Figures
Abstract
In mice, certain proteins show a highly confined expression in specific muscle groups. Also, resting and exercise/contraction-induced phosphorylation responses are higher in rat skeletal muscle with low mitochondrial content compared to muscles with high mitochondrial content, possibly related to differential reactive oxygen species (ROS)-scavenging ability or resting glycogen content. To evaluate these parameters in humans, biopsies from soleus, gastrocnemius and vastus lateralis muscles were taken before and after a 45 min inclined (15%) walking exercise bout at 69% VO2max aimed at simultaneously activating soleus and gastrocnemius in a comparable dynamic work-pattern. Hexokinase II and GLUT4 were 46–59% and 26–38% higher (p<0.05) in soleus compared to the two other muscles. The type I muscle fiber percentage was highest in soleus and lowest in vastus lateralis. No differences were found in protein expression of signalling proteins (AMPK subunits, eEF2, ERK1/2, TBC1D1 and 4), mitochondrial markers (F1 ATPase and COX1) or ROS-handling enzymes (SOD2 and catalase). Gastrocnemius was less active than soleus measured as EMG signal and glycogen use yet gastrocnemius displayed larger increases than soleus in phosphorylation of AMPK Thr172, eEF2 Thr56 and ERK 1/2 Thr202/Tyr204 when normalised to the mean relative EMG-signal. In conclusion, proteins with muscle-group restricted expression in mice do not show this pattern in human lower extremity muscle groups. Nonetheless the phosphorylation-response is greater for a number of kinase signalling pathways in human gastrocnemius than soleus at a given activation-intensity. This may be due to the combined subtle effects of a higher type I muscle fiber content and higher training status in soleus compared to gastrocnemius muscle.
Citation: Jensen TE, Leutert R, Rasmussen ST, Mouatt JR, Christiansen MLB, Jensen BR, et al. (2012) EMG-Normalised Kinase Activation during Exercise Is Higher in Human Gastrocnemius Compared to Soleus Muscle. PLoS ONE 7(2): e31054. https://doi.org/10.1371/journal.pone.0031054
Editor: Jose A. L. Calbet, University of Las Palmas de Gran Canaria, Spain
Received: September 9, 2011; Accepted: December 31, 2011; Published: February 8, 2012
Copyright: © 2012 Jensen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the Danish Medical Research Council, The Lundbeck Foundation and NovoNordisk Foundation. TJ was supported by a postdoctoral fellowship from the Danish Medical Research Council. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Endurance exercise represents an immense stress to the working muscle due to the increased ATP demand used for ion-pumping and force generation and increased production of potentially harmful by-products such as reactive oxygen species (ROS). To minimise the homeostatic disturbance, the working muscle adapts acutely by a number of mechanisms directed at increasing energy substrate uptake and/or turnover [1]. In addition, repeated exercise bouts elicit changes in gene expression patterns that lead to mitochondrial biogenesis and increased expression of ROS-handling enzymes [1], [2]. Protein phosphorylation is indisputably the most studied mechanism for muscular signal transduction and muscle contraction has been documented to elicit a plethora of protein phophorylation events to elicit adaptations to exercise [3].
Rodent muscles have been used extensively to identify and characterise the ever-expanding kinase signalling networks activated by muscle contraction. Conceptually, muscles are often divided into slow-twitch (type I) and fast-twitch (type II) fibers dictated by their myosin heavy chain (MHC) isoform expression [4]. Human muscle groups are mostly a homogenous mix of slow and fast-twitch fibers whereas rodent muscle groups exhibit a more extreme division into either type I or type II fiber-dominated muscles [5]–[10].
In both rodents and humans, many endurance-training responsive proteins are expressed in an activity-pattern dependent manner, including glucose-handling proteins and mitochondrial markers [1]. However, in mice in particular, there are clearly also a number of proteins with expression confined to certain muscle groups. For instance, the gamma3 subunit of contraction-activated 5′-AMP-activated protein kinase (AMPK) and its downstream substrate protein, TBC1D1, is lowly expressed in mouse slow-twitch oxidative soleus compared to more fast-twitch glycolytic muscles [11]–[14]. Although MHC isoform-distribution is more mixed in humans than rodents, the expression of other potential muscle group-specific proteins may be controlled by distinct transcriptional regulators [4]. It is currently unknown whether any of the muscle group-restricted proteins in mice are enriched in certain muscle-groups in humans.
