Exercise is a stimulus capable of challenging mitochondria, causing adaptation to meet the demand for adenosine triphosphate (ATP) production (8). It is well known that exercise training can elicit increases in skeletal muscle mitochondrial content and function to maximize oxidative capacity and substrate utilization for ATP synthesis (10,11,18,21). However, much less is known about the adaptations induced by exercise training on hepatic mitochondria. In the liver, mitochondrial ATP production serves other functions during exercise. The liver plays a vital role in maintaining circulating blood glucose levels through the activation of gluconeogenesis during times of fasting or exercise. Hepatic mitochondria fuel these energy costly gluconeogenic processes with ATP formation in part through the oxidation of fatty acids that are lipolyzed from hepatic and adipose stores (6).
Emerging evidence suggests that exercise training can induce adaptations in markers of hepatic mitochondrial content and function. Eight weeks of treadmill running has been shown to increase hepatic cytochrome c oxidase activity (29) and increase the activity of mitochondrial complexes I, IV, and V in the liver compared with sedentary rats (37). In addition, 10 wk of resistance training in ovariectomized rats significantly increased hepatic β-hydroxyacyl-CoA dehydrogenase (β-HAD) activity and CPT-1 mRNA expression (12). Furthermore, we have previously shown that voluntary wheel running increased several indices of hepatic mitochondrial content and function, including complete palmitate oxidation, β-HAD and citrate synthase activities, and COX IV subunit I and cytochrome c protein content in the Otsuka Long-Evans Tokushima fatty rat model (31,33). In addition, we have also found similar results in lean Fischer 344 x Brown Norway F1 hybrid rats who underwent 6 wk of voluntary wheel running, where hepatic PGC-1α mRNA expression and palmitate oxidation were increased in running compared with sedentary rats (22). In addition, rats that are bred for high running capacity, and therefore have a phenotype characteristic of an exercise-trained animal, also display higher palmitate oxidation and mitochondrial content compared with rats bred for low running capacity in a sedentary state (38). In total, these studies suggests that daily exercise leads to enhanced hepatic mitochondrial function; however, more thorough studies need to be conducted to elucidate the different aspects of mitochondrial function that are influenced by exercise training.
The purpose of this investigation was to examine and compare the impact of voluntary wheel running and daily treadmill exercise on hepatic mitochondrial content and function, as assessed by mitochondrial respiration, palmitate and pyruvate oxidation, and mitochondrial enzyme activities in healthy Sprague–Dawley rats. Endurance and interval sprint training treadmill exercise, two common forms of exercise training, were used because these two forms of exercise tend to rely on different substrate use (fatty acids vs glucose, respectively). Furthermore, we sought to maximize the hepatic gluconeogenic effect in one of two voluntary wheel running groups by removing the food just before the dark cycle, therefore causing the rats to run nightly in the fasted state. We hypothesized that the combination of exercise and fasting would maximize the need for hepatic gluconeogenesis to maintain euglycemia, resulting in additional mitochondrial adaptations in the liver. We also hypothesized that while all forms of training would have beneficial effects on hepatic mitochondria, voluntary wheel running would have the greatest impact due to a higher volume of daily exercise.
