- Open Access
Acetate supplementation modulates brain adenosine metabolizing enzymes and adenosine A2Areceptor levels in rats subjected to neuroinflammation
Journal of Neuroinflammation volume 11, Article number: 99 (2014)
Acetate supplementation reduces neuroglia activation and pro-inflammatory cytokine expression in rat models of neuroinflammation and Lyme neuroborreliosis. Because single-dose glyceryl triacetate (GTA) treatment increases brain phosphocreatine and reduces brain AMP levels, we postulate that GTA modulates adenosine metabolizing enzymes and receptors, which may be a possible mechanism to reduce neuroinflammation.
To test this hypothesis, we quantified the ability of GTA to alter brain levels of ecto-5’-nucleotidase (CD73), adenosine kinase (AK), and adenosine A2A receptor using western blot analysis and CD73 activity by measuring the rate of AMP hydrolysis. Neuroinflammation was induced by continuous bacterial lipopolysaccharide (LPS) infusion in the fourth ventricle of the brain for 14 and 28 days. Three treatment strategies were employed, one and two where rats received prophylactic GTA through oral gavage with LPS infusion for 14 or 28 days. In the third treatment regimen, an interventional strategy was used where rats were subjected to 28 days of neuroinflammation, and GTA treatment was started on day 14 following the start of the LPS infusion.
We found that rats subjected to neuroinflammation for 28 days had a 28% reduction in CD73 levels and a 43% increase in AK levels that was reversed with prophylactic acetate supplementation. CD73 activity in these rats was increased by 46% with the 28-day GTA treatment compared to the water-treated rats. Rats subjected to neuroinflammation for 14 days showed a 50% increase in levels of the adenosine A2A receptor, which was prevented with prophylactic acetate supplementation. Interventional GTA therapy, beginning on day 14 following the induction of neuroinflammation, resulted in a 67% increase in CD73 levels and a 155% increase in adenosine A2A receptor levels.
These results support the hypothesis that acetate supplementation can modulate brain CD73, AK and adenosine A2A receptor levels, and possibly influence purinergic signaling.
In the central nervous system (CNS), adenosine is a potent neuromodulator that regulates sleep, arousal, neuronal excitability, cerebral blood flow and inflammation [1, 2]. Under pathological events or increased metabolic demand, adenosine triphosphate (ATP) metabolism and adenosine levels increase with a decrease in the energy charge ratio ((ATP + 0.5*ADP)/(ATP + ADP + AMP)) . Adenosine is described as a ‘retaliatory metabolite’  since it inhibits high energy utilizing processes, reduces the cellular metabolic demand, and restores cellular energy levels. Both adenosine and ATP are ubiquitously present in most organs and tissues and have an important signaling role in inflammation [2, 5, 6]. Thus, adenosine serves as a link between cellular metabolism and inflammatory signaling.
Adenosine modulates brain activity by binding to G-protein coupled purinergic P1 or adenosine (A1, A2A, A2B, and A3) receptors . The CNS effects of adenosine are primarily mediated by inhibitory A1 and stimulatory A2A receptors . Activation of A1 receptors inhibits neuronal excitability by reducing excitatory neurotransmitter release and offers neuroprotection . While activation of peripheral A2A receptors reduces inflammation, central A2A receptor activation increases glutamate outflow and neuroinflammation [9–11]. Adenosine can be formed both inside as well as outside the cell and distinct cell-specific mechanisms for the elevation of extracellular adenosine levels exist . Under conditions of hypoxia, ischemia, inflammation, nerve stimulation or stress, astrocytes release ATP, which is enzymatically metabolized to adenosine . The rate limiting enzyme in this process is ecto-5’-nucleotidase (CD73) . Adenosine catabolism, on the other hand, is controlled by two enzymes: adenosine deaminase and adenosine kinase (AK). Adenosine deaminase converts adenosine to inosine, which is typically negligible in the central nervous system, although this may change under pathological conditions . Adenosine kinase converts adenosine to AMP following its uptake into the cell via nucleoside transporters . Because adenosine can influence neuronal activity and mediate neuroinflammation, being able to modulate adenosine levels or the receptors involved in purinergic signaling has broad therapeutic potential .
A reproducible model of neuroinflammation is generated in rats by the infusion of the bacterial endotoxin lipopolysaccharide (LPS) directly into the fourth ventricle of the brain . In brain, LPS binds to the TLR4/CD14/MD-2 receptor complex  that activates neuroglia, reduces cholinergic cell immunoreactivity , and increases the expression of the pro-inflammatory cytokine interleukin (IL)-1β . Acetate supplementation, induced with glyceryl triacetate (GTA, 6 g/kg, by oral gavage) reduces LPS-induced neuroglial activation [19, 21], IL-1β levels , and loss of cholinergic immunoreactivity . Glyceryl triacetate is an effective treatment in rat models of Canavan’s disease  and traumatic brain injury , possesses growth-arresting properties  and is shown to be safe and well tolerated in human trials for Canavan’s disease . Oral administration of GTA increase rat plasma acetate by 100-fold and brain acetyl-CoA levels by 2.2-fold compared to water treated rats . Increase in acetyl-CoA metabolism further increases brain energy stores, reduces AMP levels  and increases acetylation of nuclear histones [20, 27], which is associated with attenuation of pro-inflammatory cytokine release . In microglia and astrocyte cell cultures, acetate reverses LPS-induced hypoacetylation of histones, attenuates pro-inflammatory cytokines, increases anti-inflammatory cytokine expression, reduces nuclear factor-κB and mitogen-activated protein kinase mediated signaling, and reduces prostaglandin E2 and cyclooxygenase 1 and 2 levels [28–30].
