Evidence That Links Loss of Cyclooxygenase-2 With Increased Asymmetric Dimethylarginine

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C yclooxygenase (COX) catalyzes the conversion of arachidonic acid to prostaglandin H 2 , which is then further metabolized by downstream synthase enzymes to a range of eicosanoids. COX is expressed in 2 isoforms, constitutive COX-1 and inducible COX-2. Nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used to treat inflammation and pain and show potential to prevent cancer. COX-2 is the therapeutic target of NSAIDs, although most members of this class of drugs inhibit both isoforms of COX 1 and, as a consequence, are associated with gastrointestinal side effects. 2 NSAID-induced gastrointestinal side effects are relatively common and can be serious, limiting the use of these drugs in some patients and proving fatal in others. 3 COX-2 selective inhibitors such as Vioxx (rofecoxib) and Celebrex (celecoxib) were originally developed to target COX-2 at the site of inflammation while sparing COX-1 in the gut and so reducing the gastrointestinal side effects typical of NSAIDs. 4 However, now, cardiovascular side effects associated with COX-2 inhibition dominate concern over NSAID usage [5][6][7] and have stopped the development of new drugs in this class. The cardiovascular side effects caused by the inhibition of COX-2 are mainly myocardial infarctions, 8,9 which implies increased thrombosis and atherosclerosis and have been considered to reflect local loss of the cardioprotective hormone prostacyclin by blood vessels. However, COX-2 is only sparsely detected in blood vessels, where, by contrast, COX-1 is readily detected. COX-2 is upregulated at sites of vascular inflammation, including atherosclerotic plaques, although, even at these areas, COX-1 drives prostacyclin release. 10 Although COX-2 is largely absent from blood vessels, [11][12][13] there are key areas in the body, including the kidney, [14][15][16][17] where it is expressed constitutively. COX-2 in the kidney regulates natriuresis, diuresis, and vasodilation. [16][17][18] NSAIDs, including COX-2 selective drugs, therefore have well-documented effects on the kidney and increase blood pressure by ≈1 to 2 mm Hg in normotensive individuals and by up to 14 mm Hg in patients with hypertension. 19 In addition, they are known to dysregulate glomerular filtration and salt/water homeostasis. [20][21][22][23] Given the well-established link between impaired renal function and cardiovascular events, including myocardial infarctions, it is logical to expect that these changes in renal function may contribute to the cardiovascular side effects associated with NSAID usage. 24 However, the precise mechanism by which COX-2 regulates renal function and the relevance of COX-2 in the kidney in comparison with other cardiovascular tissues are not known, and the debate continues regarding the relative contribution of vascular prostacyclin versus renal effects to cardiovascular side effects of NSAIDs. 25 Consequently, there are no biomarkers of NSAID-induced cardiovascular risk and no avenues to protect those that might be more susceptible than the general population.
To address this issue, we have performed a transcriptomic analysis of the 4 key cardiovascular tissues, kidney, heart, aorta, and blood, from wild-type and COX-2-deficient mice. Pathway analysis revealed alterations in the kidney of genes associated with nitric oxide (NO) biology, particularly those regulating the synthesis and metabolism of the endogenous NO synthase (NOS) inhibitors asymmetrical dimethylarginine (ADMA) and monomethyl-l-arginine (l-NMMA). We went on to validate increased ADMA and l-NMMA levels in plasma of mice lacking COX-2 and in wild-type mice or healthy human volunteers taking COX-2 selective inhibitors. Our work fits well with and helps to explain recent observations showing that endothelial NO synthase (eNOS) responses are reduced in vessels from COX-2-deficient mice. 26 Because NO release from endothelial cells performs the same protective role that prostacyclin performs on platelets and blood vessels, and because it synergizes powerfully with prostacyclin in platelets, 27 our observations are the first to provide a rational explanation for how the inhibition of COX-2 in the kidney can remotely regulate vascular side effects throughout the vasculature.

Experimental Animals
Male or female COX-1 -/and COX-2 -/mice, 11 back-crossed for >7 generations onto a C57Bl/6J background (Harlan, UK) were used at 10 to 12 weeks of age. For transcriptomic studies, littermate COX-2 +/+ mice from COX-2 -/colonies were used. For other studies, wildtype mice maintained separately were used as controls. Animals were genotyped before use. 11 Mice lacking prostacyclin receptors (IP -/-), supplied by Dr Rolf Nüsing, were on a C57BL/6 background as described. 28 Animal studies were conducted in accordance with Animals (Scientific Procedures) Act 1986, which is a UK act after local ethical review.

