ライフサイエンスコーパス: reduced glutathione

1 oxidant-induced protein thiyl radicals with reduced glutathione.

2 ygen species and exhibited less depletion of reduced glutathione.

3 l but shows a >100-fold lower k cat/ K m for reduced glutathione.

4 g it to a disulfide reductase that generates reduced glutathione.

5 in the presence of a mixture of oxidized and reduced glutathione.

6 zes the reduction of oxidized glutathione to reduced glutathione.

7 d that this is correlated with the levels of reduced glutathione.

8 ation was not observed in cells treated with reduced glutathione.

9 increase in antioxidants including NADPH and reduced glutathione.

10 neurons to maintain intracellular levels of reduced glutathione.

11 ctaldehyde, which is paralleled by a loss of reduced glutathione.

12 -reducing agents, such as dithiothreitol and reduced glutathione.

13 and identified by the reaction of UQ(0) with reduced glutathione.

14 nd a marked increase in endogenous levels of reduced glutathione.

15 eurons, and MPP(+) failed to alter levels of reduced glutathione.

16 and not simulated by oxidized glutathione or reduced glutathione.

17 eversed by dithiothreitol, ascorbic acid, or reduced glutathione.

18 the oxidized Ng could be reduced by NADPH or reduced glutathione.

19 reduced rapidly by ascorbic acid but not by reduced glutathione.

20 acid, coumaric acid, acetaldehyde, total and reduced glutathione.

21 des, and TGFbeta1, and erythrocyte levels of reduced glutathione.

22 -terminal kinase activation, or depletion of reduced glutathione.

23 ivity against DPPH radicals when compared to reduced glutathione.

24 ls of oxidized glutathione with reference to reduced glutathione.

25 d to the increased production of taurine and reduced glutathione.

26 erine treatment with concomitant decrease in reduced glutathione.

27 n reactive oxygen species and a reduction in reduced glutathione.

28 ered in the presence of physiologic level of reduced glutathione (1 mmol/L), suggesting that selenocy

29 nd, glycine and the higher concentrations of reduced glutathione (1.0 and 2.0%) were able to promote

30 Plants with the lowest levels of reduced glutathione (10% of wild type) were sensitive to

31 in a 35% decrease in the hepatic content of reduced glutathione 4 days after lipopolysaccharide chal

32 The addition of reduced glutathione (8 microM) only enhanced nonenzymati

33 folding of RfBP even in the presence of 5 mM reduced glutathione, a competing ligand for As(III) spec

34 Included are reduced glutathione, adenosine monophosphate, nicotinami

35 Reduced glutathione, although subject to transport by At

36 ctivity (complexes I-IV), ATP concentration, reduced glutathione (an intracellular antioxidant) conce

37 Exposure to HNE led to a depletion of reduced glutathione and an increase in the production of

38 inetic constants of approximately 1.4 mM for reduced glutathione and approximately 6.5 microM for APS

39 evels by 50% and increased levels of ATP and reduced glutathione and Bcl-2.

40 the use of chemical trapping agents, such as reduced glutathione and cyanide, to form stable adducts

41 tol was unable to compensate for the lack of reduced glutathione and did not promote secretion of per

42 s judged by an elevated ratio of oxidized to reduced glutathione and enhanced oxidative folding in th

43 y during the acute phase of illness leads to reduced glutathione and glutamate in the residual phase

44 tion of hydrogen peroxide in the presence of reduced glutathione and glutathione reductase.

45 tion, CD34(+) AML cells have lower levels of reduced glutathione and increased levels of oxidized glu

46 ultures seeded on dicarbonyl-modified FN had reduced glutathione and increased levels of reactive oxy

47 paired cystine uptake, lowered intracellular reduced glutathione and increased oxidative stress.

48 s the pivotal residue discriminating between reduced glutathione and its conjugates.

