in humans. Am. J. Clin. Nutr. 2003, 78, 361–369.
- Suzuki, M.; Akisaka, M.; Ashitomi, I.; Higa, K.; Nozaki, H. Chronological study concerning ADL among Okinawan centenarians. Nippon Ronen Igakkai Zasshi 1995, 32, 416–423, doi:10.3143/geriatrics.32.416.
- Willcox, D.C.; Willcox, B.J.; Shimajiri, S.; Kurechi, S.; Suzuki, M. Aging gracefully: A retrospective analysis of functional status in Okinawan centenarians. Am. J. Geriat. Psychiat. 2007, 15, 252–256, doi:10.1097/JGP.0b013e31803190cc.
- Walford, R.L.; Mock, D.; Verdery, R.; MacCallum, T. Calorie restriction in biosphere 2: Alterations in physiologic, hematologic, hormonal, and biochemical parameters in humans restricted for a 2-year period. J. Gerontol. A—Biol. 2002, 57, B211–B224, doi:10.1093/gerona/57.6.B211.
- Ingram, D.K.; Zhu, M.; Mamczarz, J.; Zou, S.; Lane, M.A.; Roth, G.S.; de Cabo, R. Calorie restriction mimetics: An emerging research field. Aging Cell 2006, 5, 97–108, doi:10.1111/j.1474-9726.2006.00202.x.
- Masoro, E.J. Dietary restriction and aging. J. Am. Geriatr. Soc. 1993, 41, 994–999.
- Fontana, L.; Meyer, T.E.; Klein, S.; Holloszy, J.O. Long-term calorie restriction is highly effective in reducing the risk for atherosclerosis in humans. Proc. Natl. Acad. Sci. USA 2004, 101, 6659–6663.
- Mattison, J.A.; Roth, G.S.; Beasley, T.M.; Tilmont, E.M.; Handy, A.M.; Herbert, R.L.; Longo, D.L.; Allison, D.B.; Young, J.E.; Bryant, M.; et al. Impact of caloric restriction on health and survival in rhesus monkeys from the NIA study. Nature 2012, 489, 318–321, doi:10.1038/nature11432.
- Liao, C.Y.; Rikke, B.A.; Johnson, T.E.; Diaz, V.; Nelson, J.F. Genetic variation in the murine lifespan response to dietary restriction: From life extension to life shortening. Aging Cell 2010, 9, 92–95, doi:10.1111/j.1474-9726.2009.00533.x.
- Wijeyesekera, A.; Selman, C.; Barton, R.H.; Holmes, E.; Nicholson, J.K.; Withers, D.J. Metabotyping of long-lived mice using 1H NMR spectroscopy. J. Proteome. Res. 2012, 11, 2224–2235, doi:10.1021/pr2010154.
- Selman, C.; Kerrison, N.D.; Cooray, A.; Piper, M.D.; Lingard, S.J.; Barton, R.H.; Schuster, E.F.; Blanc, E.; Gems, D.; Nicholson, J.K.; et al. Coordinated multi-tissue transcriptional and plasma metabonomic profiles following acute caloric restriction in mice. Physiol. Genomics 2006, 27, 187–200, doi:10.1152/physiolgenomics.00084.2006.
- Wang, Y.; Lawler, D.; Larson, B.; Ramadan, Z.; Kochhar, S.; Holmes, E.; Nicholson, J.K. Metabonomic investigations of aging and caloric restriction in a life-long dog study. J. Proteome Res. 2007, 6, 1846–1854, doi:10.1021/pr060685n.
- Rezzi, S.; Martin, F.P.; Shanmuganayagam, D.; Colman, R.J.; Nicholson, J.K.; Weindruch, R. Metabolic shifts due to long-term caloric restriction revealed in nonhuman primates. Exp. Gerontol. 2009, 44, 356–362, doi:10.1016/j.exger.2009.02.008.
- Boulange, C.L.; Claus, S.P.; Chou, C.J.; Collino, S.; Montoliu, I.; Kochhar, S.; Holmes, E.; Rezzi, S.; Nicholson, J.K.; Dumas, M.E.; et al. Early metabolic adaptation in C57BL/6 mice resistant to high fat diet induced weight gain involves an activation of mitochondrial oxidative pathways. J. Proteome Res. 2013, 12, 1956–1986, doi:10.1021/pr400051s.
- West, D.B.; Boozer, C.N.; Moody, D.L.; Atkinson, R.L. Dietary obesity in nine inbred mouse strains. Am. J. Physiol. 1992, 262, R1025–R1032.