The animal protocol was approved by the Institutional Animal Care and Use Committee at the University of Missouri–Columbia and adhered to the animal care standards of the American College of Sports Medicine. Forty-six male Sprague–Dawley rats (12 wk of age) were randomly assigned (n = 8–10 per group) into sedentary (SED), voluntary wheel running (VWR), voluntary wheel running with overnight fasting (VWR-OF), treadmill endurance training (TM-END), or treadmill interval sprint training (TM-IST) groups for a 4-wk intervention. All rats were individually housed during the intervention in temperature controlled animal quarters (21°C) with a 0600- to 1800-h light cycle and an 1800- to 0600-h dark cycle. All groups were provided standard rodent chow (Formulab 5008; Purina Mills, Brentwood, MO) for ad libitum feeding in new cages at the beginning of each week. Rats assigned to the voluntary wheel running groups (VWR, VWR-OF) were housed in cages equipped with voluntary running wheels. Running wheel revolutions were monitored and counted continuously through the 4-wk intervention using VitalView software (VitalView, Version 4.2, 2007; Mini Mitter Company, Inc., Bend, OR). The food of the VWR-OF rats was pulled at 1700 h and returned the next morning at 0800 h. The TM-END and the TM-IST animals were acclimated to the treadmill for 5 d at a speed 15 m·min−1 for 5–10 min. The first week and a half of the intervention was a ramp-up phase for both treadmill groups. The TM-END group started at 20 m·min−1 for 10 min at a 12% gradient and gradually increased to 30 m·min−1 for 60 min (12% gradient), 5 d·wk−1 for the remainder of the 4-wk intervention. In a similar fashion, the TM-IST groups started with six sprints at 35 m·min−1, 1 min in duration (12% gradient), and 4.5-min rest in between sprints, then gradually increased to six 2.5-min sprints at 50 m·min−1 (12% gradient) with a 4.5-min rest in between sprints. Both treadmill groups completed the exercise training in the morning hours while still in the fed state. Body mass and food consumption were measured weekly throughout the investigation. To calculate feeding efficiency, a measurement that allows for the assessment of energy expenditure without direct or indirect calorimetry, the amount of body weight gained was divided by the amount of food consumed (g gain/g intake). At 16 wk of age, rats were anesthetized with pentobarbital sodium (100 mg·kg−1) and then exsanguinated by removing the heart 24 h after locking of wheels (VWR, VWR-OF) or the last bout of treadmill exercise (TM-END and TM-IST). Animals from each group (SED, VWR, VWR-OF, TM-END, and TM-IST) were killed after an 18-h fast. Retroperitoneal, epididymal, and omental adipose tissue fat pads were excised from exsanguinated rats and weighed.
Tissue homogenization and mitochondrial isolation procedures
Livers were quickly excised from anesthetized rats and either flash-frozen in liquid nitrogen or placed in ice-cold isolation buffer (in mM: 220 mannitol, 70 sucrose, 10 Tris base, and 1 EDTA, pH 7.4). Hepatic mitochondria were prepared as previously described (23,34). Briefly, 1 g of liver was minced in ice-cold mitochondrial isolation buffer (220 mM mannitol, 70 mM sucrose, 10 mM Tris base, and 1 mM EDTA, pH 7.4), transferred to a 30-mL glass tube, on ice, and homogenized with a Teflon pestle. The homogenate was then transferred to a 15-mL conical tube and centrifuged (1500g, 10 min, 4°C). The pellet was discarded, and the supernatant was centrifuged (8000g, 10 min, 4°C). The pellet was then resuspended in mitochondrial isolation buffer, homogenized in a glass tube using a glass pestle, and centrifuged (6000g, 10 min, 4°C). The pellet was again resuspended in mitochondrial isolation buffer containing fatty acid-free 0.1% BSA, homogenized with glass on glass homogenization, and centrifuged (4000g, 10 min, 4°C). Finally, the supernatant was discarded and the mitochondrial pellet was then split and placed in either 1000 μL of SET buffer (250 mM sucrose, 1 mM EDTA, 10 mM Trizma hydrochloride, and 2 mM ATP, pH 7.4) for palmitate and pyruvate oxidation experiments, or resuspended in MiPO3 buffer (0.5 mM EGTA, 3 mM MgCl2·6H20, 60 mM K-lactobionate, 20 mM taurine, 10 mM KH2P04, 20 mM HEPES, 110 mM sucrose, 1 g·L−1 BSA, 20 mM histidine, 20 μM vitamin E succinate, 3 mM glutathione, 1 μM leupeptine, 2 mM glutamate, 2 mM malate, and 2 mM Mg-ATP) for mitochondrial respiration. Protein concentration was determined by BCA assay.
Palmitate and pyruvate oxidation
Oxidation of [1-14C] palmitate (American Radiochemicals, St. Louis, MO), [1-14C] pyruvate (PerkinElmer, Boston, MA), and [2-14C] pyruvate (PerkinElmer) were measured in fresh isolated hepatic mitochondria preparations. The collection and measurement of 14C palmitate oxidation allowed for the estimation of complete fatty acid oxidation and was conducted as previously described (31), except a slight modification with the addition of 2 mM ADP. As previously described (23), pyruvate ([1-14C] and [2-14C]) were oxidized to 14CO2 by isolated hepatic mitochondria in the appropriate reaction buffer. [1-14C] pyruvate oxidation was used as an index of pyruvate dehydrogenase (PDH) activity, and [2-14C] pyruvate oxidation was used as an index of tricarboxylic acid (TCA) cycle flux (25).