49 valuate the ability of gallic acid, glycine, reduced glutathione and l-cysteine at 0.1, 0.5, 1.0 and

50 polynitroxyl albumin groups had hippocampal reduced glutathione and manganese superoxide dismutase a

51 Reduced glutathione and NADPH protects the brain from ox

52 hromate exposure depleted cellular levels of reduced glutathione and other free thiols to a greater e

53 ells offered protection against depletion of reduced glutathione and oxidative stress mediated by TNF

54 antification of reactive oxygen species, and reduced glutathione and oxidised content.

55 by initiating an enhanced generation of both reduced glutathione and oxidized glutathione and enhance

56 and simultaneously to quantify the levels of reduced glutathione and products of its oxidation as pot

57 rs after asphyxial cardiac arrest, levels of reduced glutathione and protein-thiols (fluorescent assa

58 h concentrations of oxidant scavengers (i.e. reduced glutathione and sodium azide) indicating a possi

59 levels of malondialdehyde and low levels of reduced glutathione and superoxide dismutase; these effe

60 This inhibition is reversed by reduced glutathione and suppressed by intracellular Zn(2

61 rovides the site for entry of electrons from reduced glutathione and that the Cys166-Cys285 disulfide

62 tic hearts, as were the ratio of oxidized to reduced glutathione and the immunohistochemical staining

63 ng to RyR1 in SR vesicles in the presence of reduced glutathione and the NO-donor NOC12, with no effe

64 NACA functioned by increasing the levels of reduced glutathione and the phase II detoxification enzy

65 tinamide nucleotides, acetoacetyl-CoA, H2O2, reduced glutathione, and 2-monoacylglycerol were not glu

66 ts, and lung homogenate EC-SOD, oxidized and reduced glutathione, and myeloperoxidase.

67 electron donors, ascorbate, dithiothreitol, reduced glutathione, and NADH, were each able to provide

68 xidative stress parameters (malondialdehyde, reduced glutathione, and superoxide dismutase) and expre

69 ibited by dialysis of the cell interior with reduced glutathione, and were markedly enhanced by inhib

70 ck(Delta19) mice, the levels of NRF2 and the reduced glutathione are constitutively low, associated w

71 In contrast, N-acetyl-l-cysteine and reduced glutathione are much less effective.

72 ic green alga Enteromorpha intestinalis uses reduced glutathione as the electron donor for the reduct

73 tected from dopamine-induced inactivation by reduced glutathione, ascorbic acid, and dithiothreitol b

74 n of p21(ras) and p21(rac), protected nigral reduced glutathione, attenuated nigral activation of NF-

75 RyR3 in the presence of reduced glutathione binds CaM with 10-15-fold higher aff

76 ion (approximately 40%) of ATP hydrolysis by reduced glutathione but not by DTT.

77 A reduction depends not only on the level of reduced glutathione, but also on the rate of NADPH produ

78 hrough the increase in soluble lens protein, reduced glutathione, catalase and SOD activity on in vit

79 ied by increased intracellular ROS level and reduced glutathione concentration in intestinal epitheli

80 significant decrease (approximately 50%) in reduced glutathione concentration, along with the rapid

81 Both products led to increased reduced glutathione concentrations in the grape juice an

82 Differences in (reduced) glutathione concentrations and the rapid develo

83 ol treatment further decreased mitochondrial reduced glutathione content and exacerbated mitochondria

84 reatment with l-buthionine-(S,R)-sulfoximine reduced glutathione content by 99% and prevented glucose

85 Superoxide dismutase activity and reduced glutathione content were not significantly diffe

86 slices of EAAC1(-/-) mice were found to have reduced glutathione content, increased oxidant levels an

87 el of the primary intracellular antioxidant, reduced glutathione, corresponding to increasing AH resi

88 d and antioxidants (superoxide dismutase and reduced glutathione) decreased following infarct.

