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The benefits of endurance exercise on general health make it desirable to identify orally active agents that would mimic or potentiate the effects of exercise to treat metabolic diseases. Although certain natural compounds, such as reseveratrol, have endurance-enhancing activities, their exact metabolic targets remain elusive. We therefore tested the effect of pathway-specific drugs on endurance capacities of mice in a treadmill running test. We found that PPARβ/δ agonist and exercise training synergistically increase oxidative myofibers and running endurance in adult mice. Because training activates AMPK and PGC1α, we then tested whether the orally active AMPK agonist AICAR might be sufficient to overcome the exercise requirement. Unexpectedly, even in sedentary mice, 4 weeks of AICAR treatment alone induced metabolic genes and enhanced running endurance by 44%. These results demonstrate that AMPK-PPARδ pathway can be targeted by orally active drugs to enhance training adaptation or even to increase endurance without exercise.
Skeletal muscle is an adaptive tissue composed of multiple myofibers that differ in their metabolic and contractile properties including oxidative slow-twitch (type I), mixed oxidative/glycolytic fast-twitch (type IIa) and glycolytic fast-twitch (type IIb) myofibers (Pette et al., 2000; Fluck et al., 2003). Type I fibers preferentially express enzymes that oxidize fatty acids, contain slow isoforms of contractile proteins and are more resistant to fatigue than glycolytic fibers. Type II fibers preferentially metabolize glucose and express the fast isoforms of contractile proteins. Endurance exercise training triggers a remodeling program in skeletal muscle that progressively enhances performance in athletes such as marathon runners, mountain climbers and cyclists. This involves change in metabolic programs and structural proteins within the myofiber that alter the energy substrate utilization and contractile properties that act to reduce muscle fatigue (Pette et al., 2000; Fluck et al., 2003). Training based adaptations in the muscle are linked to increases in the expression of genes involved in the slow-twitch contractile apparatus, mitochondrial respiration and fatty acid oxidation (Holloszy et al., 1984; Booth et al., 1991; Schmitt et al., 2003; Yoshioka et al., 2003; Mahoney et al., 2005a and b; Siu et al., 2004; Garnier et al., 2005; Short et al., 2005; Timmons et al., 2005). These adaptations that improve performance, can also protect against obesity and related metabolic disorders (Wang et al., 2004; Koves et al., 2005). Moreover, skeletal muscles rich in oxidative slow-twitch fibers are resistant to muscle wasting (Minnaard et al., 2005).
Given the numerous benefits of exercise on general health, identification of orally active agents that mimic or potentiate the genetic effects of endurance exercise is a long standing, albeit elusive medical goal. High doses of certain natural extracts such as resveratrol can improve endurance (Lagouge et al 2006). The aerobic effects of resveratrol are thought to dependent on activation of SIRT1-PGC1α coactivator complex in skeletal muscle. However, the downstream transcriptional factor(s) targeted by SIRT1/PGC1α in mediating these effects are not known. More importantly, both SIRT1/PGC1α and resveratrol each activate multiple targets and thus whether there is a specific signaling pathway that can be selectively activated by a synthetic drug to improve endurance is not known.