Pharmacological COX-2 Inhibition and Blood Pressure Measurement
Parecoxib (Pfizer, USA; 100 mg·kg -1 ·d -1 ) in drinking water was administered for 4 days to wild-type mice. Mean carotid arterial blood pressure was measured by using radiotelemetry. In brief, a 1.4F Millar MikroTip pressure catheter was inserted in the right common carotid artery of spontaneously breathing mice anesthetized with inhaled isoflurane (Abbott, USA). Animals were allowed to recover from the anesthetic, and measurements were made in conscious, unrestrained animals 21 days later. Blood pressure traces were recorded continuously with the use of the PowerLab and Chart 5 software (AD Instruments Ltd, UK). Blood was obtained by tail nick in conscious animals into 3.2% citrate and plasma separated by centrifugation.

Mouse Tissue Collection and Processing
Mice were euthanized by CO 2 narcosis. Blood collected from the inferior vena cava into heparin (10 U/mL final; Leo Laboratories, UK) or clotting-tubes (Sarstdet, UK) was centrifuged for serum/ plasma. Urine was collected by amniocentesis. Serum urea was measured by a commercial veterinary diagnostics service (IDEXX Laboratories, UK).

Microarray Analysis
Tissues were snap frozen and homogenized, and total RNA was extracted by using a silica column-based kit (Nucleospin RNA II; Machery-Nagal, UK). Samples were converted to cDNA, fragmented, labeled, and hybridized to MouseRef-8v3 BeadChip arrays (Illumina, UK). Data were quantile normalized and analyzed by using the linear models for microarray data modified t test method and Benjamini-Hochberg false discovery rate correction by using GeneSpring GX 12.1 software (Agilent, USA). Differential expressed genes with a corrected P value of q<0.05 were considered statistically significant. Focused pathway analysis was performed by examination of genes altered >1.3-fold (q<0.05) featuring in the following human Gene Ontology (http://www.geneontology.org) pathways:

Liquid-Chromatography Tandem Mass-Spectrometry Measurements
Samples were analyzed as described previously 29 with a Agilent 6400 series triple quadruple liquid-chromatography tandem massspectrometry using mobile phase (0.1% formic acid, 1% acetonitrile). The mass spectrum parameters for detection were as follows: ADMA, mass-to-charge ratio (m/z): 203.

Vasomotor Responses
Mice were euthanized by CO 2 narcosis, and the thoracic aorta was cut into 2-mm aortic rings, mounted in organ baths of a Mulvany-Halpern myograph at a resting tension of 13 kPa in Krebs with or without l-arginine (100 μmol/L; Sigma, UK) and contracted with of endothelin (ET)-1 (30 pmol/L to 30 nmol/L; Sigma, UK) or the thromboxane mimetic U46619 (1 nmol/L to 1 μmol/L). After washing, tissues were contracted with an EC 80 concentration of U46619 (30-100 nmol/L) followed by acetylcholine (1 nmol/L to 10 μmol/L) or sodium nitroprusside (SNP; 1 pmol/L to 10 μmol/L). For ET-1 studies, vessels were preincubated with the NOS inhibitor N G -nitro-l-arginine methyl ester (100 μmol/L; Sigma, UK) to exclude any effect of changes in the NO/ADMA pathway. Force was recorded via a PowerLab/800 (AD Instruments Ltd., UK) and analyzed by using Chart 6.0 acquisition system (AD Instruments Ltd, UK).

Clinical Study
Sixteen healthy young male volunteers aged 20 to 35 who had abstained from NSAID use for 14 days previously were recruited. Volunteers received standard doses of the COX-2 selective inhibitor Celebrex (celecoxib; 200 mg twice a day; Pfizer USA), or the nonselective COX-1/COX-2 inhibitor Naprosyn (naproxen; 500 mg twice a day; Roche Switzerland) for 7 days. After overnight fasting, on day 0, before the first dose, and day 7, 2 hours after the final dose, blood was collected into citrate Vacutainers (BD Diagnostics, UK) and separated by centrifugation. This study was approved by the St Thomas's Hospital Research Ethics Committee (Ref. 07/Q0702/24) and conducted according to the Declaration of Helsinki. All volunteers gave written informed consent before entering the study.