Mitochondrial respiration was assessed using high-resolution respirometry (Oroboros Oxygraph-2k; Oroboros Instruments, Innsbruck, Austria). Isolated mitochondria (100–150 μg protein) were initially placed in respiration chambers in respiration media (MiR05; sucrose, 100 mM; K-lactobionate, 60 mM; EGTA, 0.5 mM; MgCl2, 3 mM; taurine, 20 mM; KH2PO4, 10 mM; HEPES, 20 mM; adjusted to pH 7.1 with KOH at 37°C; and 1 g·L−1 fatty acid–free BSA) for the assessment of basal respiration (Basal). Oxygen flux was measured by the addition of glutamate (5 mM) and malate (2 mM) to the chambers in the absence of ADP (GM-state 2) for the assessment of state 2 respiration. Oxidative phosphorylation (OXPHOS) with electron flux through complex I was then quantified by titration of ADP (25–125 μM) (GM + ADP: state 3-complex I) for the assessment of state 3 respiration. Maximal ADP respiration with electron flux through both complex I and complex II was assessed by the addition of succinate (10 mM) (succinate: state 3-complex I + II). Finally, the maximal capacity of the electron transport system was assessed by uncoupling with the addition of FCCP (carbonyl cyanide 4-(trifluoromethoxy) phenylhydrazone, 0.25 μM) (uncoupled).
Citrate synthase and β-hydroxyacyl-CoA dehydrogenase (β-HAD) activity
Hepatic citrate synthase and β-HAD activity were measured as previously described by Srere (36) and Bass et al. (4), respectively, as well as previously described by our laboratory (31).
PEPCK, G6Pase, and PGC-1α mRNA expression
Phosphoenolpyruvate carboxykinase (PEPCK) and glucose 6-phosphatase (G6Pase) mRNA expression was quantified as previously described (32). Briefly, to examine PEPCK and G6Pase, the primer dilution mix (nuclease-free water, and both forward and reverse primers [Sigma], Fast Sybr Green Master Mix kit [ABI]) and cDNA sample (50 ng) were loaded to a 96-well microplate and placed into the Roche Light Cycle 480 system (Roche, Rotkreuz, Switzerland) for polymerization. PGC-1α gene expression was assessed by loading TaqMan Master Mix (ABI), PGC-1α primers and probe (Life Technologies), and cDNA samples (250 ng) into a 96-well microplate and placed into the ABI 7500 Fast Sequence Detection System (Applied Biosystems, Carlsbad, CA) for polymerization. Once polymerization was completed, results were quantified using the DdCT technique relative to the 18S housekeeping gene.
Western blot analyses were performed to determine the protein content of the following: OXPHOS electron transport chain complexes I through V (MitoProfile Total OXPHOS Rodent WB Antibody Cocktail; Abcam, Cambridge, MA), peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α; EMD Millipore Corp., Billerica, MA), NAD-dependent deacetylase sirtuin 1 (SIRT1; Santa Cruz Biotechnology, Santa Cruz, CA), NAD-dependent deacetylase sirtuin 3 (SIRT3; Cell Signaling, Beverly, MA), cAMP-responsive element-binding protein (CREB and phospho-CREB(Ser133); Cell Signaling), AMP-activated protein kinase (AMPK and phospho-AMPK(Thr 172); Cell Signaling), and cytochrome c (Cell Signaling). Phosphorylation status (using phosphospecific antibodies) was calculated from the density of the phosphoprotein band divided by density of the total protein using the appropriate antibody (30,31). Membranes stained with 0.1% amido-black (Sigma) were quantified to control for differences in protein loading or transfer of band densities as previously described (31).
Each outcome measure was examined in 8–10 animals per group. Differences among groups were examined by a one-way ANOVA (IBM SPSS, version 20.0; SPSS, Chicago, IL), and significant main effects (P < 0.05) were followed with Fisher LSD post hoc comparisons. Values are reported as means ± SE, and a P value of ≤0.05 denotes a statistically significant difference.
VWR and VWR-OF groups ran ∼4 km·d−1 throughout the 4-wk intervention, and while running distance did not differ between groups in weeks 1–3, the VWR-OF group maintained daily running distance in week 4, whereas the VWR running distance decreased from weeks 3 to 4 (P < 0.05; Fig. 1A). The TM-END and the TM-IST groups ran 1.8 and 0.75 km·d−1, respectively. Heart weight-to-body weight ratio was significantly higher in VWR, VWR-OF, and TM-END groups compared with SED (P < 0.05; Fig. 1B).
