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1 e than a less targeted antioxidant approach (Tempol).
2 ydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPOL).
3 ydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPOL).
4 of EDD with the superoxide dismutase mimetic TEMPOL).
5 ydroxy-2,2,6,6-tetramethylpiperydine-1-oxyl (Tempol).
6 it is rescued by infusion of the SOD mimetic tempol.
7  NMDA and kainate, and during treatment with tempol.
8  ERK was abolished by treatment of rats with tempol.
9 pinephrine (NE) are normal and unaffected by tempol.
10 rsus -46 +/- 4%; P < 0.05) and normalized by tempol.
11 n of CGP-20,712A to NE but was normalized by tempol.
12 cessary for the chemopreventative effects of tempol.
13  of mice were coinfused with the antioxidant Tempol.
14 ated in SOD2+/-, and was acutely restored by Tempol.
15 arison with those on a KD diet alone without tempol.
16 e of p53 in the chemopreventative effects of tempol.
17 ng, which was abolished by the SOD1 mimetic, tempol.
18  hypothermia, except perhaps the antioxidant tempol.
19 groups and was unaffected by the addition of tempol.
20 ers citrate buffer containing 0 mM or 100 mM TEMPOL.
21  and hatching rate were observed in 10 uM of tempol.
22  when the extender was treated with 10 uM of tempol.
23 als originate from intramolecular protons on TEMPOL.
24 nal FXR mediates the anti-obesity effects of tempol.
25 t with the reactive oxygen species scavenger Tempol.
26  by pretreating animals with the antioxidant tempol.
27 dministered the superoxide dismutase mimetic tempol.
28 or by exposure to the free radical scavenger Tempol.
29   In some pigs, superoxide dismutase mimetic TEMPOL (1 mM) or vehicle (saline) was injected intravitr
30 l injection into the hindlimb circulation of tempol (10 mg), a superoxide dismutase mimetic (DeltaMAP
31 ins compared with equimolar concentration of tempol (10 mM).
32             The superoxide dismutase mimetic tempol (10(-4) M) moderated the AngII responses of Aff f
33  during inhibition of oxidative stress using tempol (100 microM).
34 atment with the superoxide dismutase mimetic Tempol (100 um) and Tempol plus the hydrogen peroxide (H
35 mpol before shock was induced (LTA/PepG plus tempol, 100 mg/kg i.v. bolus injection, 15 mins before L
36 5 mL/kg i.v., n = 6) or tempol (control plus tempol, 100 mg/kg i.v. bolus injection, followed by an i
37                            Administration of Tempol (250 mg/kg, i.p.) 10 min prior to administration
38 tine diet (2 weeks prior to noise exposure), tempol (3 mM in drinking water 2 weeks prior to exposure
39 ed by the antioxidants ebselen (100 mum) and TEMPOL (3 mm).
40 droxy-2,2,6, 6-tetramethylpiperidine-N-oxyl (TEMPOL), 3-carboxy-proxyl, and 3-ethoxycarbonyl-proxyl,
41 ersus -34 +/- 3%; NS) and were unaffected by tempol (-32 +/- 4%; NS).
42 nd restored by coincubation of AA (37+/-2%), tempol (33+/-2%), losartan (34+/-2%), or apocynin (36+/-
43 gated to a triphenylphosphonium cation, Mito-Tempol (4) [Mito-T (4)].
44 ed hydroxytoluene, butylated hydroxyanisole, TEMPOL (4-hydroxy-2,2,6, 6-tetramethylpiperidine-N-oxyl)
45  addition of the superoxide scavenging agent tempol (4-hydroxy-2,2,6,6-tetramethyl piperidine-1-oxyl)
46  demonstrated that the nitroxide antioxidant tempol (4-hydroxy-2,2,6,6-tetramethylpiperidine-N-oxyl)
47 er the well-described nitroxide antioxidant, tempol (4-hydroxy-2,2,6,6-tetramethylpiperidine-N-oxyl),
48 id is oxidized to dehydroascorbic acid using Tempol (4-hydroxy-2,2,6,6-tetramethylpiperidinyloxy) and
49 nger, 4-hydroxytetramethylpiperidine-1-oxyl (tempol; 5 mM), was used in some experiments.
50 toTEMPO (mitochondria-targeted antioxidant), TEMPOL (a general antioxidant), apocynin (nicotinamide a
51                             Intrathecal Mito-tempol (a mitochondria-targeted O2(.-)scavenger) reduced
52                    Chronic administration of Tempol (a potent antioxidant) attenuated both SERCA oxid
53 f cells with Trolox (a soluble vitamin E) or Tempol (a radical scavenger).
