Published online before print March 18, 2002, doi: 10.1161/01.CIR.0000012748.58444.08
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(Circulation. 2002;105:1656.)
© 2002 American Heart Association, Inc.
Clinical Investigation and Reports |
Mechanisms of Increased Vascular Superoxide Production in Human Diabetes Mellitus
Role of NAD(P)H Oxidase and Endothelial Nitric Oxide Synthase
From the Departments of Cardiovascular Medicine (T.J.G., S.M., K.M.C.) and Cardiothoracic Surgery (S.M., D.G., C.R., R.P.), University of Oxford, Oxford, UK, and Departments of Medicine (T.J.G.) and Cardiovascular Surgery and Transplantology (J.S.), Jagiellonian University School of Medicine, Cracow, Poland.
Correspondence to Dr Keith Channon, MD, MRCP, Department of Cardiovascular Medicine, John Radcliffe Hospital, Oxford OX3 9DU, UK. E-mail keith.channon{at}cardiov.ox.ac.uk
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Abstract |
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Background— Increased superoxide production contributes to reduced vascular nitric oxide (NO) bioactivity and endothelial dysfunction in experimental models of diabetes. We characterized the sources and mechanisms underlying vascular superoxide production in human blood vessels from diabetic patients with coronary artery disease compared with nondiabetic patients.
Methods and Results— Vascular superoxide production was quantified in both saphenous veins and internal mammary arteries from 45 diabetic and 45 matched nondiabetic patients undergoing coronary artery bypass surgery. NAD(P)H-dependent oxidases were important sources of vascular superoxide in both diabetic and nondiabetic patients, but both the activity of this enzyme system and the levels of NAD(P)H oxidase protein subunits (p22phox, p67phox, and p47phox) were significantly increased in diabetic veins and arteries. In nondiabetic vessels, endothelial NO synthase produced NO that scavenged superoxide. However, in diabetic vessels, the endothelium was an additional net source of superoxide production because of dysfunctional endothelial NO synthase that was corrected by intracellular tetrahydrobiopterin supplementation. Furthermore, increased superoxide production in diabetes was abrogated by the protein kinase C inhibitor chelerythrine.
Conclusions— These observations suggest important roles for NAD(P)H oxidases, endothelial NO synthase uncoupling, and protein kinase C signaling in mediating increased vascular superoxide production and endothelial dysfunction in human diabetes mellitus.
Key Words: diabetes mellitus • atherosclerosis • endothelium • superoxide • nitric oxide
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Introduction |
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Superoxide production by vascular tissues and its interaction with nitric oxide (NO) play important roles in vascular pathophysiology.1,2 Superoxide reacts rapidly with NO, reducing NO bioactivity and producing the oxidative peroxynitrite radical.3,4 Abnormal vascular endothelial function and atherosclerosis are prominent features of diabetes mellitus,5 and evidence from experimental studies suggests that increased superoxide production accounts for a significant proportion of the NO deficit in diabetic vessels. In addition to NO scavenging, superoxide may alter the activity and regulation of endothelial NO synthase activity in endothelial cells6 and has other potentially proatherogenic actions on smooth muscle cell proliferation, inflammatory cell recruitment, and redox-sensitive gene expression.7
Potential sources of vascular superoxide production include NAD(P)H-dependent oxidases,8,9 xanthine oxidase,10 lipoxygenase, mitochondrial oxidases, and NO synthases.11 NAD(P)H oxidases appear to be the principal source of superoxide production in several animal models of vascular disease, including diabetes.1,8,12 Furthermore, NAD(P)H oxidase proteins and activity are present in human blood vessels, including atherosclerotic coronary arteries,13 and in saphenous veins and mammary arteries from patients with coronary artery disease,14 which suggests that this oxidase system plays an important role in vascular disease states.15
Endothelial NO synthase (eNOS), present in the vascular endothelium, produces NO by oxidation of L-arginine to L-citrulline. NO has diverse antiatherogenic actions on the vessel wall, including antioxidant effects by direct scavenging of superoxide. However, eNOS may be a source of superoxide production under certain conditions because of enzymatic "uncoupling" of L-arginine oxidation and oxygen reduction by the oxygenase and reductase domains of eNOS, respectively. Recent studies suggest that reduced availability of the cofactor tetrahydrobiopterin (BH4) may result in eNOS uncoupling and that this may be an important contributor to the imbalance between production of NO and superoxide production in vascular disease. Hyperglycemia increases NOS-dependent superoxide production in human endothelial cells,16 and recent data from animal studies suggest a possible role for BH4 in mediating the eNOS dysfunction observed in diabetic vessels17–19 and endothelial cells.20,21
Despite the importance of increased superoxide production in endothelial dysfunction and vascular disease in diabetes, the characteristics and mechanisms of vascular superoxide production in human diabetes remain poorly defined. Accordingly, we evaluated the sources and relative magnitude of superoxide production in both arteries and veins taken from patients with type II diabetes compared with vessels from matched nondiabetic patients. In particular, we sought to investigate both the NAD(P)H oxidase system and the potential role of eNOS dysfunction in contributing to vascular superoxide production.
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Methods |
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Patients and Blood Vessels
Segments of internal mammary arteries and human saphenous veins were obtained from patients undergoing routine coronary artery bypass surgery at the John Radcliffe Hospital, Oxford, UK. The Local Research Ethics Committee approved collection of tissue specimens, and all patients gave written informed consent. Patients with type II diabetes mellitus had fasting glucose >5.5 mmol/L and/or current treatment with insulin or oral hypoglycemic agents. An equal number of nondiabetic subjects were matched for other major demographic and clinical risk factors: hypercholesterolemia (total plasma cholesterol >4.8 mmol/L), smoking (current or within last 6 months), and hypertension (current treatment with antihypertensive agents). Vessels were collected immediately after surgical harvesting and transported to the laboratory in ice-cold Krebs-HEPES buffer.
Vascular Superoxide Production
Superoxide production was measured by both lucigenin-enhanced chemiluminescence and ferricytochrome c reduction by previously described and validated methods.14,22,23 Briefly, intact vessel segments were equilibrated in Krebs-HEPES gassed with 95% O2/5% CO2 for 30 minutes at 37°C. Lucigenin-enhanced chemiluminescence from intact vessels was measured in buffer (2 mL) containing low-concentration lucigenin (5 µmol/L).22 In some experiments, superoxide generation was measured in the presence of various oxidase inhibitors with 20 µmol/L lucigenin. Superoxide production was expressed as relative light units per second per milligram of vessel dry weight.