89 The protein displayed reduced glutathione-dependent phospholipid hydroperoxide

90 s a His-tagged recombinant protein catalyzes reduced glutathione-dependent reduction of APS to sulfit

91 p38 kinase because of its ability to prevent reduced glutathione depletion and scavenge hydrogen pero

92 Mitochondrial depolarization and reduced glutathione depletion occurred as well, and cell

93 diated dichlorodihydrofluorescein oxidation, reduced glutathione depletion, aconitase inactivation, T

94 Cysteine, cystine, and reduced glutathione did support bacterial growth, and no

95 These results suggest that reduced glutathione does not affect the accumulation of

96 Reduced glutathione drastically increases the warfarin s

97 wild-type mice had similar levels of hepatic reduced glutathione, endogenous reactive oxygen species,

98 The highest level of 2.0% for glycine and reduced glutathione favored protein extractability and a

99 f thiol-containing model substrates, namely, reduced glutathione (gamma-Glu-Cys-Gly) and the carrier

100 drolyze the unique N-terminal amide bonds of reduced glutathione (gamma-L-glutamyl-cysteinyl-glycine)

101 creasing glycolysis and increasing levels of reduced glutathione, generated by metabolism of glucose

102 Increased intracellular reduced glutathione/glutathione disulfide ratio and grea

103 ve at preventing a decrease in intracellular reduced glutathione:glutathione disulfide ratios, protec

104 Reduced glutathione greatly increased the rate of bindin

105 The endogenous antioxidant reduced glutathione (GSH) also potentiated IGABA in alph

106 ons of two major non-enzymatic antioxidants, reduced glutathione (GSH) and ascorbate, and completely

107 Complex formation requires reduced glutathione (GSH) and can be prevented by N-ethy

108 e is characterized by glutathione imbalance, reduced glutathione (GSH) and cysteine were quantified i

109 Reduced glutathione (GSH) and glutathione disulfide (GSS

110 superoxide dismutase (SOD), catalase (CAT), reduced glutathione (GSH) and glutathione peroxidase (GP

111 Organosulfurs, mainly reduced glutathione (GSH) and GSH conjugates, were relea

112 ion of individual ingredients disclosed that reduced glutathione (GSH) and lactobionate in UW solutio

113 ed in significant increases in the levels of reduced glutathione (GSH) and NAD(P)H:quinone oxidoreduc

114 In this study, we investigated the role of reduced glutathione (GSH) and nuclear factor-kappaB (NFk

115 re used to assess relative concentrations of reduced glutathione (GSH) and oxidized disulfide glutath

116 HPLC-BDD responses for reduced glutathione (GSH) and oxidized glutathione (GSSG

117 Intracellular levels of reduced glutathione (GSH) and oxidized glutathione (GSSG

118 Acid extracts were assayed for reduced glutathione (GSH) and oxidized glutathione (GSSG

119 The major thiol-disulfide couple of reduced glutathione (GSH) and oxidized glutathione is a

120 er on platelet aggregation and the effect of reduced glutathione (GSH) and platelet activation on sul

121 ductase (GSR) activities, while the level of reduced glutathione (GSH) and the activities of superoxi

122 rph2(rds/rds)) and compared the abundance of reduced glutathione (GSH) and the activity of mitochondr

123 This shift, in turn, caused an increase in reduced glutathione (GSH) and, ultimately, resulted in R

124 Nitro-fatty acid adducts of protein and reduced glutathione (GSH) are detected in healthy human

125 Reduced glutathione (GSH) at 24 hours was lower in mild

126 its biospecific interaction with tripeptide reduced glutathione (GSH) bioreceptor directly immobiliz

127 tamylcysteine ligase (GCLC), a rate-limiting reduced glutathione (GSH) biosynthesis enzyme.

128 The DeltagshB strain lacks reduced glutathione (GSH) but instead accumulates the pr

129 ion of free radicals requires maintenance of reduced glutathione (GSH) by NADPH.

130 ADP(+) to NADPH and promotes regeneration of reduced glutathione (GSH) by supplying NADPH to glutathi

131 Depletion of cellular reduced glutathione (GSH) by treatment of AREc32 cells w

132 This correlates with lower tissue reduced glutathione (GSH) concentration and higher NADPH

133 Erythrocyte reduced glutathione (GSH) concentration was determined 2

134 orrelated with a deficiency in intracellular reduced glutathione (GSH) concentrations in diabetic pat

135 tathione-S-Transferase (GST) activities, and reduced glutathione (GSH) content, higher level of malon

136 ralleled by increased lipid peroxidation and reduced glutathione (GSH) content.

