- Open Access
AICAR inhibits ceramide biosynthesis in skeletal muscle
Diabetology & Metabolic Syndrome volume 4, Article number: 45 (2012)
The worldwide prevalence of obesity has lead to increased efforts to find therapies to treat obesity-related pathologies. Ceramide is a well-established mediator of several health problems that arise from adipose tissue expansion. The purpose of this study was to determine whether AICAR, an AMPK-activating drug, selectively reduces skeletal muscle ceramide synthesis.
Murine myotubes and rats were challenged with palmitate and high-fat diet, respectively, to induce ceramide accrual, in the absence or presence of AICAR. Transcript levels of the rate-limiting enzyme in ceramide biosynthesis, serine palmitoyltransferase 2 (SPT2) were measured, in addition to lipid analysis. Student’s t-test and ANOVA were used to assess the association between outcomes and groups.
Palmitate alone induced an increase in serine palmitoyltransferase 2 (SPT2) expression and an elevation of ceramide levels in myotubes. Co-incubation with palmitate and AICAR prevented both effects. However, ceramide and SPT2 increased with the addition of compound C, an AMPK inhibitor. In rats fed a high-fat diet (HFD), soleus SPT2 expression increased compared with normal chow-fed littermates. Moreover, rats on HFD that received daily AICAR injections had lower SPT2 levels and reduced muscle ceramide content compared with those on HFD only.
These results suggest that AICAR reduces ceramide synthesis by targeting SPT2 transcription, likely via AMPK activation as AMPK inhibition prevented the AICAR-induced improvements. Given the role of skeletal muscle ceramide in insulin resistance, it is tempting to speculate that interventions that activate AMPK may lead to long-term ceramide reduction and improved metabolic function.
Obesity predisposes individuals to a host of health complications, including insulin resistance, hypertension, and dyslipidemia, which characterize the metabolic syndrome . Due to the massive and sustained increase in obesity and the prevalence of the metabolic syndrome worldwide in recent decades , extensive efforts have been devoted to better understand the cellular events that mediate obesity-related pathologies.
Long known to regulate apoptotic signals , the biologically active sphingolipid ceramide is more recently known to mediate several of the deleterious conditions associated with obesity, such as insulin resistance, hepatic steatosis, and cardiovascular complications [4–6]. A variety of stimuli have been found to induce ceramide biosynthesis in rodents, including high-fat diet [7–9] and inflammatory agonists [8, 10, 11]. Despite the wealth of research establishing the efficacy of ceramide inhibition in improving obesity-related morbidities , no current prescribed pharmacological therapies are known to directly inhibit ceramide biosynthesis. A potentially useful focus in exploring treatments to prevent excessive ceramide accumulation, and block ceramide-mediated pathologies related to obesity, is to identify anti-ceramide effects of currently used drugs . A promising possibility is to explore the numerous drugs prescribed to treat obesity-related diseases that are known to regulate AMP-activated protein kinase (AMPK).
Research in recent decades has elucidated the role of the prototypical metabolic regulator AMPK in ameliorating deleterious conditions associated with obesity. Indeed, AMPK-activating drugs have been shown to improve insulin resistance [13, 14], cardiovascular complications [15, 16], and hepatic steatosis , which may explain their widespread use. Interestingly, many of the benefits attributed to AMPK activation are similar to those seen with ceramide inhibition [4, 6, 18].
The metabolic functions of AMPK are increasingly clear—increased glucose uptake, increased fatty acid uptake and oxidation, and the inhibition of anabolic processes (e.g., lipogenesis) . We have previously shown that AMPK inhibits inflammatory activity by blocking the NF-κB pathway , which, in light of our recent observation that ceramide biosynthesis requires inflammatory signals , suggests a potential ceramide-specific effect of AMPK activation. Given the general oxidative effect of AMPK on fatty acids, we sought to test the hypothesis that AMPK inhibits ceramide biosynthesis in muscle. Positive results will reveal a novel mechanism to partly explain the beneficial effects of AMPK-activating drugs in treating several obesity-related pathologies.