54 e pyroptosis could be partially inhibited by Tempol (a superoxide dismutase-mimetic agent) and by gly
55 ongruently, the addition of 4-hydroxy-TEMPO (TEMPOL), a superoxide dismutase mimic that reacts with s
56  a model of FA, we examined the potential of tempol, a nitroxide antioxidant and a superoxide dismuta
57 xygen species, whereas preincubation of mito-TEMPOL, a superoxide dismutase mimetic, abolished statin
58                          Coadministration of tempol, a superoxide dismutase mimetic, ameliorated the
59                      Finally, treatment with Tempol, a superoxide dismutase mimetic, and insulin, bot
60  protein (P < 0.05), which were inhibited by Tempol, a superoxide dismutase.
61                               Treatment with Tempol, a superoxide scavenger, attenuates the augmented
62                    Chronic administration of tempol, a superoxide scavenger, reduced intraretinal oxi
63 ydroxy-2,2,6,6-tetramethylpiperidine-n-oxyl (TEMPOL,a superoxide dismutase-mimetic), N-omega-nitro-L-
64 cynin, or superoxide dismutase (SOD) mimetic tempol abolished O2- and restored BH4 levels.
65 mice with antioxidants (mitoTEMPO, apocynin, Tempol) abrogates the hypertensive, prothrombotic phenot
66                                        Thus, tempol acts as a novel chemopreventative agent in this m
67 ron spin resonance spectroscopy suggest that Tempol acts in this system by reacting directly with bot
68 icacy of 6OHDA, we have used the antioxidant Tempol adjunctively with 6OHDA.
69 on of 14 drugs in dogs, only the antioxidant tempol administered at the start of prolonged cardiac ar
70                                              Tempol administered continuously via the diet after wean
71                                     Finally, Tempol administration markedly attenuated impaired endot
72 ay 10 was equally attenuated by creatine and tempol alone or in combination.
73 OL for almost 5 h, whereas administration of TEMPOL alone results in clearance of blood redox activit
74                                              Tempol alone significantly reduced ABR threshold shifts
75 mor weights from mice administered saline or Tempol alone were 3.6 +/- 1.9 and 2.9 +/- 0.7 g, respect
76 enal superoxide levels more effectively than tempol alone.
77                                              TEMPOL also abrogated the inhibitory effect of 15-A2-Iso
78                                              Tempol also attenuated the RSNA response to 1 min interm
79                                              Tempol also normalized NF-kappaB translocation, PKC acti
80                                              Tempol also significantly decreased the AP-1-DNA binding
81                         A broad antioxidant, Tempol, also reduced oxidant stress yet did not recouple
82                            Here we show that tempol alters the gut microbiome by preferentially reduc
83  by oxidative stress, because treatment with Tempol, an superoxide dismutase mimetic, rescued kidney
84                                 The decay of Tempol and 3CP in tumor tissue was significantly faster
85                                              Tempol and Apocynin reversed the increased expression of
86  weeks prior to exposure), and creatine plus tempol and exposed to 120 dB SPL one-octave band noise c
87              Treatment with the antioxidants Tempol and MitoTEMPO reversed many proteomic signatures
88 sent study was to investigate the effects of tempol and straw size on rooster sperm post-thaw quality
89                                              Tempol and tempo are stable free radical nitroxides that
90 bsence of an environmental oxidative stress, tempol and tempo elicit distinct cellular signaling path
91                                         Both TEMPOL and TEMPOL/PNA give rise to prevention of apoptos
92 n vivo by treating mice with the antioxidant TEMPOL and the IsoLG scavenger 2-hydroxybenzylamine duri
93 ith phentolamine, antioxidant treatment with Tempol and thromboxane receptor antagonism with SQ-29548
94 roxy-2,2,6,6,-tetramethyl-1-piperidynyloxyl (Tempol) and 3-carbamoyl-2,2,5,5-tetramethylpyrrolidine-1
95  inhibitor (L-NAME), a superoxide scavenger (Tempol), and an NADPH oxidase inhibitor (apocynin), as w
96 e restored in the presence of ascorbic acid, tempol, and apocynin, which inhibits NADPH oxidase assem
97 revented by the antioxidant agents Desferal, Tempol, and dimethylsulfoxide.