137 esis that depolarization-enhanced release of reduced glutathione (GSH) contributes to this phenomenon

138 The effect of reduced glutathione (GSH) depletion by acetaminophen (AP

139 ells to toxic chemical species can result in reduced glutathione (GSH) depletion, generation of free

140 Reduced glutathione (GSH) has been determined by fluores

141 t systems involved in the export of cellular reduced glutathione (GSH) have not been identified, alth

142 as the rate of depletion of the antioxidant reduced glutathione (GSH) in a model of human respirator

143 m of the metabolism of APAP and depletion of reduced glutathione (GSH) in hepatocytes.

144 Histochemical studies show reduced glutathione (GSH) in neuroglia, whereas immunocy

145 for low-potential amperometric detection of reduced glutathione (GSH) in pH 7.2 phosphate buffer sol

146 opeptidase (FCGAP) with BOC-Leu-Met-CMAC and reduced glutathione (GSH) in the absence of Ca(2+).

147 We studied the role of reduced glutathione (GSH) in the activations of ARE-medi

148 ) increased metal donation fourfold, whereas reduced glutathione (GSH) inhibited donation by approxim

149 ng to the presence of high concentrations of reduced glutathione (GSH) inside the cells, thereby faci

150 rons and contributes to injury, we delivered reduced glutathione (GSH) into microglia, again using li

151 Injections of reduced glutathione (GSH) into the antennal lobes before

152 Sinusoidal efflux of hepatic reduced glutathione (GSH) is a key step in interorgan GS

153 Reduced glutathione (GSH) is an efficient antioxidant on

154 ition to its intracellular antioxidant role, reduced glutathione (GSH) is released by CNS cells and m

155 ciation with a decrease in the mitochondrial reduced glutathione (GSH) level and activity of MnSOD.

156 ested a significant age-related reduction of reduced glutathione (GSH) level in all brain regions exa

157 dant defense function in cells by increasing reduced glutathione (GSH) levels and decreasing ROS leve

158 in malonyldialdehyde (MDA) and a decrease in reduced glutathione (GSH) levels in cell lysates.

159 In contrast, reduced glutathione (GSH) levels were associated with th

160 as this is accompanied with higher cytosolic reduced glutathione (GSH) levels.

161 Cells were processed for reduced glutathione (GSH) measurement, RNA extraction, c

162 n construct to study the effects of Bcl-2 on reduced glutathione (GSH) metabolism.

163 Decreases in reduced glutathione (GSH) mimic the effects of biliatres

164 We previously found that reduced glutathione (GSH) or a mixture of GSH/glutathion

165 ceptor (IR) sulfhydryl groups in response to reduced glutathione (GSH) or N-acetyl-L-cysteine (NAC).

166 Reduced glutathione (GSH) plays a crucial role in hepato

167 II iron-limited cells similarly oxidized the reduced glutathione (GSH) pool, phase II iron limitation

168 pectrofluorometrically by enzymatic methods, reduced glutathione (GSH) spectrofluorometrically with O

169 ition, antioxidant activity, effect on total reduced glutathione (GSH) synthesis and protective effec

170 active oxygen species (ROS) and depletion of reduced glutathione (GSH) that together inhibited histon

171 nstrated by (a) the ability of intracellular reduced glutathione (GSH) to eliminate EPR-detectable et

172 whose shared function is the conjugation of reduced glutathione (GSH) to endo- and xenobiotics.

173 a chemical oxidant that selectively converts reduced glutathione (GSH) to its disulfide (GSSG) and pr

174 in increased ROS production and oxidation of reduced glutathione (GSH) to its oxidized form (GSSG).