- Champy, M.F.; Selloum, M.; Zeitler, V.; Caradec, C.; Jung, B.; Rousseau, S.; Pouilly, L.; Sorg, T.; Auwerx, J. Genetic background determines metabolic phenotypes in the mouse. Mamm. Genome 2008, 19, 318–331, doi:10.1007/s00335-008-9107-z.
- Ni, Y.; Su, M.; Lin, J.; Wang, X.; Qiu, Y.; Zhao, A.; Chen, T.; Jia, W. Metabolic profiling reveals disorder of amino acid metabolism in four brain regions from a rat model of chronic unpredictable mild stress. FEBS Lett. 2008, 582, 2627–2636, doi:10.1016/j.febslet.2008.06.040.
- Coleman, E.A.; Eilertsen, T.B.; Magid, D.J.; Conner, D.A.; Beck, A.; Kramer, A.M. The association between care co-ordination and emergency department use in older managed care enrollees. Int. J. Integr. Care 2002, 2, e03.
- Adams, S.H.; Hoppel, C.L.; Lok, K.H.; Zhao, L.; Wong, S.W.; Minkler, P.E.; Hwang, D.H.; Newman, J.W.; Garvey, W.T. Plasma acylcarnitine profiles suggest incomplete long-chain fatty acid beta-oxidation and altered tricarboxylic acid cycle activity in type 2 diabetic African-American women. J. Nutr. 2009, 139, 1073–1081, doi:10.3945/jn.108.103754.
- Noland, R.C.; Koves, T.R.; Seiler, S.E.; Lum, H.; Lust, R.M.; Ilkayeva, O.; Stevens, R.D.; Hegardt, F.G.; Muoio, D.M. Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control. J. Biol. Chem. 2009, 284, 22840–22852, doi:10.1074/jbc.M109.032888.
- Bauer, M.; Hamm, A.C.; Bonaus, M.; Jacob, A.; Jaekel, J.; Schorle, H.; Pankratz, M.J.; Katzenberger, J.D. Starvation response in mouse liver shows strong correlation with life-span-prolonging processes. Physiol. Genomics 2004, 17, 230–244, doi:10.1152/physiolgenomics.00203.2003.
- Dhahbi, J.M.; Mote, P.L.; Wingo, J.; Tillman, J.B.; Walford, R.L.; Spindler, S.R. Calories and aging alter gene expression for gluconeogenic, glycolytic, and nitrogen-metabolizing enzymes. Am. J. Physiol. 1999, 277, E352–E360.
- Kabe, Y.; Ohmori, M.; Shinouchi, K.; Tsuboi, Y.; Hirao, S.; Azuma, M.; Watanabe, H.; Okura, I.; Handa, H. Porphyrin accumulation in mitochondria is mediated by 2-oxoglutarate carrier. J. Biol. Chem. 2006, 281, 31729–31735, doi:10.1074/jbc.M604729200.
- Barger, J.L.; Kayo, T.; Vann, J.M.; Arias, E.B.; Wang, J.; Hacker, T.A.; Wang, Y.; Raederstorff, D.; Morrow, J.D.; Leeuwenburgh, C.; et al. A low dose of dietary resveratrol partially mimics caloric restriction and retards aging parameters in mice. PLoS One 2008, 3, 2264–2272, doi:10.1371/journal.pone.0002264.
- Rider, M.H.; Bertrand, L.; Vertommen, D.; Michels, P.A.; Rousseau, G.G.; Hue, L. 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase: head-to-head with a bifunctional enzyme that controls glycolysis. Biochem. J. 2004, 381, 561–579, doi:10.1042/BJ20040752.
- Pilloff, D.; Dabovic, K.; Romanowski, M.J.; Bonanno, J.B.; Doherty, M.; Burley, S.K.; Leyh, T.S. The kinetic mechanism of phosphomevalonate kinase. J. Biol. Chem. 2003, 278, 4510–4515.
- Richards, S.E.; Wang, Y.; Lawler, D.; Kochhar, S.; Holmes, E.; Lindon, J.C.; Nicholson, J.K. Self-modeling curve resolution recovery of temporal metabolite signal modulation in NMR spectroscopic data sets: Application to a life-long caloric restriction study in dogs. Anal. Chem. 2008, 80, 4876–4885, doi:10.1021/ac702584g.