Exercise training activates a number of transcriptional regulators as well as serine/threonine kinases in skeletal muscles that contribute to metabolic re-programming (Bassel-Duby and Olson, 2006). We and others previously identified a critical role for PPARβ/δ (henceforth referred to as PPARδ) in transcriptional regulation of skeletal muscle metabolism (Dressel et al., 2003; Luquet et al., 2003; Schuler et al., 2006; Wang et al., 2004). Over-expression of a constitutively active PPARδ (VP16-PPARδ) in skeletal muscles of transgenic mice pre-programs an increase in oxidative muscle fibers, enhancing running endurance by nearly 100% in untrained adult mice (Wang et al., 2004). One of the best understood serine/threonine kinases is AMP-activated protein kinase (AMPK), a master regulator of cellular and organismal metabolism whose function is conserved in all eukaryotes (Hardie, 2007). In mammals, AMPK has been shown to contribute to glucose homeostasis, appetite, and exercise physiology (Andersson et al., 2004; Hardie, 2007; Kubota et al., 2007; Mu et al, 2001; Minokoshi et al., 2004; Thomson et al., 2007). These observations raise the question as to whether synthetic PPARδ or AMPK agonists can re-program established fiber specification in adult muscle toward an overt endurance phenotype. We have found that the PPARδ agonist GW1516 (shown to be bioactive in humans, Sprecher et al., 2007) enables mice to run 60-75% longer and further than the non-treated controls only when combined with exercise training. This ‘super-endurance phenotype’ is linked to a transcriptional boost provided by exercise-activated AMPK resulting in a novel endurance gene signature. A more critical role of AMPK in the super-endurance phenotype is revealed in our unexpected finding that, the orally active AMPK agonist AICAR is sufficient as a single agent to improve running endurance by nearly 45% in non-exercised mice. Together these results provide new insights into the pharmacological malleability of muscle performance.
To examine whether treatment with PPARδ ligands alone can re-program the muscle transcriptome and endurance capacity, wild-type C57Bl/6J age matched cohorts were treated with vehicle or GW1516 for 4 weeks. QPCR analysis of selective target genes confirmed that drug treatment induced oxidative metabolic biomarkers such as uncoupling protein 3 (Ucp3), muscle carnitine palmitoyl transferase I (mCPT I, Cpt 1b) and pyruvate dehydrogenase kinase 4 (Pdk4) (Figure 1A). These changes in gene expression were detected as early as 4 days post-treatment as well as with drug concentrations ranging from 2-5 mg/kg/day. Moreover, in all our gene expression studies, maximal effects of PPARδ activation were detected in pre-dominantly fast-twitch (quadricep and gastrocnemius) but not slow-twitch (soleus) muscles (data not shown). In primary muscle cells cultured from wild type and PPARδ null mice (Chawla et al., 2003; Man et al., 2007), we confirmed that the induction of oxidative genes by GW1516 is mediated via selective activation of PPARδ in skeletal muscles (Supplementary Figure S1 A-C). Moreover, this is similar to the expression changes found in the same genes in muscles expressing the constitutively active VP16-PPARδ transgene (Wang et al., 2004) (Figure 1A), supporting the concept that pharmacological activation of PPARδ is sufficient to initiate an oxidative response in adult skeletal muscle. To determine the functional effects of ligand, age and weight matched cohorts of treated and control mice were subjected to an endurance treadmill performance test before (week 0) and after (week 5) treatment. Curiously, running performance was unchanged by GW1516 treatment (Figure 1B). Furthermore, long-term drug treatment of up to 5 months also did not change running endurance (data not shown). These results indicate that pharmacologic activation of the PPARδ genetic program in adult C57Bl/6J mice is insufficient to promote a measurable enhancement of treadmill endurance.
Since endurance exercise remodels the skeletal muscle to progressively alter performance (Holloszy et al., 1984; Booth et al., 1991; Schmitt et al., 2003; Yoshioka et al., 2003; Mahoney et al., 2005a and b; Siu et al., 2004; Garnier et al., 2005; Short et al., 2005; Timmons et al., 2005), we speculated whether co-administration of GW1516 in the context of exercise training might enhance anticipated changes in fiber type composition and mitochondrial biogenesis. The effect of GW1516 and exercise on fiber type composition was determined using meta-chromatic staining of cryo-sections of the gastrocnemius (Wang et al., 2004). As expected from the results of the running performance in Figure 1B, there was no significant difference in the proportion of type I fibers between vehicle and GW1516-treated sedentary mice (Figure 1C). In contrast, in trained mice, GW1516 increased the proportion of type I fibers (by ~38%) compared to the vehicle-treated sedentary mice (Figure 1C and 1D). In addition to its effects on the fiber type, exercise training increases skeletal muscle mitochondrial biogenesis, which was measured as a function of mitochondrial DNA expression levels using quantitative real time PCR (QPCR). Similar to type I fiber changes, mitochondrial DNA expression was not changed by drug alone but was increased by approximately 50% with the combination of exercise and GW1516 treatment (Figure 1E).