Vascular superoxide production was also measured by superoxide dismutase (SOD)–inhibitable ferricytochrome c reduction assays, as described previously.14,24 Briefly, equal portions of vascular homogenate were incubated in 1 mL of buffer containing ferricytochrome c (80 µmol/L) in the presence of NAD(P)H or NADH (100 µmol/L) at 37°C for 45 minutes, then absorbance was measured at 550 nm. All experiments were performed with and without SOD (400 U/mL). Superoxide production was calculated as the portion of ferricytochrome c reduction inhibited by SOD.
Oxidative Fluorescent Microtopography
In situ superoxide generation was evaluated in vascular cryosections with the oxidative fluorescent dye dihydroethidium (DHE). Cryosections (30 µm) were incubated with DHE (2 µmol/L) in PBS, with or without polyethylene glycol (PEG)-conjugated SOD, or oxidase inhibitors. Fluorescence images were obtained with a BioRad MRC 1024 scanning confocal microscope. In each case, paired segments of diabetic and nondiabetic vessels were analyzed in parallel with identical imaging parameters.
Western Immunoblotting
Portions of vascular homogenate, equalized for protein content, were separated by SDS-PAGE (12% gels) and transferred to nitrocellulose membranes. NAD(P)H oxidase components were detected with mouse monoclonal antibodies against p67phox or p47phox (Transduction Laboratories) or by rabbit polyclonal antibodies against a p22phox C-terminus peptide (generously provided by Dr Imajoh-Ohmi, Tokyo, Japan).13 Bands were detected by horseradish peroxidase–conjugated secondary antibodies and visualized by chemiluminescence.
Statistical Analysis
Data are expressed as mean±SEM. In all cases, n refers to numbers of patients. Statistical significance of differences was assessed by Student t tests. A value of P<0.05 was considered statistically significant.
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Results |
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Patient Characteristics
Vessels were obtained from a total of 90 patients (76 men, 14 women; 45 diabetics and 45 nondiabetics) undergoing coronary artery bypass grafting. Demographic and clinical characteristics, shown in Table 1, revealed that diabetic and nondiabetic patients were closely matched for these factors except for specific therapies for diabetes.
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Vascular Superoxide Generation Is Increased in Human Arteries and Veins in Diabetes
Basal superoxide production from both saphenous veins and internal mammary arteries was determined by lucigenin-enhanced chemiluminescence from intact vessel rings from diabetic and nondiabetic patients (Figure 1). Specificity for superoxide was demonstrated by coincubation with SOD (500 U/mL). In both veins and arteries, basal superoxide release was significantly elevated in vessels from patients with diabetes; in mammary arteries, total superoxide release was almost doubled.
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Role of the Endothelium in Superoxide Production in Human Blood Vessels
To investigate the importance of the endothelium in vascular superoxide production, we studied internal mammary artery segments denuded of endothelium (Figure 2). In arteries from nondiabetic patients, endothelium removal resulted in a significant increase in superoxide release, which suggests that in these vessels the net contribution of the endothelium is to reduce vascular superoxide release by production of NO. In marked contrast, endothelium removal in artery segments from diabetic patients significantly reduced superoxide release, which suggests that in diabetic vessels, the endothelium is a net contributor to total vascular superoxide production.
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To further investigate these regional differences in superoxide production in the vessel wall, we visualized vessel cryosections using the intracellular fluorescent dye DHE (Figure 2B). Oxidative fluorescent microtopography revealed superoxide generation in endothelial and medial layers and to a lesser extent in the adventitia of both veins and arteries. Medial and adventitial fluorescence was modestly increased in diabetic vessels. However, in vessel sections from patients with diabetes, endothelial cells showed strikingly increased fluorescence compared with other regions of the vessel wall when visualized with identical imaging parameters. As expected, PEG-conjugated SOD (PEG-SOD) abolished DHE fluorescence.
Sources of Vascular Superoxide in Human Diabetes
To investigate the enzymatic sources of superoxide production in diabetic and nondiabetic vessels, we measured superoxide production in response to a range of potential oxidase inhibitors and substrates (Table 2). In both diabetic and nondiabetic vessels, superoxide production was inhibited by diphenylene iodonium, an inhibitor of flavin-containing oxidases such as NAD(P)H oxidases. However, the response to inhibition of NOS with N-methyl-L-arginine was strikingly different between diabetic and nondiabetic vessels. In both veins and arteries from nondiabetic patients, NOS inhibition significantly increased superoxide release because of the loss of superoxide scavenging by NO. In contrast, NOS inhibition in diabetic vessels decreased superoxide release, which suggests that the net effect of NOS activity in these vessels is superoxide production rather than NO production. Oxypurinol, indomethacin, and rotenone had minimal or more modest effects on superoxide production. Indomethacin resulted in statistically significant inhibition in saphenous veins from nondiabetics and mammary arteries from both groups of patients. Oxypurinol inhibited superoxide release in some diabetic mammary arteries, but these effects were not consistently different between diabetic and nondiabetic vessels in all patients.
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Increased NAD(P)H Oxidase Activity and Protein Subunits in Diabetic Vessels
To investigate the potential importance of vascular NAD(P)H oxidases in mediating increased vascular superoxide production in diabetes, we compared NADH and NAD(P)H-dependent superoxide production in diabetic and nondiabetic arteries and veins. We quantified superoxide using 2 different methods: lucigenin-enhanced chemiluminescence in intact vessel rings and SOD-inhibitable ferricytochrome c reduction in vessel homogenates (Figure 3). Addition of NADH or NAD(P)H (100 µmol/L) stimulated superoxide release more than 10-fold; NADH-stimulated superoxide release was inhibited by diphenylene iodonium but not by oxypurinol, rotenone, or N-methyl-L-arginine (data not shown). NADH/NAD(P)H-stimulated superoxide production from both saphenous veins and internal mammary arteries was significantly greater in vessels from diabetic patients than from nondiabetic patients.
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Next, we investigated the relative abundance of NAD(P)H oxidase protein subunits in vessels from diabetic and nondiabetic patients using Western immunoblotting. We found increased levels of the p22phox membrane-bound subunit and the p67phox and p47phox cytosolic subunits in both saphenous veins and mammary arteries from diabetic patients (Figure 4). Relative quantification of protein bands, normalized to smooth muscle 
-actin, revealed that levels of these NAD(P)H oxidase protein subunits were almost 3-fold higher in diabetic arteries and veins than in vessels from nondiabetic patients.