Cells were maintained in DMEM + 10% fetal bovine serum (Invitrogen). For differentiation into myotubes, C2C12 myoblasts were grown to confluency and the medium was replaced with DMEM + 10% horse serum (Invitrogen). Myotubes were used for experiments on day 4 of differentiation. For lipid treatment, palmitic acid (Sigma P5585) was dissolved in ethanol and diluted to desired concentration in DMEM. Palmitate solutions were then conjugated to 2% (w/v) BSA (Sigma A9576). Cells were monitored for toxicity to the high palmitic acid concentration (0.75 mM) and no difference was observed between sample protein content. 5-amino-1-β-D-ribofuranosyl-imidazole-4-carboxamide (AICAR) (Sigma A9978) was reconstituted in DMEM. Compound C (Sigma P5499) was reconstituted in DMSO.
Male Wistar rats were kept in a temperature-controlled room with a 12:12-h light–dark cycle. Rats were fed rodent laboratory chow (8604 Harlan Teklad Rodent Diet) and water ad libitum. Treatments lasted 6 wk. During this time, rats were randomly sorted into one of four groups: no intervention (control diet; 8604 Harlan Teklad) (n=9), daily AICAR injections (n=9), high-fat diet (HFD) (n=11), or HFD with daily AICAR injections (n=10). The HFD used in this study was composed of the following (g/kg of food): 116.6 g olive oil, 232.7 g flax seed oil, 87.2 g sugar, 174.6 starch, 226.6 g casein, 4.5 g methionine, 30.7 g gelatin, 51.2 g wheat bran, 22.5 g vitamin mix (Harlan Teklad, AIN76A), 52.2. g mineral mix (Harlan Teklad, AIN76), 1.4 g choline chloride. The HFD was 60% fat (40% flax seed, 20% olive oil). AICAR injections (dissolved in 0.9% NaCl) were administered subcutaneously at a dose of 0.5 mg/g body weight each morning. To reduce confounding factors, rats in the control and HFD groups were similarly handled each morning and injected with similar volumes of saline alone. All experimental procedures involving animals were approved by and performed in compliance with the Institutional Animal Care and Use Committee of Brigham Young University.
For isolation of lipids, cell and tissue pellets were re-suspended in 900 μl ice-cold chloroform:methanol (1:2) and incubated for 15 min on ice then briefly vortexed. A portion of the suspension (prior to pelleting) was used for protein measurement (Thermo Scientific). Separation of aqueous and organic phases required addition of 400 μl of ice-cold water and 300 μl of ice-cold chloroform. The organic phase was collected into a fresh vial and lipids were dried under a gentle nitrogen stream. An Agilent high performance liquid chromatography (HPLC) system coupled with an Applied Biosystems Triple Quadrupole/Ion Trap mass spectrometer (3200 Qtrap) was used for quantification of individual phospholipids. Multiple reaction monitoring (MRM) transitions were set up for quantitative analysis of various polar lipids [20, 21]. Levels of individual lipids were quantified using spiked internal standards, including dimyristoyl phosphatidylcholine (28:0-PC), C17-ceramide, C8-glucosylceramide, which were obtained from Avanti Polar Lipids (Alabaster, AL, USA). Neutral lipids were analyzed using a sensitivity HPLC/ESI/MRM method, modified from a previous method . TAG was calculated as relative contents to the spiked d5-TAG 48:0 internal standard (CDN isotopes), while DAG was quantified using 4ME 16:0 Diether DG (Avanti) as an internal standard.
Quantitative real-time PCR
Total RNA was extracted and purified from tissues using TRIzol (Invitrogen) according to the manufacturer's recommendations. cDNA was synthesized from mRNA by reverse transcription using a commercial cDNA synthesis kit with oligo(dT) primers (iScript Select cDNA Synthesis; Bio-rad). Quantitative real-time PCR was performed by following the instructions accompanying the Qiagen Quantifast SYBER Green PCR kit and using a Qiagen QIAcube. A sample containing no cDNA was used as a non-template control to verify the absence of primer dimers. β-actin reactions were performed side by side with every sample analyzed. Changes in mRNA level of each gene for each treatment were normalized to that of the β-actin control mRNA according to Pfaffle . Sequences are included in Table 1.