The effects of GW1516 treatment and exercise, singly or in combination, on components of the oxidative metabolism of fatty acids were further analyzed by measuring the gene expression levels of selective biomarkers for fatty acid β-oxidation. As expected, we found that previously examined genes such as Ucp3, Cpt 1b and Pdk4 were up-regulated by GW1516 but showed no further induction with exercise (Figure 2A). Unexpectedly, we discovered a second set of genes that show no response to exercise or drug alone but are robustly induced by the combination. This intriguing response profile includes a series of genes involved in the regulation of fatty acid storage [such as steroyl-CoA-desaturase (Scd1), fatty acyl coenzyme A synthase (FAS, Fasn) and serum response element binding protein 1c (SREBP1c) (Srebf1c)] and fatty acid uptake [such as the fatty acid transporter (FAT) (Cd36) and lipoprotein lipase (Lpl)] (Figs. 2B, 2C and and33).
We also measured the protein levels of selective oxidative biomarkers including myoglobin, UCP3, cytochrome c (CYCS) and SCD1. In each case, a more robust up-regulation of protein expression was found by combining exercise and GW1516 treatment relative to either drug or exercise alone (Figure 2D). Altered triglycerides are one way to assess changes in muscle oxidative capacity. Triglyceride levels were unchanged in vehicle or GW1516-treated sedentary mice, but showed a striking increase with exercise. In contrast, this increase was completely reversed by GW1516 treatment presumably due to enhanced fat utilization (Supplementary Figure S1 D).
As described above, although GW1516 treatment alone induces wide spread genomic changes associated with oxidative metabolism, it fails to increase running endurance. On the other hand, drug treatment in conjunction with exercise produces an enriched remodeling program that includes a series of transcriptional and post-translational adaptations in the skeletal muscle. This suggests that exercise training serves as a key trigger to unmask a cryptic set of PPARδ target genes leading us to re-examine the ability of the drug to modulate endurance. Indeed, the same dose and duration of GW1516 treatment that previously failed to alter performance, when paired with 4 weeks of exercise training, increases running time by 68% and running distance by 70% over vehicle-treated trained mice (Figure 3A and 3B, compare Week 5). It is also important to note that comparison of running time and distance before (week 0) and after (week 5) exercise and drug treatment revealed a 100% increment in endurance capacity for individual mice, underscoring the robustness of the combination paradigm (Figure 3A and 3B). Finally, it is noteworthy that the combined effects of GW1516 and exercise reduces the epididymal fat to body weight ratio as well as fat cross-sectional area in these mice (Supplementary Figure S1 E, F) suggesting the broader systemic effects of this protocol.
To dissect the mechanism underlying the super-endurance phenotype, we conducted a comprehensive study of the muscle transcriptome induced either by ligand, exercise or the combination, which produced three overlapping networks of 96, 113 and 130 genes, respectively (Figure 3C). Approximately 50% of the target genes were common between GW1516 and exercise demonstrating that PPARδ activation partially mimics exercise. To our surprise, combined GW1516 treatment and exercise established a unique gene expression pattern that was neither an amalgamation nor a complete overlap of the individual interventions (Figure 3C). This signature included 48 new target genes (Supplementary Table S1) not regulated by either GW1516 or exercise alone while excluding 74 genes regulated by GW1516 or exercise (selective genes are listed in Supplementary Table S3). The majority of the genes in the GW1516-exercise signature were induced (108/130); the components of which are described in Figure 3D. While the largest gene subclass (32% of genes) was linked to positive regulation of aerobic capacity, additional pathways implicated in muscle remodeling and endurance were also represented in the signature (see Supplementary Table S2 for detailed description). It is noteworthy that comparative expression analysis of the 48 exclusive genes of the endurance signature (but not of either intervention alone) revealed a striking similarity to ‘untrained’ VP16-PPARδ transgenic mice (Figure 3E). This observation confirms the primary dependence of the 48 genes on PPARδ and points to the possibility that exercise-generated signals may function to synergize PPARδ transcriptional activity to levels comparable to transgenic over-expression.