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eNOS Dysfunction in Human Diabetes Mellitus
We next sought to further investigate the potential role of eNOS dysfunction in contributing to vascular superoxide production in diabetic patients. We measured superoxide production in internal mammary arteries in response to NOS inhibition and in response to BH4 supplementation. We incubated vessels with the synthetic pterin sepiapterin (10 µmol/L), which is converted to BH4 intracellularly via the pterin salvage pathway, then washed extensively to avoid potential confounding by nonspecific antioxidant effects of high extracellular BH4 concentrations. In vessels from patients with diabetes, sepiapterin significantly reduced vascular superoxide production. As observed previously with NG-monomethyl-l-arginine (L-NMMA), NOS inhibition with NG-nitro-L-arginine methyl ester (L-NAME) in this experiment again increased superoxide release from nondiabetic vessels but reduced superoxide release from diabetic vessels. Similar reductions in superoxide production after either sepiapterin or L-NAME suggest that sepiapterin was effective in abolishing the proportion of superoxide release mediated by eNOS dysfunction in diabetic vessels.
To investigate the potential importance of PKC signaling in human diabetic vessels, we preincubated vessels with the PKC inhibitor chelerythrine chloride. Chelerythrine (3 µmol/L) modestly reduced superoxide production (by <25%) in nondiabetic internal mammary artery segments (Figure 5). However, this reduction was significantly greater in vessels from diabetic patients (>60%), reducing superoxide production to levels observed in nondiabetics, which suggests that PKC inhibition abrogates the increased vascular superoxide production in diabetic patients.
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To visualize changes in eNOS-mediated endothelial superoxide production, we used oxidative fluorescent microtopography with DHE (Figure 6). Endothelial DHE fluorescence in diabetic internal mammary artery and saphenous vein tissue sections was virtually abolished by incubation with sepiapterin and by incubation with L-NAME. Importantly, DHE fluorescence in other regions of the vessel wall was unaffected in each case, providing a within-section control and demonstrating the endothelium-specific nature of the effect of NOS inhibition or cofactor supplementation. In contrast, incubation with PEG-conjugated SOD abolished all cellular fluorescence, leaving only autofluorescence from the elastic lamina.
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Discussion |
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We have used mammary arteries and saphenous veins as model systems to investigate the characteristics, sources, and mechanisms of vascular superoxide production in human diabetes mellitus. Vessels from patients with diabetes generate significantly more superoxide, from 2 principal sources: first, activity and protein levels of the vascular NAD(P)H oxidase system are increased; second, in diabetic vessels, the endothelium is a net contributor to total vascular superoxide release, rather than to scavenging of superoxide by NO production. This increased endothelial superoxide production appears to be caused by dysfunctional eNOS, mediated by availability of the cofactor BH4. Finally, these changes appear to be mediated, at least in part, by PKC signaling.
These findings are important because they reveal the mechanisms underlying increased vascular superoxide production in human diabetes, and they suggest clear associations with the endothelial dysfunction characteristic of diabetic vessels even in the absence of macroscopic atherosclerosis. The present study supports previous in vivo25 and in vitro26 data indicating that vessels from diabetic patients show marked abnormalities in endothelial function characterized by reduced NO bioactivity, and they support data from experimental models of diabetes that reveal increased superoxide production. Our findings suggest 2 important and potentially related mechanisms that underlie these functional deficits. First, increased superoxide production by NAD(P)H oxidases, in common with atherosclerosis and other preatherosclerotic states,8,12,15 likely reduces NO bioactivity by direct scavenging. NAD(P)H oxidases are expressed in vascular cells and macrophages in atherosclerotic coronary arteries,13 although the lack of overt atherosclerosis in saphenous veins and mammary arteries suggests that macrophages are less likely a major source of NAD(P)H oxidase activity in the vessels in the present study. The increased levels of the NAD(P)H oxidase protein subunits in diabetic vessels, in association with increased enzymatic activity, suggest that upregulated gene expression or posttranscriptional upregulation of protein levels is important in mediating increased NAD(P)H oxidase activity in human vascular disease. Second, in diabetic vessels, the endothelium is a significant net source of superoxide because of a profound loss of normal eNOS function, characterized by a transition from NO production to superoxide production. This observation suggests that diabetes appears to result in specific and marked defects in endothelial biology compared with other systemic risk factors for vascular disease. Indeed, the patient groups in the present study were closely matched for other risk factors and medication to reduce the confounding effects of factors that are associated with increased vascular superoxide generation. Furthermore, we observed similar abnormalities of endothelial function in both saphenous veins and mammary arteries, which suggests that the effects of diabetes on endothelial function are systemic and are not restricted to arteries that develop overt atherosclerosis.
Recent studies have highlighted the potential importance of dysfunctional eNOS regulation in vascular disease states.17,21,27,28 Our data now provide the first direct evidence for enzymatic uncoupling of dysfunctional eNOS in human endothelium, leading to increased superoxide production. Furthermore, our observation that eNOS-mediated superoxide production can be normalized by incubation with sepiapterin adds further evidence to previous in vitro and animal studies suggesting that this effect is mediated by BH4 availability. Our use of sepiapterin, followed by extensive washing, rather than high-concentration BH4 makes nonspecific superoxide scavenging by this redox-active molecule unlikely. Our findings in human vessels support a potential mechanistic relationship between increased NAD(P)H oxidase activity and eNOS dysfunction, proposed on the basis of similar findings in experimental diabetes in rats17 and in atherosclerotic apolipoprotein E knockout mice,28 in which both increased NAD(P)H oxidase activity and eNOS dysfunction contributed to increased total vascular superoxide production and reduced NO bioactivity. Peroxynitrite, generated from NO and superoxide, directly oxidizes BH4 to BH2 (dihydrobiopterin), a biopterin that does not support eNOS enzymatic activity.29 Indeed, some data suggest that competition between BH2 and BH4 for eNOS binding may increase eNOS uncoupling. Therefore, upregulation of vascular superoxide production by NAD(P)H oxidases may in turn lead to eNOS uncoupling through oxidation of BH4, which reduces NO production and further increases endothelial superoxide production. Furthermore, our data from human blood vessels add to findings in experimental models of diabetes17 and nitrate tolerance21 and recent studies of flow-mediated vasodilatation in hyperglycemia30 that suggest an important role for PKC in mediating increased NAD(P)H oxidase activity and eNOS dysfunction in human diabetes.30
In conclusion, we find that significantly increased superoxide production in human blood vessels from patients with diabetes is mediated by upregulated NAD(P)H oxidase activity and by a striking increase in endothelial superoxide production mediated by eNOS. This suggests important and potentially related roles for the NAD(P)H oxidase system and BH4-dependent eNOS uncoupling, possibly mediated by PKC signaling, in the pathophysiology of endothelial dysfunction in human diabetes mellitus.