- Kochhar, S.; Jacobs, D.M.; Ramadan, Z.; Berruex, F.; Fuerholz, A.; Fay, L.B. Probing gender-specific metabolism differences in humans by nuclear magnetic resonance-based metabonomics. Anal. Biochem. 2006, 352, 274–281, doi:10.1016/j.ab.2006.02.033.
- Pereira, S.P.; Cassell, T.B.; Engelman, J.L.; Sladen, G.E.; Murphy, G.M.; Dowling, R.H. Plasma arachidonic acid-rich phospholipids in Crohn’s disease: Response to treatment. Clin. Sci. 1996, 91, 509–512.
- Bartke, A. Insulin resistance and cognitive aging in long-lived and short-lived mice. J. Gerontol. A—Biol. 2005, 60, 133–134, doi:10.1093/gerona/60.1.133.
- Barger, J.L.; Kayo, T.; Pugh, T.D.; Prolla, T.A.; Weindruch, R. Short-term consumption of a resveratrol-containing nutraceutical mixture mimics gene expression of long-term caloric restriction in mouse heart. Exp. Gerontol. 2008, 43, 859–866, doi:10.1016/j.exger.2008.06.013.
- Newgard, C.B.; An, J.; Bain, J.R.; Muehlbauer, M.J.; Stevens, R.D.; Lien, L.F.; Haqq, A.M.; Shah, S.H.; Arlotto, M.; Slentz, C.A.; et al. A branched-chain amino acid-related metabolic signature that differentiates obese and lean humans and contributes to insulin resistance. Cell Metab. 2009, 9, 311–326, doi:10.1016/j.cmet.2009.02.002.
- Pass, G.J.; Becker, W.; Kluge, R.; Linnartz, K.; Plum, L.; Giesen, K.; Joost, H.G. Effect of hyperinsulinemia and type 2 diabetes-like hyperglycemia on expression of hepatic cytochrome p450 and glutathione s-transferase isoforms in a New Zealand obese-derived mouse backcross population. J. Pharmacol. Exp. Ther. 2002, 302, 442–450, doi:10.1124/jpet.102.033553.
- Wu, G.; Fang, Y.Z.; Yang, S.; Lupton, J.R.; Turner, N.D. Glutathione metabolism and its implications for health. J. Nutr. 2004, 134, 489–492.
- Yu, Z.; Zhai, G.; Singmann, P.; He, Y.; Xu, T.; Prehn, C.; Romisch-Margl, W.; Lattka, E.; Gieger, C.; Soranzo, N.; et al. Human serum metabolic profiles are age dependent. Aging Cell 2012, 11, 960–967, doi:10.1111/j.1474-9726.2012.00865.x.
- Biesalski, H.K.; Nohr, D. New aspects in vitamin a metabolism: The role of retinyl esters as systemic and local sources for retinol in mucous epithelia. J. Nutr. 2004, 134, 3453S–3457S.
- Zoeller, R.A.; Lake, A.C.; Nagan, N.; Gaposchkin, D.P.; Legner, M.A.; Lieberthal, W. Plasmalogens as endogenous antioxidants: Somatic cell mutants reveal the importance of the vinyl ether. Biochem. J. 1999, 338, 769–776, doi:10.1042/0264-6021:3380769.
- Wallner, S.; Schmitz, G. Plasmalogens the neglected regulatory and scavenging lipid species. Chem. Phys. Lipids 2011, 164, 573–589, doi:10.1016/j.chemphyslip.2011.06.008.
- Scott, B.L.; Bazan, N.G. Membrane docosahexaenoate is supplied to the developing brain and retina by the liver. Proc. Natl. Acad. Sci. USA 1989, 86, 2903–2907, doi:10.1073/pnas.86.8.2903.
- Pugh, T.D.; Klopp, R.G.; Weindruch, R. Controlling caloric consumption: Protocols for rodents and rhesus monkeys. Neurobiol. Aging 1999, 20, 157–165, doi:10.1016/S0197-4580(99)00043-3.
- Lee, C.K.; Allison, D.B.; Brand, J.; Weindruch, R.; Prolla, T.A. Transcriptional profiles associated with aging and middle age-onset caloric restriction in mouse hearts. Proc. Natl. Acad. Sci. USA 2002, 99, 14988–14993, doi:10.1073/pnas.232308999.
- Benjamini, Y.; Yekutieli, D. The control of the false discovery rate in multiple hypotheses testing under dependency. Ann. Stat. 2001, 29, 1165–1188, doi:10.1214/aos/1013699998.