Statistical Methods
Data are mean±standard error of the mean. Statistical significance (taken as P<0.05) was determined by using the following tests: Mann-Whitney (1 variable, 2 groups), Wilcoxon signed-rank (1 variable, 2 paired groups), Kruskal-Wallis with the Dunn post hoc test (1 variable, 3 groups), or Quades test (2 variables). All tests were performed using GraphPad Prism 6 software, with the exception of the Quades test, which was performed using R. Significance was assumed where P<0.05. No further correction has been made for multiple testing (typically <5 end points per animal). The exception is analysis of transcriptomic data where false discovery rate correction has been applied as described above.

Expression of COX-2 in the Kidney
As others have shown, 16 constitutive expression of Ptgs2 gene, which encodes the COX-2 protein, was seen in the medulla region of the kidney, with lower levels in the cortex ( Figure 1A), which others have shown is relatively sparse unless animals are salt depleted. 16 As seen by others, the loss of COX-2, but not of COX-1, resulted in renal compromise associated with increased serum urea and creatinine 30 ( Figure 1B and 1C).

Effect of COX-2 on the Transcriptome in Cardiovascular Tissues
In the blood, heart, and aorta, COX-1 activity drives prostanoid production with little or no contribution from COX-2. 11,14 Consistent with this, no genes were altered by COX-2 deletion in the blood of COX-2 -/mice, and, in the heart and aorta, only 1 gene was altered/decreased, Rgl1, in both tissues ( Table I in the online-only Data Supplement). By contrast, in the renal medulla, deletion of COX-2 altered the expression of 1018 genes by >1.5-fold ( Figure 2A; Table I in the onlineonly Data Supplement). To explore the consequences of this finding, we applied focused pathway analysis to specifically examine changes in (1) blood pressure control, (2) vascular tone, and (3) vascular hormones and identified alterations in the expression of a number of genes involved in angiotensin, ET, and NO ( Figure 2B). Changes in angiotensin genes (Anpep, Agt, Mme) were predictive of reduced activity, so they were unlikely to be implicated in the deleterious effects of COX-2 inhibitors. ET-1 and ET receptor gene expression (Edn1, Endra, Ednrb) was increased ( Figure 2B). However, levels of ET-1 in the plasma of COX-2 -/mice were not altered ( Figure IA in the online-only Data Supplement). Moreover, contractile responses in the aorta to ET-1 were not significantly altered in COX-2 -/mice ( Figure IB in the online-only Data Supplement). We therefore focused on a cluster of genes (Agxt2, Ddah2, Prmt1) related to the turnover of methylarginines such as ADMA and l-NMMA, which are inhibitors of NOS enzymes. Using quantitative polymerase chain reaction, we confirmed that in COX-2 -/renal medulla expression of Prmt1 ( Figure 2C), which drives methylarginine synthesis, 29 was increased; Ddah2, which breaks down methylarginine, was nonsignificantly increased ( Figure II in the online-only Data Supplement), whereas Agxt2, which degrades methylarginines, 29 tended to be reduced ( Figure 2D). Using quantitative polymerase chain reaction , we also observed reduced expression of Ddah1, which, like Agxt2, is responsible for methylarginine breakdown 29 ( Figure 2E).

Effect of COX-2 on Plasma Methylarginines and eNOS Responses in Mouse Aorta
Plasma levels of ADMA and l-NMMA were increased in COX-2 -/-, but not COX-1 -/mice ( Figure 3A and 3B). Plasma SDMA levels were not changed in COX-2 -/mice (Table II in the online-only Data Supplement). Arginases, like NOS, use l-arginine as a substrate and can be altered in inflammatory conditions. However, in the renal medulla, Arg1 was not expressed and Arg2 was not altered in COX-2 -/mice ( Figure IIIA in the online-only Data Supplement). In addition, in the aorta, Arg2 was not expressed in and Arg1 was not altered in COX-2 -/mice  Increased plasma levels of methylarginines are associated in other models with reduced eNOS activity in vessels ex vivo 31 and hypertension in vivo. Aorta from COX-2 -/mice had a reduced eNOS response to acetylcholine ( Figure 5A). However, their response to the NO-donor SNP that relaxes vessels via NO independently of the endothelium was not altered ( Figure 5B), nor was their contractile response to U46619 ( Figure V in the online-only Data Supplement). The reduced eNOS responses in the aorta of COX-2 -/mice were reversed in the presence of l-arginine (100 μmol/L; Figure 5C). No effect of l-arginine ( Figure 5D) was seen on response to SNP. These effects were not due to local changes in aortic Nos3, Ddah1, Ddah2, or Agxt2 gene expression ( Figure VI in the online-only Data Supplement).

