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1 at appears to be related to the formation of superoxide anion.
2 cells, utilize molecular oxygen to generate superoxide anion.
3 e activated in response to the production of superoxide anion.
4 was decreased with a concomitant increase in superoxide anion.
5 rmed the identity of the reaction product as superoxide anion.
6 inone (DMNQ), which generates a low level of superoxide anion.
7 It also directly detoxifies superoxide anion.
8 eactive oxygen species by disproportionating superoxide anion.
9 he reaction product of nitric oxide (NO) and superoxide anion.
10 luding at 37 degrees C or in the presence of superoxide anion.
11 ress with enhanced endothelial production of superoxide anion.
12 major defense against ROS by detoxifying the superoxide anion.
13 ng damage mediated by detrimental actions of superoxide anion.
14 s formed in the reaction of nitric oxide and superoxide anion.
15 en peroxide generation but was unaffected by superoxide anion.
16 f other stimuli to catalyze the formation of superoxide anion.
17 ired vascular function through production of superoxide anion.
18 ells, indicating eNOS as a primary source of superoxide anion.
19 effects of corresponding ROS, H(2)O(2), and superoxide anion.
20 es the assembly of NADPH oxidase to generate superoxide anion.
21 ntrols and was accompanied by an increase in superoxide anion.
22 ir reaction with dissolved oxygen to produce superoxide anions.
23 o interfere with NADH oxidation and generate superoxide anions.
24 s low, leading to an increased production of superoxide anions.
25 medullae, suggesting increased generation of superoxide anions.
26 roxide dismutases (SOD) that act to detoxify superoxide anions.
27 a secretion by PBMC in response to exogenous superoxide anions.
28 gen peroxide, a stable dismutated product of superoxide anions.
29 ikewise is associated with the production of superoxide anions.
30 ne NADPH oxidases that produce extracellular superoxide anion, a reactive oxygen species that is read
32 It was hypothesized that a specific ROS, superoxide anion, acts as an intracellular signaling mol
33 ight provide a preorganized binding site for superoxide anion, an obligatory intermediate in the two-
35 se wave velocity, measurement of circulating superoxide anion and C-reactive protein, as well as bloo
36 NADPH oxidases, leading to production of the superoxide anion and decreased availability of nitric ox
37 hagocytes are defective in the generation of superoxide anion and downstream reactive oxidant species
38 e reaction of OG with the E1o-h gave rise to superoxide anion and hydrogen peroxide (reactive oxygen
39 the data suggest the novel observation that superoxide anion and hydrogen peroxide are produced sepa
40 w cytometry that 1,6-BPQ and 3,6-BPQ produce superoxide anion and hydrogen peroxide in MCF-10A cells.
42 ric reducing antioxidant power (FRAP), ABTS, superoxide anion and hydroxyl radical scavenging tests.
43 SLDLPVLRW, FVPY) were found able to scavenge superoxide anion and hydroxyl radicals, organic nitro-ra
44 by disrupting electron transport, generating superoxide anion and inactivating bacterial oxidative de
45 tress as measured by increased generation of superoxide anion and increased expression of nitrotyrosi
46 dant and nitrating agent readily formed from superoxide anion and nitric oxide generated by mitochond
47 power, DPPH (2,2-diphenyl-1-picrylhydrazyl), superoxide anion and nitric oxide radical scavenging.