The SED and VWR groups both weighed significantly more than the VWR-OF, TM-END, and TM-IST groups (Table 1). The SED group also developed significantly larger total fat pad (retroperitoneal, epididymal, and omental) mass than any exercise group (VWR, VWR-OF, TM-END, TM-IST; P ≤ 0.05), with VWR also being greater than the VWR-OF, TM-END, and TM-IST groups (P ≤ 0.05; Table 1). VWR rats consumed significantly more food per week than all other groups, whereas the SED group consumed significantly more food than the VWR-OF, TM-END, and TM-IST groups (Table 1). In addition, food consumption relative to body weight was significantly greater in the VWR rats compared with the SED, VWR-OF, TM-END, and TM-IST groups. Furthermore, both the SED and the VWR groups had significantly higher feeding efficiency than either treadmill group (TM-END and TM-IST; Table 1).
Markers of hepatic mitochondrial function
OXPHOS with electron flux through complex I (GM + ADP: state 3-complex I) and maximal uncoupled mitochondrial respiration (FCCP: uncoupled) were significantly (P < 0.05) increased in all four exercise groups compared with SED animals (Fig. 2A). In addition, maximal ADP respiration with electron flux through both complex I and complex II (succinate: state 3-complex I + II) was significantly increased in the VWR and VWR-OF groups but not in the treadmill-trained animals. [1-14C] pyruvate oxidation, an index of PDH activity, was significantly greater in the VWR-OF, TM-END, and TM-IST groups compared with SED (P ≤ 0.05; Fig. 2B). Furthermore, [2-14C] pyruvate oxidation, an index of TCA cycle flux, tended to be higher in the exercise groups compared with the SED rats as reflected by 30%–40% increases in the VWR, TM-END, and TM-IST groups, but this did not reach statistical significance (P = 0.075; Fig. 2C). Moreover, changes in [1-14C] palmitate oxidation did not reach statistical significance despite a 40% increase in the VWR compared with the SED group (Fig. 2D). However, incomplete palmitate oxidation was significantly reduced in VWR-OF, TM-END, and TM-IST animals compared with the SED group (P < 0.05; Fig. 2E). In addition, citrate synthase activity in whole liver homogenate was significantly higher in the VWR group compared with SED (P < 0.05, Table 1), whereas β-HAD activity did not differ among groups (Table 1).
Markers of hepatic mitochondrial content and biogenesis
Hepatic cytochrome c protein content, a marker of mitochondrial content, was significantly increased in the VWF-OF group only (P < 0.05 vs SED; Fig. 3A). PCG-1α protein content was assessed because of its role in mitochondrial biogenesis. Neither 4 wk of voluntary wheel running nor treadmill training was sufficient to alter hepatic PGC-1α protein content (Fig. 3B). In addition, no differences were detected among groups for hepatic SIRT-1 protein content (Fig. 3C), a protein responsible for deacetylating and increasing PGC-1α activation. We then measured hepatic SIRT3, a mitochondrial deacetylase that activates numerous mitochondrial proteins, to assess the potential activation of multiple mitochondrial proteins in response to exercise. SIRT3 protein content measured in isolated mitochondria was approximately twofold higher in the VWR, VWR-OF, and TM-END groups compared with the SED group (P < 0.05, Fig. 3D). Despite the increase in mitochondrial SIRT3, we found no differences in the acetylation status of the mitochondrial proteins with a Western blot for acetylated lysine (data not shown). There are reservations regarding the sensitivity of this technique, and it is possible that the acetylation status of specific mitochondrial proteins was changed but not detected using this method. An examination of the protein content of individual complexes in the electron transport chain (OXPHOS), as they are markers of mitochondrial content and potential targets of SIRT-3, revealed no significant effect of the various exercise training interventions (Fig. 3E). Finally, we also witnessed no differences in hepatic AMPK activation (phosphorylation status) among any of the exercise groups (data not shown).
Gluconeogenesis and the transcription factor CREB
To determine whether the VWR-OF treatment was effective in stimulating a pathway unique to gluconeogenesis, we measured the phosphorylation and activation of CREB, a transcription factor that up-regulates gluconeogenic genes. Voluntary wheel running with overnight fasting and treadmill endurance running caused greater than twofold increases in the ratio of phosphorylated CREB to CREB protein content compared with SED group (P ≤ 0.05; Fig. 4A). PGC-1α, PEPCK, and G6Pase mRNA expression were measured to examine whether the increases in phosphorylated CREB protein content resulted in the up-regulation of genes important to mitochondrial biogenesis and gluconeogenesis. PGC-1α gene expression followed a similar trend as phosphorylated CREB protein content, with increases seen in VWR-OF and TM-END animals (P < 0.05; Fig. 4B). In addition, PEPCK mRNA expression was significantly elevated only in the VWR-OF rats compared with the SED (Fig. 4C). G6Pase mRNA expression did not differ among groups (Fig. 4D).