Effect of Loss of the Prostacyclin Receptor (IP) on Renal Gene Expression and Plasma ADMA Levels
Prostacyclin, which acts via cell surface IP receptors, is an important COX-derived mediator in the cardiovascular system. To establish the relative role of prostacyclin, in comparison with the myriad of other COX products, in our study, we performed experiments using IP -/mice. None of our genes of interest (Prmt1, Agxt2, Ddah1, Ddah2, or Arg2) were altered in the renal medulla from IP -/mice ( Figure

Effect of Inhibition of COX-2 in Healthy Human Volunteers
In direct corroboration of our findings in mice, the inhibition of COX-2 with standard anti-inflammatory doses of celecoxib (200 mg twice a day) for 7 days (n=8) increased ADMA levels in healthy human volunteers (Table). Naproxen (500 mg twice a day), which inhibits COX-2, but also inhibits COX-1, similarly increased ADMA levels in volunteers taking the drug for 7 days (n=8; Table).

Discussion
The notion that COX-2 is constitutively expressed in the kidney is not new and is, in fact, based on observations made as early as 1994, 32 well before selective COX-2  inhibitors were introduced to the clinic. Similarly, the idea that the inhibition of COX-2 in the kidney could explain the cardiovascular side effects of NSAIDs has been suggested. [18][19][20] However, this view has been somewhat sidelined by the idea that vascular COX-2 drives prostacyclin throughout the systemic circulation, 7 and, until our recent studies, 14,33 the relative importance of the kidney in comparison with large vessels had not been specifically addressed. Using a COX-2 luciferase knock-in mouse, we performed an unbiased systems-based analysis of COX-2 expression in an extensive panel of organs and tissues in the mouse and found that renal COX-2 was localized to an intense hot spot in the center of the kidney, aligned to the inner region of the renal medulla. Here, we validated our earlier report and used polymerase chain reaction to show that the COX-2 (Ptgs2) gene is highly enriched in the medulla in comparison with the renal cortex. This is in line with what is known about COX-2 in the kidney, which under normal or highsalt conditions is predominantly expressed in the medulla region, particularly in the interstitial fibroblasts. 14,16 Although COX-2 expression and activity are low relative to those of COX-1 in other cardiovascular structures, such as the heart and major blood vessels, conditional knockout mice where either endothelial 26 or cardiomyocyte 34 COX-2 is deleted have been used to implicate a role of COX-2 in cardiovascular function in these structures; although, in the heart, the findings with conditional knockout mice were questioned and suggested to be confounded by the nonspecific effects of tamoxifen/cre toxicity. 35 Nevertheless, to identify the gross effect of COX-2 at these sites in comparison with the renal medulla and to identify the novel mechanisms of NSAIDs, we investigated the effects of COX-2 gene deletion on the transcriptome. In line with constitutive COX-2 gene activity that we recently reported, 14 we found that only 1 gene is altered in the heart and aorta of COX-2 -/mice, whereas >600 genes were changed by >1.5fold in the renal medulla by COX-2 deletion. Clearly, these findings implicate a dominant role for constitutive COX-2 in the kidney in comparison with the heart or aorta. This may suggest that endothelial cells outside large vessels, potentially in the renal circulation, mediate the effects previously reported. 26 Because of the large number of genes altered in the renal medulla by COX-2 deletion, we chose to apply a focused gene pathway analysis of transcripts Methylarginine (ADMA, l-NMMA, and SDMA) and creatinine levels in the plasma of patients before (control) and after 7 days of standard anti-inflammatory dosing with naproxen or celecoxib (n=8). Data are represented as mean±SEM. P values by a Wilcoxon signed rank test in comparison with baseline values for each individual. ADMA indicates asymmetrical dimethylarginine; l-NMMA, monomethyl-l-arginine; SDMA, symmetrical dimethylarginine; and SEM, standard error of the mean. relating to control of blood pressure, vascular tone, and vascular hormones to extract leads for understanding how renal COX-2 can regulate systemic cardiovascular homeostasis. Using this approach, we identified a number of groups of genes, for example, related to ET and angiotensin signaling. Angiotensin genes were altered in a way that would not predict cardiovascular side effects and so were not pursued in this study. Changes in ET-1 genes may well be important in the effects of NSAIDs in some settings, but, in our model using healthy mice, the changes we found in the renal medulla did not ultimately affect plasma ET-1 levels or vascular responses to ET-1 in the aorta ex vivo. We therefore focused our study around genes altered that regulate the synthesis and metabolism of the endogenous eNOS inhibitors ADMA and l-NMMA. The kidney is a major site of methylarginine synthesis and clearance from the circulation and changes to these pathways have the potential to systemically regulate vascular health. Specifically, Prmt1, first identified because of its association with the TIS21 gene, 36 methylates arginine residues in proteins leading to the release of mature ADMA and l-NMMA after proteolysis, was increased by COX-2 deletion, whereas both Agxt2 37 and Ddah1 31 , enzymes that metabolize methylarginines, were decreased in COX-2 -/renal medulla.