Recent rat studies have also suggested that both the resting and in situ contraction-induced phosphorylation of a number of kinases correlates inversely with the mitochondrial content of different parts of the tibialis anterior muscle [15]. This might relate to higher ROS-production per mitochondria in less oxidative muscle [16], [17]. To our knowledge, no study has attempted to compare basal and exercise-stimulated kinase phosphorylation in different human muscle-groups at a comparable work-load.
Here, the expression of selected proteins, some of which show muscle group-confined expression in mice, was evaluated in human soleus, lateral gastrocnemius and vastus lateralis-part (VL) of the quadriceps femoris muscle. Furthermore, a human inclined walking exercise model was employed with the aim of comparing resting and exercise-induced kinase responses in human soleus and gastrocnemius muscle at a comparable level of activation.
Results
A schematic overview of the experimental protocol is shown in figure 1. All subjects completed a 15% inclined 45 min uphill walking bout covering a mean distance of 4770 m and corresponding to a 715 m elevation. This elicited a mean oxygen uptake of 69.1±1.6 %VO2 max and changes in various blood metabolites and hormones typical of whole-body exercise at this intensity including increased lactate and catecholamines and lower insulin (table 1).
The measured fibertype-distribution in the biopsies obtained from human soleus, gastrocnemius and VL showed a roughly 20% higher mean type I fiber content and equally lower type IIa fiber content in soleus compared to gastrocnemius and VL (figure 2A). Figure 2B and table 2 also show representative blots and lists the total protein measurements performed on the current biopsy-material. HXII content was higher in soleus compared to gastrocnemius (p<0.01) and VL (p<0.001) and GLUT4 content higher in soleus compared to gastrocnemius (p<0.05). In addition, a strong trend towards a differential expression of the mitochondrial superoxide-converting enzyme, SOD2 was found (p = 0.07 by 1-way ANOVA). All remaining proteins measured, including signalling proteins (AMPK subunits, ERK, eEF2, TBC1D1, TBC1D4), mitochondrial markers (F1 ATPase, COXI) and the hydrogen peroxide-inactivating Catalase-enzyme showed no significant differences in relative expression between muscles. A much used loading control, actin, tended to be higher in soleus compared to gastrocnemius (mean 28% lower) and VL (mean 7% lower). Given that the quantifications for multiple proteins in these samples and coomassie-staining indicates equal protein loading, this may suggest that actin is a poor loading control for comparison between muscles. Overall, the mouse pattern of high enrichment of certain proteins within specific muscle groups is unlikely to be present in humans.
A) Mean fibertype distribution and B) representative blots of relative protein expression in human soleus (S), lateral gastrocnemius (G) and vastus lateralis (VL) as indicated. ** p<0.01 fibertype-difference soleus vs. VL. n = 7–8 for fibertype-determinations and n = 10 for western blotting.
Soleus was significantly more active than gastrocnemius measured as both %EMGmax (Fig. 3A) and glycogen use (Fig. 3B). Total glycogen tended to be higher in gastrocnemius compared to soleus muscle although this was not significant (Fig. 3B). VL was only minimally activated by the current exercise regimen. Measured as %total glycogen use, the numbers were 70%, 57% and 2% for soleus, gastrocnemius and VL-muscle, respectively.
Relative work-load during exercise-bout evaluated by A) % of maximal EMG and B) glycogen content in human soleus (SOL), lateral gastrocnemius (Gast) and vastus lateralis (VL) before and after inclined walking exercise at ∼70% VO2max. Measured phosphorylations of C) ERK1/2, D) AMPK and E) eEF2 normalised per total protein in SOL, Gast and VL before and after exercise. F) EMG-normalised phosphorylation per total protein in gastroc. vs. SOL. G) Representative blots. §/§§§ p<0.05/0.001 vs. soleus. *** p<0.001 exercise-effect vs. rest within muscle. ††† p<0.001 muscle-effect, n = 10.
ERK, AMPK and eEF2 phosphorylation were all significantly higher after exercise in soleus and gastrocnemius, but not in VL (Fig. 3C–E). Interestingly, despite the fact that gastrocnemius was less active than soleus, the absolute mean activation after exercise tended to be greater in gastrocnemius than soleus for all signalling outcomes measured. When normalised to %EMGmax, gastrocnemius showed a significantly higher general kinase-responsiveness to exercise compared to soleus (Fig. 3F, p<0.001, representative blots in Fig. 3G).