It is well known that exercise training increases mitochondrial content (11) as well as improves mitochondrial function (10,18,21) in skeletal muscle. Surprisingly, little is known about the effects exercise training has on hepatic mitochondria. To our knowledge, this is the first study to examine the effects of multiple modalities of exercise training (voluntary wheel running and treadmill training) on hepatic mitochondrial content and function in healthy rats. A novel finding of this study is that different exercise modalities resulted in greater hepatic mitochondrial respiration and that each modality elicits effects on different indices of mitochondrial function. It also was found that exercise-induced increases in indices of hepatic mitochondrial function were not dependent on increases in hepatic mitochondrial content.
One of the most accurate methods used to assess mitochondrial function is the measurement of mitochondrial respiration (27). Here, we report novel findings that regardless of the training stimuli, the exercise intensity, or the fasting state of the animal, all four exercise groups (VWR, VWR-OF, TM-END, and TM-IST) significantly increased ADP-stimulated OXPHOS and maximal uncoupled hepatic mitochondrial respiration. These findings contradict those by Ascensao et al. (3), who found that state 3 and state 4 respiration were lower after 5 wk of treadmill training compared with the sedentary condition. Discrepancies between findings may be due to differences in respiration protocols. Furthermore, we found that mitochondrial respiration increased despite a lack of change in protein content in the electron transport chain complexes for our treadmill training groups compared with the SED group. These data suggest that complex activities increased independent of content. Findings from Sun et al. (37) demonstrate that 8 wk of treadmill training increased the activity of complexes I, IV, and V in the liver compared with sedentary rats. Unfortunately, OXPHOS protein content was not measured in their study to determine whether there is a correlation between complex content and function.
In the current study, palmitate oxidation tended to be elevated only in the VWR group (+40%) compared with the sedentary rats, whereas there was no apparent changes in the other exercising groups. Given our previously observations with 6, 16, and 36 wk of voluntary wheel running showing increases in hepatic palmitate oxidation (22,31,33), it is possible that 4 wk of exercise training is insufficient to elicit increases in this index of hepatic mitochondrial function. However, we found that voluntary wheel running in combination with overnight fasting and treadmill training (END and IST) resulted in significant decreases in incomplete palmitate oxidation. This is a unique observation given that it previously has been demonstrated that incomplete fatty acid oxidation products are linked to metabolic dysfunction and insulin resistance (19,20).
Both carbohydrate and fatty acid sources are ultimately transformed to acetyl-CoA and feed into the TCA cycle. Endurance exercise training has been shown to increase TCA cycle flux in skeletal muscle (5). Here, we found that VWR, TM-END, and TM-IST groups tended (P = 0.075) to increase [2-14C] pyruvate oxidation, an index of TCA cycle flux. In addition, the VWR-OF, TM-END, and TM-IST groups exhibited significant increases in [1-14C] pyruvate oxidation, an index of PDH activity, compared with the SED rats. The increase in PDH activity in these groups suggests greater reliance on carbohydrate as an energy source compared with the SED and VWR groups. The factors driving these differences in substrate oxidation are unknown but may be related to differences in substrate utilization patterns due to the various exercise modalities and disparities in food intake. The ratio of phosphorylated CREB to total CREB protein content is another sign of different metabolic regulation between groups. Phosphorylated CREB was not elevated in the VWR rats (group which had the greatest food intake) but was elevated in the VWR-OF and TM-END groups compared with the SED rats. CREB is a transcription factor that, once phosphorylated, is activated and up-regulates gluconeogenic genes during times of metabolic stress (2,16). Therefore, the increased phosphorylated CREB protein content suggests that VWR-OF and TM-END interventions resulted in greater reliance on gluconeogenic processes. This is further supported by the finding that PEPCK mRNA expression was significantly elevated in the VWR-OF groups. Conversely, G6Pase mRNA expression was not elevated in any group. This observation that some exercise stimuli (VWR-OF and TM-END) increase the ratio of phosphorylated CREB to CREB protein content and PEPCK mRNA expression (VWR-OF only), but not G6Pase, may suggest that gluconeogenic genes do not all respond in the same manner. Evidence of these differences in gluconeogenic enzyme responses to different stimuli has been previously reported (14).