- Kim, S.Y.; Volsky, D.J. PAGE: parametric analysis of gene set enrichment. BMC Bioinformatics 2005, 8, 144–156.
- NCBI-GEO. Available online: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE50789 (accessed on 28 June 2013).
- Baur, P.; Martin, F.P.; Gruber, L.; Bosco, N.; Brahmbhatt, V.; Collino, S.; Guy, P.; Montoliu, I.; Rozman, J.; Klingenspor, M.; et al. Metabolic phenotyping of the Crohn’s disease-like IBD etiopathology in the TNF(DeltaARE/WT) mouse model. J. Proteome Res. 2011, 10, 5523–5535, doi:10.1021/pr2007973.
- Folch, J.; Lees, M.; Sloane Stanley, G.H. A simple method for the isolation and purification of total lipides from animal tissues. J. Biol. Chem. 1957, 226, 497–509.
- Wiklund, S.; Johansson, E.; Sjostrom, L.; Mellerowicz, E.J.; Edlund, U.; Shockcor, J.P.; Gottfries, J.; Moritz, T.; Trygg, J. Visualization of GC/TOF-MS-based metabolomics data for identification of biochemically interesting compounds using OPLS class models. Anal. Chem. 2008, 80, 115–122, doi:10.1021/ac0713510.
|Table A1. Body weight for the control and CR strains. Data are reported as mean ± SE values for the body weight gain calculated from Week 8 onwards. Control and CR groups are plotted with dot and square shapes, respectively. Differences of body weight gain were statistically significant between CR and control group were tested by ANOVA and Bonferroni post-tests (*** p <0.001).|
|129S1/SvlmJ||Control||22.8 ± 1.26||23.7 ± 1.41||27.4 ± 3.66||29.0 ± 4.17||28.8 ± 4.04||28.1 ± 3.85||28.2 ± 4.35||28.2 ± 4.11|
|CR||22.5 ± 0.43||22.8 ± 0.41||25.2 ± 1.33||26.5 ± 1.40||27.0 ± 1.28||25.3 ± 1.32||24.1 *** ± 1.35||23.7 *** ± 1.37|
|C57BL6/J||Control||24.4 ± 2.11||24.1 ± 1.47||26.6 ± 1.98||28.5 ± 2.24||28.4 ± 2.39||28.7 ± 2.39||29.5 ± 2.37||30.5 ± 2.55|
|CR||25.6± 1.53||25.6 ± 1.05||26.1 ± 1.01||27.4± 0.96||27.6± 1.13||27.3± 1.01||23.6 *** ± 0.71||23.6 *** ± 0.77|
|C3H/HeJ||Control||25.8± 1.03||28.3 ± 1.14||30.1 ± 1.59||31.6 ± 1.99||32.9 ± 2.83||33.4 ± 3.14||33.6 ± 3.77||33.7 ± 3.73|
|CR||24.2 ***± 0.82||22.1 *** ± 0.72||22.8 *** ± 0.89||24.2 *** ± 0.76||26.7 *** ± 0.73||28.4 *** ± 0.83||28.4 *** ± 0.73||28.4 *** ± 0.78|
|CBA/J||Control||26.3 ± 0.90||29.3 ± 0.95||29.7 ± 0.99||29.8 ± 1.17||34.5 ± 1.54||35.6 ± 1.41||35.9 ± 1.21||35.9 ± 1.36|
|CR||25.1 *** ± 1.27||21.6 *** ± 1.04||21.4 *** ± 0.99||21.4 *** ± 0.96||24.0 *** ± 0.59||25.6 *** ± 1.04||25.7 *** ± 1.45||26.5 *** ± 3.67|
|DBA/2J||Control||24.9 ± 0.79||27.2 ± 1.54||27.8 ± 1.11||30.2 ± 1.85||31.7 ± 2.09||31.9 ± 2.27||32.1 ± 2.24||31.4 ± 2.48|
|CR||24.4 ± 1.05||22.1 *** ± 1.11||22.8 *** ± 1.22||24.1 *** ± 1.36||25.5 *** ± 1.41||25.9 *** ± 1.53||25.8 *** ± 1.55||25.0 *** ± 1.54|
|JC3F1/J||Control||27.8 ± 0.79||33.6 ± 0.55||35.7 ± 0.60||36.6 ± 1.03||36.1 ± 0.99||36.3 ± 0.94||38.3 ± 1.22||37.5 ± 1.04|
|CR||28.4 ± 0.94||26.2 *** ± 0.67||27.3 *** ± 1.05||28.0 *** ± 1.11||27.5 *** ± 1.24||27.2 *** ± 1.45||29.2 *** ± 1.59||28.4 *** ± 1.47|
|Table A2. Number of genes changed in expression for each strain. Values reported are p value and fold change (FC).|