Based on this data, we postulated that acetate supplementation modulates the levels of adenosine metabolizing enzymes and adenosine receptors, which may be a possible mechanism by which GTA exerts its anti-inflammatory and neuroprotective effects. To begin to test this hypothesis, we quantified the ability of GTA to alter brain levels and activity of CD73, and the levels of AK and adenosine A2A receptors. We also examined how protein levels and activity differed using both prophylactic and interventional GTA treatment strategies. Prophylactic acetate supplementation prevented the LPS-induced reduction of brain CD73, increased CD73 activity, and prevented the LPS-induced increase of AK and A2A receptor levels. Interventional GTA treatment increased CD73 similar to the prophylactic treatment, but reduced CD73 activity. Furthermore, in contrast to the prophylactic treatment, interventional GTA increased A2A receptor levels compared to the water-treated controls. These data support the hypothesis that acetate supplementation can modulate adenosine metabolizing enzymes and A2A receptor expression levels in the brain and possibly enhance the effects of endogenous adenosine.
Glyceryl triacetate, buffer reagents, β-glycerophosphate, erythro-9-(2-hydroxy-3-nonyl) adenine, α, β-methyleneadenosine 5’-diphosphate, and 2-mercaptoethanol were purchased from Sigma (Sigma, St. Louis, MO, USA). A mouse anti-human CD73 antibody and a horseradish peroxidase (HRP)-conjugated goat anti-mouse IgG antibody were obtained from AbD Serotec (AbD Serotec, Raleigh, NC, USA). A HRP-conjugated goat anti-mouse IgG antibody was purchased from Jackson ImmunoResearch (Jackson ImmunoResearch, Westgrove, PA, USA). A mouse anti-adenosine receptor A2A antibody was obtained from Upstate (Upstate, Billerica, MA, USA). A goat anti-adenosine kinase antibody, mouse anti-α tubulin antibody, HRP-conjugated donkey anti-goat IgG antibody, and HRP-conjugated goat anti-mouse IgM antibody were obtained from Santa Cruz Biotechnology (Santa Cruz Biotechnology, Santa Cruz, CA, USA). Absolute ethanol was from Pharmco (Pharmco, Brookfield, CT, USA).
This study was conducted in accordance with the NIH Guidelines for the Care and Use of Laboratory Animals (NIH Publication No. 80-23) under an approved University protocol using male Sprague-Dawley rats (Charles River, Wilmington, MA, USA). All rats were allowed to acclimate in our facility for at least seven days prior to inclusion in the study. The surgical implantation of cannulas and the induction of neuroinflammation were performed as described previously . A solution of artificial cerebrospinal fluid (aCSF) or LPS (20.0 ng/μL, E coli, 055:B5, Sigma, St. Louis, MO, USA) dissolved in aCSF (Harvard Apparatus, Holliston, MA, USA) was infused continually at a rate of 0.25 μL/hr via the osmotic mini-pump for a period of 14 or 28 days [31, 32]. The rats were divided into three separate experiments: a 14- and 28-day prophylactic treatment study, and a 28-day interventional treatment study. During the 14- and 28-day prophylactic treatment studies, rats were treated daily with water or glyceryl triacetate (GTA) at a dose of 6 g/kg by oral gavage. In the 28-day interventional study, rats did not begin receiving daily doses of either water or GTA until 14 days after the start of the LPS infusion. Interventional treatment was started on day 14 due to neuroglia activation being significantly elevated above controls at this time .
Extraction of rat brain tissue
Rats were anesthetized with isoflurane, euthanized by decapitation, and then the brains were removed and dissected anterior to the middle carotid artery in the coronal plane . The postmortem interval for the sample extraction did not exceed 1.5 min. The dissected brains were placed in a tube containing 3 mL of ice cold extraction buffer (50 mM Tris buffer (pH 7.4) containing 150 mM sodium chloride, 1 mM EGTA, 1 mM sodium orthovanadate, 5 mM zinc chloride, 100 mM sodium fluoride, 1 mM PMSF, one complete, EDTA-free tablet (Roche Applied Science, Indianapolis, IN, USA) per 50 mL, and 0.1% Igepal CA-630). The sample was allowed to sit on ice for 10 min, then homogenized using probe sonication. Homogenized samples were centrifuged at 4°C for 20 min at 4,500 x g and the cytosolic portion was aliquotted into small volumes and stored at -80°C until use.
Western blot analysis
Samples were prepared by boiling in loading buffer composed of 95% Laemmli sample buffer containing 5% 2-mercaptoethanol. The separation was performed on 50 μg of protein using a 15% Tris-HCl gel with an electrophoresis separation of 100 volts for 135 min. The protein was transferred onto a 0.45 μm nitrocellulose membrane at 100 volts for 90 min in ice. Primary antibodies against CD73 (1:1,000 dilution), A2AR (1:1000 dilution), adenosine kinase (1:200 dilution), and α-tubulin (1:1,500 dilution) were prepared in 20 mM Tris buffer, pH 7.4, containing 150 mM NaCl, 0.05% Tween 20 (TTBS), and 5% nonfat dried milk. The nitrocellulose membranes were incubated with primary antibody overnight at 4°C, then incubated with HRP-linked secondary antibody for 90 min at room temperature. Secondary antibodies goat anti-mouse IgG (1:20,000 dilution), goat anti-mouse IgG (1:10,000 dilution), donkey anti-goat IgG (1:10,000 dilution), and goat anti-mouse IgM (1:10,000 dilution) (Santa Cruz Biotechnology, Santa Cruz, CA, USA) were prepared in TTBS buffer. Protein bands were detected using either SuperSignal™ West Pico or West Femto Chemiluminescent Substrates (Pierce, Rockford, IL, USA) and analyzed in a UVP Bioimaging System equipped with VisionWorks™ imaging software (version 4.5, Upland, CA, USA, http://www.UVP.com). Protein concentration was measured using the Bradford assay . Optical densities of the proteins of interest are normalized to the optical density of the loading control α-tubulin and all the western blot data are expressed as percentage over controls.