To define the interaction between COX-2 and the methylarginine pathways and to validate biologically our gene expression data, we measured the levels of ADMA, SDMA, and l-NMMA. ADMA and l-NMMA are both competitive inhibitors of eNOS, whereas SDMA is biologically inactive and not cleared by DDAH1. COX-1 -/mice exhibited normal renal, plasma, and urinary levels of each methylarginine. In contrast, the plasma levels of ADMA and l-NMMA were increased, whereas l-arginine was unchanged, in samples from COX-2 -/mice. These findings are in line with others showing increased methylarginines in models where the activity of PRMT1 is elevated and AGXT2 is reduced. 29 We found that SDMA is not significantly increased in COX-2 -/mouse plasma, implicating an additional functional role for reduced DDAH1 in this model. It should be noted that nonrenal factors may act together with events in the kidney to regulate plasma ADMA in COX-2 -/mice.
After demonstrating that COX-2 deletion increases ADMA and l-NMMA, we next sought to establish if this could be recapitulated with a therapeutically relevant COX-2 selective drug in wild-type mice. We chose parecoxib, which is the prodrug of valdecoxib and a licensed therapy for acute pain. It is highly COX-2 selective, 1 and, because it is water soluble, it can be easily administered to mice in drinking water. Similar to our findings in COX-2 -/mice, pharmacological COX-2 inhibition by parecoxib produced an increase in circulating levels of ADMA and l-NMMA. This further supports our findings, confirming that increased levels of endogenous NOS inhibitors is not a developmental consequence of COX-2 deletion; rather, it is an acute biochemical consequence of the loss of COX-2 enzyme activity.
We have shown previously that the global heterozygous deletion of the Ddah1 gene results in increased levels of plasma ADMA and l-NMMA and increased blood pressure 31 similar in magnitude to that seen in the current study. Further, we have demonstrated that plasma increases of ADMA and l-NMMA in Ddah1-deficient mice, in the concentration range shown here in COX-2 -/mice, were associated with vascular dysfunction manifesting as reduced acetylcholine-induced vasodilator responses in endothelium intact segments of aorta. 31 In the aorta, acetylcholine-induced vasodilation is mediated predominately by NO derived from eNOS, with no role for local prostacyclin release. Thus, in this work, the loss of acetylcholine-induced vasodilation was attributed to the inhibition of eNOS as a direct consequence of increased ADMA and l-NMMA. 31 In the current study, we have taken a similar approach and found that aorta from COX-2 -/mice had a reduced eNOS-dependent response to acetylcholine, but a normal response to the endothelial-independent NO donor SNP. This observation is consistent with recent work from others showing reduced eNOS activity in the aorta of COX-2 -/mice, 26 although, in that study, a role for natural eNOS inhibitors was not addressed. ADMA and l-NMMA are competitive inhibitors of eNOS, and, as such, their effects are reversed when the natural substrate, l-arginine, is increased in the system. 38 To establish the specific role of ADMA and l-NMMA in the loss of eNOS function in the aorta, in our study, we assessed the ability of l-arginine to rescue the vascular dysfunction. In wild-type mouse aorta, l-arginine did not amplify acetylcholine-induced vasodilation, consistent with l-arginine availability not being rate limiting in healthy blood vessels. 39 In contrast, l-arginine reversed the impairment in endothelial function present in aorta from COX-2 -/mice; returning acetylcholine-dependent vasodilation to wild-type levels, without affecting smooth muscle sensing of NO. It must be remembered that this effect cannot be explained by any loss of COX-2 activity locally within the vessel, because, in this tissue, COX-1, and not COX-2, is expressed. 11,14 Rather, this is explained by changes in kidney function, leading to increased circulating ADMA and l-NMMA, which then act in a endocrine manner on the endothelium in the systemic circulation. Our findings that the reduced eNOS activity seen in vessels from COX-2 -/mice could be prevented by exogenous l-arginine clearly implicate a role for ADMA and l-NMMA and are in line with others showing that ADMA and l-NMMA specifically and actively accumulate in endothelial cells and that this results in decreased eNOS activity ex vivo, which is reversible by l-arginine. 