What might be the molecular interface between mechanical exercise and PPARδ transcription? Exercise training is known to activate multiple kinases; among which, AMPK has profound effects on skeletal muscle gene expression and oxidative metabolism (Chen et al., 2003, Reznick et al., 2006). Indeed, mice defective for AMPK signaling in muscle exhibit reduced capacity for voluntary running (Mu et al, 2001; Thomson et al., 2007). As previously observed (Durante et al., 2002; Frøsig et al., 2004), we found increased AMPK activation in the quadriceps of exercised mice relative to the sedentary controls (Figure 4A). Furthermore and unexpectedly, AMPK is constitutively activated in muscles of VP16-PPARδ transgenic mice in absence of exercise or drug (Figure 4B). In contrast, in our experiments GW1516 treatment alone does not activate AMPK in either sedentary or exercise trained muscles, as previously suggested by some (Tareda et al., 2006), but not by others (Kramer et al., 2007). Taken together these results strongly suggest that the ability to promote endurance in mice is associated with activation of both AMPK and PPARδ.
According to this hypothesis selective co-activation of AMPK and PPARδ would induce gene expression changes that mimic those triggered by combined exercise and PPARδ as well as VP16-PPARδ over-expression. To investigate this possibility, we compared the transcriptional changes induced in skeletal muscle by combined exercise and GW1516 treatment with that of combined AMPK activator (the cell permeable AMP analog AICAR) and GW1516 treatment. It is noteworthy that simultaneous GW1516 and AICAR treatment created a unique gene expression signature in the quadriceps of untrained C57Bl/6J mice (Supplementary Figure S2) that shares 40% of the genes with that of combined GW1516 treatment and exercise (Figure 4C). Classification of the 52 genes common to the two signatures (Figure 4D, listed in Supplementary Table S4) revealed that the majority of the targets were linked to oxidative metabolism. Quantitative expression analysis of selective oxidative genes by QPCR showed that several of these biomarkers including Scd1, ATP citrate lyase (Acly), hormone sensitive lipase (HSL) (Lipe), muscle fatty acid binding protein (mFABP, Fabp3), Lpl and Pdk4 were induced in a synergistic fashion by GW1516 and AICAR in the quadriceps (Figure 4E-4J). It is also noteworthy that all of the above genes were induced in quadriceps of untrained VP16-PPARδ mice where AMPK is constitutively active (Supplementary Figure S1 G). Collectively, these results show that interaction between AMPK and PPARδ substantially contributes to re-programming of the skeletal muscle transcriptome during exercise.
The above described pathway crosstalk raised the possibility that AMPK directly regulates the transcriptional activity of PPARδ in skeletal muscles. An analysis of the effects of GW1516 and AICAR on gene expression in primary muscle cells isolated from wild type and PPARδ null mice revealed that synergism is completely dependent on PPARδ and lost in the null cells (Figure 5A-D). These observations show that AMPK enhances a subset of ligand-dependent PPARδ transcriptional targets in a cell-autonomous fashion.