Sample brain extracts were diluted in ice cold assay buffer (50 mM Tris buffer (pH 7.4 at 37°C) containing 20 mM β-glycerophosphate and 20 μM erythro-9-(2-hydroxy-3-nonyl) adenine) to a protein concentration of 3.33 μg/μL. Each sample (500 μg protein) was assayed in duplicate, with one assay containing 400 μM α, β-methylene adenosine 5’-diphosphate (AMPCP) in the buffer, as a control to inhibit the activity of CD73, and the other without AMPCP. Samples were pre-incubated at 37°C for 10 min, and the assay was started by adding 1 mM AMP and incubating for 30 min at 37°C. The reaction was stopped with 3 M perchloric acid and placed on ice before being centrifuged at 18,100 × g for 5 min at 4°C. The adenosine formed as a result of AMP breakdown by CD73 was then converted into its fluorescent derivative and quantified using HPLC with fluorescence detection as described . Adenosine levels from the control reaction were subtracted from the experimental reaction to calculate CD73 activity in units of nmol adenosine/mg protein/min.
When comparing two groups, an unpaired t-test with a two-tailed P value was used to calculate statistical differences using GraphPad InStat statistical software (Version 3.10, Graph Pad Software, Inc., San Diego, CA, USA, http://www.graphpad.com). When comparing more than two groups, a One Way ANOVA with a Tukey’s post-hoc test was performed using the same statistical software. All results are expressed as means ± SD with significance set at P ≤0.05.
To test the hypothesis that acetate supplementation modulates brain adenosine metabolizing enzymes (CD73 and AK) and adenosine A2A receptor levels, we measured the levels of these proteins and the activity of CD73 in three parallel studies. In studies one and two, rats were subject to neuroinflammation for either 14 or 28 days and received prophylactic acetate supplementation throughout the duration of the experiment. A third study was performed in which a group of rats were subjected to 28 days of neuroinflammation, and acetate supplementation was started interventionally on day 14 following the start of the LPS infusion.
Fourteen day prophylactic acetate supplementation
We measured the levels of CD73, AK, and A2A receptor and the activity of CD73 in rats after a 14-day study period. In this study, there were three groups of rats. Group one received sham surgery with aCSF infusion and oral water which served as the control group (n = 6), group two received a LPS infusion dissolved in aCSF with oral water (n = 12), and group three received LPS and were treated with daily oral doses of GTA (6 g/kg body weight) (n = 6). Protein bands for CD73, AK, A2AR, and α-tubulin corresponding to molecular weights 68, 48, 45, and 55 kDa respectively, were quantified using western blot analysis (Figures 1A, 2A, and 3A). We found that LPS significantly reduced CD73 levels by 38%, while rats that received LPS plus GTA did not differ from controls (95% ± 11) (Figure 1B). Since CD73 is the rate-limiting enzyme for adenosine formation  and changes in its activity are observed in inflammatory conditions , we measured CD73 activity in these samples. The activity of CD73 did not significantly differ between control and rats subjected to neuroinflammation. However, rats receiving LPS plus GTA had a significant increase in activity by 31% compared to controls and rats subjected to LPS (Figure 1C). Further, no significant differences in AK levels were observed between the groups (Figure 1D). Based on these data, we measured A2A receptor levels and found that LPS infusion causes a significant increase by 50% compared to controls, while acetate supplementation prevented the LPS-induced increase leaving A2A receptor at control levels (Figure 1E). These results demonstrate that prophylactic acetate supplementation has the capacity to prevent LPS-induced changes in CD73 and A2A receptor levels, and is also able to increase CD73 activity. Although it is not clear whether acetate supplementation achieves an increase in CD73 activity through changes in gene expression or enzyme modification, both may be involved. These data do, however, suggest that acetate supplementation can modulate adenosine metabolizing enzymes and A2A receptor levels.
Twenty-eight day prophylactic acetate supplementation
A 28-day study was performed to examine the long-term effect of acetate supplementation on brain adenosine metabolizing enzymes (CD73 and AK) and A2A receptor levels. The infusion and treatment groups were identical to those described above except that the GTA treatment and LPS infusion were continued for a total of 28 days. In this study, we found that LPS significantly reduced CD73 levels by 28% of controls, which was not evident in rats that received acetate supplementation (Figure 2B). There was no difference in CD73 activity between controls and rats subjected to neuroinflammation, but LPS-treated rats receiving acetate supplementation showed a significant increase in activity (46%) compared to controls and rats subjected to neuroinflammation (Figure 2C). Twenty eight-day LPS infusion resulted in a significant increase in AK levels (43%) compared to control rats. We found no change in AK levels in rats subjected to neuroinflammation and treated with prophylactic acetate supplementation (Figure 2D). No difference in A2A receptor levels was observed between groups (Figure 2E). These results demonstrate that long-term prophylactic acetate supplementation is able to prevent LPS-induced changes in CD73 and AK levels, and increase CD73 activity using a 28-day prophylactic treatment strategy. Collectively, these studies suggest that neuroinflammation modulates adenosine metabolizing enzymes, which can be prevented with prophylactic acetate supplementation.