Discussion
This study examined protein expression and kinase-signalling in 3 different muscle-groups of the lower extremity in humans. Our first aim was to assess whether signalling proteins like AMPK and TBC1D1 and 4, previously found to display muscle-group specific expression in mice, differed between human muscle groups. This was clearly not the case and in general protein expression was found to be similar in different lower extremity human muscles. The second aim was to examine whether resting and exercise-stimulated kinase-signalling differed between human muscles at a given rate of activation as previously shown in rats. Surprisingly, despite comparable expression of mitochondrial marker proteins, glycogen content and only a trend towards lower SOD2 content in gastrocnemius, the latter muscle displayed a ∼60% greater mean exercise-induced increase in phosphorylation-response for the 3 kinase-signalling pathways measured compared to soleus at a given level of EMG-defined muscle activation.
A number of endurance-training responsive proteins have previously been measured in distinct human muscle groups, including GLUT4 and various markers of mitochondrial content [6], [7], [21]–[23]. In general, our results of only subtle differences between muscle groups are in agreement with these studies. This implies that protein expression in human vastus lateralis, the most commonly studied muscle in human exercise-studies, is likely to be generally representative of other muscle groups. The most differentially expressed protein in our study, HXII showed 46–58% higher expression in soleus compared to other muscles. HXII expression is often observed to be very sensitive to endurance-training in humans [24], and the elevated HXII content in soleus is probably reflective of its function as a postural muscle. Of note, some of our total protein measurements (Catalase, COXI, GLUT4, SOD2) show a tendency towards a ∼20% lower level in vastus lateralis compared to the other muscles. Based on the mean standard deviation for these four proteins, a minimum sample size of 17 would be needed to detect differences of this magnitude at the α = 0.05 level by western blotting in future studies. However, even if our sample size is insufficient, the differences between muscle groups for most proteins examined seem to be small (<20%).
During preparation of this manuscript, a study was published measuring selected proteins including TBC1D1 and TBC1D4 in 12 different rat muscles [25]. Similar to humans, TBC1D4 expression was not different and TBC1D1 expression showed a ∼30% difference in expression range between different hindlimb-muscles. This is in stark contrast to the muscle-type confined expression in mice where TBC1D4 is enriched in slow-oxidative muscle and TBC1D1 in fast-twitch glycolytic muscle [12]. Based on this, mice may be unique in their muscle-type restricted expression. Since transgenic mice are a major tool used to chart signalling pathways in muscle-research, this obviously calls for caution when generalising signalling concepts from mice to humans or even other rodent species like rats.
Studies by David Hood's group showed that mitochondrial content was inversely correlated with the resting and in situ contraction-stimulated phosphorylation of a number of kinases in rat tibialis anterior muscle [15], [16]. A putative causal link between kinase phosphorylation and mitochondrial content might be muscle group-specific differences in ROS-mediated signalling. ROS is produced during exercise [2], [26]. In the present study, the lack of difference in SOD2 and catalase-expression did not support that a poorer maintenance of redox-status in gastrocnemius contributed to the higher kinase responsiveness in gastrocnemius compared to soleus.
In rats and humans, low glycogen has been shown to correlate with increased basal phosphorylation and/or exercise or insulin-activation of some kinases including AMPK and Akt [27]–[29]. This occurs by a poorly defined mechanism that does not appear to involve increased skeletal muscle ROS-production in situations with low glycogen in exercising humans [30]. In the present study, the greater exercise-induced kinase-signalling response in gastrocnemius compared to soleus could not be explained by differences in muscle glycogen which tended to be higher in gastrocnemius than soleus muscle.
Endurance-training of rats or humans has been reported to reduce phosphorylations in response to exercise of a number of signalling proteins including AMPK, TBC1D4, mTOR, S6K1, S6 and ERK at the same absolute work-intensity [31]–[35] although the mechanism has not been resolved. Soleus is more posturally active in daily life than gastrocnemius muscle and some of our measured proteins, HXII and GLUT4, would suggest that soleus has, as expected, been more habitually active than gastrocnemius. Thus, it is tempting to ascribe the lower activation-sensitivity in soleus vs. gastrocnemius to a training effect in soleus vs. gastrocnemius in our study. While this phenomenon could relate to an improved maintenance of cellular energy charge for some kinases such as AMPK [34], this does not explain why kinases with other activation-mechanisms would behave similarly. Given that phosphatases can be reversibly inactivated by ROS and affect kinase-activation [36] and the previously discussed link between kinase-activation and mitochondrial ROS, we suspected that reactive oxygen species might be involved. However, our data showing equal mitochondrial enzymes and ROS-handling enzymes in soleus and gastrocnemius clearly do not support this hypothesis. Fascinatingly, endurance-trained athletes have been reported to exhibit a much higher phosphorylation of several proteins including AMPK, S6 and p38 MAPK than resistance trained athletes in response to acute maximal isokinetic leg extension (resistance training) exercise [37]. The opposite is also true in that strength-athletes show a greater kinase-responsiveness than endurance-athletes for some of the same kinases (AMPK, p38 MAPK) after 1 h of moderate-high intensity cycling [37]. Since the greater kinase-responsiveness of endurance-athletes to resistance exercise likely occurs despite higher mitochondrial content and perhaps even a higher percentage of type I fibers with lower intrinsic mitochondrial ROS production as suggested in rat [17], this again appears to be more than a mere function of mitochondrial ROS production. How this regimen-specific attenuation of kinase-responsiveness by training is brought about will be an interesting topic for future studies.