We found that voluntary wheel running led to increases in cytochrome c protein content as well as citrate synthase activity (VWR group only). These findings are in agreement with previous rodent exercise training studies (9,14). Interestingly, Haase et al. (14) found that 5 wk of treadmill training increased cytochrome c in wild-type mice. This effect was abolished in PGC-1α knockout mice, indicating the potential necessity of PGC-1α for increases in cytochrome c. However, in the current study, hepatic PGC-1α protein content and protein content of the deacetylase SIRT-1 was not different among groups, yet the protein content of cytochrome c was elevated in the VWR groups. One possibility for this discrepancy is that there was already enough SIRT-1 protein content in liver and that the activity of this preexisting deactylase increased and activated PGC-1α without a need for increased PGC-1α protein levels. Future work is needed to examine the transcriptional regulation of changes in hepatic mitochondrial function induced by exercise.
Posttranslational modifications could be another factor playing a role in exercise-induced hepatic mitochondrial changes. In response to metabolic stressors, SIRT3 deacetylates and activates certain complexes in the electron transport chain as well as key proteins and enzymes involved in ATP production (1,7,13,17,24). Furthermore, it has been shown that in the absence of SIRT 3, hepatic ATP levels drop more than 50%, suggesting that SIRT 3 is essential for maintaining ATP levels (1). There is also some evidence that SIRT3 is capable of activating AMPK (26,28,35), which can initiate energy producing processes such as fatty acid oxidation (15). Here, increases in SIRT3 protein content in the VWR, VWR-OF, and TM-END groups suggest that these exercise interventions may be enhancing hepatic mitochondrial function through SIRT3-dependent deacetylation of mitochondrial proteins. However, Western blot analysis for acetylated-lysine content in the mitochondrial proteins failed to detect significant differences among the groups. Future investigation is warranted to examine the role of SIRT3 in exercise-induced hepatic mitochondrial adaptations.
Hepatic gluconeogenesis is an energy costly process and requires increases in mitochondrial respiration to generate ATP. The VWR-OF group was added to the current investigation to determine whether fasting in combination with exercise training would invoke the need for increased hepatic gluconeogenesis and further hepatic mitochondrial adaptations over VWR alone. Both the VWR-OF and the VWR resulted in similar increases in hepatic mitochondrial state 3-complex I + II and maximal uncoupled respiration. However, VWR-OF animals exhibited significant increases in [1-14C] pyruvate oxidation and significant reductions in incomplete palmitate oxidation compared with SED animal, which were not apparent in the VWR rats. Moreover, VWR-OF was the only intervention to significantly increase hepatic cytochrome c protein content. Furthermore, the VWR-OF group had greater PEPCK and PGC-1α mRNA expression than the VWR group, likely due to the greater increases seen in CREB phosphorylation. These data suggest that 4 wk of wheel running in a fasting condition evokes greater stimulation of gluconeogenic processes, likely leading to enhancement of hepatic mitochondrial content and function.
In conclusion, results from the present investigation indicate that various forms of exercise training increase indices of hepatic mitochondria metabolism and that these changes are not entirely dependent on changes in mitochondrial content. Regardless of the training stimuli, the exercise intensity, or the fasting state of the animal, exercise significantly improved hepatic mitochondrial respiration. Furthermore, exercise in the setting of a fasting condition appeared to up-regulate genes related to gluconeogenesis and mitochondrial biogenesis, suggesting potentially greater hepatic mitochondrial adaptation with more prolonged exercise training.
This work was supported by the National Institutes of Health grant nos. T32 AR 048523-07 (JAF and EMM), DK-088940 (JPT), and VHA-CDA2 1299-02 (RSR). The authors thank Tzu-Wen Liu, Timothy Tan, Raisa Buenaventura, and Kelly Stromsdorfer for excellent technical assistance to this work. This work was supported with resources and the use of facilities at the Harry S. Truman Memorial Veterans’ Hospital in Columbia, MO. The authors have no conflicts of interest to disclose. The results of the present study do not constitute endorsement by the American College of Sports Medicine.
1. Ahn BH, Kim HS, Song S, et al. A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis. Proc Natl Acad Sci U S A
. 2008; 105 (38): 14447–52.