Interventional acetate supplementation
The effect of interventional acetate supplementation (starting at 14 days post-LPS infusion until the 28th day of LPS infusion) on adenosine metabolizing enzymes (CD73 and AK) and A2A receptor levels was examined. Treatment with GTA was begun on day 14 because this is the earliest time when neuroglia activation, based on significant morphological changes in astrocytes and microglia, has been documented  in this model. However, the inflammatory signaling starts as early as 6 days following LPS infusion . LPS-treated rats that received an interventional acetate treatment showed a significant increase in CD73 levels (by 67%) when compared to rats that received water (Figure 3B) but demonstrated a significantly lower CD73 activity (by 12%, Figure 3C). There was no significant difference in AK levels between rats receiving water and rats receiving acetate supplementation (Figure 3D). Interventional acetate supplementation resulted in a significant increase in A2A receptor levels (155%) compared to controls (Figure 3E). These results demonstrate that acetate supplementation is able to modulate CD73 and A2A receptor following an interventional treatment strategy. While an increase in CD73 activity was not correlated to an increase in CD73 protein levels as seen with prophylactic treatment, it may be that the mechanism by which acetate exerts its effects takes longer to alter the activity of the enzyme.
Acetate supplementation elevates plasma acetate (approximately 19 mM) , brain acetate (approximately 11 mM) , and acetyl Co-A (approximately 9 μM) levels . This increase in brain acetyl-CoA metabolism increases brain phosphocreatine levels and reduces AMP levels, suggesting a potential role in altering brain purine metabolism . In order to integrate GTA-induced changes in energy levels  with the potential to alter purinergic metabolism, we investigated the effect that acetate supplementation had on purinergic enzymes and receptors in a rat model of neuroinflammation. These studies suggest that acetate supplementation was able to modulate brain ecto-5’-nucleotidase (CD73) and adenosine kinase (AK), as well as the levels of the adenosine A2A receptor, which may describe a mechanism by which acetate exerts its observed anti-inflammatory and potentially neuroprotective effects. The premise that bioenergetic stimulation can influence neuroinflammation has been demonstrated in various animal models of Alzheimer’s disease and Parkinson’s disease, as well as in Parkinson’s disease patients . Acetyl-L-carnitine, like acetate, bolsters mitochondrial metabolism in astrocytes and is neuroprotective in a rat model of traumatic brain injury . Similarly, the closest metabolic correlate of acetate supplementation the ketogenic diet, also modulates brain mitochondrial metabolism and is neuroprotective [39, 40] through a mechanism involving adenosine . With 14- and 28-day prophylactic acetate supplementation we found that GTA was able to prevent LPS-induced reduction in CD73 levels in addition to increasing CD73 activity (Figures 1 and 2). This suggests that GTA can increase brain adenine nucleotide metabolism and potentially elevate extracellular levels of adenosine. In this regard, interferon-β used for treatment of multiple sclerosis also increases the expression of CD73 [42, 43]. Interventional acetate supplementation increased CD73 levels however lower CD73 activity was observed with GTA as compared to the LPS group (Figure 3). Cortical stab wound and focal cerebral ischemia models of brain injury have demonstrated a biphasic alteration in CD73 expression and activity, where an initial decrease is followed by a distinct increase in expression and activity of CD73 during the post-injury period [44–46]. Thus, this suggests that the 14 days of interventional GTA treatment may not be sufficient to elevate CD73 activity. Although during CD73 activity measurements, the non-specific phosphatase activity was inhibited by β-glycerophosphate and the non-CD73 related nucleotidase activity was subtracted from samples by AMCP, involvement of other alkaline phosphatases and intracellular cellular nucleotidases that are not completely inhibited by AMCP cannot be ruled out . Furthermore, different CD73 isoforms in distinct brain regions  have been reported which may differentially contribute and interfere with the whole brain CD73 activity analysis in the current study.
Another key enzyme that regulates extracellular levels of adenosine is AK. Although intracellular, the low Km of AK for adenosine (1.5-2.4 μM)  combined with the bidirectional and equilibrative nature of adenosine transporters, allows AK to control adenosine uptake. We found that 28 days of LPS-infusion increased AK levels as seen during traumatic brain injury and epilepsy [15, 49] (Figure 2). This increase was prevented by the long-term prophylactic treatment, which suggests that GTA in presence of LPS is able to enhance extracellular adenosine availability by preventing the increase in its uptake and conversion to AMP. However, this may lead to a scenario where, elevated adenosine levels become more susceptible to adenosine deaminase mediated degradation to inosine. Since these alterations may be cell-type specific, an in depth in vitro analysis of all purinergic enzymes is required to develop a comprehensive view of how acetate alters brain adenosine metabolism.