To more directly examine this connection, we utilized reporter gene expression assays. Co-transfection of either catalytic AMPK α1 or α2 subunits but not control vector with PPARδ increased the basal (Figure 5E) and GW1516-dependent transcriptional activity (Figure 5F) of PPARδ in inducing a PPRE-driven reporter gene in AD293 cells. It should be noted that AMPK over-expression or GW1516 treatment did not change reporter activity in transfections excluding the PPARδ expression vector (data not shown) negating the possibility of an effect via RXR. Additionally, in AD293 cells co-transfected with Flag-PPARδ and with either catalytic AMPK α1 or α2 subunits, we discovered that each of the AMPK subunits co-immunoprecipitated as a complex with Flag-PPARδ (Figure 5G). Furthermore, Flag-PPARδ co-immunoprecipitated endogenous AMPKα subunits from AD293 cells confirming a tight physical interaction between the nuclear receptor and the kinase (Figure 5H). Despite this association, AMPK failed to increase PPARδ phosphorylation. In vivo orthophosphate labeling of PPARδ in AD 293 cells in the presence or absence of either AMPK alpha isoform under the same conditions where AMPK promotes PPARδ-dependent transcription revealed no change in overall PPARδ phosphorylation (Figure 5I). These data suggest PPARδ phosphorylation is not increased by AMPK in vivo. However, co-transfection of AMPKα2 and co-activator PGC1α (a previously reported direct substrate of AMPK) cooperatively interact to further induce both the basal and ligand-dependent transcriptional activity of PPARδ (Figure 5J). Strikingly, we did not detect physical interaction between Flag-PGC1α and AMPK (Figure 5K), though both independently interacted with PPARδ. Collectively, these observations suggest that AMPK may be present in a transcriptional complex with PPARδ where it can potentiate receptor activity via direct protein-protein interaction and/or by phosphorylating co-activators such as PGC1α.
Our findings show that pharmacologic activation of PPARδ in adult mice can increase running endurance only in conjunction with exercise signals. The central role for AMPK in this process is especially underscored by the observations that it is both robustly stimulated by exercise as well as is constitutively active in muscles of VP16-PPARδ transgenic mice that exhibit endurance without exercise. Further, AMPK can integrate multiple transcriptional programs by interacting not only with PPARδ but also other transcriptional regulators of metabolism (e.g. PGC1α, PPARα) (Hong et al., 2003; Leff, 2003; Bronner et al., 2004; Jäger et al., 2007). This raises the interesting question as to whether chemical activation of AMPK is sufficient to increase running endurance without exercise.
To test this idea we treated C57B/6J mice with AICAR (500mg/kg/day) for 4 weeks. AICAR increased phosphorylation of AMPK α subunit and acetyl CoA carboxylase (ACC) as well as increased expression of UCP3 in quadriceps confirming effective activation of AMPK signaling (Figure 6A). Interestingly, 4 weeks of drug treatment decreased epididymal fat mass to body weight ratio and increased oxygen consumption without changing body weight (Figure 6B-E), supporting the speculation that AICAR may positively regulate endurance. Indeed, in a treadmill endurance test ACIAR-treated mice ran longer (~23%) and further (~44%) compared to vehicle-treated mice revealing that increase in endurance can be achieved without exercise (Figure 6F). Furthermore, global gene expression analysis of quadriceps revealed that AICAR treatment alone up-regulated a set of 32 genes linked to oxidative metabolism (Figure 6G and Supplementary Table S5). Notably, 30 of these 32 genes were also up-regulated in VP16-PPARδ transgenic mice suggesting that stimulation of oxidative genes by AMPK may depend on PPARδ (Supplementary Table S5). To test this possibility, we utilized wild type and PPARδ null primary muscle cells. Treatment of wild type primary cells with AICAR (for 72 hr) increased expression of key oxidative biomarker genes (Scd1, fasn (FAS), Ppargc 1a, Pdk4) (Figure 6H). In contrast, AICAR failed to increase the expression of the above genes in PPARδ null cells, demonstrating the requirement of the receptor for transcriptional effects of AMPK on oxidative genes.
In this study, we show that the AMP-mimetic AICAR can increase endurance in sedentary mice by genetically reprogramming muscle metabolism in a PPARδ-dependent manner. We also found that a PPARδ agonist in combination with exercise synergistically induces fatigue resistant type I fiber specification and mitochondrial biogenesis ultimately enhancing physical performance. These changes correlate with an unexpected but interesting establishment of a muscle endurance gene signature that is unique to the drug-exercise paradigm. Such a signature is an outcome of molecular crosstalk and perhaps a physical association between exercise-activated AMPK and PPARδ. These findings identify a novel pharmacologic strategy to re-program muscle endurance by targeting AMPK-PPARδ signaling axis with orally active ligands.