AMPK is an attractive drug target to treat insulin resistance since its activation is likely sufficient to increase glucose uptake in muscle cell culture and mouse muscle [38]–[40] and to drive mitochondrial biogenesis [41]. AMPK is a heterotrimeric αβγ protein-complex and some AMPK activators like AICAR and A-769662 have been shown to require certain AMPK subunits to elicit biological effects [11], [13], [42]. In rodent muscle, AMPK subunit expression differs markedly between muscle groups as does the expression of potential downstream effectors of contraction and insulin-stimulated glucose uptake like TBC1D1 and 4 [11]–[13], [43]. We found near equal expression of these proteins in different human muscle groups, implying that AMPK-dependent signalling mechanisms are likely conserved between most human skeletal muscles.
In conclusion, humans do not exhibit the extreme muscle-specific expression of signalling proteins like AMPK and TBC1D1 and 4 seen in mice. Human gastrocnemius shows a greater phosphorylation response of a number of kinases to exercise at a given degree of EMG-verified activation than soleus. This probably reflects a difference in training-status and muscle fiber type composition between the muscles but occurs despite similar expression of mitochondrial markers, ROS-handling enzymes and glycogen content.
Methods
Subjects
10 young moderately trained male subjects [26±2 yr, 184±2 cm, 85±2 kg, o2peak = 58±2 ml·(kg·min)−1] gave their informed written consent to participate in the study, which was approved by the Copenhagen Ethics Committee (reg. no. H-KF277313) and conformed to the Helsinki II Declaration (1996).
Protocol
Pre-test day.
The subjects underwent one day of pre-testing and 2 separate experimental days (see Figure 1 for graphic overview). On the pre-test day, anthropometric measurements and maximal oxygen uptake was determined in the fed condition. Upon arrival, the subjects rested in the supine position for 15 min after which resting pulmonary VO2 was determined. The subject then undertook an inclined (15%) treadmill test at increasing speeds to determine VO2max (starting at 6 km/h and increasing 1 km/h every minute until exhaustion) and calculate the experimental walking speed. The 15% incline was shown in a pilot experiment to activate both soleus and gastrocnemius muscle measured as electromyography (EMG) signal during exercise (data not shown).
Experimental day 1.
On both experimental days the subjects arrived in the morning after an overnight fast. On day 1, the subjects' maximal voluntary EMG was determined for soleus, gastrocnemius and vastus lateralis muscles, and subsequently EMG was recorded with the same surface electrodes during the experimental work-bout (15% incline, walking speed corresponding to 65–70% VO2 max, for 45 min).
Relevant parts of a given subject's legs were shaven, sandpapered and wiped with ethanol after which electrodes were placed in pairs approx. 2 cm. centre–to-centre above soleus, gastrocnemius and vastus lateralis muscles in addition to a reference electrode on the tibia. Maximal EMG responses (highest of 3–5 attempts) were determined for soleus, gastrocnemius and vastus lateralis during a maximal isometric knee extension, a standing isometric loaded heel raise and a sitting isometric heel raise with the knee at a 90° angle. The experimental bout started approx. 90 min after arrival. During the experimental work-bouts, EMG (sampling rate 1000 Hz) was recorded at 5–15 min, 20–30 min and 35–45 min.
Experimental day 2.
