ライフサイエンスコーパス: alpha-tocopherol

1 teract with chromanol (the active segment of alpha-tocopherol).

2 hemagglutinin and AS03B adjuvant (5.93 mg of alpha-tocopherol).

3 receiving memantine alone or memantine plus alpha tocopherol.

4 SigmaCLA, PUFA, omega3, omega6, retinol and alpha-tocopherol.

5 ism is a mechanism for regulating whole-body alpha-tocopherol.

6 on for 7-fold longer than that recorded with alpha-tocopherol.

7 influence the radical scavenging activity of alpha-tocopherol.

8 doing so, TTP regulates body-wide levels of alpha-tocopherol.

9 rotein-lipid interaction in the transport of alpha-tocopherol.

10 s is dynamic and responds to the presence of alpha-tocopherol.

11 with the typical chain-breaking antioxidant alpha-tocopherol.

12 red with other vitamin E isoforms, including alpha-tocopherol.

13 nship of isochromans compared to HT, BHT and alpha-tocopherol.

14 d beta-carotene, lutein plus zeaxanthin, and alpha-tocopherol.

15 r was inversely associated with lycopene and alpha-tocopherol.

16 d in the order of methyl gallate>gallic acid>alpha-tocopherol.

17 ascorbic acid, butylated hydroxylanisole and alpha-tocopherol.

18 ion (AS, 50.8 mg) were observed for milk RRR-alpha-tocopherol.

19 ture rate was observed with lower intakes of alpha-tocopherol.

20 ck of oxidised cholesterol and small loss of alpha-tocopherol.

21 c acid, but the highest activity belonged to alpha-tocopherol.

22 elimination rate (0.36/h) were found for RRR-alpha-tocopherol.

23 a-carotene more effectively than did BHT and alpha-tocopherol.

24 ible to degradation compared with lutein and alpha-tocopherol.

25 omes were associated with a higher intake of alpha-tocopherol.

26 ommercial butylated hydroxytoluene (BHT) and alpha-tocopherol.

27 ox(R) T 70 EU being more effective than pure alpha-tocopherol.

28 rom administered oral d3- and intravenous d6-alpha-tocopherols.

29 ) nanoemulsions loading different amounts of alpha-tocopherol (0-40%) were produced.

30 o the reported findings in vivo, addition of alpha-tocopherol (0-75%) did not interfere with the anti

31 tein + zeaxanthin, 0.46; lycopene, 0.32; and alpha-tocopherol, 0.47.

32 mmol TE/kg), and high amounts (mg/100 g) of alpha-tocopherol (11.6-21.0), beta-carotene (0.49-0.65)

33 Data from 561 participants were analyzed (alpha tocopherol = 140, memantine = 142, combination = 1

34 encapsulated hexadeuterium-labeled (d6)-RRR-alpha-tocopherol (15 mg) with 240 mL nonfat (0.2 g fat),

35 .3 mg/100 g), vitamin A (486.7 ug/100 g) and alpha-tocopherol (174.5 ug/100 g).

36 owers, these last samples also being rich in alpha-tocopherol (~18 mg/100 g dw).

37 asterol (1229.0mgkg(-1) of dry material) and alpha-tocopherol (21.8mgkg(-1) of dry material).

38 , in which stigmasterol, rosmarinic acid and alpha-tocopherol (237.7, 180.1 and 53.6 mg/100 g, respec

39 Among different stereoisomers of all-rac-alpha-tocopherol, 2R-stereoisomers have higher biologica

40 ene (755 and 332mug/g of oil, respectively), alpha-tocopherol (308mug/g of oil), total phenols (13.6m

41 4-87.43% of Recommended Daily Intake (RDI)), alpha-tocopherol (38.90-51.87% RDI), manganese (>100% RD