|Gene Symbol||Gene Title||p-value (129)||FDR (129)||FC (129)||p-value (B6)||FDR (B6)||FC (B6)||p-value (C3H)||FDR (C3H)||FC (C3H)||p-value (CBA)||FDR (CBA)||FC (CBA)||p-value (DBA)||FDR (DBA)||FC (DBA)||p-value (F1)||FDR (F1)||FC (F1)|
|4931406C07Rik||RIKEN cDNA 4931406C07 gene||0.000||0.003||−1.380||0.001||0.030||−1.290||0.004||0.071||−1.290||0.000||0.000||−1.900||0.000||0.003||−1.680||0.000||0.009||−1.400|
|9530008L14Rik||RIKEN cDNA 9530008L14 gene||0.000||0.002||−2.010||0.000||0.013||−1.430||0.001||0.031||−1.310||0.000||0.000||−1.840||0.000||0.008||−1.890||0.000||0.001||−1.390|
|Acadm||Acyl-Coenzyme A dehydrogenase, medium chain||0.000||0.000||−1.850||0.000||0.003||−1.430||0.001||0.030||−1.270||0.009||0.033||−1.210||0.002||0.088||−1.510||0.000||0.007||−1.430|
|Acss2||acyl-CoA synthetase short-chain family member 2||0.006||0.099||4.230||0.000||0.014||4.340||0.000||0.002||3.600||0.000||0.002||2.400||0.000||0.001||5.640||0.000||0.001||6.270|
|Adh4||alcohol dehydrogenase 4 (class II), pi polypeptide||0.000||0.011||−1.570||0.002||0.035||−1.460||0.007||0.106||−1.310||0.000||0.002||−2.250||0.000||0.034||−1.800||0.000||0.001||−1.640|
|Aldoc||aldolase C, fructose-bisphosphate||0.000||0.000||4.140||0.000||0.001||2.230||0.004||0.074||1.590||0.000||0.000||2.190||0.000||0.001||2.080||0.002||0.062||1.780|
|Ass1||argininosuccinate synthetase 1||0.000||0.005||2.330||0.001||0.026||1.670||0.000||0.003||2.010||0.000||0.000||5.340||0.000||0.000||2.950||0.001||0.032||2.010|
|Atp5g1||ATP synthase, H+ transporting, mitochondrial F0 complex, subunit c1 (subunit 9)||0.001||0.022||1.600||0.003||0.043||1.510||0.000||0.000||1.410||0.000||0.000||1.770||0.000||0.017||1.830||0.000||0.006||1.520|
|Chrna2||cholinergic receptor, nicotinic, alpha polypeptide 2 (neuronal)||0.000||0.001||−5.230||0.000||0.002||−3.170||0.000||0.003||−2.670||0.000||0.000||−4.260||0.002||0.078||−4.090||0.002||0.052||−1.960|
|D16H22S680E||DNA segment, Chr 16, human D22S680E, expressed||0.000||0.016||1.640||0.000||0.000||2.140||0.000||0.012||1.570||0.000||0.000||1.760||0.000||0.029||1.700||0.001||0.029||1.310|
|Dlat||dihydrolipoamide S-acetyltransferase (E2 component of pyruvate dehydrogenase complex)||0.001||0.026||1.530||0.000||0.009||1.470||0.001||0.022||1.830||0.000||0.004||−1.710||0.000||0.029||1.960||0.001||0.039||1.970|
|Echdc1||enoyl Coenzyme A hydratase domain containing 1||0.005||0.090||1.780||0.000||0.002||1.790||0.002||0.051||1.680||0.000||0.000||−2.410||0.000||0.024||1.890||0.005||0.100||1.970|
|Eci1||enoyl-Coenzyme A delta isomerase 1||0.000||0.000||−2.720||0.000||0.000||−1.800||0.002||0.049||−1.440||0.005||0.022||1.310||0.000||0.030||−1.620||0.004||0.087||−1.520|
|Fbxo18||F-box protein 18||0.000||0.009||1.590||0.000||0.013||1.410||0.000||0.010||1.400||0.000||0.000||2.160||0.004||0.121||1.260||0.000||0.011||1.430|
|Fdps||farnesyl diphosphate synthetase||0.001||0.038||6.470||0.001||0.023||5.310||0.000||0.011||3.510||0.009||0.033||1.920||0.000||0.000||7.660||0.000||0.009||4.870|
|Fh1||fumarate hydratase 1||0.000||0.021||1.740||0.000||0.011||1.440||0.000||0.001||1.910||0.002||0.011||1.430||0.000||0.004||2.080||0.000||0.003||2.010|
