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J. Biol. Chem., Vol. 282, Issue 48, 35069-35077, November 30, 2007
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1
1







2
From the
Departments of
Nutrition, ¶Environmental Sciences and Engineering, and **Biostatistics, University of North Carolina, Chapel Hill, North Carolina 27599, the
Jackson Laboratory, Bar Harbor, Maine 04609, ||Columbia University College of Physicians & Surgeons, New York, New York 10025, and the 
Medical Research Council Clinical Sciences Centre, Imperial College of London, London W12 0NN, United Kingdom
Received for publication, January 17, 2007 , and in revised form, September 4, 2007.
| ABSTRACT |
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| INTRODUCTION |
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During fasting (a) the appearance in the circulation of glucose from the gastrointestinal tract is low, (b) the concentrations of circulating glucose and insulin are low, (c) circulating glucose is used for energy rather than storage, and (d) the circulating glucose used is replenished largely by liver glucose production, via gluconeogenesis and glycogenolysis. Thus, whole body glucose utilization may be lowered during fasting by decreasing glucose production. Whether fasting glucose production is decreased in long-lived mice is currently unknown.
Adiponectin, a hormone produced by adipose tissue, can lower glucose utilization by decreasing glucose production (14–16). Adiponectin is elevated in many long-lived mice (17, 18). The elevation of adiponectin in long-lived mice may also stimulate fatty acid utilization through its intracellular target, AMP-activated protein kinase (AMPK)3 (19–21).
Reducing the utilization of glucose for energy may increase longevity by lowering the production of oxygen radicals from the mitochondria (22, 23). The link between glucose utilization and oxygen radical production is demonstrable in bovine aortic endothelial cells (24). Compared with 5 mM glucose, the incubation of aortic endothelia in 30 mM glucose doubled the rate of glucose utilization and tripled reactive oxygen species. The elevation of reactive oxygen species by 30 mM glucose was blocked by 4-hydroxycyanocinnamic acid (4-OHCA), an inhibitor of pyruvate transport into the mitochondria. The link between low glucose utilization and longevity is supported by the observation that fasting glucose utilization in mice, rats, dogs, and humans, respectively, 20, 12, 4, and 2 mg/kg/min, correlates with the difference in longevity between these species (25–28).
In the present study, we set out to determine whether fasting glucose utilization is reduced in long-lived mice. We measured glucose utilization after food withdrawal in free moving long-lived Snell dwarf mice (29). We also investigated the mechanisms underlying the reduction of glucose utilization and whether low glucose and high fatty acid utilization could reduce oxygen radical production.
| EXPERIMENTAL PROCEDURES |
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Glucose Utilization in Vivo—Due to the small size of Snell dwarf mice, glucose utilization was measured by single injection of tracer instead of the primed infusion technique (30). Trace amounts of carbon-3-labeled [3H]glucose (PerkinElmer Life Sciences) in saline (50–100 µl) were injected directly into the circulation of conscious free moving mice through the ophthalmic plexus (31). Blood samples (10–20 µl) were collected from the tail tip at 3, 6, 9, 12, 15, 18, and 21 min after injection for the measurement of (a) glucose by a hand-held glucose meter and (b) radioactivity by scintillation counter (15, 16). The glucose meter (Johnson & Johnson) showed comparable accuracy and reproducibility to colorimetric assays. High-performance liquid chromatography analysis was performed to verify that the radioactivity measured in dried plasma by scintillation counter represented [3H]glucose. We used an Agilent 1100 high-performance liquid chromatography system connected to a beta-RAM Model 2B Detector (IN/US Systems) and an Aminex HPX-87C polystyrene divinylbenzene resin column (Bio-Rad) at 80 °C using a 0.6 ml/min flow of water. Blood collected immediately before [3H]glucose injection was used to measure insulin and adiponectin by radioimmunoassay (Linco) and Western blot analysis, respectively (17). Mutant and control mice were always paired for the measurement of glucose utilization.
Calculations—The disappearance of radioactivity in plasma exhibited single phase exponential kinetics according to ln(Ei) =-kt + ln(Eo), where Ei is [3H]glucose in plasma at time i, k is the fractional elimination constant (min-1), t is the time after [3H]glucose injection (min), and Eo is the initial [3H]glucose in plasma at time 0. Glucose utilization was calculated by multiplying k with the total pool of circulating glucose (Q) and dividing by the body weight (32). The pool of circulating glucose was estimated from the initial dilution of the tracer.