Gastrocnemius was extracted from euthanized mice and flash frozen then stored at −80. Tissues were later lysed and protein content was determined using a BCA protein assay (Pierce, Rockford, IL, USA) and sample volumes were adjusted so that precisely 50 μg of protein was loaded into each lane. After addition of sample buffer, samples were resolved by SDS-PAGE, transferred to nitrocellulose, and immunoblotted with anti-SPT2 antibody (Abcam, Cambridge, MA, USA) using methods described previously . After incubation with primary antibody, blots were incubated with a horseradish peroxidase-conjugated secondary antibody. Horseradish peroxidase activity was assessed with ECL solution (Thermo Scientific, Rockford, IL, USA) and exposed to film.
Data are presented as the mean ± SEM. Data were compared by ANOVA with Tukey’s post-hoc analysis (Graphpad Prism; La Jolla, CA). Significance was set at P<0.05.
AICAR selectively blocks sphingolipid accumulation in muscle cells
AMPK activation is known to increase rates of mitochondrial fatty acid oxidation . Based on these observations, we anticipated a general reduction in accumulated intracellular lipids when cells were treated with palmitate and AICAR when compared with palmitate treatment alone. AICAR is a well-established AMPK activator. We found that levels of the glycerolipids triacylglycerol (TAG) and diacylglycerol (DAG) (Figure 1A and B, respectively) were significantly increased in C2C12 myotubes in response to prolonged palmitate treatment. AICAR addition to palmitate incubations had no significant effect on TAG and DAG levels. Similar to these glycerolipids, palmitate induced a robust increase in ceramides and glucosylceramides (Figure 1C and D, respectively), which have both been implicated in mediating lipid-induced insulin resistance [26, 27]. However, whereas AICAR treatment had little effect of TAG and DAG, AICAR treatment blunted ceramide and glucosylceramides accrual to such a degree that levels returned to vehicle-treated conditions (Figure 1C and D). Despite its well-established ability to activate AMPK, AICAR may have off-target effects. To more confidently establish the importance of AMPK in mediating the sphingolipid-specific effects of AICAR, we included compound C, a specific AMPK inhibitor. The addition of compound C to palmitate and AICAR treatments completely reversed the protective effect of AICAR with ceramides (Figure 1C) and glucosylceramides (Figure 1D).
AICAR prevents lipid-induced transcription of SPT2 in muscle cells
Given our findings that AICAR inhibited the synthesis of ceramide and its downstream metabolite, glucosylceramide, we sought to determine whether AICAR alters expression of enzymes involved in de novo sphingolipid biosynthesis. In support of previous findings , palmitate elicited a significant increase in transcript expression of multiple enzymes, including ceramide synthase 6 (CerS6), CerS2, and, finally, serine palmitoyltransferase 2 (SPT2) (Figure 2). The observations regarding SPT2 are doubly noteworthy—SPT2 acts as the rate-limiting enzyme in de novo sphingolipid synthesis and it was the only enzyme whose transcript level was significantly blunted with inclusion of AICAR into the palmitate-enriched media (Figure 2). Interestingly, addition of the AMPK-inhibitor compound C elicited a pronounced increase in SPT2 and CerS6 transcript levels.