42 MAG (0.5wt%) suppressed the effectiveness of alpha-tocopherol (40muM) in SSO.

43 Viable seeds contained higher levels of alpha-tocopherol (6.7 mg/100 g), lipids (23.11 g/100 g,

44 30 +/- 11 h), and the minimum estimated (2)H-alpha-tocopherol absorbed (24% +/- 16%) did not vary bet

45 pants with higher serum lipids, but the (2)H-alpha-tocopherol absorbed was not dependent on the plasm

46 but MetS participants had lower estimated d6-alpha-tocopherol absorption (+/-SEM) than did healthy pa

47 xidative stress that limits small intestinal alpha-tocopherol absorption and/or impairs hepatic alpha

48 d soil water contents, with the exception of alpha-tocopherol accumulation.

49 noids, thereby enabling the determination of alpha-tocopherol acetate in plant samples.

50 Enano), which were composed of EGCG, PC, (+) alpha-tocopherol acetate, and surfactant.

51 Remarkably alpha-tocopherol acted as a pro-oxidant at 25 and 40 deg

52 re useful biomarkers to noninvasively assess alpha-tocopherol adequacy, especially in populations wit

53 0 and 37% decreased risk of incident asthma (alpha-tocopherol: adjusted odds ratio = 0.52; 95% confid

54 acid in an acylglycerol structure protected alpha-tocopherol against thermal degradation, which was

55 alpha-Tocopherol alone significantly increased the heali

56 was to determine the extent to which plasma alpha-tocopherol (alpha-T) or gamma-tocopherol (gamma-T)

57 s expected, alpha-tocotrienol (alpha-T3) and alpha-tocopherol (alpha-T) were the predominant tocol is

58 Determining the human vitamin E [alpha-tocopherol (alpha-T)] requirement is difficult, an

59 To test whether the alpha-tocopherol (alpha-Toc) form of vitamin E, a regula

60 (DCP) as well as different concentration of alpha-tocopherol (alpha-TOC) on mean size, polydispersit

61 inherent reactivity of RSSH to match that of alpha-tocopherol (alpha-TOH), nature's premier radical-t

62 In contrast, phenolic RTAs such as alpha-tocopherol (alpha-TOH), the most potent form of vi

63 ee 8-h urine collections (0-24 h) and plasma alpha-tocopherol, alpha-CEHC, and alpha-CMBHC concentrat

64 The major vitamin E components were alpha-tocopherol, alpha-tocotrienol, gamma-tocotrienol a

65 The presumptive function for alpha-tocopherol (alphatoc) in membranes is to protect p

66 des both tocopherols and tocotrienols, where alpha-tocopherol (alphaTOC) is the most bioavailable for

67 y developed, extremely sensitive fluorogenic alpha-tocopherol analogue (H4BPMHC), we report herein th

68 ,2,5,7,8-pentamethyl-6-hydroxy-chromanol, an alpha-tocopherol analogue lacking the phytyl tail).

69 Plasma unlabeled alpha-tocopherol and (2)H-alpha-tocopherol were measured

70 uca and G. vermiculophylla and stigmasterol, alpha-tocopherol and 24-methylenecholesterol in C. tomen

71 alpha-Tocopherol and alpha-tocopherol/selenium combinati

72 idant activity especially when combined with alpha-tocopherol and are suggested for protection of foo

73 t (fatty acids, chlorophylls, beta-carotene, alpha-tocopherol and ascorbic acid) content and composit

74 rgistic antioxidant effect was found between alpha-tocopherol and beta-carotene.