98 holine responses were improved (P<0.05) with Tempol, and histochemistry revealed oxidative stress in
99 a diet supplemented with a stable nitroxide, Tempol, and showed that the progression of neuromuscular
100        PNA enhances the therapeutic index of TEMPOL, and the recycling antioxidant that results from
101 apocynin, and the nonspecific ROS scavenger, tempol, are shown to reduce oxidative stress and improve
102     These results encourage further study of Tempol as a chemopreventive, to reduce the incidence of
103 ormed two types of adducts (LT and OLT) with TEMPOL as characterised by HPLC.
104 ubation with the antioxidants mito-TEMPO and TEMPOL, as well as inhibitors of xanthine oxidase and ar
105  and reactive oxygen species (ROS) scavenger tempol, as well as mitochondrial NCX (mNCX) blocker CGP-
106 n a frozen glycerol-water mixture doped with TEMPOL at ~1.4 K using spin diffusion enhanced saturatio
107 racellular application of the ROS scavenger, Tempol, attenuated the Ang II-induced increase in neuron
108                    Pretreatment of rats with tempol augmented the hypotension but attenuated the rena
109    Another group of rats was pretreated with tempol before shock was induced (LTA/PepG plus tempol, 1
110 , polarity or partitioning of the spin probe TEMPOL-benzoate (TB), as proved by EPR measurements and
111 er (xestospongin C), or ROS scavengers (PBN, tempol), but not by an mGluR1 antagonist (LY367385) or N
112                   The free radical scavenger Tempol, but not other classes of antioxidants, reduced o
113 tor of cAMP; -56 +/- 4%); were normalized by tempol; but were unaffected by ICI-118,551 (selective be
114                 Agents such as the nitroxide Tempol can facilitate the oxidation of the semiquinone t
115                      These results show that tempol can significantly delay tumor formation in Fancd2
116                 Interestingly, however, only tempol caused increased extracellular signal-regulated k
117 tion of the clusters by the stable nitroxide TEMPOL caused their disassembly, potently inhibited the
118 ng and the reactive oxygen species inhibitor Tempol completely reversed the decline in Ser(P)(473)-AK
119 is inhibited by the antioxidants ebselen and TEMPOL, consistent with the concept that it requires an
120 metry of the adduct formation is two mole of TEMPOL consumed for one mole of LH and one mole of LOOH.
121 ydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPOL) consumption by using ESR allows to follow the an
122  by an infusion of 1.5 mL/kg i.v., n = 6) or tempol (control plus tempol, 100 mg/kg i.v. bolus inject
123                                              Tempol decreased ACh-mediated vasodilatation of medial c
124                                     However, tempol decreased basal production of superoxide anion in
125      In BSO-treated rats' supplementation of tempol decreased oxidative stress, normalized BP, and re
126                                              Tempol decreased the level of Ang II-induced aortic supe
127                             More strikingly, tempol delayed the onset of epithelial tumors and increa
128 he animals that had first been injected with TEMPOL developed only stage 2 to stage 4 cataracts (the
129                                              Tempol did not affect the increase in nitrite/nitrate ca
130 ikewise, the antioxidants dithiothreitol and tempol did not reverse permeabilization.
131      Notably, delaying administration of the Tempol diet one month after TBI could also enhance survi
132 , and forebrain of animals maintained on the Tempol diet, IRP1 was converted from a cytosolic aconita
133                               Oxypurinol and Tempol diminished the leak in NOS1(-/-) cardiomyocytes.
134         Here we show for the first time that tempol dramatically reduced STAT1 and 3 phosphorylation.
135 ted with the STAT1 activator, IFN-gamma, and tempol during I/R injury.
136                             The antioxidants tempol, ebselen, and deferoxamine inhibited CO-induced O
137             Mice treated with antibiotics or tempol exhibited altered bile acid composition, with a n
138     In contrast, except for one antioxidant (Tempol), explorations of 14 different drugs added to the
139 olate-antioxidant conjugate 4-hydroxy-Tempo (tempol)-folate to target folate receptors, which are hig
140 nce revealed the successful targeting of the tempol-folate conjugate to the kidney and other tissues
141                            Administration of tempol-folate protected the renal function of mice after
142  model of renal ischemia-reperfusion injury, tempol-folate reduced renal superoxide levels more effec
143               In contrast, mice administered Tempol followed by 6OHDA had an average tumor weight of
144 ine (BSO), an oxidant, with and without 1 mM tempol for 2 wk.