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Acknowledgments |
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This work was supported by grants from the Garfield Weston Trust and the British Heart Foundation (to Dr Channon) and by a Wellcome Trust International Research Development Award (to Drs Guzik and Channon).
Received November 13, 2001; revision received January 29, 2002; accepted January 29, 2002.
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References |
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1. Kojda G, Harrison D. Interactions between NO and reactive oxygen species: pathophysiological importance in atherosclerosis, hypertension, diabetes and heart failure. Cardiovasc Res. 1999; 43: 562–571.
2. Cai H, Harrison DG. Endothelial dysfunction in cardiovascular diseases: the role of oxidant stress. Circ Res. 2000; 87: 840–844.
3. Gryglewski RJ, Palmer RM, Moncada S. Superoxide anion is involved in the breakdown of endothelium-derived vascular relaxing factor. Nature. 1986; 320: 454–456.
4. White CR, Brock TA, Chang L-Y, et al. Superoxide and peroxynitrite in atherosclerosis. Proc Natl Acad Sci U S A. 1994; 91: 1044–1048.
5. Pieper GM. Review of alterations in endothelial nitric oxide production in diabetes: protective role of arginine on endothelial dysfunction. Hypertension. 1998; 31: 1047–1060.
6. Peterson TE, Poppa V, Ueba H, et al. Opposing effects of reactive oxygen species and cholesterol on endothelial nitric oxide synthase and endothelial cell caveolae. Circ Res. 1999; 85: 29–37.
7. Wolin MS. Interactions of oxidants with vascular signaling systems. Arterioscler Thromb Vasc Biol. 2000; 20: 1430–1442.
8. Rajagopalan S, Kurz S, Munzel T, et al. Angiotensin II-mediated hypertension in the rat increases vascular superoxide production via membrane NAD/NAD(P)H oxidase activation. J Clin Invest. 1996; 97: 1916–1923.
9. Ushio-Fukai M, Zafari AM, Fukui T, et al. p22phox is a critical component of the superoxide-generating NADH/NAD(P)H oxidase system and regulates angiotensin II-induced hypertrophy in vascular smooth muscle cells. J Biol Chem. 1996; 271: 23317–23321.
10. White CR, Darley-Usmar V, Berrington WR, et al. Circulating plasma xanthine oxidase contributes to vascular dysfunction in hypercholesterolemic rabbits. Proc Natl Acad Sci U S A. 1996; 93: 8745–8749.
11. Vasquez-Vivar J, Kalyanaraman B, Martasek P, et al. Superoxide generation by endothelial nitric oxide synthase: the influence of cofactors. Proc Natl Acad Sci U S A. 1998; 95: 9220–9225.
12. Warnholtz A, Nickenig G, Schulz E, et al. Increased NADH-oxidase-mediated superoxide production in the early stages of atherosclerosis: evidence for involvement of the renin-angiotensin system. Circulation. 1999; 99: 2027–2033.
13. Azumi H, Inoue N, Takeshita S, et al. Expression of NADH/NAD(P)H oxidase p22phox in human coronary arteries. Circulation. 1999; 100: 1494–1498.
14. Guzik TJ, West NEJ, Black E, et al. Vascular superoxide production by NAD(P)H oxidase: association with endothelial dysfunction and clinical risk factors. Circ Res. 2000; 86: e85–e90.
15. Griendling KK, Sorescu D, Ushio-Fukai M. NAD(P)H oxidase: role in cardiovascular biology and disease. Circ Res. 2000; 86: 494–501.
16. Cosentino F, Hishikawa K, Katusic ZS, et al. High glucose increases nitric oxide synthase expression and superoxide anion generation in human aortic endothelial cells. Circulation. 1997; 96: 25–28.
17. Hink U, Li H, Mollnau H, et al. Mechanisms underlying endothelial dysfunction in diabetes mellitus. Circ Res. 2001; 88: e14–e22.
18. Shinozaki K, Kashiwagi A, Nishio Y, et al. Abnormal biopterin metabolism is a major cause of impaired endothelium-dependent relaxation through nitric oxide/O2-imbalance in insulin-resistant rat aorta. Diabetes. 1999; 48: 2437–2445.
19. Pieper GM. Acute amelioration of diabetic endothelial dysfunction with a derivative of the nitric oxide synthase cofactor, tetrahydrobiopterin. J Cardiovasc Pharmacol. 1997; 29: 8–15.
20. Meininger CJ, Marinos RS, Hatakeyama K, et al. Impaired nitric oxide production in coronary endothelial cells of the spontaneously diabetic BB rat is due to tetrahydrobiopterin deficiency. Biochem J. 2000; 349: 353–356.
21. Munzel T, Li H, Mollnau H, et al. Effects of long-term nitroglycerin treatment on endothelial nitric oxide synthase (NOS III) gene expression, NOS III-mediated superoxide production, and vascular NO bioavailability. Circ Res. 2000; 86: e7–e12.
22. Skatchkov MP, Sperling D, Hink U, et al. Validation of lucigenin as a chemiluminescent probe to monitor vascular superoxide as well as basal vascular nitric oxide production. Biochem Biophys Res Comm. 1999; 254: 319–324.
23. Li Y, Zhu H, Kuppusamy P, et al. Validation of lucigenin (bis-N-methylacridinium) as a chemilumigenic probe for detecting superoxide anion radical production by enzymatic and cellular systems. J Biol Chem. 1998; 273: 2015–2023.
24. Pritchard KA Jr, Groszek L, Smalley DM, et al. Native low-density lipoprotein increases endothelial cell nitric oxide synthase generation of superoxide anion. Circ Res. 1995; 77: 510–518.
25. Vita JA, Treasure CB, Nabel EG, et al. Coronary vasomotor response to acetylcholine relates to risk factors for coronary artery disease. Circulation. 1990; 81: 491–497.
26. Huraux C, Makita T, Kurz S, et al. Superoxide production, risk factors, and endothelium-dependent relaxations in human internal mammary arteries. Circulation. 1999; 99: 53–59.
27. Maier W, Cosentino F, Lutolf RB, et al. Tetrahydrobiopterin improves endothelial function in patients with coronary artery disease. J Cardiovasc Pharmacol. 2000; 35: 173–178.
28. Laursen JB, Somers M, Kurz S, et al. Endothelial regulation of vasomotion in apoE-deficient mice: implications for interactions between peroxynitrite and tetrahydrobiopterin. Circulation. 2001; 103: 1282–1288.