On day 2, a venous catheter was inserted in the forearm antecubital vein for blood sampling. After 60 min of rest, 5 mm incisions were made for each biopsy (1/muscle) above the soleus, lateral head of the gastrocnemius and the vastus lateralis-part of the quadriceps muscles on both legs under local anaesthesia (Xylocaine 2%, Astra-Zenica, Sweden). After an additional 30 min, a resting blood sample and needle biopsy was taken from each of the three muscles in one leg (randomised with respect to dominant leg and biopsy-order), after which the experimental work-bout was begun (15% incline, walking speed corresponding to 65–70% VO2 max, 45 min). Blood samples were collected at 15, 30 and 45 min. After completing the work bout, biopsies were taken from the second non-biopsied leg, and divided for histochemistry and biochemical analyses. The last biopsy was frozen in liquid N2 within 3 min after work termination.
Pulmonary gas analysis
During the incremental maximal walking test, expired air was collected in Douglas bags and analysed as previously described [18].
EMG analysis
EMGmax was calculated as the largest 1 s root mean square value obtained (average of ten 100-ms segments) during the maximum contractions. EMG recorded during the walking exercise was calculated as root mean square amplitudes (100 ms segments) and expressed relative to the maximal EMG response (% EMGmax). Resting EMG was subtracted from all values. No differences were found between the three recording periods, indicating no development of muscle fatigue. Therefore, data is presented as average of the three periods recorded during the work-bout.
Blood and plasma analyses
Plasma epinephrine, nor-epinephrine and insulin concentrations were analysed by means of radioimmunoassay kits (High sensitive 2-Cat RIA, Labor Diagnostika Nord GmbH & Co., Germany and Insulin RIA DSL-1600, Diagnostic Systems Laboratories Inc., Webster, TX, USA). The plasma FFA concentration and the blood concentration of glucose and lactate were measured using an automatic analyzer (Hitachi automatic analyzer 912; Boehringer Mannheim, Ingelheim, Germany).
Muscle fiber typing
Fibertype composition of the different muscles was determined using histochemical ATPase staining of cryosections, as described previously [19].
Muscle glycogen
Glycogen content was determined as glycosyl units after acid hydrolysis of freeze dried dissected muscle biopsy specimens [19].
Muscle preparation
All materials were from Sigma-Aldrich (St. Louis, MO, USA) unless stated otherwise. Freeze dried and dissected muscle biopsies were homogenized 1∶15 w/v using a Tissuelyser II (Qiagen, USA) in ice-cold buffer containing 50 mM HEPES (pH 7.5), 150 mM NaCl, 20 mM sodium pyrophosphate, 20 mM β-glycerophosphate, 10 mM NaF, 2 mM sodium orthovanadate, 2 mM EDTA, 1% NP-40, 10% glycerol, 2 mM PMSF, 1 mM MgCl2, 1 mM CaCl2, 10 µg/ml leupeptin, 10 µg/ml aprotinin, and 3 mM benzamidine. Homogenates were rotated end over end for 30 min at 4°C and then cleared by centrifugation at 16.000 g at 4°C for 20 min. Protein content in the supernatant was measured in triplicate by the bicinchoninic acid method, accepting a 5% coefficient of variance (Pierce Rockford, IL). Then, the lysates were diluted in Milli-Q ultrapure water and 6×laemlii-buffer (340 mM TRIS-base pH 6.8, 11% SDS, 20% glycerol, 0.05% bromophenol blue and 225 mM freshly added DTT) to the same protein concentration.