145 t of animals on a K-deficient (KD) diet with tempol for 7 days significantly decreased the production
146 L/PNA maintains redox-active blood levels of TEMPOL for almost 5 h, whereas administration of TEMPOL
147 oss (NIHL), we measured the effectiveness of tempol (free radical scavenger) and creatine (enhances c
148 motility, VAP and VSL increased in the 10 uM tempol group.
149 ,6,6-tetramethylpiperidine hydrochloride), a TEMPOL-H (OT-674) derivative, is a new catalytic antioxi
150 oxy-2,2,6,6-tetramethyl-1-hydroxypiperidine (TEMPOL-H) as a probe in conjunction with superoxide dism
151             Oxidized but not reduced TEMPOL (TEMPOL-H) was an effective radioprotector in cultured ra
152  enhancements as large as 50 are achieved on TEMPOL/H(2)O solutions at room temperature.
153                         In the control rats, tempol had no effect on these responses.
154 aled oxidative stress in KW animals, whereas Tempol had no impact and reactive oxygen species stainin
155  the Lake cryopreservation medium with 10 uM tempol improved cryo-survival.
156           TEMPOL/PNA is also less toxic than TEMPOL in mice, allowing administration of higher doses
157                           The level of total TEMPOL in the aqueous humor of rabbits at 15 minutes aft
158 t chronic supplementation of the antioxidant Tempol in the diet of mice can reduce body weight withou
159 containing 0 (control), 5, 10, 15 and 20 muM tempol (in two different straw size, 0.25 and 0.5).
160 y 6-OHDA than the non-recycling antioxidant, TEMPOL, in a murine model of catecholaminergic oxidative
161                                      Dietary tempol increased the mean tumor-free survival time of Fa
162                                 Both SOD and TEMPOL increased the signal intensity of the .OH adduct
163                                              Tempol inhibited the effects of IP(3) but not those of a
164 suggest that the chemopreventative effect of tempol is not solely due to the reduction of oxidative s
165                  The free radical scavenger, tempol, is known to have cardioprotective properties, al
166                              Moreover, 10 uM tempol led to lower ROS compared to other groups.
167 manner that was inhibited by bradykinin, AA, tempol, losartan, or apocynin.
168 ter incubation with the superoxide scavenger TEMPOL, maximal EDD improved by approximately 65% in Eln
169                                              Tempol may also find applications to reduce the risk of
170 l, suggesting that the protective effects of tempol may partly operate by decreasing the phosphorylat
171 suggested that SMG-1 was responsible for the tempol-mediated enhancement of p53 serine 18 phosphoryla
172 y in p53-deficient mice and the finding that tempol-mediated resistance to oxidative insult was p53-d
173   Administration of the superoxide scavenger TEMPOL, NAD(P)H oxidase inhibitor (apocynin), or anti-TN
174 ts, and administration of the O2*- scavenger TEMPOL, NAD(P)H oxidase inhibitor (apocynin), or anti-TN
175      In the presence of superoxide scavenger TEMPOL, NAD(P)H oxidase inhibitor apocynin, p38 kinase i
176                                              Tempol normalized basal VO2 and VCO2 and improved the wo
177           We also examined the effect of ICV Tempol on the RVLM of CHF rabbits.
178 s of a membrane-permeable radical scavenger (tempol) on the circulatory failure and MODS (kidney, liv
179 pyrroline N-oxide) or the O(2)(*-) scavenger Tempol or an SOD mimic (AEOL10113) resulted in a decreas
180 ations were inhibited by treatment with mito-tempol or apocynin or by inhibiting EGFR expression or a
181 ta with either superoxide dismutase (SOD) or tempol or apocynin significantly improved acetylcholine-
182 pletely restored by coincubation with tiron, tempol or apocynin.
183 ic arteries, which is rescued by SOD mimetic tempol or gene transfer of SOD3.