175 Reduced glutathione (GSH) was determined by a colorimetr

176 lthough a similar rapid depletion of hepatic reduced glutathione (GSH) was found in both GstP1/P2((+/

177 Dithiothreitol (DTT) or reduced glutathione (GSH) was required for optimal activ

178 minations of oxidized glutathione (GSSG) and reduced glutathione (GSH) were performed in monolayer cu

179 reduction of glutathione disulfide (GSSG) to reduced glutathione (GSH) with the accompanying oxidatio

180 Reduced glutathione (GSH), a component of University of

181 nicotinamide dinucleotide phosphate (NADPH), reduced glutathione (GSH), and shear-induced adenosine t

182 emical quantification of oxidized (GSSG) and reduced glutathione (GSH), biomarkers of oxidative stres

183 of endogenous thiol pools, most importantly, reduced glutathione (GSH), by NADPH.

184 We showed that diminishing reduced glutathione (GSH), by treatment with 1-chloro-2,

185 tathione (GSSG), and total glutathione (GT), reduced glutathione (GSH), catalase (CAT), peroxidase (P

186 cetyl-p-benzoquinone imine, higher levels of reduced glutathione (GSH), centrilobular inflammation, a

187 hibition of K(+) channels of glomus cells by reduced glutathione (GSH), dithiothreitol (DTT) and by c

188 In the corresponding reaction, with reduced glutathione (GSH), equimolar amounts of selenodi

189 causes oxidative stress through depletion of reduced glutathione (GSH), increases the passive K+ perm

190 induction of oxidative stress, depletion of reduced glutathione (GSH), inhibition of IKK activity le

191 ighly sensitive and inexpensive detection of reduced glutathione (GSH), over its oxidized form (GSSG)

192 rs of NOx formation, levels of intracellular-reduced glutathione (GSH), protein nitrosothiols, and th

193 but the levels of an endogenous antioxidant, reduced glutathione (GSH), remained subnormal in the ret

194 a, interleukin (IL)-1beta, IL-6, IL-8, IL10, reduced glutathione (GSH), superoxide dismutase (SOD), a

195 of cancer cells by producing an antioxidant, reduced glutathione (GSH), through HIF-1-mediated metabo

196 ferase (GST) and non-enzymatic antioxidant - reduced glutathione (GSH), vitamin E and C generation in

197 Detoxification of methylglyoxal requires reduced glutathione (GSH), which accumulates to high lev

198 recycling of oxidized glutathione (GSSG) to reduced glutathione (GSH), which is due to the augmented

199 obenzoate oxidation used in the detection of reduced glutathione (GSH).

200 t hypoxia and oxidative stress by preserving reduced glutathione (GSH).

201 an ISC and that this coordination depends on reduced glutathione (GSH).

202 to the pentose phosphate pathway to generate reduced glutathione (GSH).

203 An effect similar to DHLA was observed with reduced glutathione (GSH).

204 duction of glutathione disulfide (GSSG) into reduced glutathione (GSH).

205 n done with the physiological reducing agent reduced glutathione (GSH).

206 M and APAP lead to a significant decrease in reduced glutathione (GSH)/glutathione disulfide (GSSG) r

207 er oxidative stress, the mean value for the [reduced glutathione (GSH)]/[oxidized glutathione (GSSG)]

208 l concentrations of either E2 (200 nM) or of reduced glutathione (GSH; 325 microM) can protect SK-N-S

209 hermore, cells sorted according to differing reduced-glutathione (GSH) contents exhibited differing s

210 Additionally, blood glutathione (reduced glutathione [GSH], glutathione disulfide [GSSG],

211 ynthesis (cysteine: higher in AD, p < 0.001; reduced glutathione [GSH]: higher in AD, p < 0.001); (3)

212 ); and antioxidants, the sum of oxidized and reduced glutathione (GSSG and GSH) can be measured with

213 lood pressure, lipid panel, oxidized (GSH) & reduced glutathione (GSSG) were also evaluated for each

214 ificant increase in the ratio of oxidised to reduced glutathione (GSSG/GSH).

215 ow a similar pattern of responses to applied reduced glutathione, GSSG and MRP1 inhibitors (indometha

216 sported glutathione disulfide (GSSG) but not reduced glutathione in agreement with a 3-fold stimulati

217 lian SOD1, wSOD-1 exhibits a requirement for reduced glutathione in CCS-independent activation.