75 The recovery of alpha-tocopherol and beta-sitosterol from the deodorizer

76 ions was also studied and high recoveries of alpha-tocopherol and beta-sitosterol, up to 99.20% and 9

77 alpha-Tocopherol and beta-tocopherol contents of the chi

78 ned wheat and yellow-grained tritordeum were alpha-tocopherol and beta-tocotrienol, whereas spring ba

79 corbic acid and Trolox) and two hydrophobic (alpha-tocopherol and BHT) antioxidants were measured by

80 ) and conventional extraction (CE) extracts, alpha-tocopherol and BHT, respectively, as compared to t

81 APH-derived radicals in ORAC assay more than alpha-tocopherol and BHT.

82 Myrtus communis phenolic compounds (McPCs), alpha-tocopherol and Butylated hydroxytoluene (BHT) were

83 isease incidence, yield and fruit vitamin C, alpha-tocopherol and carotenoids content for Monroe, Opt

84 Appreciable amounts of alpha-tocopherol and cholesterol were also found (126+/-

85 Healthy women received intravenous d6-alpha-tocopherol and consumed d3-alpha-tocopherol with a

86 protein (TTP) preferentially selects dietary alpha-tocopherol and facilitates its transport through t

87 on furan formation from linolenic acid while alpha-tocopherol and FeSO4 promoted furan formation.

88 her higher first-trimester concentrations of alpha-tocopherol and gamma-tocopherol were associated wi

89 ation of retinyl acetate, retinyl palmitate, alpha-tocopherol and gamma-tocopherol, reverse phase hig

90 is proven in homogenous lipids using natural alpha-tocopherol and hydroxytyrosol as antioxidants, cal

91 pharmacokinetics of stereoisomers of all-rac-alpha-tocopherol and investigated the discrimination and

92 he change in TTP localization is specific to alpha-tocopherol and is time- and dose-dependent.

93 There was no synergistic relation between alpha-tocopherol and MCTs.

94 ifferential catabolism of the intravenous d6-alpha-tocopherol and oral d3-alpha-tocopherol doses show

95 antioxidant, even with higher activity than alpha-tocopherol and other carotenoids.

96 off-flavour volatile compound production and alpha-tocopherol and polyphenols losses, and thus, highe

97 Nevertheless, the amount of alpha-tocopherol and polyunsaturated fatty acid were fou

98 ent and soaking temperature increased, while alpha-tocopherol and polyunsaturated fatty acids decreas

99 in lung lysates to greater extents than did alpha-tocopherol and prednisolone.

100 e present study is to evaluate the effect of alpha-tocopherol and selenium on gingival fibroblasts (G

101 -I, amide-II, amide-III, beta-sheet protein, alpha-tocopherol and Soybean Kunitz Trypsin Inhibitor.

102 Total oil, oleic acid, alpha-tocopherol and squalene contents were found to ran

103 S03B (AS03B is an Adjuvant System containing alpha-tocopherol and squalene in an oil-in-water emulsio

104 c and carnosic acids are more efficient than alpha-tocopherol and synthetic antioxidants for the pres

105 n Mt-abi5 seeds, evident from an increase in alpha-tocopherol and upregulation of genes related to pr

106 significantly impaired by co-incubation with alpha-tocopherol (and vice versa).

107 rients (alpha-linolenic acid, beta-carotene, alpha-tocopherol) and carbohydrates, whereas the post-ha

108 oxidants (alpha- and beta-carotenes, lutein, alpha-tocopherol), and gelling effect.

109 averaged 1.57-6.75 times higher and retinol, alpha-tocopherol, and 25(OH)D 0.30-0.84 times lower in c

110 he concentrations of 7 carotenoids, retinol, alpha-tocopherol, and gamma-tocopherol with risk of pros

111 d with retinol and inversely associated with alpha-tocopherol, and risk of aggressive prostate cancer

112 Low intakes and low serum concentrations of alpha-tocopherol are associated with an increased rate o

113 with antioxidants N-acetylcysteine amide or alpha-tocopherol as indicated by restored synaptic vesic

114 ted the highest content in tocopherols, with alpha-tocopherol as the most abundant.

115 to the antioxidant effect of astaxanthin and alpha-tocopherol, as their concentrations decreased as s

116 oxidant type (EDTA, ascorbic acid, catechin, alpha tocopherol, ascorbic acid palmitate) on the physic

117 transferase converting gamma-tocopherol into alpha-tocopherol) associated with the observed trait var

118 The alpha-tocopherol association with overall mortality was

119 Maternal plasma alpha-tocopherol at 10-12 weeks gestation was positively

120 ish oil, all esters were more effective than alpha-tocopherol at 2 mmol/kg concentration but were not

121 esters were more effective than both BHT and alpha-tocopherol at 2 mmol/kg concentration.