2. Altarejos JY, Montminy M. CREB and the CRTC co-activators: sensors for hormonal and metabolic signals. Nat Rev Mol Cell Biol
. 2011; 12 (3): 141–51.
3. Ascensao A, Goncalves IO, Lumini-Oliveira J, et al. Endurance training and chronic intermittent hypoxia modulate in vitro salicylate-induced hepatic mitochondrial dysfunction. Mitochondrion
. 2012; 12 (6): 607–16.
4. Bass A, Brdiczka D, Eyer P, Hofer S, Pette D. Metabolic differentiation of distinct muscle types at the level of enzymatic organization. Eur J Biochem
. 1969; 10 (2): 198–206.
5. Befroy DE, Petersen KF, Dufour S, Mason GF, Rothman DL, Shulman GI. Increased substrate oxidation and mitochondrial uncoupling in skeletal muscle of endurance-trained individuals. Proc Natl Acad Sci U S A
. 2008; 105 (43): 16701–6.
6. Burgess SC, He T, Yan Z, et al. Cytosolic phosphoenolpyruvate carboxykinase does not solely control the rate of hepatic gluconeogenesis in the intact mouse liver. Cell Metab
. 2007; 5 (4): 313–20.
7. Cimen H, Han MJ, Yang Y, Tong Q, Koc H, Koc EC. Regulation of succinate dehydrogenase activity by SIRT3 in mammalian mitochondria. Biochemistry
. 2010; 49 (2): 304–11.
8. Constable SH, Favier RJ, McLane JA, Fell RD, Chen M, Holloszy JO. Energy metabolism in contracting rat skeletal muscle: adaptation to exercise
training. Am J Physiol
. 1987; 253 (2 Pt 1): C316–22.
9. da Silva LA, Pinho CA, Rocha LG, Tuon T, Silveira PC, Pinho RA. Effect of different models of physical exercise
on oxidative stress markers in mouse liver. Appl Physiol Nutr Metab
. 2009; 34 (1): 60–5.
10. Daussin FN, Rasseneur L, Bouitbir J, et al. Different timing of changes in mitochondrial functions following endurance training. Med Sci Sports Exerc
. 2012; 44 (2): 217–24.
11. Davies KJ, Packer L, Brooks GA. Biochemical adaptation of mitochondria, muscle, and whole-animal respiration to endurance training. Arch Biochem Biophys
. 1981; 209 (2): 539–54.
12. Domingos MM, Rodrigues MF, Stotzer US, et al. Resistance training restores the gene expression of molecules related to fat oxidation and lipogenesis in the liver of ovariectomized rats. Eur J Appl Physiol
. 2012; 112 (4): 1437–44.
13. Green MF, Hirschey MD. SIRT3 weighs heavily in the metabolic balance: a new role for SIRT3 in metabolic syndrome. J Gerontol A Biol Sci Med Sci
. 2013; 68 (2): 105–7.
14. Haase TN, Ringholm S, Leick L, et al. Role of PGC-1alpha in exercise
and fasting-induced adaptations in mouse liver. Am J Physiol Regul Integr Comp Physiol
. 2011; 301 (5): R1501–9.
15. Hardie DG, Carling D. The AMP-activated protein kinase-fuel gauge of the mammalian cell? Eur J Biochem
. 1997; 246 (2): 259–73.
16. Herzig S, Long F, Jhala US, et al. CREB regulates hepatic gluconeogenesis through the coactivator PGC-1. Nature
. 2001; 413 (6852): 179–83.
17. Hirschey MD, Shimazu T, Goetzman E, et al. SIRT3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation. Nature
. 2010; 464 (7285): 121–5.
18. Holloszy JO. Adaptation of skeletal muscle to endurance exercise
. Med Sci Sports
. 1975; 7 (3): 155–64.
19. Koves TR, Li P, An J, et al. Peroxisome proliferator-activated receptor-gamma co-activator 1alpha-mediated metabolic remodeling of skeletal myocytes mimics exercise
training and reverses lipid-induced mitochondrial inefficiency. J Biol Chem
. 2005; 280 (39): 33588–98.
20. Koves TR, Ussher JR, Noland RC, et al. Mitochondrial overload and incomplete fatty acid oxidation
contribute to skeletal muscle insulin resistance. Cell Metab
. 2008; 7 (1): 45–56.