Contribution of Gluconeogenesis and Glycogenolysis to Glucose Production—Plasma glucose produced by gluconeogenesis and glycogenolysis was measured in free moving Snell dwarf and control mice by measuring 2H enrichment of plasma glucose on carbons 5 and 2 (33). Enrichment (
5%) of body water by 2H2O was achieved by intraperitoneal injection of 2H2O (0.015 x body weight) and the provision of 5% 2H2O drinking water at 10 a.m. The 2H2O enrichment of body water was confirmed by mixing plasma, collected 1–3 p.m., with calcium carbide to form acetylene gas (34). Acetylene gas was analyzed by GC/MS using an EC5 Alltech Econo-CAP column (30 m x 0.32 mm, film thickness of 1 µm) at 200 °C. Acetylene and [2H]acetylene were measured by monitoring m/z 26 and 27, respectively. To measure 2H enrichment of circulating glucose on carbons 5 and 2, plasma (100 µl) was deproteinated by ZnSO4/Ba(OH)2 and deionized through an AG-1-X8 (COO- form) over an AG-50W-X8 (H+ form) resin column (Bio-Rad). For the measurement of 2H labeling of glucose on carbon 5, glucose (50 µg) was converted to xylose. Oxidation yielded formaldehyde that contained carbon 5 of glucose and its hydrogen. Six formaldehydes in NH4OH were condensed to produce solid hexamethylenetetramine (HMT). HMT was dissolved in dichloromethane and analyzed by GC/MS using an EC5 Alltech Econo-CAP column (30 m x 0.32 mm, film thickness of 1 µm) operated at 60 °C for 1 min followed by an increase to 300 °C at 10 °C/min under 2 ml/min He2 gas. HMT and [2H]HMT were measured by single ion monitoring of m/z 140 and 141, respectively. For the measurement of 2H labeling of glucose on carbon 2, glucose (10–20 µg) was reduced to sorbitol with NaHB4. The hydrogen on carbon 2 was transferred to lactate using sorbitol dehydrogenase and lactate dehydrogenase (Sigma). Lactate was derivatized and analyzed by GC/MS using a Pal A200 autosampler (Leap) and a Trace GC-2000 attached to a TSQ 7000 mass analyzer (ThermoFinnigan) under He2 gas (2 ml/min). In vivo measurements of gluconeogenesis were estimated by using carbon 5/carbon 2 enrichment instead of carbon 5/body water 2H2O to eliminate the diluting effect of glucose absorption from the gastrointestinal tract.
Glucose in Stomach Contents—Stomach contents were isolated from Snell dwarf and control mice after euthanasia and analyzed for glucose (35). In brief, stomach contents (50–250 mg) were digested in 1 N NaOH, and protein was precipitated out with 1 N perchloric acid. Glycogen was precipitated out of solution in ethanol and digested with 1 mg/ml amyloglucosidase (Sigma) in 0.5 M sodium acetate (pH 4.5) for 4 h at 55 °C before glucose was measured by colorimetric assay (Waco).
Body Composition—Percent body fat and body water were measured in conscious mice by magnetic resonance imaging using an Echo magnetic resonance imaging-100 QNMR system. Percentages of body fat and body water were also estimated from the radioactivity in a sample of plasma 1 h after 3H2O injection for verification.
Glucose Production in Vitro—Glucose production in McArdle 7777 rat hepatoma cells was determined as previously described with minor modifications (14). Cells were thawed from liquid nitrogen storage upon rat tail collagen I-coated plates. Cells equilibrated for 24 h in high glucose (25 mM) Dulbecco's Modified Eagle Medium (DMEM) supplemented with 2.5% fetal bovine serum (FBS) and 2.5% horse serum (HS). After equilibration, cells were split into 12-well plates at a density of 2.5 x 104 cells/well and allowed 2–3 h for adherence. The media was changed to serum-free low glucose (5 mM) DMEM. After 8 h, adipocyte conditioned media (ACM) with or without adiponectin (ACM-adiponectin) was added. Media and cell lysates were collected 8 h later. Colorimetric assay kits were used to determine glucose in the media (Waco) and cell protein content (Pierce). ACM-adiponectin was produced by depleting adiponectin from ACM by immunoprecipitation using rabbit antisera produced with the peptide antigen EDDVTTTEELAPALV, representing adiponectin residues 18–32. Preimmune rabbit serum was used as a control.