50 y F(2)-isoprostanes (P < 0.001) and monocyte superoxide anion and tumor necrosis factor release compa
51 inding that nicotine significantly increased superoxide anions and 3-nitrotyrosine-positive proteins,
53 c complexes are not effective in scavenging superoxide anions and are not effectively reduced by asc
54 ltered cellular redox state due to increased superoxide anions and establish a new relationship betwe
55 153), an enzyme mediating the dismutation of superoxide anions and examined the in vitro and in vivo
56 A medium resulted in increased production of superoxide anions and H(2)O(2), transduction of the PI 3
57 superoxide dismutase and catalase to quench superoxide anions and hydrogen peroxide, respectively, i
58 somes was determined against the toxicity of superoxide anions and hydroxyethyl radicals in HepG2 cel
59 n excess, iron is toxic because it generates superoxide anions and hydroxyl radicals that react readi
60 mechanisms involving increased generation of superoxide anions and suggest that hypoxia-evoked CA eff
62 ate immunity (phagocytosis and production of superoxide anion) and pathogen challenge were used to ev
63 ntaneous generation of hydrogen peroxide and superoxide anion, and decreased ATP, as well as subseque
64 at least four individual RONS (NO, H(2)O(2), superoxide anion, and peroxynitirte), induced apoptotic
65 denced by increased levels of monocyte IL-6, superoxide anion, and plasma CRP, sICAM, sCD40L, and nit
67 tein kinase (MAPK) activation, generation of superoxide anion, and Toll-like receptor 4 expression wa
68 e in circulating endothelial cell sloughing, superoxide anion, and vasoconstriction in diabetic rats
69 at all 15 strains exhibit elevated levels of superoxide anions, and we show that elevated levels of r
71 Hp disrupt NADPH oxidase targeting such that superoxide anions are released into the extracellular mi
72 Reactive oxygen species (ROS), particularly superoxide anion, are well known to inhibit NO, and ther
75 in) generation of both hydrogen peroxide and superoxide anion, as defined with oxidation-sensitive dy
76 endothelial NADPH oxidase and generation of superoxide anion at the extracellular surface of the cel
78 rom peritoneal lavage fluids did not produce superoxide anion, but did produce an anti-inflammatory a
79 and subsequent cell death was dependent upon superoxide anion, but independent of hydrogen peroxide,
80 s of AT1R protein and measured production of superoxide anion by brain tissue under basal conditions
82 Corroboratively, we found that scavenging of superoxide anion by Mn(III) tetrakis (4-benzoic acid) po
83 nhibitors of the extracellular production of superoxide anion by preventing the up-regulation of the
84 d the generation of NAD(P)H oxidase-mediated superoxide anions by increasing the translocation and me
85 not only generate hydrogen peroxide but also superoxide anions by transferring aldehyde-derived elect
86 d by diminished activation and intracellular superoxide anion concentration, and reduced leukocyte ad
87 genously produced hydrogen peroxide, but not superoxide anions, contributed to the formation of oxidi
88 ously that inactivation of catecholamines by superoxide anions contributes to the loss of vascular re
94 e have hypothesized that the balance between superoxide anion efflux through inner membrane anion cha
96 a cleavage is blocked under conditions where superoxide anion formation is blocked or monocytes are t
100 inhibited nitroblue tetrazolium reduction of superoxide anion generated in a xanthine-xanthine oxidas
101 uman Burkitt's lymphoma cells are exposed to superoxide anion, generated as a flux from xanthine and
102 ) deficiency, the catalytic component of the superoxide anion-generating NADPH oxidase complex, is ad
103 (18 +/- 12% of control, n = 4) and increased superoxide anion generation (358 +/- 37%, p = 0.003).
104 ha-primed cells causes major upregulation of superoxide anion generation (O(2)(-)) yet no incremental
105 VEGF and angiogenin 1 together with reduced superoxide anion generation and an increase in MnSOD com
106 nin, which abolished both agonist-stimulated superoxide anion generation and degranulation, had no ef
107 y assess the relative rates of mitochondrial superoxide anion generation in isolated islets in respon
108 this end, PMN transendothelial migration and superoxide anion generation were assessed with LAP patie
109 PLD activation, myeloperoxidase release, and superoxide anion generation, and that PLD activation occ
110 ion and the augmentation of the fMLP-induced superoxide anion generation, by all priming agents were
112 NADPH oxidase 4 (NOX4), a source of cellular superoxide anions, has multiple biological functions tha
113 Reactive oxygen species (ROS), including superoxide anions, hydrogen peroxide and hydroxyl radica
114 ases, reactive species levels (nitric oxide, superoxide anion, hydroxyl radical scavenger capacity) a
115 f different ROS including hydrogen peroxide, superoxide anion, hydroxyl radical, and lipid peroxides.