21. Krieger DA, Tate CA, McMillin-Wood J, Booth FW. Populations of rat skeletal muscle mitochondria after exercise
and immobilization. J Appl Physiol
. 1980; 48 (1): 23–8.
22. Laye MJ, Rector RS, Borengasser SJ, et al. Cessation of daily wheel running differentially alters fat oxidation capacity in liver, muscle, and adipose tissue. J Appl Physiol (1985)
. 2009; 106 (1): 161–8.
23. Morris EM, Meers GM, Booth FW, et al. PGC-1alpha overexpression results in increased hepatic fatty acid oxidation
with reduced triacylglycerol accumulation and secretion. Am J Physiol Gastrointest Liver Physiol
. 2012; 303 (8): G979–92.
24. Nogueiras R, Habegger KM, Chaudhary N, et al. Sirtuin 1 and sirtuin 3: physiological modulators of metabolism. Physiol Rev
. 2012; 92 (3): 1479–514.
25. Noland RC, Koves TR, Seiler SE, et al. Carnitine insufficiency caused by aging and overnutrition compromises mitochondrial performance and metabolic control. J Biol Chem
. 2009; 284 (34): 22840–52.
26. Palacios OM, Carmona JJ, Michan S, et al. Diet and exercise
signals regulate SIRT3 and activate AMPK and PGC-1alpha in skeletal muscle. Aging (Albany NY)
. 2009; 1 (9): 771–83.
27. Perry CG, Kane DA, Lanza IR, Neufer PD. Methods for assessing mitochondrial function
in diabetes. Diabetes
. 2013; 62 (4): 1041–53.
28. Pillai VB, Sundaresan NR, Kim G, et al. Exogenous NAD blocks cardiac hypertrophic response via activation of the SIRT3-LKB1-AMP-activated kinase pathway. J Biol Chem
. 2010; 285 (5): 3133–44.
29. Quiles JL, Huertas JR, Manas M, Ochoa JJ, Battino M, Mataix J. Dietary fat type and regular exercise
affect mitochondrial composition and function depending on specific tissue in the rat. J Bioenerg Biomembr
. 2001; 33 (2): 127–34.
30. Rector RS, Thyfault JP, Laye MJ, et al. Cessation of daily exercise
dramatically alters precursors of hepatic steatosis in Otsuka Long-Evans Tokushima fatty (OLETF) rats. J Physiol
. 2008; 586 (Pt 17): 4241–9.
31. Rector RS, Thyfault JP, Morris RT, et al. Daily exercise
increases hepatic fatty acid oxidation
and prevents steatosis in Otsuka Long–Evans Tokushima fatty rats. Am J Physiol Gastrointest Liver Physiol
. 2008; 294 (3): G619–26.
32. Rector RS, Uptergrove GM, Borengasser SJ, et al. Changes in skeletal muscle mitochondria in response to the development of type 2 diabetes or prevention by daily wheel running in hyperphagic OLETF rats. Am J Physiol Endocrinol Metab
. 2010; 298 (6): E1179–87.
33. Rector RS, Uptergrove GM, Morris EM, et al. Daily exercise
vs. caloric restriction for prevention of nonalcoholic fatty liver disease in the OLETF rat model. Am J Physiol Gastrointest Liver Physiol
. 2011; 300 (5): G874–83.
34. Ruiz-Ramirez A, Chavez-Salgado M, Peneda-Flores JA, Zapata E, Masso F, El-Hafidi M. High-sucrose diet increases ROS generation, FFA accumulation, UCP2 level, and proton leak in liver mitochondria. Am J Physiol Endocrinol Metab
. 2011; 301 (6): E1198–207.
35. Shi T, Fan GQ, Xiao SD. SIRT3 reduces lipid accumulation via AMPK activation in human hepatic cells. J Dig Dis
. 2010; 11 (1): 55–62.
36. Srere PA. Citrate synthase. Methods Enzymology
. 1969; 13: 3–5.
37. Sun L, Shen W, Liu Z, Guan S, Liu J, Ding S. Endurance exercise
causes mitochondrial and oxidative stress in rat liver: effects of a combination of mitochondrial targeting nutrients. Life Sci
. 2010; 86 (1–2): 39–44.
38. Thyfault JP, Rector RS, Uptergrove GM, et al. Rats selectively bred for low aerobic capacity have reduced hepatic mitochondrial oxidative capacity and susceptibility to hepatic steatosis and injury. J Physiol
. 2009; 587 (Pt 8): 1805–16.