AICAR prevents high-fat diet-induced SPT2 expression in vivo
Having established an anti-ceramide effect of AICAR in cultured muscle cells, we next explored this relationship in whole muscle. Male Wistar rats were fed a normal chow or high-fat diet for 6 wk. During this period, animals further received daily injections of AICAR (0.5 mg/g BW) or vehicle (saline). Given our observations that SPT2 was affected by both the lipid-laden and AICAR conditions in cells, we analyzed SPT2 expression in the muscles of rats in the control, HFD, and HFD+AICAR conditions. We found that SPT2 transcript levels increased by roughly 60% in the muscle of animals fed a HFD when compared with those receiving normal laboratory chow (Figure 3A). Importantly, prolonged AICAR injections prevented this effect, with SPT2 levels falling slightly lower than control conditions (Figure 3A). These findings were further supported by similar results with SPT2 protein levels (Figure 3B). However, the increased SPT2 transcription was insufficient to significantly increase muscle ceramide levels in rats on HFD compared with normal chow, which only tended to increase (p=0.068) (Figure 4). Nevertheless, ceramide content from muscles of rats fed a HFD while receiving AICAR injections was significantly lower than those on HFD alone (Figure 4).
The purpose of this study was to elucidate the targeted effect of AICAR on inhibiting de novo ceramide biosynthesis in skeletal muscle. Our data suggest that AICAR treatment, which is known to potently activate AMPK, inhibits ceramide accumulation in lipid-laden conditions by inhibiting lipid-induced expression of the rate-limiting enzyme SPT2. These findings were particularly robust in murine myotubes, which showed a dramatic increase in SPT2 expression and ceramides with palmitate exposure and a complete reversal of both trends with AICAR inclusion. Additionally, and suggestive of the importance of AMPK, the addition of the AMPK inhibitor compound C increased transcript levels of SPT2 (Figure 2) and both sphingolipids (Figure 1C and D). Less dramatic were the data from muscle from HFD-fed and AICAR-treated rats. While SPT2 expression was increased in muscle from HFD-fed rats compared with those receiving normal chow and decreased in the muscle of rats receiving AICAR injection in conjunction with HFD, actual ceramides only significantly differed between the HFD and HFD plus AICAR groups, nonetheless suggesting an in vivo effect of AICAR on ceramide inhibition (Figure 4).
A likely explanation for the lack of a more robust increase in muscle ceramides in the HFD-fed group is the saturation state of the lipids in the HFD. Previous studies that have shown increased muscle ceramide in HFD-fed models have used a HFD that is largely lard based and is, subsequently, much higher in saturated fats than the HFD used in this study, which was almost completely unsaturated (flax and olive oil). Saturated fat is not only a substrate for ceramide, but it also activates the biosynthetic pathway [8, 28], while unsaturated fats, particularly the mono-unsaturated oleic acid, do not . In contrast to the in vivo findings, our use of palmitate in the cell culture provided a strong induction of ceramide biosynthesis. While the concentration used is not physiological (0.75 mM), it is widely used as a method to potently activate ceramide biosynthetic pathways.
Our findings of an anti-ceramide effect of AICAR in skeletal muscle corroborate previous observations in non-muscle tissues. Blazquez et al.  found that long-term stimulation of AMPK via AICAR treatment in astrocytes inhibited SPT activity and reduced ceramides. Collectively, these data highlight a novel specificity of AMPK activation to target ceramide synthesis in various cell types. Further, a possible mechanism for AMPK-induced inhibition of ceramide biosynthesis is the anti-inflammatory effects of AMPK. We recently found that ceramide biosynthesis requires NF-κB activation , which is inhibited by AMPK. Cacicedo et al.  observed that active AMPK prevents the inflammatory effects of both saturated fatty acids (SFA) and TNFα in endothelial cells. In particular, they found that the SFA- and TNFα-induced 2- to 4-fold increase in NF-κB reporter gene expression was prevented with both AICAR treatment and constitutively active AMPK .
Many prominent AMPK-activating drugs like metformin and thiazolidinediones (TZD) possess anti-inflammatory activity [31, 32]. Thus, given previous findings, it is not surprising that both metformin and TZD reduce ceramide accumulation [33, 34], though whether the activation of AMPK is necessary for the drugs’ anti-inflammatory and anti-ceramide actions is unknown.