122 and half-life for beta-carotene, lutein and alpha-tocopherol at 4 degrees C and non-vacuumed were 2.

123 e susceptible to degradation than lutein and alpha-tocopherol at 40 degrees C in the presence of air,

124 AX and alpha-tocopherol (AT) degradation followed a zero-order

125 They also had lower plasma d6-alpha-tocopherol AUC from 0 to 72 h, as well as maximal

126 MetS participants had lower d6-alpha-tocopherol AUC from t = 0-12 h (AUC0- t final) in

127 Percentages of d6-alpha-tocopherol AUC0- t final in both the chylomicron (

128 ascorbic acid and fat-soluble antioxidants (alpha-tocopherol, beta-carotene and lutein), in vitro ga

129 and Muscat de Hambourg the highest levels of alpha-tocopherol, beta-carotene and monoterpenols, well-

130 on pre-supplementation fasting serum in the Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC)

131 rom 5 nested case-control studies within the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study

132 k of overall and site-specific cancer in the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study

133 k of overall and site-specific cancer in the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study

134 tal, and Ovarian Cancer Screening Trial, the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study,

135 is of 29 092 participants in the ATBC Study (Alpha-Tocopherol, Beta-Carotene Cancer Prevention) that

136 effect of permitted antioxidants, including alpha-tocopherol, beta-carotene, ascorbyl palmitate, asc

137 he vitamin E profile of silverskin comprises alpha-tocopherol, beta-tocopherol, -tocopherol, delta-to

138 We reported previously that alpha-tocopherol bioavailability in healthy adults is hi

139 valent to the Recommended Dietary Allowance, alpha-tocopherol bioavailability is unaffected by dairy

140 Regardless of health status, d6-alpha-tocopherol bioavailability was unaffected by incre

141 ng dietary fat intake is expected to improve alpha-tocopherol bioavailability, which could be benefic

142 spective cohort study, higher baseline serum alpha-tocopherol biochemical status was associated with

143 (beta-carotene-capsanthin) (1:9) and (1:1), (alpha-tocopherol-capsanthin) (1:9), (lutein-lycopene) (9

144 Levels of photoprotective molecules (alpha-tocopherol, carotenoids, and anthocyanins) increas

145 The alpha-tocopherol-carrying niosomes with mean diameter of

146 shows both liver and intestine have roles in alpha-tocopherol catabolism.

147 Human vitamin E (alpha-tocopherol) catabolism is a mechanism for regulati

148 increased requirements.We hypothesized that alpha-tocopherol catabolites alpha-carboxyethyl hydroxyc

149 ples were analyzed by LC/MS to determine the alpha-tocopherol catabolites and alpha-carboxyethyl hydr

150 ients with mild to moderate AD, 2000 IU/d of alpha tocopherol compared with placebo resulted in slowe

151 Muscle alpha-tocopherol concentration was over 3.5-fold higher

152 imes (12.6 +/- 2.5 h) of maximum plasma (2)H-alpha-tocopherol concentrations (0.82% +/- 0.59% total a

153 Doubling of alpha-tocopherol concentrations and PAF-AH activity was

154 These data suggest that plasma alpha-tocopherol concentrations are more dependent on me

155 It is noticeable that the highest alpha-tocopherol concentrations induce the generation of

156 Unlabeled alpha-tocopherol concentrations were higher in older adu

157 ased significantly post-challenge but fillet alpha-tocopherol concentrations were increased significa

158 locked nucleotide acid gapmer duplex with an alpha-tocopherol-conjugated complementary RNA (Toc-HDO)

159 d Arabidopsis (Arabidopsis thaliana) leaves, alpha-tocopherol constitutes the main tocopherol form, w

160 on treatment with alpha-tocopherol, TTP- and alpha-tocopherol-containing vesicles translocate to the

161 The alpha-tocopherol content decreased in all treatments at

162 The alpha-tocopherol content seems to be the most important

163 oil degradation, fatty acid composition and alpha-tocopherol content was investigated.