Retroviral Transduction in Vitro—A DNA construct encoding a dominant negative AMPK mutant (DN-AMPK) was used to generate a 5'-EcoRI/3'-SacII DN-AMPK fragment (36). The fragment was cloned into a retroviral shuttle vector pML2(EGFP-N1) producing DN-AMPK-pML2(EGFP-N1). HEK293 cells were transfected with a 3:1 ratio of DN-AMPK-pML2(EGFP-N1) and pCL-Eco, encoding the ecotropic envelope protein (Imgenex), using FuGENE transfection reagent (Roche Applied Science). HEK293 cells were incubated at 37 °C for 48 h. Media was changed, and cells were placed at 32 °C for 48 h to allow for retroviral production. The media containing virus (6 ml) was mixed with Polybrene (2.67 µg) and centrifuged at 3500 rpm for 5 min at room temperature. The supernatant was introduced to actively growing hepatoma cells (2 ml/well of 6-well plate) for 12–18 h at 37 °C. Medium was replaced with DMEM/FBS/HS. Overexpression of DN-AMPK was verified by EGFP and PCR (data not shown). The pML2(EGFP-N1) construct was used as a control for effects of retroviral transduction.
Fatty Acid Utilization in Vivo—Trace amounts of carbon-1-labeled [14C]oleic acid (PerkinElmer Life Sciences) were dried under nitrogen gas and allowed to equilibrate in plasma for 1 h at 37 °C. The utilization of circulating oleic acid was measured in conscious free moving Snell dwarf and control mice by injecting [14C]oleic acid directly into the circulation through the ophthalmic plexus. Blood samples (25–50 µl) were collected from the tail tip at 5, 15, 30, 55, and 70 min after injection to measure (a) free fatty acids by colorimetric assay (Waco) and (b) radioactivity by scintillation counting (16). To verify that the radioactivity in plasma represented [14C]oleic acid, high-performance liquid chromatography analysis was performed at room temperature on a Zorbax SB-Aq column (Agilent) under 1.5 ml/min 90:9:1 acetonitrile:water:acetic acid. GC/MS analysis revealed oleic acid represented
15–16% of circulating fatty acids in Snell dwarf and control mice in the 0- and 70-min blood samples (37). Snell dwarf and control mice were always paired for the measurement of fatty acid utilization. The measurement of glucose and fatty acid utilization by [3H]glucose and [14C]oleic injection was based on similar tracer analysis assumptions, including: 1) the tracer is homogeneously mixed in the circulation, 2) the tracer is metabolically indistinguishable from glucose or oleic acid, and 3) the production of [14C]oleic acid or [3H]glucose by isotope exchange is insignificant.
Intracellular Triacylglycerol and Acetyl-CoA Carboxylase—Intracellular triacylglycerol content in liver and heart was determined by homogenizing freeze-clamped tissue stored at -80 °C in 2:1 chloroform/methanol. Briefly, tissue homogenates were mixed with 0.9% NaCl before the lipid extract was dried and analyzed for triacylglycerol by enzymatic colorimetric assay (Waco). Liver acetyl-CoA carboxylase (ACC) and phosphorylated ACC was measured by Western blot analysis (17). Antibodies against ACC were commercially available (Cell Signaling).
Protein Carbonyl Content—Protein carbonyl groups were derivatized with 2,4-dinitrophenylhydrazine, producing dinitrophenylhydrazone products that were quantified by spectrophotometric analysis (38). Mouse liver and McArdle 7777 rat hepatoma cells were analyzed according to the manufacturer's protocol for the Protein Carbonyl Assay Kit (Cayman Chemical). Mouse liver (50–150 mg) was homogenized in 2.5 M hydrochloric acid with or without 2,4-dinitrophenylhydrazine. Rat hepatoma cells were scraped off collagen-coated plates, split in two tubes, and centrifuged at 14,000 rpm for 5 min at 4 °C. Cell pellets were either dissolved in 2,4-dinitrophenylhydrazine or 2.5 M HCl. Samples were vortexed and incubated in the dark for 1 h at room temperature. Homogenates received 20% trichloroacetic acid and incubated on ice for 5 min. Samples were centrifuged at 14,000 rpm for 10 min at 4 °C. Pellets were dissolved in 10% trichloroacetic acid and incubated 5 min on ice. Samples were centrifuged at 14,000 rpm for 10 min at 4 °C. Pellets were dissolved in ethanol:ethyl acetate (1:1). Samples were centrifuged at 14,000 rpm for 10 min at 4 °C. Pellets were resuspended in guanidine-HCl and centrifuged at 14,000 rpm for 10 min at 4 °C. The supernatant was split and analyzed by a spectrophotometer (415 nm). Protein concentrations were determined by BCA assay (Pierce).