116 ectroscopic evidence of the participation of superoxide anion in a related chemical model reaction th
119 d molecular pattern, activates production of superoxide anion in leukocytes without the need for phag
120 ngiotensin II increased lucigenin-detectable superoxide anion in LV tissue in a manner that was inhib
121 inished NADPH oxidase-mediated production of superoxide anion in response to bacteria by MyD88-/- pha
122 days significantly increased the release of superoxide anion in response to the calcium ionophore A2
123 ormation of nitrotyrosine, nitric oxide, and superoxide anion in retinal vascular endothelial cells a
126 Paraquat-induced ROS production (including superoxide anions) in BV-2 cells was accompanied by tran
127 abrogated cell chemotaxis and the release of superoxide anions induced by the bacterial formylpeptide
128 potent oxidant generated by nitric oxide and superoxide anions, instigates GTPCH1 ubiquitination and
129 e capacity is reduced in conditions in which superoxide anion is increased, and this is associated wi
130 at pomegranate extract reduced mitochondrial superoxide anion levels and increased mitochondrial func
132 ide synthase (eNOS) expression and increased superoxide anion levels in both vessels and HPAECs.
134 f proliferating fibroblasts led to increased superoxide anion levels, juxtanuclear accumulation of ub
138 kinase C (PKC) contributes to generation of superoxide anion (O(-)(2)) after fluid percussion brain
141 ense hBVR, with 66% reduced BVR activity, to superoxide anion (O(2)()) formed by menadione is attenua
142 re we show that Fe(2+) induces generation of superoxide anion (O(2)()) in endosomes, reduces protein-
145 ochrome bc(1) complex (bc(1)) also catalyzes superoxide anion (O(2)(*)) generation upon oxidation of
149 me activity, and cellular NO levels, whereas superoxide anion (O(2)(-)) production was significantly
150 ed that diabetic monocytes produce increased superoxide anion (O(2)(-)), and alpha-tocopherol (AT) su
151 neutrophils and HL-60 cells fail to produce superoxide anion (O(2)(-)), which is partially attributa
152 rved with NADH may involve the generation of superoxide anion (O(2)(-).) as they were attenuated to j
153 espiratory burst" of NADPH oxidase-dependent superoxide anion (O(2)(-*)) production that is required
154 hate (NADPH) oxidase activity causes reduced superoxide anion (O(2)(.)) radical production leading to
155 ective effect by scavenging of mitochondrial superoxide anion (O(2)(.-)) and intramitochondrial free
157 , which decreases NO synthesis and increases superoxide anion (O(2)(.-)) production by the enzyme.
158 idase and could provide high local levels of superoxide anion (O(2)), that when dismutated would gene
159 maintain the steady-state concentrations of superoxide anion (O(2)*-) and hydrogen peroxide (H(2)O(2
160 tive (reduced) oxygen species (ROS), such as superoxide anion (O-2.) and/or hydrogen peroxide (H2O2).
163 e of this study was to determine the role of superoxide anions (O(2)(-)) in mononuclear phagocyte-ind
164 diated tissue injury involves the release of superoxide anions (O(2)(-)), the present study examined
165 HUVECs to high glucose (30 mmol/l) increased superoxide anions (O(2).(-)) and prostacyclin synthase n
169 ed inhibition, indicating the involvement of superoxide anion (O2(*-)) in the inactivation process.