184               Treatment with the antioxidant TEMPOL or lung-specific overexpression of ecSOD prevente
185 tetramethylpiperidine1-oxyl (tempol) or Mito-tempol or MitoQ in the presence or absence of PEG-catala
186      Treatment with the superoxide scavenger tempol or the isoketal scavenger 2-hydroxybenzylamine (2
187       Administration of the SOD mimetic mito-tempol or the NADPH oxidase inhibitor apocynin attenuate
188 RPM2+/+ mice with the free radical scavenger Tempol or the PARP1 inhibitor 3-aminobenzamide attenuate
189 ion of L-arginine or a superoxide scavenger, tempol or tiron, attenuated sympathetic vasoconstriction
190 ydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPOL or TPL) in the ischemic isolated rat heart, allow
191 ydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPOL) or mice overexpressing lung-specific extracellul
192 ydroxyl-2,2,6,6-tetramethylpiperidine1-oxyl (tempol) or Mito-tempol or MitoQ in the presence or absen
193  blocked by the antioxidant 4-hydroxy-TEMPO (TEMPOL) or the mitochondrial uncoupler carbonyl cyanide
194 reduced by intracerebroventricular losartan, tempol, or apocynin in CHF rabbits but not in sham rabbi
195 restored by coincubation with ascorbic acid, Tempol, or apocynin.
196 olished by intracerebroventricular losartan, tempol, or apocynin.
197 ed by treatment of the superoxide scavenger, TEMPOL, or by overexpression of manganese superoxide dis
198  prevented by losartan, superoxide scavenger TEMPOL, or NADPH oxidase inhibitor apocynin.
199 asone, the reactive oxygen species scavenger tempol, or the glial inhibitor minocycline attenuated th
200 of ceramide levels in the ileum and serum in tempol- or antibiotic-treated mice fed a HFD resulted in
201 osure of the protein to the stable nitroxide TEMPOL oxidizes and degrades the cluster and drastically
202                                              Tempol, oxypurinol, or SB203850 decreased O2- in all gro
203  by preincubation with Tiron, ascorbic acid, Tempol, oxypurinol, or SB203850, an inhibitor of p38 kin
204  73 arbitrary units (a.u.); before vs. after tempol; P < 0.05).
205 4-hydroxy-2,2,6,6-tetramethylpiperidinyloxy (TEMPOL) partially recovered impaired endothelial functio
206                                              Tempol plus catalase further decreased ACh-mediated vaso
207 roxide dismutase mimetic Tempol (100 um) and Tempol plus the hydrogen peroxide (H(2)O(2)) scavenger c
208                              Both TEMPOL and TEMPOL/PNA give rise to prevention of apoptosis and to t
209                                              TEMPOL/PNA is also less toxic than TEMPOL in mice, allow
210                                              TEMPOL/PNA is more effective against depression of activ
211 PC12 cells treated with 6-OHDA, but in vivo, TEMPOL/PNA maintains redox-active blood levels of TEMPOL
212 eridine-1-oxyl and polynitroxylated albumin (TEMPOL/PNA), an antioxidant complex that facilitates rec
213            On the other hand, tempo, but not tempol, potently activated stress-activated protein kina
214                                 Furthermore, TEMPOL pretreatment prevented nicotine effects on stimul
215 t with the reactive oxygen species scavenger Tempol prevented FRD-induced apoptosis in WT mice.
216 iredoxin-6 overexpression or the SOD mimetic tempol, prevented chromatin SUMO3 depletion, HDR loss of
217                              We suggest that Tempol protected IRP2(-/-) mice by disassembling the cyt
218                     Treatment with L-NAME or TEMPOL protected retinal neurons and confirmed the invol
219 we investigate the relaxation effects of the TEMPOL radicals used for the hyperpolarization process a
220 in modulating the cardioprotective effect of tempol, rats were injected with the STAT1 activator, IFN
221                      O(2)(-) scavenging with Tempol reduced flow-induced vasodilatation from all grou
222                                              Tempol reduced oxidative stress and thereby restored D1
223    The permeant superoxide dismutase mimetic tempol reduced the effects of AngII400 on the SBP (-1.7
224                                              Tempol reduced the incidence of hematopoietic neoplasms
225       When combined with caspase inhibition, tempol reduced the production of ROS and provided an add
226 IKKbeta(-/-) cells, BCL10 silencing, but not Tempol, reduced the CGN-induced increases in KC, phospho
227                              The antioxidant tempol reduces obesity in mice.
228 atment of the cerebral microcirculation with tempol restored impaired nNOS-dependent vasodilatation i
229                Infusion of the ROS scavenger tempol restored sympatholysis in these rats.
230 Addition of the superoxide radical scavenger tempol restored the ability of bradykinin, enalaprilat,
231                    Intracameral injection of TEMPOL resulted in a decrease of nearly 70% in the level
232 ical, 2,2,6, 6-tetramethyl-1-piperidinyloxy (TEMPOL), resulted in protection of plasma Fe-TF against
233 f AMPKalpha1(-/-) mice with the antioxidant, tempol, resulted in decreased reticulocyte counts and im
234  chromatography demonstrated that conjugated tempol retained its efficacy to scavenge superoxide in p
235                                  Addition of tempol reversed the defects in responsiveness to enalapr
236  of MG132 or a superoxide dismutase mimetic, tempol, reversed the diabetes mellitus-induced reduction
237 ng showed that Ang II elicited losartan- and TEMPOL-sensitive superoxide production in arterioles.