Extracellular adenosine is an endogenous agonist for four different G protein-coupled (A1, A2A, A2B, and A3) receptors, of which the A1 and A2A receptors have the greatest relevance in the central nervous system [50, 51]. The A1 receptor signal cascade generally suppresses neuronal activity, inhibits synaptic transmission, and reduces the activation and response of microglia [52, 53]. Adenosine A2A receptors, on the other hand are known to mediate LPS-induced neuroinflammation and neuronal dysfunction [9, 10, 54]. Antagonists of the A2A receptors have been shown to be anti-inflammatory in a number of CNS disorders [52, 54–56], mainly secondary to their inhibitory effects on the glutamate outflow and resulting excitotoxicity [9, 10]. In specific regard to our model, it was found that the A2A receptor inhibitor caffeine attenuates LPS-induced neuroinflammation . We found that at 14 days, LPS-induced neuroinflammation caused a significant increase in A2A receptor levels compared to controls (Figure 1), in line with our previous findings that show an increase in IL-1β expression , which is known to increase A2A receptor levels . Fourteen-day prophylactic acetate supplementation prevented this LPS-induced increase (Figure 1) in A2A receptors, which is in agreement with results demonstrating that GTA attenuates LPS-induced pro-inflammatory cytokine release . Since blockade of A2A receptor prevents IL-1β induced exacerbation of neuronal toxicity , acetate supplementation has a combined effect of reducing IL-1β levels and A2A receptors that can offer robust neuroprotection by attenuating neuroinflammation. However, interventional acetate supplementation unlike the prophylactic treatment increased A2A receptor levels (Figure 3). The reason for this difference is not yet clear, but a bidirectional effect of A2A receptors in neuroinflammation has been described . It is possible that 14 days of interventional acetate supplementation started after significant increases in neuroglia activation have already occurred may not be sufficient to counteract the LPS-induced elevation in A2A receptor levels. However, the ability of the A2A receptors to control neuroinflammation is dependent on local glutamate levels and is critical in determining whether their stimulation results in anti-inflammatory or pro-inflammatory effects . Distinct pathological stages after injury respond to different A2A receptor modulators. For example, during early spinal cord injury A2A receptor agonists offer neuroprotection, while A2A receptor knockout was neuroprotective only during later injury stages . Thus, an alternative reasoning may be that the increase in A2A receptors observed with interventional GTA may be beneficial in enhancing the effects of endogenous adenosine that may contribute towards the anti-inflammatory effect of acetate supplementation. However, to make this determination a thorough investigation of temporal changes in inflammatory markers, A2A receptors, and local glutamate levels with LPS and GTA is required. Further, the protective effects of adenosine A2A receptor agonists and antagonists against spinal cord injury are mediated through their effects in the periphery and the CNS, respectively , hence it will be interesting to study how GTA alters peripheral purinergic signaling. A limitation of the interventional study was the lack of the aCSF control group, which would have allowed us to determine whether the increase in A2A receptors was indeed an elevation from control levels. Thus, future studies that examine the effect of interventional GTA strategy for longer treatment duration with adequate controls are necessary. Regardless, this study demonstrates that prophylactic acetate supplementation does prevent the LPS-induced increase in A2A receptor levels, which may help to explain the mechanism by which GTA confers its anti-inflammatory effects.
We previously reported that, acetate supplementation increases histone acetylation  and reverses LPS-induced histone H3 at lysine 9 (H3K9) hypoacetylation in a model of neuroinflammation . Histone hyperacetylation alters gene expression and also induces anti-inflammatory effects [61, 62]. Therefore, it is reasonable to speculate that acetate induced histone acetylation may be a potential underlying mechanism involved in the modulation of adenosine metabolizing enzymes CD73 and AK as well as the levels of the adenosine A2A receptors, especially at the level of gene transcription. Future studies will determine the link between acetate-induced histone acetylation changes and alteration in the levels of these proteins. Using specific histone acetyltransferase inhibitors to block the effect of acetate on histone acetylation will allow us to determine its role in altering levels of adenosine metabolizing enzymes and receptors. Further, by studying if acetylated H3K9 is associated with the gene promoters of adenosine metabolizing enzyme and receptor will determine if acetate-induced alteration in their expression is controlled by chromatin remodeling.
Since adenosine is a potent endogenous modulator of neuronal activity and inflammation, development of therapeutic strategies that modulate adenosine metabolism may offer treatment alternatives for neuroinflammation and neurodegenerative disorders. This study attempts to identify the underlying mechanism of action and a treatment regimen for glyceryl triacetate that has been shown to be anti-inflammatory in rat models of neuroinflammation and Lyme neuroborreliosis. In conclusion, both prophylactic and interventional acetate supplementation can modulate adenosine metabolizing enzymes and A2A receptor levels supporting our hypothesis. Future experimentation is needed to determine the specific brain regions, cell types, and mechanisms involved in altering brain adenosine metabolism with acetate supplementation.
artificial cerebrospinal fluid
α,β-methylene adenosine 5′-diphosphate
analysis of variance
- A2A receptor:
adenosine A2A receptor
adenosine A2A receptor
central nervous system
ethylene glycol bis (2-aminoethyl ether)-N, N, N’, N’-tetraacetic acid
high performance liquid chromatography
Tris-buffered saline containing Tween 20.
Cunha RA: Neuroprotection by adenosine in the brain: From A (1) receptor activation to A (2A) receptor blockade. Purinergic Signal. 2005, 1: 111-134. 10.1007/s11302-005-0649-1.
Dunwiddie TV, Masino SA: The role and regulation of adenosine in the central nervous system. Annu Rev Neurosci. 2001, 24: 31-55. 10.1146/annurev.neuro.24.1.31.
Shepel PN, Ramonet D, Stevens P, Geiger JD: Purine level regulation during energy depletion associated with graded excitatory stimulation in brain. Neurol Res. 2005, 27: 139-148. 10.1179/016164105X21832.
Newby AC: Adenosine and the concept of retaliatory metabolites. Trends Biochem Sci. 1984, 9: 42-44. 10.1016/0968-0004(84)90176-2.
Di Virgilio F, Ceruti S, Bramanti P, Abbracchio MP: Purinergic signalling in inflammation of the central nervous system. Trends Neurosci. 2009, 32: 79-87. 10.1016/j.tins.2008.11.003.