|Foxa3||forkhead box A3||0.002||0.042||−1.940||0.000||0.001||−1.980||0.000||0.005||−2.580||0.000||0.002||−1.820||0.000||0.011||−2.020||0.000||0.001||−2.440|
|Gls2||glutaminase 2 (liver, mitochondrial)||0.000||0.001||3.080||0.000||0.000||2.430||0.000||0.000||2.210||0.000||0.000||2.700||0.000||0.025||2.050||0.000||0.003||2.080|
|Got1||glutamate oxaloacetate transaminase 1, soluble||0.000||0.009||3.130||0.000||0.001||2.310||0.000||0.000||4.230||0.000||0.002||4.020||0.004||0.121||4.300||0.000||0.000||4.130|
|Gsta4||glutathione S-transferase, alpha 4||0.000||0.000||2.510||0.000||0.000||2.690||0.003||0.070||1.400||0.000||0.000||1.910||0.000||0.035||1.510||0.000||0.018||1.760|
|Gstm2||glutathione S-transferase, mu 2||0.001||0.040||2.110||0.000||0.007||1.680||0.002||0.054||1.800||0.001||0.006||1.730||0.000||0.004||3.020||0.000||0.001||2.680|
|Gstm6||glutathione S-transferase, mu 6||0.001||0.023||2.030||0.000||0.002||2.030||0.000||0.015||2.300||0.002||0.009||1.840||0.000||0.001||3.030||0.000||0.000||2.880|
|Heatr1||HEAT repeat containing 1||0.000||0.001||2.110||0.000||0.011||1.520||0.000||0.000||1.690||0.002||0.009||1.370||0.000||0.003||1.550||0.000||0.001||1.750|
|Hgd||homogentisate 1, 2-dioxygenase||0.006||0.101||1.340||0.000||0.011||1.280||0.000||0.000||1.630||0.000||0.000||2.140||0.000||0.022||1.820||0.000||0.002||1.760|
|Hsd3b5||hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 5||0.009||0.129||−2.140||0.003||0.043||−13.12||0.000||0.002||−3.790||0.000||0.002||−2.400||0.000||0.003||−5.730||0.000||0.019||−12.07|
|Hsp90aa1||heat shock protein 90, alpha (cytosolic), class A member 1||0.002||0.044||−1.790||0.000||0.001||−2.030||0.000||0.016||−1.740||0.000||0.000||−3.640||0.006||0.149||−2.390||0.000||0.008||−2.220|
|Ikbkg||inhibitor of kappaB kinase gamma||0.000||0.002||−1.480||0.000||0.000||−1.640||0.005||0.085||−1.370||0.000||0.000||−1.750||0.002||0.080||−1.690||0.002||0.050||−1.380|
|Klc4||kinesin light chain 4||0.000||0.001||1.750||0.000||0.001||1.460||0.000||0.003||1.490||0.001||0.004||1.410||0.000||0.032||1.550||0.000||0.006||1.370|
|Lonp2||lon peptidase 2, peroxisomal||0.000||0.000||−2.040||0.000||0.000||−1.950||0.001||0.028||−1.450||0.001||0.005||−1.380||0.000||0.004||−1.790||0.000||0.002||−1.550|
|Mdh2||malate dehydrogenase 2, NAD (mitochondrial)||0.003||0.063||1.540||0.002||0.032||1.540||0.000||0.017||1.590||0.000||0.000||1.810||0.004||0.126||2.030||0.001||0.043||2.080|
|Mmd||monocyte to macrophage differentiation-associated||0.000||0.000||−1.760||0.001||0.023||−1.270||0.004||0.075||−1.320||0.000||0.002||−1.780||0.001||0.064||−1.300||0.000||0.001||−1.570|
|Mthfd1||methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase||0.003||0.068||1.510||0.000||0.008||1.680||0.000||0.022||1.410||0.000||0.000||2.820||0.001||0.054||1.740||0.009||0.137||1.380|
|Nadsyn1||NAD synthetase 1||0.000||0.008||1.790||0.000||0.008||1.610||0.004||0.072||1.380||0.000||0.000||1.570||0.003||0.099||1.610||0.000||0.024||1.360|