Transgenic over-expression as well as knockout studies have identified PPARδ and AMPK as key regulators of type I fiber specification and endurance adaptations during exercise (Mu et al, 2001; Röckl et al., 2007; Thomson et al., 2007; Wang et al., 2004). Whether and how these endogenously expressed regulators can be targeted to re-program adult muscle without exercise has been a subject of unresolved speculation. We found that the AMPK activator AICAR increased oxygen consumption and endurance in untrained adult mice in part by stimulating PPARδ-dependent oxidative genes. Despite a demonstrated role for PPARδ in endurance, 5 week treatment with a potent and selective agonist failed to alter either fiber type composition or endurance revealing that direct and pharmacologic activation of PPARδ is insufficient to enhance running performance. In contrast, transgenic over-expression of activated PPARδ at birth pre-programs the nascent myofibers to trans-differentiate into slow-twitch fibers, thus imparting a high basal endurance capacity to adult transgenic mice. Apparently, once fiber type specification is complete in adults the potential plasticity of muscle to synthetic activation of a single transcriptional pathway is constrained. Along these lines, the unexpected yet successful re-programming of endurance in untrained adults with synthetic AMP-mimetic might be linked to the ability of AMPK to simultaneously target multiple transcriptional programs governed by its substrates such as PGC1α, PPARα and PPARδ triggering a genetic effect akin to exercise (Hong et al., 2003; Leff, 2003; Bronner et al., 2004; Jäger et al., 2007).
Interestingly, the recalcitrance of adult skeletal muscle endurance to manipulation by PPARδ agonist alone is relieved by combining drug treatment with exercise. Indeed, this strategy generates an endurance gene signature that is unique from either paradigm alone reflecting a crosstalk between exercise and PPARδ signaling (Supplementary Table S2). While exercise activates a cascade of signaling events, we feel AMPK is central to this genetic adaptation for several reasons. First, AMPK is a metabolic sensor that detects low ATP levels (such as occur during exercise) and in turn increases oxidative metabolism (Mu et al., 2001, Reznick et al., 2006). Second, long term effects of AMPK are in part mediated via regulation of gene expression (Reznick et al., 2006). Third, exercise induces activation and nuclear import of AMPK, where it can potentially interact with transcription factors (this study and McGee et al., 2003). And finally, transgenic mice defective for AMPK activation exhibit reduced voluntary exercise (Mu et al, 2001; Thomson et al., 2007), making it an attractive exercise cue that modulates receptor signaling.
The notion that exercise-activated AMPK interacts with PPARδ in regulating gene expression is supported by our demonstration that AMPK associates with PPARδ and dramatically increases basal and ligand-dependent transcription via the receptor. Despite physical interaction, we found that AMPK does not induce PPARδ phosphorylation in metabolic labeling studies. Interestingly, AMPK and its previously reported substrate PGC1α synergistically increased PPARδ transcription, suggesting indirect regulation of receptor function by AMPK via co-regulator modification. Nevertheless, we cannot rule out the possible regulation of PPARδ by AMPK via direct protein-protein interaction. Indeed, regulation of other transcription factors by AMPK via similar mechanisms has been previously demonstrated (Hong et al., 2003; Leff, 2003; Bronner et al., 2004). A physiological validation of AMPK-PPARδ interaction comes from our observation that GW1516 and AICAR (AMPK activator) synergistically induces several endurance related genes in wild type but not in PPARδ null primary muscle cells. More importantly, treatment of animals with AICAR and GW1516 creates a gene signature in skeletal muscle that replicates up to 40% of the genetic effects of combined exercise and GW1516 treatment. Notably, the shared genes between the two profiles are linked to oxidative metabolism, angiogenesis and glucose sparing, pathways that are directly relevant to muscle performance (Figure 4D, listed in Supplementary Table S4).