29. Milstien S, Katusic Z. Oxidation of tetrahydrobiopterin by peroxynitrite: implications for vascular endothelial function. Biochem Biophys Res Comm. 1999; 263: 681–684.
30. Beckman JA, Goldfine AB, Gordon MB, et al. Inhibition of protein kinase C beta prevents impaired endothelium-dependent vasodilation caused by hyperglycemia in humans. Circ Res. 2002; 90: 107–111.
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 J. G. Lopez-Lopez, J. Moral-Sanz, G. Frazziano, M. J. Gomez-Villalobos, J. Flores-Hernandez, E. Monjaraz, A. Cogolludo, and F. Perez-Vizcaino Diabetes induces pulmonary artery endothelial dysfunction by NADPH oxidase induction Am J Physiol Lung Cell Mol Physiol, November 1, 2008; 295(5): L727 - L732. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. Xue, Q. Qian, A. Adaikalakoteswari, N. Rabbani, R. Babaei-Jadidi, and P. J. Thornalley Activation of NF-E2-Related Factor-2 Reverses Biochemical Dysfunction of Endothelial Cells Induced by Hyperglycemia Linked to Vascular Disease Diabetes, October 1, 2008; 57(10): 2809 - 2817. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 X. W. Cheng, T. Murohara, M. Kuzuya, H. Izawa, T. Sasaki, K. Obata, K. Nagata, T. Nishizawa, M. Kobayashi, T. Yamada, et al. Superoxide-Dependent Cathepsin Activation Is Associated with Hypertensive Myocardial Remodeling and Represents a Target for Angiotensin II Type 1 Receptor Blocker Treatment Am. J. Pathol., August 1, 2008; 173(2): 358 - 369. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. Antoniades, C. Shirodaria, T. Van Assche, C. Cunnington, I. Tegeder, J. Lotsch, T. J. Guzik, P. Leeson, J. Diesch, D. Tousoulis, et al. GCH1 Haplotype Determines Vascular and Plasma Biopterin Availability in Coronary Artery Disease: Effects on Vascular Superoxide Production and Endothelial Function J. Am. Coll. Cardiol., July 8, 2008; 52(2): 158 - 165. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 N. Sasaki, T. Yamashita, T. Takaya, M. Shinohara, R. Shiraki, M. Takeda, N. Emoto, A. Fukatsu, T. Hayashi, K. Ikemoto, et al. Augmentation of Vascular Remodeling by Uncoupled Endothelial Nitric Oxide Synthase in a Mouse Model of Diabetes Mellitus Arterioscler Thromb Vasc Biol, June 1, 2008; 28(6): 1068 - 1076. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
T. Fujii, M. Onimaru, Y. Yonemitsu, H. Kuwano, and K. Sueishi Statins restore ischemic limb blood flow in diabetic microangiopathy via eNOS/NO upregulation but not via PDGF-BB expression Am J Physiol Heart Circ Physiol, June 1, 2008; 294(6): H2785 - H2791. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 T. A. Schwann, A. Zacharias, C. J. Riordan, S. J. Durham, A. S. Shah, and R. H. Habib Does radial use as a second arterial conduit for coronary artery bypass grafting improve long-term outcomes in diabetics? Eur. J. Cardiothorac. Surg., May 1, 2008; 33(5): 914 - 923. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y.-J. Chen, J. Li, and J. Quilley Deficient renal 20-HETE release in the diabetic rat is not the result of oxidative stress Am J Physiol Heart Circ Physiol, May 1, 2008; 294(5): H2305 - H2312. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
F. Cosentino, P. Francia, G. G. Camici, P. G. Pelicci, M. Volpe, and T. F. Luscher Final Common Molecular Pathways of Aging and Cardiovascular Disease: Role of the p66Shc Protein Arterioscler Thromb Vasc Biol, April 1, 2008; 28(4): 622 - 628. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 F Cosentino, D Hurlimann, C Delli Gatti, R Chenevard, N Blau, N J Alp, K M Channon, M Eto, P Lerch, F Enseleit, et al. Chronic treatment with tetrahydrobiopterin reverses endothelial dysfunction and oxidative stress in hypercholesterolaemia Heart, April 1, 2008; 94(4): 487 - 492. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. M. Kim, H. Kattach, C. Ratnatunga, R. Pillai, K. M. Channon, and B. Casadei Association of atrial nicotinamide adenine dinucleotide phosphate oxidase activity with the development of atrial fibrillation after cardiac surgery. J. Am. Coll. Cardiol., January 1, 2008; 51(1): 68 - 74. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. Blouet, F. Mariotti, V. Mathe, D. Tome, and J.-F. Huneau Nitric Oxide Bioavailability and Not Production Is First Altered During the Onset of Insulin Resistance in Sucrose-Fed Rats Experimental Biology and Medicine, December 1, 2007; 232(11): 1458 - 1464. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. E. Vendrov, Z. S. Hakim, N. R. Madamanchi, M. Rojas, C. Madamanchi, and M. S. Runge Atherosclerosis Is Attenuated by Limiting Superoxide Generation in Both Macrophages and Vessel Wall Cells Arterioscler Thromb Vasc Biol, December 1, 2007; 27(12): 2714 - 2721. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 P. Dandona, A. Chaudhuri, and P. Mohanty Macronutrients, Advanced Glycation End Products, and Vascular Reactivity Diabetes Care, October 1, 2007; 30(10): 2750 - 2751. [Full Text] [PDF]
|
|
|
|
|
|
B. P. Choudhary, C. Antoniades, A. F. Brading, A. Galione, K. Channon, and D. P. Taggart Diabetes Mellitus as a Predictor for Radial Artery Vasoreactivity in Patients Undergoing Coronary Artery Bypass Grafting J. Am. Coll. Cardiol., September 11, 2007; 50(11): 1047 - 1053. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 R. Muniyappa, M. Montagnani, K. K. Koh, and M. J. Quon Cardiovascular Actions of Insulin Endocr. Rev., August 1, 2007; 28(5): 463 - 491. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 G. Li, E. J. Barrett, M. O. Barrett, W. Cao, and Z. Liu Tumor Necrosis Factor-{alpha} Induces Insulin Resistance in Endothelial Cells via a p38 Mitogen-Activated Protein Kinase-Dependent Pathway Endocrinology, July 1, 2007; 148(7): 3356 - 3363. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. Rajesh, P. Mukhopadhyay, S. Batkai, G. Hasko, L. Liaudet, V. R. Drel, I. G. Obrosova, and P. Pacher Cannabidiol attenuates high glucose-induced endothelial cell inflammatory response and barrier disruption Am J Physiol Heart Circ Physiol, July 1, 2007; 293(1): H610 - H619. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 Authors/Task Force Members, L. Ryden, E. Standl, M. Bartnik, G. V. d. Berghe, J. Betteridge, M.-J. de Boer, F. Cosentino, B. Jonsson, M. Laakso, et al. Guidelines on diabetes, pre-diabetes, and cardiovascular diseases: full text: The Task Force on Diabetes and Cardiovascular Diseases of the European Society of Cardiology (ESC) and of the European Association for the Study of Diabetes (EASD) Eur. Heart J. Suppl., June 1, 2007; 9(suppl_C): C3 - C74. [Full Text] [PDF]