Immunoblotting procedures
Total protein and phosphorylation were measured by standard immunoblotting techniques, largely as described previously [20]. For a given measurement, equal volumes and protein amounts of all samples were separated by SDS-PAGE (PROTEAN Tetra, BioRad, USA) using self-cast 15-well minigels (5–10% acrilamide, 5 gels per full sample set) cast from the same solution. Then, regions of interest were identified based on the molecular weight markers, cut from the gels and semidry-transferred (TE-77, Amersham Biosciences, USA) onto the same PVDF-membrane (Immobilon-P, 0.45 µM, Millipore, USA) for subsequent blocking and antibody-probing. If uneven transfer was suspected based on the molecular weight markers or ECL signal obtained, the blots were ponceau-stained to verify this and all samples rerun for the measurement in question. Primary antibodies used were glucose transporter 4 (GLUT4, Pierce, USA, cat#PA5-1065), hexokinase II (HXII, Santa Cruz, USA, cat#28889), Cytochrome c oxidase I (COXI, Invitrogen, USA, cat# 459600), F1 ATPase (Santa Cruz, USA, cat#16689), SOD2 (Millipore, USA, cat#06-984), Catalase (Abcam, USA, cat#52477), TBC1D1 (provided by C. MacKintosh, University of Dundee, UK), TBC1D4 (Upstate, USA, cat#07-741), alpha1, alpha2, beta1 and beta2 AMPK (provided by D. G. Hardie, University of Dundee, UK), gamma3 AMPK (Zymed, USA, cat#52-5717), eukaryotic elongation factor 2 (eEF2) total (Santa Cruz, USA, cat# 13004), extracellular receptor activated protein kinase (ERK) 1/2 total (Cell Signaling Technology, USA, cat#9102), pan-actin (Sigma, USA, cat#A2668), phospho-ERK 1/2 Thr202/Tyr204 (Cell Signaling Technology, cat#9101), phospho-Thr56 eEF2 (Cell Signaling Technology, USA, cat#2331), phospho-Thr172 AMPK (Cell Signaling Technology, USA, cat#2531). Horse-radish peroxidise-conjugated secondary antibodies were from Dako (Glostrup, Denmark). Band intensity was quantified by Kodak imaging software (Kodak 1D version 3.5, USA). Loading was optimised for signal and linearity for all antibodies prior to use. Coomassie-staining after development was performed by submersion of PVDF membranes for ∼10 min in 0.5% Coomassie Blue G-250 in 50% ethanol/10% acetic acid, removal of excess coomassie-stain with distilled water followed by destaining in 50% ethanol/10% acetic acid until bands were clearly visible. The strong band above 150 kDa was quantified. Half and double protein amounts were loaded for one vastus lateralis sample to show that the signal was in the dynamic range.
Statistics
Statistical evaluation was performed using SigmaPlot 11.0 (Systat Software Inc., USA) by 1-way ANOVA for protein expression data (muscle), two-way ANOVA with repeated measures (muscle×time) for rest vs. exercise, and one-way ANOVA with repeated measures for blood data. When ANOVA revealed significant differences, a Tukey's post hoc test was used to correct for multiple comparison. For the global comparison of EMG-normalised data in Figure 3F, the normality-test failed and the data-set was instead analysed using Wilcoxon's signed rank test. The significance level was set at p<0.05. All data are expressed as mean ± SEM.
Acknowledgments
We acknowledge Betina Bolmgren and Irene Beck Nielsen for their skilled technical assistance.
Author Contributions
Conceived and designed the experiments: TJ RL SR BJ ER. Performed the experiments: TJ RL SR JM MC BJ ER. Analyzed the data: TJ RL SR JM MC BJ. Contributed reagents/materials/analysis tools: BJ ER. Wrote the paper: TJ BJ ER.
References
- 1. Wojtaszewski JF, Richter EA (2006) Effects of acute exercise and training on insulin action and sensitivity: focus on molecular mechanisms in muscle. Essays Biochem 42: 31–46.
- 2. Gomez-Cabrera MC, Domenech E, Vina J (2008) Moderate exercise is an antioxidant: upregulation of antioxidant genes by training. Free Radic Biol Med 44: 126–131.
- 3. Rose AJ, Richter EA (2005) Skeletal Muscle Glucose Uptake During Exercise: How is it Regulated? Physiology 20: 260–270.
- 4. Spangenburg EE, Booth FW (2003) Molecular regulation of individual skeletal muscle fibre types. Acta Physiol Scand 178: 413–424.
- 5. Akimoto T, Ribar TJ, Williams RS, Yan Z (2004) Skeletal muscle adaptation in response to voluntary running in Ca2+/calmodulin-dependent protein kinase IV (CaMKIV) deficient mice. Am J Physiol Cell Physiol 287: C1311–C1319.
- 6. Vandenborne K, Walter G, Ploutz-Snyder L, Staron R, Fry A, et al. (1995) Energy-rich phosphates in slow and fast human skeletal muscle. Am J Physiol 268: C869–C876.
- 7. Gregory CM, Vandenborne K, Dudley GA (2001) Metabolic enzymes and phenotypic expression among human locomotor muscles. Muscle Nerve 24: 387–393.
- 8. Hintz CS, Lowry CV, Kaiser KK, McKee D, Lowry OH (1980) Enzyme levels in individual rat muscle fibers. Am J Physiol 239: C58–C65.
- 9. Luginbuhl AJ, Dudley GA, Staron RS (1984) Fiber type changes in rat skeletal muscle after intense interval training. Histochemistry 81: 55–58.
