ライフサイエンスコーパス: reduced glutathione

1 ygen species and exhibited less depletion of reduced glutathione.

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

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

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

5 zes the reduction of oxidized glutathione to reduced glutathione.

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

7 neurons to maintain intracellular levels of reduced glutathione.

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

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

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

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

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

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

14 and not simulated by oxidized glutathione or reduced glutathione.

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

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

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

18 K-edge spectrum is similar to that of fully reduced glutathione.

19 which was also significantly antagonized by reduced glutathione.

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

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

22 ivity against DPPH radicals when compared to reduced glutathione.

23 increase in antioxidants including NADPH and reduced glutathione.

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

25 erine treatment with concomitant decrease in reduced glutathione.

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

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

28 oxidant-induced protein thiyl radicals with reduced glutathione.

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

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

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

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

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

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

35 Included are reduced glutathione, adenosine monophosphate, nicotinami

36 Reduced glutathione, although subject to transport by At

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

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

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

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

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

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

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

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

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

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

50 Reduced glutathione and NADPH protects the brain from ox

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

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

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

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

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

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

57 lso produces NADPH needed for maintenance of reduced glutathione and reductive biosynthesis.

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 This stimulation was enhanced by reduced glutathione as is its drug transport, and oxidiz

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

90 The protein displayed reduced glutathione-dependent phospholipid hydroperoxide

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

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

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

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

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

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

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 r reducing power, containing only 30% of the reduced glutathione found in unfractionated cells.

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

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

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

103 Increased intracellular reduced glutathione/glutathione disulfide ratio and grea

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

105 Reduced glutathione greatly increased the rate of bindin

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

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

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

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

110 Reduced glutathione (GSH) and glutathione disulfide (GSS

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

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

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

118 HPLC-BDD responses 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 Reduced glutathione (GSH) inhibited Ca2+-stimulated [3H]

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

150 The presence of intracellular reduced glutathione (GSH) inhibited the beta-NAD+-activa

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

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

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

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

155 Reduced glutathione (GSH) is an efficient antioxidant on

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 Reduced glutathione (GSH) was determined by a colorimetr

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

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

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

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

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

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

183 y efflux (countertransport) of intracellular reduced glutathione (GSH), and whether hydrophobic gluta

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

233 sults from exposure to H2O2, nor oxidized or reduced glutathione levels were responsible for activati

234 Finally, reduced glutathione levels were significantly lower in I

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

236 lation of manganese superoxide dismutase and reduced glutathione levels.

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

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

239 asts from oxidative stress through increased reduced glutathione levels.

240 -1beta), tumor necrosis factor-alpha, IL-10, reduced glutathione, malonaldehyde, and nitrate/nitrite

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

242 For example, reduced glutathione mediates zinc transfer from enzymes

243 Like reduced glutathione, N-acetyl-L-cysteine, L-cysteine met

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

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

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

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

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

249 by treatment with GSSG, while treatment with reduced glutathione or other sulfhydryl-reducing agents

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

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

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

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

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

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

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

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

260 Reduced glutathione prevented peroxynitrite-induced FeOx

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

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

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

264 y absorption near-edge structure spectrum of reduced glutathione resembles that of cysteine, whereas

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

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

267 We find that reduced glutathione stabilizes an interdomain associatio

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

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

270 m disulfides in the presence of oxidized and reduced glutathione, the native disulfides were not form

271 in a significant depletion of intracellular reduced glutathione (thiol) content at 72 and 96 h and d

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