|
|
|
|
 |
|
 C. Shirodaria, C. Antoniades, J. Lee, C. E. Jackson, M. D. Robson, J. M. Francis, S. J. Moat, C. Ratnatunga, R. Pillai, H. Refsum, et al. Global Improvement of Vascular Function and Redox State With Low-Dose Folic Acid: Implications for Folate Therapy in Patients With Coronary Artery Disease Circulation, May 1, 2007; 115(17): 2262 - 2270. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. K. Bendall, R. Rinze, D. Adlam, A. L. Tatham, J. de Bono, and K. M. Channon Endothelial Nox2 Overexpression Potentiates Vascular Oxidative Stress and Hemodynamic Response to Angiotensin II: Studies in Endothelial-Targeted Nox2 Transgenic Mice Circ. Res., April 13, 2007; 100(7): 1016 - 1025. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Hattori, S. Hattori, X. Wang, H. Satoh, N. Nakanishi, and K. Kasai Oral Administration of Tetrahydrobiopterin Slows the Progression of Atherosclerosis in Apolipoprotein E-Knockout Mice Arterioscler Thromb Vasc Biol, April 1, 2007; 27(4): 865 - 870. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Z. Guo, Z. Xia, J. Jiang, and J. H. McNeill Downregulation of NADPH oxidase, antioxidant enzymes, and inflammatory markers in the heart of streptozotocin-induced diabetic rats by N-acetyl-L-cysteine Am J Physiol Heart Circ Physiol, April 1, 2007; 292(4): H1728 - H1736. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. Dikalov, K. K. Griendling, and D. G. Harrison Measurement of Reactive Oxygen Species in Cardiovascular Studies Hypertension, April 1, 2007; 49(4): 717 - 727. [Full Text] [PDF]
|
|
|
|
|
|
T. Thum, D. Fraccarollo, M. Schultheiss, S. Froese, P. Galuppo, J. D. Widder, D. Tsikas, G. Ertl, and J. Bauersachs Endothelial Nitric Oxide Synthase Uncoupling Impairs Endothelial Progenitor Cell Mobilization and Function in Diabetes Diabetes, March 1, 2007; 56(3): 666 - 674. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
E. Takimoto and D. A. Kass Role of Oxidative Stress in Cardiac Hypertrophy and Remodeling Hypertension, February 1, 2007; 49(2): 241 - 248. [Full Text] [PDF]
|
|
|
|
|
|
X. Gao, S. Belmadani, A. Picchi, X. Xu, B. J. Potter, N. Tewari-Singh, S. Capobianco, W. M. Chilian, and C. Zhang Tumor Necrosis Factor-{alpha} Induces Endothelial Dysfunction in Leprdb Mice Circulation, January 16, 2007; 115(2): 245 - 254. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J.-H. Oak and H. Cai Attenuation of Angiotensin II Signaling Recouples eNOS and Inhibits Nonendothelial NOX Activity in Diabetic Mice Diabetes, January 1, 2007; 56(1): 118 - 126. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 T. Hayashi, H. Matsui-Hirai, A. Miyazaki-Akita, A. Fukatsu, J. Funami, Q.-F. Ding, S. Kamalanathan, Y. Hattori, L. J. Ignarro, and A. Iguchi Endothelial cellular senescence is inhibited by nitric oxide: Implications in atherosclerosis associated with menopause and diabetes PNAS, November 7, 2006; 103(45): 17018 - 17023. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C. Antoniades, C. Shirodaria, N. Warrick, S. Cai, J. de Bono, J. Lee, P. Leeson, S. Neubauer, C. Ratnatunga, R. Pillai, et al. 5-Methyltetrahydrofolate Rapidly Improves Endothelial Function and Decreases Superoxide Production in Human Vessels: Effects on Vascular Tetrahydrobiopterin Availability and Endothelial Nitric Oxide Synthase Coupling Circulation, September 12, 2006; 114(11): 1193 - 1201. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. W. A. Smit and J. A. Romijn Acute insulin resistance in myocardial ischemia: causes and consequences. Seminars in Cardiothoracic and Vascular Anesthesia, September 1, 2006; 10(3): 215 - 219. [Abstract] [PDF]
|
|
|
|
|
|
T. Szerafin, N. Erdei, T. Fulop, E. T. Pasztor, I. Edes, A. Koller, and Z. Bagi Increased Cyclooxygenase-2 Expression and Prostaglandin-Mediated Dilation in Coronary Arterioles of Patients With Diabetes Mellitus Circ. Res., September 1, 2006; 99(5): e12 - 317. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. Oelze, A. Warnholtz, J. Faulhaber, P. Wenzel, A. L. Kleschyov, M. Coldewey, U. Hink, O. Pongs, I. Fleming, S. Wassmann, et al. NADPH Oxidase Accounts for Enhanced Superoxide Production and Impaired Endothelium-Dependent Smooth Muscle Relaxation in BK{beta}1-/- Mice Arterioscler Thromb Vasc Biol, August 1, 2006; 26(8): 1753 - 1759. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. W.Y. Chung, Y. N. Hsiang, L. A. Matzke, B. M. McManus, C. van Breemen, and E. B. Okon Reduced Expression of Vascular Endothelial Growth Factor Paralleled With the Increased Angiostatin Expression Resulting From the Upregulated Activities of Matrix Metalloproteinase-2 and -9 in Human Type 2 Diabetic Arterial Vasculature Circ. Res., July 21, 2006; 99(2): 140 - 148. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Picchi, X. Gao, S. Belmadani, B. J. Potter, M. Focardi, W. M. Chilian, and C. Zhang Tumor Necrosis Factor-{alpha} Induces Endothelial Dysfunction in the Prediabetic Metabolic Syndrome Circ. Res., July 7, 2006; 99(1): 69 - 77. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