- 10. Allen DL, Harrison BC, Sartorius C, Byrnes WC, Leinwand LA (2001) Mutation of the IIB myosin heavy chain gene results in muscle fiber loss and compensatory hypertrophy. Am J Physiol Cell Physiol 280: C637–C645.
- 11. Barnes BR, Marklund S, Steiler TL, Walter M, Hjalm G, et al. (2004) The 5′-AMP-activated protein kinase gamma3 isoform has a key role in carbohydrate and lipid metabolism in glycolytic skeletal muscle. J Biol Chem 279: 38441–38447.
- 12. Pehmoller C, Treebak JT, Birk JB, Chen S, MacKintosh C, et al. (2009) Genetic disruption of AMPK signaling abolishes both contraction- and insulin-stimulated TBC1D1 phosphorylation and 14-3-3 binding in mouse skeletal muscle. Am J Physiol Endocrinol Metab 297: E665–E675.
- 13. Treebak JT, Birk JB, Hansen BF, Olsen GS, Wojtaszewski JF (2009) A-769662 activates AMPK beta1-containing complexes but induces glucose uptake through a PI3-kinase-dependent pathway in mouse skeletal muscle. Am J Physiol Cell Physiol 297: C1041–C1052.
- 14. Taylor EB, An D, Kramer HF, Yu H, Fujii NL, et al. (2008) Discovery of TBC1D1 as an insulin-, AICAR-, and contraction-stimulated signaling nexus in mouse skeletal muscle. J Biol Chem 283: 9787–9796.
- 15. Ljubicic V, Hood DA (2009) Specific attenuation of protein kinase phosphorylation in muscle with a high mitochondrial content. Am J Physiol Endocrinol Metab 297: E749–E758.
- 16. Ljubicic V, Hood DA (2008) Kinase-specific responsiveness to incremental contractile activity in skeletal muscle with low and high mitochondrial content. Am J Physiol Endocrinol Metab 295: E195–E204.
- 17. Anderson EJ, Neufer PD (2006) Type II skeletal myofibers possess unique properties that potentiate mitochondrial H(2)O(2) generation. Am J Physiol Cell Physiol 290: C844–C851.
- 18. Frosig C, Jorgensen SB, Hardie DG, Richter EA, Wojtaszewski JF (2004) 5′-AMP-activated protein kinase activity and protein expression are regulated by endurance training in human skeletal muscle. Am J Physiol Endocrinol Metab 286: E411–E417.
- 19. Hoeg LD, Sjoberg KA, Jeppesen J, Jensen TE, Frosig C, et al. (2011) Lipid-induced insulin resistance affects women less than men and is not accompanied by inflammation or impaired proximal insulin signaling. Diabetes 60: 64–73.
- 20. Rose AJ, Broholm C, Kiillerich K, Finn SG, Proud CG, et al. (2005) Exercise rapidly increases eukaryotic elongation factor 2 phosphorylation in skeletal muscle of men. J Physiol 569: 223–228.
- 21. Daugaard J, Richter E (2004) Muscle- and fibre type-specific expression of glucose transporter 4, glycogen synthase and glycogen phosphorylase proteins in human skeletal muscle. Pfl++gers Archiv European Journal of Physiology 447: 452–456.
- 22. Houmard JA, Weidner ML, Gavigan KE, Tyndall GL, Hickey MS, et al. (1998) Fiber type and citrate synthase activity in the human gastrocnemius and vastus lateralis with aging. J Appl Physiol 85: 1337–1341.
- 23. Hickey MS, Weidner MD, Gavigan KE, Zheng D, Tyndall GL, et al. (1995) The insulin action-fiber type relationship in humans is muscle group specific. Am J Physiol 269: E150–E154.
- 24. Frosig C, Rose AJ, Treebak JT, Kiens B, Richter EA, et al. (2007) Effects of endurance exercise training on insulin signaling in human skeletal muscle: interactions at the level of phosphatidylinositol 3-kinase, Akt, and AS160. Diabetes 56: 2093–2102.
- 25. Castorena CM, Mackrell JG, Bogan JS, Kanzaki M, Cartee GD (2011) Clustering of GLUT4, TUG and RUVBL2 Protein Levels Correlate with Myosin Heavy Chain Isoform Pattern in Skeletal Muscles, but AS160 and TBC1D1 Levels Do Not. J Appl Physiol. [Epub ahead of print].
- 26. Jackson MJ (2011) Control of reactive oxygen species production in contracting skeletal muscle. Antioxid Redox Signal 15: 2477–86.