|Ndufs8||NADH dehydrogenase (ubiquinone) Fe-S protein 8||0.000||0.000||1.530||0.008||0.085||1.270||0.001||0.025||1.260||0.006||0.025||−1.210||0.004||0.126||1.310||0.000||0.016||1.260|
|Ngef||neuronal guanine nucleotide exchange factor||0.000||0.002||2.140||0.000||0.000||2.100||0.000||0.003||1.470||0.000||0.000||1.930||0.003||0.094||1.360||0.001||0.027||1.340|
|Nkiras2||NFKB inhibitor interacting Ras-like protein 2||0.009||0.129||1.460||0.001||0.023||1.340||0.000||0.009||1.330||0.000||0.000||1.890||0.001||0.051||1.430||0.000||0.010||1.490|
|Nol8||nucleolar protein 8||0.002||0.043||−1.550||0.003||0.044||−1.390||0.000||0.010||−1.650||0.000||0.002||−1.680||0.003||0.094||−1.660||0.001||0.027||−1.730|
|Paox||polyamine oxidase (exo-N4-amino)||0.000||0.014||2.960||0.000||0.008||2.930||0.000||0.002||2.240||0.000||0.000||1.530||0.000||0.001||2.390||0.000||0.000||2.480|
|Paqr9||progestin and adipoQ receptor family member IX||0.000||0.003||−4.730||0.000||0.000||−3.590||0.001||0.025||−1.610||0.000||0.000||−3.550||0.005||0.131||−3.970||0.000||0.008||−1.770|
|Pcca||propionyl-Coenzyme A carboxylase, alpha polypeptide||0.000||0.018||1.510||0.000||0.005||1.330||0.000||0.001||1.390||0.000||0.000||1.840||0.001||0.045||1.450||0.000||0.009||1.480|
|Pctp||phosphatidylcholine transfer protein||0.000||0.000||−3.120||0.000||0.000||−1.610||0.001||0.040||−1.850||0.000||0.001||−2.950||0.000||0.027||−1.960||0.001||0.024||−1.380|
|Pdilt||protein disulfide isomerase-like, testis expressed||0.000||0.003||−3.470||0.001||0.023||−2.850||0.000||0.018||−2.100||0.000||0.000||−3.690||0.003||0.102||−2.180||0.009||0.135||−1.580|
|Pdzk1||PDZ domain containing 1||0.000||0.002||−1.550||0.001||0.028||−1.410||0.000||0.002||−1.470||0.004||0.018||−1.300||0.001||0.061||−1.480||0.000||0.009||−1.310|
|Pgam1||phosphoglycerate mutase 1||0.000||0.014||1.680||0.000||0.003||1.420||0.000||0.005||1.390||0.003||0.016||1.400||0.000||0.005||1.640||0.000||0.003||1.500|
|Pgk1||phosphoglycerate kinase 1||0.001||0.034||1.450||0.000||0.002||1.180||0.000||0.006||1.230||0.000||0.000||1.700||0.000||0.036||1.410||0.001||0.044||1.290|
|Pla2g16||phospholipase A2, group XVI||0.000||0.006||2.180||0.002||0.033||1.840||0.000||0.003||1.590||0.000||0.000||2.210||0.000||0.038||2.060||0.000||0.005||1.930|
|Ppif||peptidylprolyl isomerase F (cyclophilin F)||0.000||0.004||1.790||0.001||0.024||1.390||0.001||0.027||1.320||0.000||0.000||2.080||0.001||0.048||1.580||0.000||0.006||1.330|
|Ppp1r3g||protein phosphatase 1, regulatory (inhibitor) subunit 3G||0.000||0.013||2.540||0.000||0.001||8.450||0.000||0.018||3.460||0.000||0.000||3.080||0.001||0.066||2.750||0.001||0.045||4.010|
|Retsat||retinol saturase (all trans retinol 13,14 reductase)||0.000||0.000||−3.880||0.000||0.000||−1.590||0.001||0.026||−1.640||0.007||0.027||−1.400||0.001||0.047||−1.820||0.004||0.091||−1.450|
|Rilp||Rab interacting lysosomal protein||0.009||0.128||1.410||0.000||0.010||1.350||0.007||0.105||1.420||0.000||0.000||2.060||0.000||0.008||1.630||0.002||0.049||1.310|
|Sdhd||succinate dehydrogenase complex, subunit D, integral membrane protein||0.001||0.039||1.570||0.003||0.049||1.250||0.000||0.002||1.270||0.000||0.000||1.990||0.000||0.004||1.710||0.001||0.027||1.340|