Glucose versus Fatty Acid Utilization in Vitro—Rat hepatoma cells were thawed from frozen vials into DMEM/FBS/HS. Cells were allowed to adhere overnight onto plastic tissue culture plates and split into 12-well plates (2.5 x 104 cells/well). Medium was removed after 24 h, and cells were treated with high glucose media (20 or 40 mM). The final media contained 0 or 0.5 mM oleic acid, 1% fat-free bovine serum albumin, 0.1 mM L-carnitine, and 0, 0.1 or 1.0 mM etomoxir (Sigma). Glucose and oleic acid in the media offered cells two sources of calories.
Steady-State Levels of H2O2 per ATP in Bovine Aortic Endothelial Cells—Bovine aortic endothelial cells were plated at 5 x 104 cells/well in DMEM/30 mM glucose and HS/FBS for 16 h followed by DMEM/5 mM glucose for 8 h. Cell medium was replaced with DMEM/5 mM glucose/1 mM carnitine/0.1 mM oleate/[14C]oleate/1% bovine serum albumin (fatty acid free). 4-Hydroxycyanocinnamic acid (Bruker) was included in the final media at concentrations indicated. Cells were harvested after 8 h to measure steady-state levels of H2O2 by colorimetric assay (BioAssay Systems) and ATP by luminescence assay (Promega). The media was mixed with perchloric acid (5:1) to isolate 14C-labeled acid-soluble metabolites (ketone bodies) and estimate β-oxidation (39).
Statistical Analysis—Student's t test was used to identify significant differences when data within groups showed a normal distribution and Wilcoxon-Rank Sum test was used when data did not show a normal distribution. p values less than 0.05 were considered significant.
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| RESULTS |
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The utilization rate of plasma glucose was 60% lower in Snell dwarf mice than their litter mate controls (3.6 ± 0.4 versus 9.2 ± 1.0 mg/kg/min, p < 0.05, Fig. 2A). During the measurement of glucose utilization, the stomach of Snell dwarf and control mice contained small amounts of amylase digestible starch (Fig. 2B). Therefore, in addition to gluconeogenesis and glycogenolysis, the absorption of glucose from the gastrointestinal tract may have contributed to the production of plasma glucose. Snell dwarf and control mice were 21–25% body fat by magnetic resonance imaging. The level of radioactivity measured in plasma after 3H2O injection supported that percent body fat was similar between Snell dwarf and control mice. We further investigated (a) the mechanisms that suppressed glucose utilization and (b) the possible link between low glucose utilization and longevity.
Low utilization of plasma glucose indicates a low rate of glucose production is needed to maintain a stable concentration of circulating glucose. Thus, we inquired whether the production of plasma glucose was suppressed by the inhibition of gluconogenesis and glycogenolysis, the main sources of glucose in the fasting state. 2H labeling of plasma glucose by 2H2O indicated that 50% of endogenous glucose production was derived by gluconeogenesis and 50% by glycogenolysis in both Snell dwarf and control mice. Therefore, glucose production in Snell dwarf mice was suppressed by a mechanism that did not change the percentage of glucose from gluconeogenesis and glycogenolysis.
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Our observations in Snell dwarfs and hepatoma cells suggested that the switch from glucose to fatty acid utilization after food withdrawal may reduce oxygen radical production. We are unaware of any previous studies that tested whether the aerobic metabolism of glucose can lead to greater oxygen radical production than the aerobic metabolism of fatty acids. Thus, we also measured steady-state levels of H2O2 per ATP in primary bovine aortic endothelial cells. 4-OHCA, a pyruvate transport inhibitor, lowered H2O2 per ATP (Fig. 5C). 4-OHCA increased fatty acid oxidation, estimated by ketone body production (data not shown).
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| DISCUSSION |
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The elevation of adiponectin in Snell dwarf mice may increase insulin inhibition of glucose production and thereby contribute to the reduction of fasting glucose utilization. Euglycemic clamp experiments previously showed that rapid elevation of adiponectin, 3-fold over baseline, increases insulin inhibition of glucose production without altering insulin-mediated glucose uptake (15). Euglycemic clamp experiments showed the same result in adiponectin transgenic mice that exhibit a chronic 3-fold elevation of adiponectin (16). The reduction of fasting glucose utilization observed in adiponectin transgenic mice, in the present study, suggests that the 3-fold elevation of adiponectin in Snell dwarfs is exerting an inhibitory effect on glucose production during fasting (Fig. 2A). In vitro data, presented here and elsewhere, obtained under conditions that resemble the fasting state (low glucose and insulin), support the hypothesis that adiponectin lowers glucose production during fasting (14).