Previous studies have tangentially explored the relationship between AMPK and ceramides in skeletal muscle. Holland et al.  found that adiponectin, long known to improve insulin sensitivity and activate AMPK , potently stimulates ceramide conversion to sphingosine 1-phosphate (S1P), which opposes several of ceramide’s deleterious effects in the cell . Interestingly, S1P induces AMPK activation, which explains the observation by Holland et al.  that ceramide activates AMPK in muscle cells. Given our findings that AMPK inhibits ceramide biosynthesis in muscle, these studies collectively suggest a self-regulating mechanism, wherein ceramide is converted to S1P, which activates AMPK and, in turn, inhibits ceramide biosynthesis.
In conclusion, these experiments reveal that the AMPK activator AICAR reduces expression of SPT2 in skeletal muscle and prevents ceramide biosynthesis in hyperlipidemic conditions. Given the wide range of AMPK-activating drugs currently used to mitigate obesity-induced pathologies, our findings suggest that ceramide inhibition may be an important and novel mechanism that mediates several health benefits derived from AMPK activation.
Co-first authors: Katherine A. Erickson and Melissa E. Smith.
Dandona P, Aljada A, Chaudhuri A, Mohanty P, Garg R: Metabolic syndrome: a comprehensive perspective based on interactions between obesity, diabetes, and inflammation. Circulation. 2005, 111: 1448-1454. 10.1161/01.CIR.0000158483.13093.9D.
Shaw JE, Sicree RA, Zimmet PZ: Global estimates of the prevalence of diabetes for 2010 and 2030. Diabetes Res Clin Pr. 2010, 87: 4-14. 10.1016/j.diabres.2009.10.007.
Aggarwal BB, Higuchi M: Role of ceramide in tumour necrosis factor-mediated apoptosis and nuclear factor-kappa B activation. Biochem Soct T. 1997, 25: 1166-1171.
Bikman BT, Summers SA: Sphingolipids and hepatic steatosis. Adv Exp Med Biol. 2011, 721: 87-97. 10.1007/978-1-4614-0650-1_6.
Holland WL, Knotts TA, Chavez JA, Wang LP, Hoehn KL, Summers SA: Lipid mediators of insulin resistance. Nutr Rev. 2007, 65: S39-S46.
Park TS, Rosebury W, Kindt EK, Kowala MC, Panek RL: Serine palmitoyltransferase inhibitor myriocin induces the regression of atherosclerotic plaques in hyperlipidemic ApoE-deficient mice. Pharmacol Res. 2008, 58: 45-51. 10.1016/j.phrs.2008.06.005.
Bikman BT, Guan Y, Shui G, Siddique MM, Holland WL, Kim JY, Fabrias G, Wenk MR, Summers SA: Fenretinide prevents lipid-induced insulin resistance by blocking ceramide biosynthesis. J Biol Chem. 2012, doi:10.1074/jbc.M1112.359950.
Holland WL, Bikman BT, Wang LP, Yuguang G, Sargent KM, Bulchand S, Knotts TA, Shui G, Clegg DJ, Wenk MR, et al: Lipid-induced insulin resistance mediated by the proinflammatory receptor TLR4 requires saturated fatty acid-induced ceramide biosynthesis in mice. J Clin Invest. 2011, 121: 1858-1870. 10.1172/JCI43378.
Blachnio-Zabielska A, Baranowski M, Zabielski P, Gorski J: Effect of high fat diet enriched with unsaturated and diet rich in saturated fatty acids on sphingolipid metabolism in rat skeletal muscle. J Cell Physiol. 2010, 225: 786-791. 10.1002/jcp.22283.
Barber SA, Perera PY, Vogel SN: Defective ceramide response in C3H/HeJ (Lpsd) macrophages. J Immunol. 1995, 155: 2303-2305.
MacKichan ML, DeFranco AL: Role of ceramide in lipopolysaccharide (LPS)-induced signaling. LPS increases ceramide rather than acting as a structural homolog. J Biol Chem. 1999, 274: 1767-1775. 10.1074/jbc.274.3.1767.