|Selenbp1||selenium binding protein 1||0.000||0.001||2.430||0.000||0.000||2.240||0.000||0.005||1.800||0.003||0.015||1.810||0.004||0.121||1.530||0.000||0.000||1.800|
|Slc25a11||solute carrier family 25 (mitochondrial carrier oxoglutarate carrier), member 11||0.000||0.003||1.530||0.000||0.005||1.390||0.004||0.081||1.240||0.010||0.035||1.180||0.000||0.029||1.290||0.000||0.002||1.460|
|Slc25a12||solute carrier family 25 (mitochondrial carrier, Aralar), member 12||0.001||0.022||1.810||0.000||0.001||1.800||0.003||0.064||1.420||0.000||0.000||1.920||0.000||0.006||1.780||0.001||0.029||1.510|
|Slc25a20||solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20||0.000||0.001||−2.090||0.000||0.003||−1.590||0.002||0.052||−1.500||0.000||0.001||−2.070||0.001||0.053||−1.310||0.000||0.003||−1.620|
|Slc2a4||solute carrier family 2 (facilitated glucose transporter), member 4||0.006||0.102||2.460||0.000||0.002||3.060||0.007||0.111||1.750||0.004||0.018||2.000||0.000||0.018||2.410||0.000||0.003||2.820|
|Slc3a1||solute carrier family 3, member 1||0.000||0.002||3.170||0.000||0.001||1.740||0.001||0.032||2.740||0.000||0.000||3.020||0.000||0.009||2.100||0.000||0.001||2.630|
|Stt3b||STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)||0.000||0.002||−1.310||0.000||0.000||−1.410||0.001||0.027||−1.220||0.000||0.000||−1.440||0.003||0.106||−1.330||0.000||0.006||−1.260|
|Tsc22d1||TSC22 domain family, member 1||0.000||0.004||−3.210||0.000||0.001||−2.840||0.007||0.111||−1.660||0.000||0.002||−2.940||0.000||0.006||−2.640||0.004||0.088||−1.610|
|Tubb4b||tubulin, beta 4B class IVB||0.000||0.000||−2.190||0.000||0.000||−2.220||0.000||0.022||−1.680||0.001||0.007||−1.410||0.005||0.141||−1.510||0.004||0.087||−1.500|
|Txndc15||thioredoxin domain containing 15||0.001||0.024||−1.350||0.001||0.018||−1.280||0.000||0.017||−1.170||0.000||0.000||−1.750||0.003||0.096||−1.380||0.000||0.006||−1.490|
|Ube2d2a||ubiquitin-conjugating enzyme E2D 2A||0.002||0.048||−1.260||0.000||0.001||−1.310||0.001||0.033||−1.250||0.000||0.000||−1.930||0.003||0.094||−1.210||0.002||0.047||−1.350|
|Ube2e2||ubiquitin-conjugating enzyme E2E 2||0.000||0.000||−2.060||0.000||0.002||−1.780||0.003||0.066||−1.370||0.000||0.000||−2.310||0.000||0.009||−1.860||0.000||0.023||−1.420|
|Ubxn4||UBX domain protein 4||0.000||0.000||−1.660||0.000||0.000||−2.200||0.000||0.001||−1.500||0.010||0.035||−1.260||0.000||0.004||−1.720||0.000||0.003||−1.410|
|Ugt2b35||UDP glucuronosyltransferase 2 family, polypeptide B35||0.000||0.008||−1.660||0.000||0.003||−1.520||0.000||0.004||−1.840||0.000||0.000||−2.630||0.001||0.062||−2.000||0.000||0.007||−1.690|
|Table A3. O-PLS-DA model summary for discriminating plasma metabolic profiles based on targeted MS profiling and NMR analysis on the six tested animal strains.|
|NMR Diffusion edited||Q2Y||0.22||0.60||0.33||0.50||0.19||0.64|
|Table A4. O-PLS-DA model summary for discriminating for 1H-NMR profiling of urine, liver tissues for the C57BL6/J strain.|
phase liver tissue
phase liver tissue
© 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).