238        DHE staining showed that CRP produced TEMPOL-sensitive superoxide production in the arteriolar
239 eeks after x-ray, rabbits irradiated without TEMPOL showed either stage 5 (complete posterior subcaps
240 r PBN and the superoxide-selective scavenger TEMPOL significantly attenuated nicotine-induced hyperlo
241     Compared to vehicle treated CHF rabbits, Tempol significantly decreased AT1R protein expression (
242 Finally, suppressing O(2)(-) production with tempol significantly increased renal K excretion measure
243 ravenous nicotine self-administration study, TEMPOL significantly reduced nicotine-taking behavior wi
244                           Both valsartan and tempol substantially attenuated mitochondrial lipid pero
245 FN-gamma abrogated the protective effects of tempol, suggesting that the protective effects of tempol
246 contractions to AngII that are normalized by tempol (superoxide dismutase mimetic), whereas contracti
247                     Furthermore, addition of tempol (superoxide dismutase-mimetic) which is a superox
248                     Oxidized but not reduced TEMPOL (TEMPOL-H) was an effective radioprotector in cul
249 ydroxyl-2,2,6,6-tetramethylpiperidin-1-oxyl (tempol) throughout exposure to intermittent hypoxia impr
250 tion in HF-SED was normalized by apocynin or TEMPOL to LF-SED and HF-RUN.
251 effect may be associated with the ability of TEMPOL to protect against radiation-produced peroxides b
252  Moreover, with the treatment of antioxidant tempol to suppress RNS, not only are DNA lesions signifi
253 elin-1 that was normalized by ifetroban plus tempol together.
254                      Addition of catalase to Tempol-treated arterioles eliminated flow-induced vasodi
255                                           In Tempol-treated arterioles, flow-induced vasodilatation w
256     The reduction in oxidative DNA damage in tempol-treated FA fibroblasts and mice suggests that its
257 ue-Dawley, untreated Ren2, and valsartan- or tempol-treated Ren2 rats.
258  show lower diet-induced obesity, similar to tempol-treated wild-type mice.
259 arp apical ROMK staining was observed in the tempol-treated WT or gp91(-/-) mice.
260                                 Furthermore, tempol treatment did not adversely affect the repopulati
261                                     Further, tempol treatment does not decrease weight gain in Fxr(De
262 tribution in WT, gp91(-/-), and WT mice with tempol treatment in response to K restriction.
263                                 In contrast, tempol treatment in WT mice abolished whereas deletion o
264                  Its increased levels during tempol treatment inhibit FXR signalling in the intestine
265                             In contrast, the tempol treatment not only increased channel activity to
266                                              Tempol treatment of cancer-prone p53-deficient mice resu
267                                              Tempol treatment reduced ROS, restored mitochondrial mem
268                                Surprisingly, tempol treatment specifically increased serine 18 phosph
269 m gp91(-/-) mice and completely abolished by tempol treatment.
270 conditions that were improved by apocynin or tempol treatment.
271 tan or superoxide dismutase/catalase mimetic tempol treatment.
272 rylated STAT1 and STAT3 and examined whether tempol was able to affect STAT activation after in vivo
273                                              TEMPOL was effective in protecting against lens epitheli
274                  Consistent with these data, tempol was found to be noncytotoxic, whereas tempo induc
275                                              Tempol was given to each mouse for 7 days by an intraper
276 adioprotector in cultured rabbit lenses, and TEMPOL was nearly completely bioreduced in the plasma an
277 nsion, whereas a similar dose of nontargeted TEMPOL was not effective.
278                 In vitro studies showed that TEMPOL was reduced rapidly by ascorbic acid but not by r
279          The latter process was inhibited by tempol, which recombines with the hSOD1-derived tryptoph
280 binding to Brca1 promoter by the antioxidant Tempol, which reduces NADH levels, relieved CtBP1-mediat
281                                 Furthermore, Tempol, which restored SERCA activity and decreased oxid

 
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