K. Sachidanandam, A. Harris, J. Hutchinson, and A. Ergul Microvascular versus macrovascular dysfunction in type 2 diabetes: differences in contractile responses to endothelin-1. Experimental Biology and Medicine, June 1, 2006; 231(6): 1016 - 1021. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Shimoni, D. Hunt, K. Chen, T. Emmett, and G. Kargacin Differential autocrine modulation of atrial and ventricular potassium currents and of oxidative stress in diabetic rats Am J Physiol Heart Circ Physiol, May 1, 2006; 290(5): H1879 - H1888. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 D. Feliers, Y. Gorin, G. Ghosh-Choudhury, H. E. Abboud, and B. S. Kasinath Angiotensin II stimulation of VEGF mRNA translation requires production of reactive oxygen species Am J Physiol Renal Physiol, April 1, 2006; 290(4): F927 - F936. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C. Vecchione, A. Aretini, G. Marino, U. Bettarini, R. Poulet, A. Maffei, M. Sbroggio, L. Pastore, M. T. Gentile, A. Notte, et al. Selective Rac-1 Inhibition Protects From Diabetes-Induced Vascular Injury Circ. Res., February 3, 2006; 98(2): 218 - 225. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
T. J. Rabelink and T. F. Luscher Endothelial Nitric Oxide Synthase: Host Defense Enzyme of the Endothelium? Arterioscler Thromb Vasc Biol, February 1, 2006; 26(2): 267 - 271. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
T. J. Guzik, J. Sadowski, B. Guzik, A. Jopek, B. Kapelak, P. Przybylowski, K. Wierzbicki, R. Korbut, D. G. Harrison, and K. M. Channon Coronary Artery Superoxide Production and Nox Isoform Expression in Human Coronary Artery Disease Arterioscler Thromb Vasc Biol, February 1, 2006; 26(2): 333 - 339. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Fortuno, G. San Jose, M. U. Moreno, O. Beloqui, J. Diez, and G. Zalba Phagocytic NADPH Oxidase Overactivity Underlies Oxidative Stress in Metabolic Syndrome Diabetes, January 1, 2006; 55(1): 209 - 215. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. Q. Liu, I. N. Zelko, E. M. Erbynn, J. S. K. Sham, and R. J. Folz Hypoxic pulmonary hypertension: role of superoxide and NADPH oxidase (gp91phox) Am J Physiol Lung Cell Mol Physiol, January 1, 2006; 290(1): L2 - L10. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
P. M. Thule, A. G. Campbell, D. J. Kleinhenz, D. E. Olson, J. J. Boutwell, R. L. Sutliff, and C. M. Hart Hepatic insulin gene therapy prevents deterioration of vascular function and improves adipocytokine profile in STZ-diabetic rats Am J Physiol Endocrinol Metab, January 1, 2006; 290(1): E114 - E122. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
L. M. Bevers, B. Braam, J. A. Post, A. J. van Zonneveld, T. J. Rabelink, H. A. Koomans, M. C. Verhaar, and J. A. Joles Tetrahydrobiopterin, but Not L-Arginine, Decreases NO Synthase Uncoupling in Cells Expressing High Levels of Endothelial NO Synthase Hypertension, January 1, 2006; 47(1): 87 - 94. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 L. G. Kevin, E. Novalija, and D. F. Stowe Reactive Oxygen Species as Mediators of Cardiac Injury and Protection: The Relevance to Anesthesia Practice Anesth. Analg., November 1, 2005; 101(5): 1275 - 1287. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. K. Bendall, N. J. Alp, N. Warrick, S. Cai, D. Adlam, K. Rockett, M. Yokoyama, S. Kawashima, and K. M. Channon Stoichiometric Relationships Between Endothelial Tetrahydrobiopterin, Endothelial NO Synthase (eNOS) Activity, and eNOS Coupling in Vivo: Insights From Transgenic Mice With Endothelial-Targeted GTP Cyclohydrolase 1 and eNOS Overexpression Circ. Res., October 28, 2005; 97(9): 864 - 871. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. G. Herman and S. Moncada Therapeutic potential of nitric oxide donors in the prevention and treatment of atherosclerosis Eur. Heart J., October 1, 2005; 26(19): 1945 - 1955. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C. Antoniades, D. Tousoulis, C. Vasiliadou, C. Pitsavos, C. Chrysochoou, D. Panagiotakos, C. Tentolouris, K. Marinou, N. Koumallos, and C. Stefanadis Genetic Polymorphism on Endothelial Nitric Oxide Synthase Affects Endothelial Activation and Inflammatory Response During the Acute Phase of Myocardial Infarction J. Am. Coll. Cardiol., September 20, 2005; 46(6): 1101 - 1109. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
T. Munzel, A. Daiber, V. Ullrich, and A. Mulsch Vascular Consequences of Endothelial Nitric Oxide Synthase Uncoupling for the Activity and Expression of the Soluble Guanylyl Cyclase and the cGMP-Dependent Protein Kinase Arterioscler Thromb Vasc Biol, August 1, 2005; 25(8): 1551 - 1557. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. E. Barbato, B. S. Zuckerbraun, M. Overhaus, K. G. Raman, and E. Tzeng Nitric oxide modulates vascular inflammation and intimal hyperplasia in insulin resistance and the metabolic syndrome Am J Physiol Heart Circ Physiol, July 1, 2005; 289(1): H228 - H236. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Taniyama, H. Hitomi, A. Shah, R. W. Alexander, and K. K. Griendling Mechanisms of Reactive Oxygen Species-Dependent Downregulation of Insulin Receptor Substrate-1 by Angiotensin II Arterioscler Thromb Vasc Biol, June 1, 2005; 25(6): 1142 - 1147. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. Satoh, S. Fujimoto, Y. Haruna, S. Arakawa, H. Horike, N. Komai, T. Sasaki, K. Tsujioka, H. Makino, and N. Kashihara NAD(P)H oxidase and uncoupled nitric oxide synthase are major sources of glomerular superoxide in rats with experimental diabetic nephropathy Am J Physiol Renal Physiol, June 1, 2005; 288(6): F1144 - F1152. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Ergul, J. S. Johansen, C. Stromhaug, A. K. Harris, J. Hutchinson, A. Tawfik, A. Rahimi, E. Rhim, B. Wells, R. W. Caldwell, et al. Vascular Dysfunction of Venous Bypass Conduits Is Mediated by Reactive Oxygen Species in Diabetes: Role of Endothelin-1 J. Pharmacol. Exp. Ther., April 1, 2005; 313(1): 70 - 77. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. F. Dominiczak, D. Graham, M. W. McBride, N. J.R. Brain, W. K. Lee, F. J. Charchar, M. Tomaszewski, C. Delles, and C. A. Hamilton Cardiovascular Genomics and Oxidative Stress Hypertension, April 1, 2005; 45(4): 636 - 642. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