Abbracchio MP, Burnstock G, Verkhratsky A, Zimmermann H: Purinergic signalling in the nervous system: an overview. Trends Neurosci. 2009, 32: 19-29. 10.1016/j.tins.2008.10.001.
Masino SA, Kawamura M, Wasser CA, Pomeroy LT, Ruskin DN: Adenosine, ketogenic diet and epilepsy: the emerging therapeutic relationship between metabolism and brain activity. Curr Neuropharmacol. 2009, 7: 257-268. 10.2174/157015909789152164.
Boison D, Chen JF, Fredholm BB: Adenosine signaling and function in glial cells. Cell Death Differ. 2010, 17: 1071-1082. 10.1038/cdd.2009.131.
Chen JF, Pedata F: Modulation of ischemic brain injury and neuroinflammation by adenosine A2A receptors. Curr Pharm Des. 2008, 14: 1490-1499. 10.2174/138161208784480126.
Chen JF, Sonsalla PK, Pedata F, Melani A, Domenici MR, Popoli P, Geiger J, Lopes LV, de Mendonca A: Adenosine A2A receptors and brain injury: broad spectrum of neuroprotection, multifaceted actions and “fine tuning” modulation. Prog Neurobiol. 2007, 83: 310-331. 10.1016/j.pneurobio.2007.09.002.
Paterniti I, Melani A, Cipriani S, Corti F, Mello T, Mazzon E, Esposito E, Bramanti P, Cuzzocrea S, Pedata F: Selective adenosine A2A receptor agonists and antagonists protect against spinal cord injury through peripheral and central effects. J Neuroinflammation. 2011, 8: 31-10.1186/1742-2094-8-31.
Parkinson FE, Xiong W, Zamzow CR: Astrocytes and neurons: different roles in regulating adenosine levels. Neurol Res. 2005, 27: 153-160.
Fredholm BB: Adenosine, an endogenous distress signal, modulates tissue damage and repair. Cell Death Differ. 2007, 14: 1315-1323. 10.1038/sj.cdd.4402132.
Thompson LF, Eltzschig HK, Ibla JC, Van De Wiele CJ, Resta R, Morote-Garcia JC, Colgan SP: Crucial role for ecto-5’-nucleotidase (CD73) in vascular leakage during hypoxia. J Exp Med. 2004, 200: 1395-1405. 10.1084/jem.20040915.
Boison D: Adenosine kinase, epilepsy and stroke: mechanisms and therapies. Trends Pharmacol Sci. 2006, 27: 652-658. 10.1016/j.tips.2006.10.008.
Fredholm BB, Chen JF, Cunha RA, Svenningsson P, Vaugeois JM: Adenosine and brain function. Int Rev Neurobiol. 2005, 63: 191-270.
Hauss-Wegrzyniak B, Dobrzanski P, Stoehr JD, Wenk GL: Chronic neuroinflammation in rats reproduces components of the neurobiology of Alzheimer’s disease. Brain Res. 1998, 780: 294-303. 10.1016/S0006-8993(97)01215-8.
Fujihara M, Muroi M, Tanamoto K, Suzuki T, Azuma H, Ikeda H: Molecular mechanisms of macrophage activation and deactivation by lipopolysaccharide: roles of the receptor complex. Pharmacol Ther. 2003, 100: 171-194. 10.1016/j.pharmthera.2003.08.003.
Reisenauer CJ, Bhatt DP, Mitteness DJ, Slanczka ER, Gienger HM, Watt JA, Rosenberger TA: Acetate supplementation attenuates lipopolysaccharide-induced neuroinflammation. J Neurochem. 2011, 117: 264-274. 10.1111/j.1471-4159.2011.07198.x.
Soliman ML, Smith MD, Houdek HM, Rosenberger TA: Acetate supplementation modulates brain histone acetylation and decreases interleukin-1beta expression in a rat model of neuroinflammation. J Neuroinflammation. 2012, 9: 51-10.1186/1742-2094-9-51.
Brissette CA, Houdek HM, Floden AM, Rosenberger TA: Acetate supplementation reduces microglia activation and brain interleukin-1beta levels in a rat model of Lyme neuroborreliosis. J Neuroinflammation. 2012, 9: 249-10.1186/1742-2094-9-249.
Arun P, Madhavarao CN, Moffett JR, Hamilton K, Grunberg NE, Ariyannur PS, Gahl WA, Anikster Y, Mog S, Hallows WC, Denu JM, Namboodiri AM: Metabolic acetate therapy improves phenotype in the tremor rat model of Canavan disease. J Inherit Metab Dis. 2010, 33: 195-210. 10.1007/s10545-010-9100-z.
Arun P, Ariyannur PS, Moffett JR, Xing G, Hamilton K, Grunberg NE, Ives JA, Namboodiri AM: Metabolic acetate therapy for the treatment of traumatic brain injury. J Neurotrauma. 2010, 27: 293-298. 10.1089/neu.2009.0994.
Tsen AR, Long PM, Driscoll HE, Davies MT, Teasdale BA, Penar PL, Pendlebury WW, Spees JL, Lawler SE, Viapiano MS, Jaworski DM: Triacetin-based acetate supplementation as a chemotherapeutic adjuvant therapy in glioma. Int J Cancer. 2014, 134: 1300-1310. 10.1002/ijc.28465.
Segel R, Anikster Y, Zevin S, Steinberg A, Gahl WA, Fisher D, Staretz-Chacham O, Zimran A, Altarescu G: A safety trial of high dose glyceryl triacetate for Canavan disease. Mol Genet Metab. 2011, 103: 203-206. 10.1016/j.ymgme.2011.03.012.