While not all genes regulated by either exercise (data not shown) or exercise-PPARδ interaction (non-overlapping signature, Figure 4D) are AMPK dependent, two key findings assign a critical role for the kinase in promoting endurance compared to other known exercise signals (Bassel-Duby and Olson, 2006, Goodyear et al., 1996, Lagouge et al., 2006). First, AMPK is constitutively active in VP16-PPARδ transgenic muscles that exhibit endurance without exercise. Second, AMPK activation by AICAR was sufficient to increase running endurance without additional exercise signals. Strikingly, majority of the oxidative genes (30 out of 32) up-regulated by AICAR are active in super-endurance VP16-PPARδ mice and perhaps are the core set of genes required to improve muscle performance. Interestingly, AICAR failed to induce oxidative gene expression in PPARδ null muscle cells, indicting the requirement of PPARδ, at least for regulation of oxidative metabolism by AMPK. Collectively, these findings demonstrate a molecular partnership between AMPK and PPARδ in re-programming skeletal muscle transcriptome and endurance (Figure 6I) that can be readily exploited by orally active AMPK drugs to replace exercise.
In humans, endurance exercise leads to physiological adaptations in the cardio-pulmonary, endocrine and neuromuscular systems (Jones et al., 2000; Lucia et al., 2001). While our current investigation focused on skeletal muscle, extra-muscular effects of PPARδ, AMPK and exercise may also contribute to increased endurance. Although, potentiation of extra-muscular adaptations by PPARδ and AMPK agonists remain to be studied, we found that drug treatment can reduce epididymal fat mass, possibly conferring additional systemic benefits. It is noteworthy that PPARδ is important for normal cardiac contractility as well as for the endocrine function of adipose tissue (Wang et al., 2003; Cheng et al., 2004). Similarly, the activation of AMPK by metformin is thought to mediate its ability to lower blood glucose levels (Shaw et al, 2005). In addition to increasing performance in athletes, exercise has beneficial effects in a wide range of patho-physiological conditions such as respiratory disorders, cardiovascular abnormalities, type 2 diabetes and cancer risk. Therefore, understanding the effects of exercise on normal physiology as well as identifying pharmaceutically targetable pathways that can boost these effects is crucial. In this study, we revealed that synthetic PPARδ activation and exercise or more importantly AMPK activation alone, provides a robust transcriptional cue that re-programs the skeletal muscle genome and dramatically enhances endurance. We believe that the strategy of re-organizing the preset genetic imprint of muscle (as well as other tissues) using exercise mimetic drugs has therapeutic potential in treating certain muscle diseases such as wasting and frailty as well as obesity where exercise is known to be beneficial.
Male C57B/6J mice (8 wks old) were randomly divided into 4 cohorts comprising (i) vehicle-treated & sedentary (V), (ii) GW1516-treated & sedentary (GW), (iii) vehicle-treated & exercise trained (Tr) and (iv) GW1516-treated & exercise trained (Tr+GW) (N=9). Mice in all groups were acclimated to moderate treadmill running (10 m/min for 15 min) every other day for 1 week. After acclimation, basal running endurances for the 4 groups were determined using a treadmill running test, where the speed was gradually increased from 0 to 15 m/min and then maintained constant until exhaustion (Week 0). Following the initial test, the mice in the exercise groups were subjected to 4 weeks (5 days/week) of exercise training. The mice were trained on a treadmill inclined at 5 degrees, with progressively increasing intensity and time. At the end of 4 weeks, all exercise-trained mice were running for 50 min/day at 18 m/min. During the 4 weeks, mice from both the sedentary and trained groups were either treated with vehicle or GW1516 (5 mg/kg/day). At the end of the drug treatment and/or training protocol (Week 5) 6 mice per group were subjected to the running test. Three mice in each group were not subjected to treadmill test to confirm that changes observed in the skeletal muscle were not due to the acute run, but related to the exercise training. It should be noted that the above interventions do not affect body weight and food intake in mice (data not shown).