Bikman BT, Summers SA: Ceramides as modulators of cellular and whole-body metabolism. J Clin Invest. 2011, 121: 4222-4230. 10.1172/JCI57144.
Winder WW, Hardie DG: AMP-activated protein kinase, a metabolic master switch: possible roles in type 2 diabetes. Am J Physiol. 1999, 277: E1-10.
Cleasby ME, Dzamko N, Hegarty BD, Cooney GJ, Kraegen EW, Ye JM: Metformin prevents the development of acute lipid-induced insulin resistance in the rat through altered hepatic signaling mechanisms. Diabetes. 2004, 53: 3258-3266. 10.2337/diabetes.53.12.3258.
Stocker DJ, Taylor AJ, Langley RW, Jezior MR, Vigersky RA: A randomized trial of the effects of rosiglitazone and metformin on inflammation and subclinical atherosclerosis in patients with type 2 diabetes. Am Heart J. 2007, 153: 445-e441-446
Marquie G: Metformin action on lipid metabolism in lesions of experimental aortic atherosclerosis of rabbits. Atherosclerosis. 1983, 47: 7-17. 10.1016/0021-9150(83)90066-7.
Lin HZ, Yang SQ, Chuckaree C, Kuhajda F, Ronnet G, Diehl AM: Metformin reverses fatty liver disease in obese, leptin-deficient mice. Nat Med. 2000, 6: 998-1003. 10.1038/79697.
Summers SA: Ceramides in insulin resistance and lipotoxicity. Prog Lipid Res. 2006, 45: 42-72. 10.1016/j.plipres.2005.11.002.
Bikman BT, Zheng D, Reed MA, Hickner RC, Houmard JA, Dohm GL: Lipid-induced insulin resistance is prevented in lean and obese myotubes by AICAR treatment. Am J Physiol Regul Integr Comp Physiol. 2010, 298: R1692-1699. 10.1152/ajpregu.00190.2009.
Fei W, Shui G, Gaeta B, Du X, Kuerschner L, Li P, Brown AJ, Wenk MR, Parton RG, Yang H: Fld1p, a functional homologue of human seipin, regulates the size of lipid droplets in yeast. J Cell Biol. 2008, 180: 473-482. 10.1083/jcb.200711136.
Chan R, Uchil PD, Jin J, Shui G, Ott DE, Mothes W, Wenk MR: Retroviruses human immunodeficiency virus and murine leukemia virus are enriched in phosphoinositides. J Virol. 2008, 82: 11228-11238. 10.1128/JVI.00981-08.
Shui G, Guan X, Low CP, Chua GH, Goh SYJ, Yang H, Wenk MR: Toward one step analysis of cellular dynamic lipidome using liquid chromatography coupled with mass spectrometry: application to saccharomyces cerevisiae and schizosaccharomyces pombe lipidomics. Mol Biosyst. 2010, doi:10.1039/B913353D.
Pfaffl MW: A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29: e45-10.1093/nar/29.9.e45.
Bikman BT, Zheng D, Pories WJ, Chapman W, Pender JR, Bowden RC, Reed MA, Cortright RN, Tapscott EB, Houmard JA, et al: Mechanism for improved insulin sensitivity after gastric bypass surgery. J Clin Endocrinol Metab. 2008, 93: 4656-4663. 10.1210/jc.2008-1030.
Winder WW, Holmes BF, Rubink DS, Jensen EB, Chen M, Holloszy JO: Activation of AMP-activated protein kinase increases mitochondrial enzymes in skeletal muscle. J Appl Physiol. 2000, 88: 2219-2226.
Tagami S, Inokuchi Ji J, Kabayama K, Yoshimura H, Kitamura F, Uemura S, Ogawa C, Ishii A, Saito M, Ohtsuka Y, et al: Ganglioside GM3 participates in the pathological conditions of insulin resistance. J Biol Chem. 2002, 277: 3085-3092. 10.1074/jbc.M103705200.