I. S. Thrainsdottir, T. Aspelund, G. Thorgeirsson, V. Gudnason, T. Hardarson, K. Malmberg, G. Sigurdsson, and L. Ryden The Association Between Glucose Abnormalities and Heart Failure in the Population-Based Reykjavik Study Diabetes Care, March 1, 2005; 28(3): 612 - 616. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. A. Summers and D. H. Nelson A Role for Sphingolipids in Producing the Common Features of Type 2 Diabetes, Metabolic Syndrome X, and Cushing's Syndrome Diabetes, March 1, 2005; 54(3): 591 - 602. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C. Rask-Madsen and G. L. King Proatherosclerotic Mechanisms Involving Protein Kinase C in Diabetes and Insulin Resistance Arterioscler Thromb Vasc Biol, March 1, 2005; 25(3): 487 - 496. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. Bauersachs and A. Schafer Tetrahydrobiopterin and eNOS dimer/monomer ratio-a clue to eNOS uncoupling in diabetes? Cardiovasc Res, March 1, 2005; 65(4): 768 - 769. [Full Text] [PDF]
|
|
|
|
|
|
A. Huang, Y.-Y. Zhang, K. Chen, K. Hatakeyama, and J. F. Keaney Jr Cytokine-Stimulated GTP Cyclohydrolase I Expression in Endothelial Cells Requires Coordinated Activation of Nuclear Factor-{kappa}B and Stat1/Stat3 Circ. Res., February 4, 2005; 96(2): 164 - 171. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
N. Lu, B. G. Helwig, R. J. Fels, S. Parimi, and M. J. Kenney Central Tempol alters basal sympathetic nerve discharge and attenuates sympathetic excitation to central ANG II Am J Physiol Heart Circ Physiol, December 1, 2004; 287(6): H2626 - H2633. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J.-M. Li and A. M Shah Endothelial cell superoxide generation: regulation and relevance for cardiovascular pathophysiology Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2004; 287(5): R1014 - R1030. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J.-D. Luo, Y.-Y. Wang, W.-L. Fu, J. Wu, and A. F. Chen Gene Therapy of Endothelial Nitric Oxide Synthase and Manganese Superoxide Dismutase Restores Delayed Wound Healing in Type 1 Diabetic Mice Circulation, October 19, 2004; 110(16): 2484 - 2493. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 R. Stocker and J. F. Keaney Jr. Role of Oxidative Modifications in Atherosclerosis Physiol Rev, October 1, 2004; 84(4): 1381 - 1478. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
K. Witte, J. Hachenberger, M. F. Castell, C. F. Vahl, and C. Haller Nitric Oxide-Sensitive Soluble Guanylyl Cyclase Activity Is Preserved in Internal Mammary Artery of Type 2 Diabetic Patients Diabetes, October 1, 2004; 53(10): 2640 - 2644. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. Wassmann, K. Wassmann, and G. Nickenig Modulation of Oxidant and Antioxidant Enzyme Expression and Function in Vascular Cells Hypertension, October 1, 2004; 44(4): 381 - 386. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Prasad and A. A. Quyyumi Renin-Angiotensin System and Angiotensin Receptor Blockers in the Metabolic Syndrome Circulation, September 14, 2004; 110(11): 1507 - 1512. [Full Text] [PDF]
|
|
|
|
|
|
T. J. Guzik, J. Sadowski, B. Kapelak, A. Jopek, P. Rudzinski, R. Pillai, R. Korbut, and K. M. Channon Systemic Regulation of Vascular NAD(P)H Oxidase Activity and Nox Isoform Expression in Human Arteries and Veins Arterioscler Thromb Vasc Biol, September 1, 2004; 24(9): 1614 - 1620. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 G.T. Chew and G.F. Watts Coenzyme Q10 and diabetic endotheliopathy: oxidative stress and the 'recoupling hypothesis' QJM, August 1, 2004; 97(8): 537 - 548. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. Veerareddy, C.-L. M. Cooke, P. N. Baker, and S. T. Davidge Gender differences in myogenic tone in superoxide dismutase knockout mouse: animal model of oxidative stress Am J Physiol Heart Circ Physiol, July 1, 2004; 287(1): H40 - H45. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. Q. Liu and R. J. Folz Extracellular superoxide enhances 5-HT-induced murine pulmonary artery vasoconstriction Am J Physiol Lung Cell Mol Physiol, July 1, 2004; 287(1): L111 - L118. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
F Violi, L Loffredo, L Musella, and A Marcoccia Should antioxidant status be considered in interventional trials with antioxidants? Heart, June 1, 2004; 90(6): 598 - 602. [Abstract] [Full Text] [PDF]
|
|
|
|
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D. Sigaudo-Roussel, C. Demiot, B. Fromy, A. Koitka, G. Leftheriotis, P. Abraham, and J. L. Saumet Early Endothelial Dysfunction Severely Impairs Skin Blood Flow Response to Local Pressure Application in Streptozotocin-Induced Diabetic Mice Diabetes, June 1, 2004; 53(6): 1564 - 1569. [Abstract] [Full Text] [PDF]
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A M Shah and K M Channon Free radicals and redox signalling in cardiovascular disease Heart, May 1, 2004; 90(5): 486 - 487. [Full Text] [PDF]
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B. Erdos, J. A. Snipes, A. W. Miller, and D. W. Busija Cerebrovascular Dysfunction in Zucker Obese Rats Is Mediated by Oxidative Stress and Protein Kinase C Diabetes, May 1, 2004; 53(5): 1352 - 1359. [Abstract] [Full Text] [PDF]
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I. Eskurza, K. D. Monahan, J. A. Robinson, and D. R. Seals Ascorbic acid does not affect large elastic artery compliance or central blood pressure in young and older men Am J Physiol Heart Circ Physiol, April 1, 2004; 286(4): H1528 - H1534. [Abstract] [Full Text] [PDF]
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 B. Erdos, S. A. Simandle, J. A. Snipes, A. W. Miller, and D. W. Busija Potassium Channel Dysfunction in Cerebral Arteries of Insulin-Resistant Rats Is Mediated by Reactive Oxygen Species Stroke, April 1, 2004; 35(4): 964 - 969. [Abstract] [Full Text] [PDF]
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N. J. Alp and K. M. Channon Regulation of Endothelial Nitric Oxide Synthase by Tetrahydrobiopterin in Vascular Disease Arterioscler Thromb Vasc Biol, March 1, 2004; 24(3): 413 - 420. [Abstract] [Full Text]
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