172 5-Epi-LXA4 (0.1-100 nM) inhibited neutrophil superoxide anion (O2(-)) generation in a concentration-
173 decreased, eNOS becomes uncoupled to produce superoxide anion (O2(-)) instead of NO, which contribute
175 The mediator of the restrictive signal is superoxide anion (O2(-)) released by membrane NAD(P)H ox
176 active site in class I b RNRs that requires superoxide anion (O2(.-) ), rather than dioxygen (O2 ),
177 Therefore, we have examined the effect of superoxide anion (O2) on IP3R-mediated Ca(2+) signaling.
182 n in MCF-7 cells increased the generation of superoxide anion (O2*-) in anthracycline-treated cell ex
183 thelial function by modulating levels of the superoxide anion (O2*-) in the extracellular space.
185 cholesterol decreased NO (*NO) and increased superoxide anion (O2*-) production and increased ATP-bin
186 o induce NAD(P)H oxidase to produce vascular superoxide anion (O2*-) production, which has been impli
187 oxide synthase (eNOS) activity, which allows superoxide anion (O2*-)) to be generated rather than nit
189 here was an increase in lucigenin-detectable superoxide anion (O2-) in cardiac tissues from nNOS-/- c
190 We hypothesized that in states in which superoxide anion (O2-) is increased, especially in the m
191 thromboxane prostanoid receptors (TP-Rs), or superoxide anion (O2-) mediates enhanced contractions of
195 blasts contain a substantial NAD(P)H oxidase superoxide anion (O2-)-generating system activated by an
198 as NoxA1ds) potently inhibited Nox1-derived superoxide anion (O2.-) production in a reconstituted No
200 ct of donor-ion charge on reduction of O2 to superoxide anion (O2.-), is obtained using an isostructu
201 itric oxide (NO) and NAD(P)Hoxidase produces superoxide anions (O2 (-) , quenching NO) we propose tha
204 body's defence against microbes: it produces superoxide anions (O2-, precursors to bactericidal react
205 g/24 hours) on platelet free radical (NO and superoxide anion [O2*-] activity) with and without coadm
206 ater molecules on the nucleophilicity of the superoxide anion, O2(*-), has been investigated in detai
208 ein kinase (MAPK) in mediating the effect of superoxide anions on PTK expression and ROMK (Kir 1.1) c
209 ogen peroxide, ozone, hydroxyl radicals, and superoxide anions), only H2O2 and ozone were found to be
210 ces concomitantly enhanced the production of superoxide anion, only the fungicidal activity of collag
212 tration of superoxide dismutase (to scavenge superoxide anions) or L-N(G)-nitroarginine methyl ester
217 te (NADPH) oxidase generates vast amounts of superoxide anion, precursor to bactericidal reactive oxy
218 ide dismutase mimetic, a potent scavenger of superoxide anions, prevented IH-induced c-fos, AP-1 and
220 inum and glass were tested and the amount of superoxide anion produced by NADPH oxidase was measured
223 42 and in the Rho GTPase-dependent functions superoxide anion production and actin polymerization.
224 veolin-1, whereas it significantly increased superoxide anion production and activated extracellular
225 ubated with eosinophils, it potently induced superoxide anion production and degranulation; 5 nM tryp
226 Furthermore, IL-6 time dependently increased superoxide anion production and ONOO- formation; the lat
230 DO45D-40 and S. pneumoniae 39937 and induced superoxide anion production by polymorphonuclear neutrop
232 )) expression and activity are essential for superoxide anion production in activated human monocytes
234 n, as well as increased TNF-alpha, IL-6, and superoxide anion production in inflammatory MC subsets.
235 uthern and Western blotting and by measuring superoxide anion production in membrane fractions in the
236 ication of NMDA and kainate did not increase superoxide anion production in nondiabetic or diabetic r
240 dinucleotide phosphate oxidase activity and superoxide anion production via downregulation of Rac1.
243 amily kinases, small GTPase Rac2, neutrophil superoxide anion production, and for Listeria monocytoge
244 2 resulted in increased Ca(2+) mobilization, superoxide anion production, and GTPase activity in neut
245 destalilization which leads to Ca(2+) rise, superoxide anion production, ATP drop and late NADP(H) d
246 ophore, phorbol ester, or H(2)O(2) exhibited superoxide anion production, which was blocked by additi
250 ubstrate for oxidation by O2, leading to the superoxide anion radical (in d) and the radical (in b).