Glucose production can be suppressed by the reduction of gluconeogenesis or glycogenolysis (45, 46). Our in vivo isotope labeling analysis indicated that the suppression of glucose production in Snell dwarfs is mediated without any change in the percent glucose from gluconeogenesis and glycogenolysis. Our in vitro isotope-labeling studies also indicated that adiponectin lowers glucose production without altering the percent glucose from gluconeogenesis and glycogenolysis. Thiazolidinediones, pharmacologic agents widely prescribed for the treatment of insulin resistance in type-2 diabetics, increase adiponectin and lower fasting glucose utilization (47, 48). These observations support that elevated adiponectin may contribute to the reduction of glucose production in Snell dwarfs and possibly other long-lived models that exhibit elevated adiponectin (17, 18).
Previous studies in mice show that adiponectin suppression of glucose production can be blocked by the ablation of the AMPK gene (49). We showed that the inhibition of glucose production by adiponectin in vitro was blocked by the expression of a dominant negative AMPK mutant (36). Studies in isolated hepatocytes showed the inhibition of AMPK can block adiponectin suppression of mRNA encoding phosphoenol-pyruvate carboxykinase and glucose-6-phosphatase, two rate-limiting enzymes in gluconeogenesis (20).
AMPK activation by adiponectin may also play a role in the elevation of fatty acid utilization in Snell dwarf mice. AMPK phosphorylates ACC and malonyl-CoA decarboxylase, lowering malonyl-CoA, a precursor in fatty acid synthesis and potent inhibitor of mitochondrial carnitine palmitoyltransferase-1, the long-chain fatty acyl-CoA transporter (50). In the present study, increased phosphorylation of ACC is consistent with the elevation of fatty acid utilization and the reduction of intracellular lipid stores in Snell dwarf liver and heart (Fig. 4). Gene expression array data in Snell dwarf and other long-lived mice, including the Ames dwarf, little, and growth hormone receptor-null mice, support the conclusion that fatty acid oxidation is elevated in these long-lived mice (51).
Whether the aerobic metabolism of glucose leads to more oxygen radical production than fatty acid oxidation is not known. We present three results that suggest glucose and fatty acid oxidation could differentially affect oxygen radical production: 1) low glucose and high fatty acid utilization correlated with a low level of oxygen radical damage in Snell dwarf mice (Fig. 5A), 2) oxygen radical damage increased with the elevation of glucose, the absence of fatty acids from the media and pharmacologic inhibition of fatty acid oxidation in hepatoma cells (Fig. 5B), and 3) pharmacologic inhibition of glucose oxidation lowered H2O2 per ATP in bovine aortic endothelial cells (Fig. 5C).
Aerobic metabolism of nutrients for ATP is associated with oxygen radical production and secondary chemical modifications of DNA, lipids, and proteins, potentially accelerating aging (52). Oxygen radicals modify the side chains of lysine, arginine, proline, and histidine residues, resulting in the appearance of protein carbonyl groups, a chemical modification that increases with aging (53). In the present study, reduced protein carbonyl content in Snell dwarf mouse liver is consistent with a decrease in oxygen radical production (Fig. 5A). Other studies also indicate that oxidative damage is reduced in Snell dwarfs. (54, 55).
Our data in hepatoma cells suggest that high glucose utilization can increase oxygen radical levels in vitro (Fig. 5B). We raised glucose utilization by increasing the concentration of glucose and reducing the concentration of fatty acids in the media or adding etomoxir, an inhibitor of fatty acid oxidation and stimulator of glucose utilization (56). Etomoxir effects in HepG2 cells support that the reduction of fatty acid utilization elevates oxygen radical damage (57).