218 ctivity, which can be provided by endogenous reduced glutathione in chromaffin granules.

219 ncrease in malondialdehyde and a decrease in reduced glutathione in most organs, as well as liver (in

220 treatment significantly increased levels of reduced glutathione in the liver and lowered levels of o

221 glutathione and a decrease in mitochondrial reduced glutathione in the WT, but not in the MT-TG, dia

222 mitation on the capacity for regeneration of reduced glutathione in this compartment may contribute t

223 DNTB reacted rapidly with reduced glutathione in vitro and was associated with a d

224 ol, Tris(2-carboxyethyl)phosphine (TCEP), or reduced glutathione increased the fraction of anomalousl

225 Here we show that depletion of reduced glutathione is an alternative trigger of synchro

226 Intracellular-reduced glutathione is consumed in detoxication of DNCB,

227 n be partially reduced by monothiols such as reduced glutathione, L-cysteine or N-acetyl-L-cysteine a

228 which correlated with a greater decrease in reduced glutathione level in Raji clones expressing GSTP

229 modulation of trace elements, alteration in reduced glutathione level, glutathione-s-transferase and

230 e poorly and exhibit oxidative stress due to reduced glutathione levels and impaired expression of se

231 rly [altered oxidized glutathione (GSSG) and reduced glutathione levels and ratio; increased reactive

232 ne potential (DeltaPsim), and superoxide and reduced glutathione levels in individual dopaminergic an

233 d with 100% oxygen had decreased hippocampal reduced glutathione levels vs. sham (15.3 +/- 0.4 vs. 20

234 SOD-1 activity and reduced glutathione levels were higher, whereas malondia

235 Finally, reduced glutathione levels were significantly lower in I

236 but not female, 17-day-old rats to maintain reduced glutathione levels within cerebral cortex acutel

237 thiobarbituric acid reactive substances and reduced glutathione levels, tissue markers of oxidative

238 stress in PrEC cells, possibly by increasing reduced glutathione levels.

239 lation of manganese superoxide dismutase and reduced glutathione levels.

240 observed, along with a decrease in cellular reduced glutathione levels.

241 asts from oxidative stress through increased reduced glutathione levels.

242 -1beta), tumor necrosis factor-alpha, IL-10, reduced glutathione, malonaldehyde, and nitrate/nitrite

243 ility of natural host defenses to regenerate reduced glutathione may explain failure of recovery from

244 For example, reduced glutathione mediates zinc transfer from enzymes

245 AIIt-mediated liposome aggregation, whereas reduced glutathione, nitrate, or nitrite had no effects.

246 but was significantly enhanced by 500 microM reduced glutathione or 100 microM dithiothreitol, agents

247 by preincubation with antioxidants including reduced glutathione or by expression of a dominant-negat

248 atment with the reductants dithiothreitol or reduced glutathione or by incubation with the thioredoxi

249 cell apoptosis is blocked by the addition of reduced glutathione or N-acetylcysteine.

250 Treatment of PTP1B with diamide and reduced glutathione or with only glutathione disulfide (

251 fect on longevity, protein carbonyl content, reduced glutathione, or glutathione disulfide content, a

252 T); oxidative stress (malondialdehyde [MDA], reduced glutathione/oxidative glutathione ratio [GSH/GSS

253 the cellular contents of total glutathione, reduced glutathione, oxidized glutathione, and intracell

254 nce of oxidants to antioxidants, measured as reduced glutathione, oxidized glutathione, and their rat

255 nse enzyme activities rather than changes in reduced glutathione, oxidized glutathione, ascorbate and

256 sympathetic neuronal marker profiles, tissue-reduced glutathione/oxidized glutathione (GSH/GSSG) rati

257 in bronchial epithelial cells, and increased reduced glutathione/oxidized glutathione following Cl2 e

258 ficantly lower mean plasma concentrations of reduced glutathione (P < 0.0001), GluCys (P < 0.0001), a

259 positive correlation with concentrations of reduced glutathione (p=0.006) and ATP (p=0.03).