251 as superoxide dismutase (SOD), which removes superoxide anion radical (O(2)(-)) and prevents the prod
252 n aqueous solutions, EBN does not react with superoxide anion radical (O2(-*)) to form EBN/(*)OOH to
254 previously shown that redox agents including superoxide anion radical and nitrogen dioxide can react
255 oxide is not the dissolved oxygen but rather superoxide anion radical generated from the reaction of
257 ensor, further support that nitric oxide and superoxide anion radical quickly react resulting in near
258 hat mulberry polyphenolics may act as potent superoxide anion radical scavengers and reducing agents.
259 ing power (0.03-38.45 muM ascorbic acid) and superoxide anion radical scavenging activity (16.53-62.8
260 According to DPPH, hydroxyl radical and superoxide anion radical scavenging activity assays, the
262 eactive oxygen species by disproportionating superoxide anion radical to oxygen and hydrogen peroxide
263 a oxidative injury of complexes I and II and superoxide anion radical-induced hydroxyl radical produc
265 omplexes of manganese (Mn) that can scavenge superoxide anion radicals and provide a backup for super
266 PD-E were found to inhibit the production of superoxide anion radicals by reducing xanthine oxidase a
267 a nonheme iron metalloenzyme that detoxifies superoxide anion radicals O(2)(*-) in some microorganism
269 ant plants also generated elevated levels of superoxide anion radicals, H2O2, and carbonylated protei
270 s were also inhibited by DMS, while only the superoxide anion release was blocked by the phosphatidyl
272 vascular cell adhesion molecule and monocyte superoxide anion release, and interleukin-1 release in T
273 ein (CRP), LDL oxidation, monocyte function (superoxide anion release, cytokine release, and adhesion
274 r agents (e.g., iron cations, cyanide anion, superoxide anion) released, and as affected by the state
275 an increase in the stimulated production of superoxide anion replicating the phenotype of LAgP PMNs.
277 erric reducing antioxidant power (FRAP), the superoxide anion scavenging activity assay (SA), and cor
279 against peroxyl radicals, hydroxyl radicals, superoxide anion, singlet oxygen, and peroxynitrite were
281 essened by decreasing either nitric oxide or superoxide anion, suggesting that ONOO(-) was responsibl
282 d T497A/S1179D eNOS generated 2-3 times more superoxide anion than WT eNOS, and both basal and stimul
283 oreductase) is generally thought to generate superoxide anion that participates in cell signaling and
284 on induced a rapid increase of intracellular superoxide anion that was maximal at the time of NF-kB a
288 ygen species by catalyzing the conversion of superoxide anion to hydrogen peroxide and molecular oxyg
289 ymes that catalyze the disproportionation of superoxide anion to oxygen and hydrogen peroxide to guar
290 positioned for electrostatic guidance of the superoxide anion to the narrow active site channel.
291 metabolism and, together with production of superoxide anions via quinone reduction under high oxyge
292 in kinase C (PKC) activity and production of superoxide anion were increased in the cerebral arteries
293 ally oxidized to fluorescent ethidium by the superoxide anion, whereas mice lacking UCP2 exhibited in
294 in both cases correlated with resistance to superoxide anion, whereas only LHCBM1 is also involved i
295 hibition of the dextrose-induced increase in superoxide anions, whereas inhibition of endothelin expr
296 produces reactive oxygen species, including superoxide anions, which cause DNA damage unless removed
297 ochondrial damage can lead to the release of superoxide anions, which then react with nitric oxide to
298 consistent with interaction of the incoming superoxide anion with a positive charge at or near the f
299 se mimetic, which has been shown to scavenge superoxide anion with highly specific and enhanced catal
300 iation with reduced myocardial generation of superoxide anion (WT versus DDAH-I, 465.7+/-79.8 versus
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