Bhatt DP, Houdek HM, Watt JA, Rosenberger TA: Acetate supplementation increases brain phosphocreatine and reduces AMP levels with no effect on mitochondrial biogenesis. Neurochem Int. 2013, 62: 296-305. 10.1016/j.neuint.2013.01.004.
Soliman ML, Rosenberger TA: Acetate supplementation increases brain histone acetylation and inhibits histone deacetylase activity and expression. Mol Cell Biochem. 2011, 352: 173-180. 10.1007/s11010-011-0751-3.
Soliman ML, Combs CK, Rosenberger TA: Modulation of inflammatory cytokines and mitogen-activated protein kinases by acetate in primary astrocytes. J Neuroimmune Pharmacol. 2013, 8: 287-300. 10.1007/s11481-012-9426-4.
Soliman ML, Ohm JE, Rosenberger TA: Acetate reduces PGE2 release and modulates phospholipase and cyclooxygenase levels in neuroglia stimulated with lipopolysaccharide. Lipids. 2013, 48: 651-662. 10.1007/s11745-013-3799-x.
Soliman ML, Puig KL, Combs CK, Rosenberger TA: Acetate reduces microglia inflammatory signaling in vitro. J Neurochem. 2012, 123: 555-567. 10.1111/j.1471-4159.2012.07955.x.
Lee H, Villacreses NE, Rapoport SI, Rosenberger TA: In vivo imaging detects a transient increase in brain arachidonic acid metabolism: a potential marker of neuroinflammation. J Neurochem. 2004, 91: 936-945. 10.1111/j.1471-4159.2004.02786.x.
Rosenberger TA, Villacreses NE, Hovda JT, Bosetti F, Weerasinghe G, Wine RN, Harry GJ, Rapoport SI: Rat brain arachidonic acid metabolism is increased by a 6-day intracerebral ventricular infusion of bacterial lipopolysaccharide. J Neurochem. 2004, 88: 1168-1178. 10.1046/j.1471-4159.2003.02246.x.
Bradford MM: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976, 72: 248-254. 10.1016/0003-2697(76)90527-3.
Bhatt DP, Chen X, Geiger JD, Rosenberger TA: A sensitive HPLC-based method to quantify adenine nucleotides in primary astrocyte cell cultures. J Chromatogr B Analyt Technol Biomed Life Sci. 2012, 889–890: 110-115.
Brisevac D, Bjelobaba I, Bajic A, Clarner T, Stojiljkovic M, Beyer C, Andjus P, Kipp M, Nedeljkovic N: Regulation of ecto-5’-nucleotidase (CD73) in cultured cortical astrocytes by different inflammatory factors. Neurochem Int. 2012, 61: 681-688. 10.1016/j.neuint.2012.06.017.
Mathew R, Arun P, Madhavarao CN, Moffett JR, Namboodiri MA: Progress toward acetate supplementation therapy for Canavan disease: glyceryl triacetate administration increases acetate, but not N-acetylaspartate, levels in brain. J Pharmacol Exp Ther. 2005, 315: 297-303. 10.1124/jpet.105.087536.
Beal MF: Mitochondrial dysfunction and oxidative damage in Alzheimer’s and Parkinson’s diseases and coenzyme Q10 as a potential treatment. J Bioenerg Biomembr. 2004, 36: 381-386.
Scafidi S, Racz J, Hazelton J, McKenna MC, Fiskum G: Neuroprotection by acetyl-L-carnitine after traumatic injury to the immature rat brain. Dev Neurosci. 2010, 32: 480-487.
Bough KJ, Wetherington J, Hassel B, Pare JF, Gawryluk JW, Greene JG, Shaw R, Smith Y, Geiger JD, Dingledine RJ: Mitochondrial biogenesis in the anticonvulsant mechanism of the ketogenic diet. Ann Neurol. 2006, 60: 223-235. 10.1002/ana.20899.
Ruskin DN, Masino SA: The nervous system and metabolic dysregulation: emerging evidence converges on ketogenic diet therapy. Front Neurosci. 2012, 6: 33.
Masino SA, Kawamura M, Ruskin DN, Gawryluk J, Chen X, Geiger JD: Purines and the Anti-Epileptic Actions of Ketogenic Diets. Open Neurosci J. 2010, 4: 58-63. 10.2174/1874082001004010058.
Airas L, Niemela J, Yegutkin G, Jalkanen S: Mechanism of action of IFN-beta in the treatment of multiple sclerosis: a special reference to CD73 and adenosine. Ann N Y Acad Sci. 2007, 1110: 641-648. 10.1196/annals.1423.067.
Niemela J, Ifergan I, Yegutkin GG, Jalkanen S, Prat A, Airas L: IFN-beta regulates CD73 and adenosine expression at the blood–brain barrier. Eur J Immunol. 2008, 38: 2718-2726. 10.1002/eji.200838437.
Bjelobaba I, Parabucki A, Lavrnja I, Stojkov D, Dacic S, Pekovic S, Rakic L, Stojiljkovic M, Nedeljkovic N: Dynamic changes in the expression pattern of ecto-5’-nucleotidase in the rat model of cortical stab injury. J Neurosci Res. 2011, 89: 862-873. 10.1002/jnr.22599.
Braun N, Lenz C, Gillardon F, Zimmermann M, Zimmermann H: Focal cerebral ischemia enhances glial expression of ecto-5’-nucleotidase. Brain Res. 1997, 766: 213-226. 10.1016/S0006-8993(97)00559-3.