Superoxide anions are produced during ATP production by oxidative phosphorylation as electrons from NADH and FADH2 leak across the inner mitochondrial membrane and react directly with O2, forming superoxide, instead of with O2 and hydrogen ions to form water (58). Hydrogen peroxide (H2O2) is formed from superoxide anions by superoxide dismutase (59). In bovine aortic endothelial cells, 4-OHCA, an inhibitor of glucose oxidation, lowered H2O2 per ATP (Fig. 5C). Energy from glucose metabolism may generate more superoxide anions than fatty acid metabolism, because 1) NADH is oxidized by complex I, the site of highest electron leakage and superoxide anion synthesis and 2) glucose is oxidized by a higher NADH to FADH2 ratio (60–62). Glucose yields 38 ATP from an NADH to FADH2 ratio of 10:2 {4 ATP from substrate level phosphorylation (2 by glycolysis, 2 by Krebs cycle), 30 ATP from 10 NADH (2 by glycolysis and 8 by Krebs cycle), and 4 ATP from 2 FADH2 (2 by Krebs cycle)}. Palmitic acid, a long-chain fatty acid, yields 112 ATP from an NADH to FADH2 ratio of 28:14 {84 ATP from 28 NADH (7 by β-oxidation, 21 by Krebs cycle) and 28 ATP from 14 FADH2 (7 by β-oxidation, 7 by Krebs cycle)}. Fatty acids also activate uncoupling proteins, which reduce oxygen radical production by depolarizing the inner mitochondrial membrane (63). A shift in substrate utilization may underlie the reduction of oxygen radical production in human myotubes exposed to adiponectin (64). However, further research is needed to resolve whether ATP production from glucose is actually a greater source of oxygen radicals than ATP production from fatty acids.
The suppression of glucose utilization in Snell dwarf mice was also linked to the reduction of circulating glucose. In clinical studies, both fasting glucose and hemoglobin A1c increase with aging even in the absence of diabetes (65). Thus, we postulated that the reduction of circulating glucose in the long-lived mice may reduce the frequency of glycations. A previous study showed that both circulating glucose and hemoglobin A1c are reduced in young calorie restricted rats (66). However, in the present study hemoglobin A1c was 4–5% in both Snell dwarf and control mice. We did not check the levels of N-carboxymethyllysine, pentosidine, or methylglyoxal to confirm that other glycation end-products were not reduced in Snell dwarfs.
Our measurements of fasting glucose utilization represent the first data obtained by a single injection of [3H]glucose in mice. This method shows that fasting glucose utilization in mice is
10 mg/kg/min. Fasting glucose utilization values obtained by constant infusion of [3H]glucose, a widely used technique, tend to be higher. Fasting glucose utilization values may be higher when measured by constant infusion of tracer because of the surgery needed to insert an intravenous catheter into a mouse. After all, elevated carbohydrate metabolism and insulin resistance are characteristic features of the surgical recovery phase (67). The administration of anticoagulants, needed to maintain an open catheter in mice, may also increase carbohydrate metabolism, because anticoagulants, like heparin, disrupt cell-associated lipoprotein lipase activity and can thereby lower fatty acid metabolism (68). These factors may not be an issue when intravenous catheters are used in larger organisms.
Many studies suggest that energy expenditure per unit body weight does not differ between long-lived and control mice. For example, based on daily food intake, the average energy expenditure in Ames dwarf mice and control mice is
325 cal/kg/min (69). Our measurements indicate that fasting glucose utilization in mice is
10 mg/kg/min (40 cal/kg/min). Thus, we estimate that fasting glucose utilization accounts for 15–20% of the total daily energy expenditure in control mice and 5–7% in Snell dwarfs. The concept that total energy expenditure per body weight is not reduced in long-lived models is corroborated in calorie restricted rats (70).
In summary, Snell dwarf mice exhibit reduced glucose utilization and elevated fatty acid utilization during fasting. High levels of circulating adiponectin may contribute to the switch in substrate utilization. The reduction of glucose utilization and elevation of fatty acid utilization during fasting may increase longevity in Snell dwarf mice by decreasing oxygen radical production.
| FOOTNOTES |
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1 Both authors contributed equally to this work. ![]()
2 To whom correspondence should be addressed: Dept. of Nutrition, School of Medicine, School of Public Health, University of North Carolina, Chapel Hill, NC 27599-7461. Tel.: 919-966-7235; Fax: 919-966-7216; E-mail: terrycombs{at}unc.edu.
3 The abbreviations used are: AMPK, AMP-activated protein kinase; 4-OHCA, 4-hydroxycyannocinnamic acid; ACC, acetyl-CoA carboxylase; ACM, adipocyte-conditioned media; FBS, fetal bovine serum; GC/MS, gas chromatography and mass spectrometry; HMT, hexamethylenetetramine; HS, horse serum; DMEM, Dulbecco's modified Eagle's medium; DN, dominant negative; EGFP, enhanced green fluorescent protein. ![]()
| ACKNOWLEDGMENTS |
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