260 m34) of Sec tRNA([Ser]Sec), and consequently reduced glutathione peroxidase 1 expression.

261 urce of cysteine; however, in the absence of reduced glutathione, pertussis toxin was not efficiently

262 Reduced glutathione prevented peroxynitrite-induced FeOx

263 nt Zn(2+) release from the vesicles, whereas reduced glutathione prevents TRPM7-dependent cytosolic Z

264 , whilst oxidized Tim10 cannot be reduced by reduced glutathione, reduced Tim10 is effectively oxidiz

265 The generation of reduced glutathione requires NADPH, and we therefore exa

266 sults suggest that the autism LCLs exhibit a reduced glutathione reserve capacity in both cytosol and

267 s of histones, tubulin, and lumican and (ii) reduced glutathione S-transferase, annexin, and dermatop

268 We find that reduced glutathione stabilizes an interdomain associatio

269 age loss of freely diffusing thiols (chiefly reduced glutathione) that have been derivatized with the

270 esence of a low concentration of diamide and reduced glutathione, the kinase was rapidly and reversib

271 of AMPKalpha1, which maintains high level of reduced glutathione to keep reduction-oxidation reaction

272 In the presence of reduced glutathione to mimic the cellular environment, C

273 duced a significant increase in the ratio of reduced glutathione to oxidized glutathione consistent w

274 e stress (significantly lower redox ratio of reduced glutathione to oxidized glutathione) in children

275 vated lipid peroxidation, decreased ratio of reduced glutathione to oxidized glutathione, and up-regu

276 Addition of 3 to 5 mM reduced glutathione to the cis chamber caused dose-depen

277 Superoxide dismutase activity, the reduced glutathione-to-glutathione disulfide ratio, and

278 with a significant decrease in the ratio of reduced glutathione-to-oxidized glutathione (GSH/GSSG),

279 Cooking time changed just for reduced glutathione-treated rice, as a result of their w

280 two endogenous channel effectors, MgATP and reduced glutathione, using the planar lipid bilayer meth

281 Mg2+ deprivation causes release of neuronal reduced glutathione via a mechanism involving excessive

282 The K(m) value for reduced glutathione was 11muM for both GGT1 and GGT5.

283 d 1.0 +/- 0.2 mM in normal prostate, whereas reduced glutathione was 2.0 +/- 0.3 mM and 0.8 +/- 0.3 m

284 Reduced glutathione was also depleted, indicating increa

285 No significant effect of GLN on lung tissue-reduced glutathione was observed.

286 Total reduced glutathione was significantly higher than contro

287 ant activity was enhanced by the addition of reduced glutathione, was proteinase K sensitive and heat

288 s (ROS) levels was reduced whereas levels of reduced glutathione were elevated in TIGAR-expressing ce

289 e, cystathionine, cysteine, and oxidized and reduced glutathione were measured in 20 children with au

290 ric acid-reactive substance and oxidized and reduced glutathione were measured on frozen brains.

291 idual species via exchange with oxidized and reduced glutathione were measured.

292 intracellular and extracellular oxidized and reduced glutathione were temporally associated with eGPx

293 ing in HepG2 cells by MR was associated with reduced glutathione, where it functions as a cofactor fo

294 Alcohol further depletes mitochondrial reduced glutathione, which exacerbates depolarization an

295 iotics and oxidatively produced compounds to reduced glutathione, which facilitates their metabolism,

296 ucing equivalents, which generates NADPH and reduced glutathione, which in turn activates sentrin/SUM

297 nd NAD-binding (KTN) domains that sense both reduced glutathione, which inhibits Kef activity, and gl

298 PI activity was inhibited by incubation with reduced glutathione while bacterial TPI was unaffected.

299 roteins also shared the same specificity for reduced glutathione, with no activity against either gam

300 iciencies are up to 100-fold higher than for reduced glutathione, with typical K(m) values of about 1