Bikman BT: A role for sphingolipids in the pathophysiology of obesity-induced inflammation. Cell Mol Life: CMLS. 2012, doi:10.1007/s00018-00012-00917-00015.
Shi H, Kokoeva MV, Inouye K, Tzameli I, Yin H, Flier JS: TLR4 links innate immunity and fatty acid-induced insulin resistance. J Clin Invest. 2006, 116: 3015-3025. 10.1172/JCI28898.
Blazquez C, Geelen MJ, Velasco G, Guzman M: The AMP-activated protein kinase prevents ceramide synthesis de novo and apoptosis in astrocytes. FEBS Lett. 2001, 489: 149-153. 10.1016/S0014-5793(01)02089-0.
Cacicedo JM, Yagihashi N, Keaney JF, Ruderman NB, Ido Y: AMPK inhibits fatty acid-induced increases in NF-kappaB transactivation in cultured human umbilical vein endothelial cells. Biochem Biophys Res Commun. 2004, 324: 1204-1209. 10.1016/j.bbrc.2004.09.177.
Bikman BT, Zheng D, Kane DA, Anderson EJ, Woodlief TL, Price JW, Dohm GL, Neufer PD, Cortright RN: Metformin improves insulin signaling in obese rats via reduced IKKbeta action in a fiber-type specific manner. Journal of obesity. 2010, 2010: doi:10.1155/2010/970865.
Ruderman N, Prentki M: AMP kinase and malonyl-CoA: targets for therapy of the metabolic syndrome. Nat Rev Drug Discov. 2004, 3: 340-351. 10.1038/nrd1344.
Todd MK, Watt MJ, Le J, Hevener AL, Turcotte LP: Thiazolidinediones enhance skeletal muscle triacylglycerol synthesis while protecting against fatty acid-induced inflammation and insulin resistance. Am J Physiol Endocrinol Metab. 2007, 292: E485-493.
Smith AC, Mullen KL, Junkin KA, Nickerson J, Chabowski A, Bonen A, Dyck DJ: Metformin and exercise reduce muscle FAT/CD36 and lipid accumulation and blunt the progression of high-fat diet-induced hyperglycemia. Am J Physiol Endocrinol Metab. 2007, 293: E172-181. 10.1152/ajpendo.00677.2006.
Holland WL, Miller RA, Wang ZV, Sun K, Barth BM, Bui HH, Davis KE, Bikman BT, Halberg N, Rutkowski JM, et al: Receptor-mediated activation of ceramidase activity initiates the pleiotropic actions of adiponectin. Nat Med. 2011, 17: 55-63. 10.1038/nm.2277.
Kadowaki T, Yamauchi T, Kubota N, Hara K, Ueki K, Tobe K: Adiponectin and adiponectin receptors in insulin resistance, diabetes, and the metabolic syndrome. J Clin Invest. 2006, 116: 1784-1792. 10.1172/JCI29126.
Takabe K, Paugh SW, Milstien S, Spiegel S: “Inside-out” signaling of sphingosine-1-phosphate: therapeutic targets. Pharmacol Rev. 2008, 60: 181-195. 10.1124/pr.107.07113.
The authors would like to acknowledge Marjean Garowski and Connie Provost for their excellent clerical assistance, and Doug C. Berry for his technical equipment support.
The authors declare no competing interests.
KAE and MES assisted with cell treatments, RT-qPCR, lipid extraction, and manuscript preparation. TSA and JTP performed lipid analysis. MJE, ESB, AEH, MAB, BJT, MOT assisted with RT-qPCR and lipid extraction. CRH managed the animal study and assisted with manuscript preparation. BTB was involved in experimental planning, all experiments, and manuscript preparation. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Erickson, K.A., Smith, M.E., Anthonymuthu, T.S. et al. AICAR inhibits ceramide biosynthesis in skeletal muscle. Diabetol Metab Syndr 4, 45 (2012). https://doi.org/10.1186/1758-5996-4-45
- Metabolic syndrome