Nedeljkovic N, Bjelobaba I, Subasic S, Lavrnja I, Pekovic S, Stojkov D, Vjestica A, Rakic L, Stojiljkovic M: Up-regulation of ectonucleotidase activity after cortical stab injury in rats. Cell Biol Int. 2006, 30: 541-546. 10.1016/j.cellbi.2006.03.001.
Cunha RA, Brendel P, Zimmermann H, Ribeiro JA: Immunologically distinct isoforms of ecto-5’-nucleotidase in nerve terminals of different areas of the rat hippocampus. J Neurochem. 2000, 74: 334-338.
Arch JR, Newsholme EA: Activities and some properties of 5’-nucleotidase, adenosine kinase and adenosine deaminase in tissues from vertebrates and invertebrates in relation to the control of the concentration and the physiological role of adenosine. Biochem J. 1978, 174: 965-977.
Aronica E, Zurolo E, Iyer A, de Groot M, Anink J, Carbonell C, van Vliet EA, Baayen JC, Boison D, Gorter JA: Upregulation of adenosine kinase in astrocytes in experimental and human temporal lobe epilepsy. Epilepsia. 2011, 52: 1645-1655. 10.1111/j.1528-1167.2011.03115.x.
Fredholm BB, IJzerman AP, Jacobson KA, Klotz KN, Linden J: International union of pharmacology. XXV. Nomenclature and classification of adenosine receptors. Pharmacol Rev. 2001, 53: 527-552.
Klotz KN: Adenosine receptors and their ligands. Naunyn Schmiedebergs Arch Pharmacol. 2000, 362: 382-391. 10.1007/s002100000315.
Fredholm BB, Chen JF, Masino SA, Vaugeois JM: Actions of adenosine at its receptors in the CNS: insights from knockouts and drugs. Annu Rev Pharmacol Toxicol. 2005, 45: 385-412. 10.1146/annurev.pharmtox.45.120403.095731.
Haselkorn ML, Shellington DK, Jackson EK, Vagni VA, Janesko-Feldman K, Dubey RK, Gillespie DG, Cheng D, Bell MJ, Jenkins LW, Homanics GE, Schnermann J, Kockanek PM: Adenosine A1 receptor activation as a brake on the microglial response after experimental traumatic brain injury in mice. J Neurotrauma. 2010, 27: 901-910. 10.1089/neu.2009.1075.
Rebola N, Simoes AP, Canas PM, Tome AR, Andrade GM, Barry CE, Agostinho PM, Lynch MA, Cunha RA: Adenosine A2A receptors control neuroinflammation and consequent hippocampal neuronal dysfunction. J Neurochem. 2011, 117: 100-111. 10.1111/j.1471-4159.2011.07178.x.
Brothers HM, Marchalant Y, Wenk GL: Caffeine attenuates lipopolysaccharide-induced neuroinflammation. Neurosci Lett. 2010, 480: 97-100. 10.1016/j.neulet.2010.06.013.
Wei CJ, Li W, Chen JF: Normal and abnormal functions of adenosine receptors in the central nervous system revealed by genetic knockout studies. Biochim Biophys Acta. 2011, 1808: 1358-1379. 10.1016/j.bbamem.2010.12.018.
Trincavelli ML, Costa B, Tuscano D, Lucacchini A, Martini C: Up-regulation of A (2A) adenosine receptors by proinflammatory cytokines in rat PC12 cells. Biochem Pharmacol. 2002, 64: 625-631. 10.1016/S0006-2952(02)01222-4.
Simoes AP, Duarte JA, Agasse F, Canas PM, Tome AR, Agostinho P, Cunha RA: Blockade of adenosine A2A receptors prevents interleukin-1beta-induced exacerbation of neuronal toxicity through a p38 mitogen-activated protein kinase pathway. J Neuroinflammation. 2012, 9: 204-10.1186/1742-2094-9-204.
Dai SS, Zhou YG: Adenosine 2A receptor: a crucial neuromodulator with bidirectional effect in neuroinflammation and brain injury. Rev Neurosci. 2011, 22: 231-239.
Li Y, Oskouian RJ, Day YJ, Rieger JM, Liu L, Kern JA, Linden J: Mouse spinal cord compression injury is reduced by either activation of the adenosine A2A receptor on bone marrow-derived cells or deletion of the A2A receptor on non-bone marrow-derived cells. Neuroscience. 2006, 141: 2029-2039. 10.1016/j.neuroscience.2006.05.014.
Adcock IM: HDAC inhibitors as anti-inflammatory agents. Br J Pharmacol. 2007, 150: 829-831. 10.1038/sj.bjp.0707166.
Strahl BD, Allis CD: The language of covalent histone modifications. Nature. 2000, 403: 41-45. 10.1038/47412.
This publication was made possible by Grants from the National Institutes of Health (NIH) (P20RR17699 and P30GM103329) and the North Dakota EPSCoR through the NSF (EPS-0447679).
The authors declare that they do not have competing interests associated with the publication of this manuscript.
DPB, MDS, JDG, and TAR participated in the research design and wrote or contributed to the writing of the manuscript. The experiments and data analysis were performed by DPB, and MDS. All authors read and approved the final version of the manuscript.
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Smith, M.D., Bhatt, D.P., Geiger, J.D. et al. Acetate supplementation modulates brain adenosine metabolizing enzymes and adenosine A2Areceptor levels in rats subjected to neuroinflammation. J Neuroinflammation 11, 99 (2014) doi:10.1186/1742-2094-11-99
- adenosine kinase
- adenosine A2A receptor
- glyceryl triacetate