- 27. Derave W, Ai H, Ihlemann J, Witters LA, Kristiansen S, et al. (2000) Dissociation of AMP-activated protein kinase activation and glucose transport in contracting slow-twitch muscle. Diabetes 49: 1281–1287.
- 28. Kawanaka K, Nolte LA, Han DH, Hansen PA, Holloszy JO (2000) Mechanisms underlying impaired GLUT-4 translocation in glycogen-supercompensated muscles of exercised rats. Am J Physiol Endocrinol Metab 279: E1311–E1318.
- 29. Wojtaszewski JFP, MacDonald C, Nielsen JN, Hellsten Y, Hardie DG, et al. (2003) Regulation of 5′AMP-activated protein kinase activity and substrate utilization in exercising human skeletal muscle. Am J Physiol Endocrinol Metab 284: E813–E822.
- 30. Hellsten Y, Svensson M, Sjodin B, Smith S, Christensen A, et al. (2001) Allantoin formation and urate and glutathione exchange in human muscle during submaximal exercise. Free Radic Biol Med 31: 1313–1322.
- 31. McConell GK, Manimmanakorn A, Lee-Young RS, Kemp BE, Linden KC, et al. (2008) Differential attenuation of AMPK activation during acute exercise following exercise training or AICAR treatment. J Appl Physiol 105: 1422–1427.
- 32. Benziane B, Burton TJ, Scanlan B, Galuska D, Canny BJ, et al. (2008) Divergent cell signaling after short-term intensified endurance training in human skeletal muscle. Am J Physiol Endocrinol Metab 295: E1427–38.
- 33. Nielsen JN, Mustard KJ, Graham DA, Yu H, MacDonald CS, et al. (2003) 5′-AMP-activated protein kinase activity and subunit expression in exercise-trained human skeletal muscle. J Appl Physiol 94: 631–641.
- 34. Lee-Young RS, Canny BJ, Myers DE, McConell GK (2009) AMPK activation is fiber type specific in human skeletal muscle: effects of exercise and short-term exercise training. J Appl Physiol 107: 283–289.
- 35. Yu M, Stepto NK, Chibalin AV, Fryer LG, Carling D, et al. (2003) Metabolic and mitogenic signal transduction in human skeletal muscle after intense cycling exercise. J Physiol 546: 327–335.
- 36. Wright VP, Reiser PJ, Clanton TL (2009) Redox modulation of global phosphatase activity and protein phosphorylation in intact skeletal muscle. J Physiol 587: 5767–5781.
- 37. Coffey VG, Zhong Z, Shield A, Canny BJ, Chibalin AV, et al. (2006) Early signaling responses to divergent exercise stimuli in skeletal muscle from well-trained humans. FASEB J 20: 190–192.
- 38. Fryer LG, Foufelle F, Barnes K, Baldwin SA, Woods A, et al. (2002) Characterization of the role of the AMP-activated protein kinase in the stimulation of glucose transport in skeletal muscle cells. Biochem J 363: 167–174.
- 39. Costford SR, Kavaslar N, Ahituv N, Chaudhry SN, Schackwitz WS, et al. (2007) Gain-of-function R225W mutation in human AMPKgamma3 causing increased glycogen and decreased triglyceride in skeletal muscle. PLoS ONE 2: e903.
- 40. Jørgensen SB, Viollet B, Andreelli F, Frosig C, Birk JB, et al. (2004) Knockout of the alpha2 but Not alpha1 5′-AMP-activated Protein Kinase Isoform Abolishes 5-Aminoimidazole-4-carboxamide-1-beta-4-ribofuranosidebut Not Contraction-induced Glucose Uptake in Skeletal Muscle. J Biol Chem 279: 1070–1079.
- 41. Garcia-Roves PM, Osler ME, Holmstrom MH, Zierath JR (2008) Gain-of-function R225Q mutation in AMP-activated protein kinase gamma 3 subunit increases mitochondrial biogenesis in glycolytic skeletal muscle. J Biol Chem 283: 35724–34.
- 42. Scott JW, van Denderen BJ, Jorgensen SB, Honeyman JE, Steinberg GR, et al. (2008) Thienopyridone drugs are selective activators of AMP-activated protein kinase beta1-containing complexes. Chem Biol 15: 1220–1230.
- 43. Chen Z, Heierhorst J, Mann RJ, Mitchelhill KI, Michell BJ, et al. (1999) Expression of the AMP-activated protein kinase beta1 and beta2 subunits in skeletal muscle. FEBS Lett 460: 343–348.