In another study, male C57B/6J mice (8 wks old) were treated with GW1516 (5 mg/kg/day, oral gavage), AICAR (250 mg/kg/day, i.p.) or the combination of the two drugs for 6 days for gene expression analysis. Additionally, C57B/6J mice (8 wks old) were also treated with AICAR (500mg/kg/day, i.p.) for 4 weeks for treadmill running tests.
The animals were euthanized by carbon dioxide asphyxiation 72 hrs after the last bout of exercise. Gastrocnemius and quadriceps were isolated, frozen and stored at -80°C until further analysis. In GW1516/AICAR study, quadriceps were similarly collected on the 6th day 4 hr after drug treatment.
RNA was extracted from gastrocnemius or quadriceps using Trizol and analyzed for gene expression using real time quantitative PCR. Protein homogenates were prepared from quadriceps and analyzed by western blotting with myoglobin (Dako), UCP3 (Affinity Bioreagents), CYCS (Santacruz), SCD1 (Santacruz), tubulin (Sigma), phospho-, total-AMPK α and phospho-ACC antibodies (Cell Signaling).
Genome-wide analysis was performed in quadriceps from V, GW, Tr and Tr+GW mice and from V, GW, AICAR and AICAR+GW mice as well as from wild type and VP16-PPARδ transgenic mice. Preparation of in vitro transcription products, oligonucleotide array hybridization, and scanning were performed by using Affymetrix high-density oligonucleotide array mouse genome 430A 2.0 chips according to Affymetrix protocols. To minimize discrepancies due to variables, the raw expression data were scaled by using Affymetrix MICROARRAY SUITE 5.0 software, and pairwise comparisons were performed. The trimmed mean signal of all probe sets was adjusted to a user-specified target signal value (200) for each array for global scaling. No specific exclusion criteria were applied. Additional analysis was performed by using the freeware program BULLFROG 7 (Zapala et al., 2002) and the Java-based statistical tool VAMPIRE (Hsiao et al, 2004).
Primary muscle cells were isolated from wild type and PPARδ null mice as previously described (Rando and Blau, 1994). These cells were treated with drugs as described in the figure legends. AD 293 cells were cultured in DMEM containing 10% serum and penicillin/streptomycin cocktail. Transfections with CMX-Flag, CMV-myc, pTAP, CMX-Flag PPARδ, pTAP-PPARδ, CMX-Tk-PPRE, CMX-βGAL, CMV-myc-hAMPK (α1 and α2 subunits) or CMX-Flag PGC1α were performed using Lipofectamine 2000. Skeletal muscle C2C12 cells were cultured in DMEM containing 20% serum and penicillin/streptomycin cocktail. For differentiation, cells at 80% confluence were switched to a differentiation medium (DMEM + 2% serum) for 4 days to obtain differentiated myotubules. Drug treatments are described in figure legends.
Flag-PPARδ or Flag-PGC1α was immuno-precipitated from cell lysates with Anti-Flag conjugated agarose beads (Sigma). For co-immunoprecipitation experiments SDS was excluded from the lysis buffer. Western blotting was performed with rabbit Anti-Flag, AMPK α subunit or PPARδ antibodies. For metabolic labeling, transfected AD 293 cells were treated with p32 for 2 hr before immunoprecipitation.
Data was analyzed using either one way ANOVA with an appropriate post hoc test for comparison of multiple groups, or using unpaired student’s t-test for comparison between two groups as described in figure legends.
The global gene expression data presented in this manuscript has been deposited in the NCBI Gene Expression Omnibus under the GEO series accession number GSE11805.
We thank Drs H. Cho, G.D. Barish and C.H. Zhang for valuable suggestions and discussion of the manuscript; and S. Ganley and E. Ong for administrative assistance. R.M.E is an investigator of the Howard Hughes Medical Institute at the Salk Institute for Biological Studies and March of Dimes Chair in Molecular and Developmental Biology. V.A.N. is supported by a Ruth L. Kirschstein National Research Service Award from the National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR053803-03). This work was supported by the Howard Hughes Medical Institute, Hilblom Foundation, and National Institutes of Health (HD027183 and DK057978).
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