40 Finally, to establish if the phenomenon demonstrated in mice, ie, that loss/inhibition of COX-2 results in increased circulating levels of ADMA also occurs in humans, we performed a clinical study in which healthy male volunteers were treated with standard doses of the selective COX-2 inhibitor celecoxib or naproxen, a dual COX-1/COX-2 inhibitor. 1 At therapeutic doses, both of these drugs inhibit COX-2 by ≈ 80%. 1 Creatinine levels were increased to a similar level by celecoxib and naproxen treatment highlighting the effect of COX-2 inhibition on renal function. In direct corroboration of our findings in mice, both celecoxib and naproxen increased ADMA levels. These observations suggest that, in humans, after even short-term inhibition of February 17, 2015 COX-2, renal dysfunction, including the reduction in filtration drive, increases the levels of ADMA. It is important to note, however, that ADMA, l-NMMA, and SDMA are similarly cleared by the kidney. Thus, the finding that ADMA is increased without a concomitant increase in other methylarginines suggests that some additional specific pathways may be altered by COX-2 inhibition. We recognize that the relative change in ADMA levels in our human study was much lower than seen in either COX-2 -/mice or in wild-type mice treated with a COX-2 inhibitor. We do not suggest that, in this small sample size with healthy volunteers, the increase would be sufficient to adversely affect cardiovascular function, simply that, it provides a proof-of-concept study and that, in a much larger cohort, such as the Framingham study 41 and in patients with inflammation or cardiovascular disease, this small but significant increase could account for the equally small but significant increase in cardiovascular events seen in patients taking anti-inflammatory drugs, including COX-2 inhibitors. Indeed, as reported in the Framingham study 41 in large populations, even relatively small changes in ADMA levels are associated with significant increases in the risk of cardiovascular events, and the plasma levels of ADMA and l-NMMA, which others have shown specifically can accumulate in endothelial cells, 40 are highly correlated with cardiovascular disease in a range of human clinical studies. [42][43][44][45][46] This is relevant because COX-2 selective drugs, including celecoxib and rofecoxib, increase the risk of cardiovascular events even in healthy individuals -that is to say, in those people without overt evidence of cardiovascular disease, requiring medication, or recent previous events, because these individuals were excluded from trials. Furthermore, although the efficacy trials for COX-2 inhibitors were performed in patients with arthritis, 47 who are commonly in a category of increased risk of cardiovascular disease owing to general inflammation and age, the Adenomatous Polyp Prevention on Vioxx (APPROVE) 48 (rofecoxib) and Adenoma Prevention With Celecoxib (APC) 49 (celecoxib) trials were conducted on volunteers without arthritis. In both the APPROVE and APC trials, increased cardiovascular events were noted, which in the case of rofecoxib lead to the withdrawal of the drug.
The differences seen in ADMA in COX-2 -/mice and human volunteers taking NSAIDs for 1 week are probably explained by the duration and extent of loss of COX-2 activity. The relatively small increase in ADMA seen in humans versus mice administered inhibitors is less obviously explained, but it could be due to species differences and the fact that humans are outbred, and so responses are likely to be more variable. In addition, mice treated with parecoxib were chronically instrumented, which may also influence responses.
Methylarginines inhibit eNOS, reducing NO released across the entire vascular tree. NO performs functions similar to prostacyclin in vessels and platelets. Moreover, NO and prostacyclin synergize strongly to inhibit platelet activation. 27 Our data provide the first explanation for how the inhibition of COX-2 in the kidney can lead to reduced vascular function and firmly establish a COX-2/eNOS axis involving ADMA. Our results also show that ADMA and other methylarginines are potential biomarkers for the cardiovascular risk in patients taking traditional NSAIDs, and COX-2 selective inhibitors, as well. In addition, if endogenous inhibitors of NOS are mechanistically involved in the cardiovascular toxicity associated with COX-2 inhibitor use in humans, then there is the very clear potential for l-arginine to be used as a preventative treatment in at-risk patients. 50 Moreover, the potential for genetic mutations in genes such as PRMT1, DDAH1, and AGXT2 to be associated with increased risk of cardiovascular side effects in patients taking NSAIDs should be considered.