164 tudy suggested that PSO nanoemulsion loading alpha-tocopherol could be introduced as delivery system

165 co-ingested 15 mg hexadeuterium-labeled RRR-alpha-tocopherol (d6-alpha-T) with nonfat, reduced-fat,

166 tunately, both phenolic derivatives favoured alpha-tocopherol decay in rapeseed oil.

167 er FO-ILEs containing MCTs and/or additional alpha-tocopherol decrease the inflammatory response to a

168 , dietary supplementation of the antioxidant alpha-tocopherol decreased reactive oxygen species but h

169 Moreover, the oxidative stability and alpha-tocopherol degradation were also assessed on optim

170 observed for (lutein-delta-tocopherol) and (alpha-tocopherol-delta-tocopherol).

171 The linear ranges for alpha-tocopherol determination were 5x10(-7)-4x10(-5) an

172 ch as the lipophilic antioxidants of BHT and alpha-Tocopherol did not show any activity.

173 nseed oil, palmitic acid, linoleic acid, and alpha-tocopherol, did not interfere with the Yb(3+) phot

174 Maternal alpha-tocopherol dietary supplementation prevented NTD a

175 intravenous d6-alpha-tocopherol and oral d3-alpha-tocopherol doses shows both liver and intestine ha

176 is exalted and BHT regenerates twice as much alpha-tocopherol due to a nucleophilic addition of short

177 25-hydroxyvitamin D2, 25-hydroxyvitamin D3, alpha-tocopherol (E), gamma-tocopherol (E), and phylloqu

178 emonstrated when extracts were combined with alpha-tocopherol, effects explained by the solubility of

179 he retention of the total tocochromanols and alpha-tocopherol equivalent decreased after extrusion (6

180 tioxidant activity (213.96 +/- 11.12 umol/mL alpha-tocopherol equivalent) and notable DNA protection

181 tamin A (retinol equivalents) and vitamin E (alpha-tocopherol equivalents) from both infant food and

182 ently FO- and 50:50 FO:MCT-ILE plus 500 mg/L alpha-tocopherol (FO + AT and 50:50 + AT, respectively).

183 he long-term health benefits of higher serum alpha-tocopherol for overall and chronic disease mortali

184 pherol concentrations (0.82% +/- 0.59% total alpha-tocopherol), fractional disappearance rates (0.63

185 c solvents, such as toluene, BHT regenerates alpha-tocopherol from tocopheryl radical, whereas in pol

186 The unsaponifiable lipid was comprised of alpha-tocopherol, fucosterol and 24-methylenecholesterol

187 and 60 degrees C) on the phenolic compounds (alpha-tocopherol, gamma-oryzanol) and on the fatty acids

188 henolic acids (TPA) in glutinous rice, while alpha-tocopherol, gamma-tocopherol and polyunsaturated f

189 tography quantified serum levels of retinol, alpha-tocopherol, gamma-tocopherol and six carotenoids (

190 in, zeaxanthin, beta-cryptoxanthin, retinol, alpha-tocopherol, gamma-tocopherol, and vitamin C.

191 alpha-tocopherol, gamma-tocopherol, delta-tocopherol, be

192 This change in the alpha tocopherol group translates into a delay in clinic

193 Almonds and hazelnuts were abundant in alpha-tocopherol (>4-fold the RDI for tocopherol equival

194 factors, we found that men with higher serum alpha-tocopherol had significantly lower all-cause morta

195 In addition, (2)H-alpha-tocopherol half-lives were correlated with lipids

196 alpha-Tocopherol has been used as an immune supplement i

197 d that medium-chain triglycerides (MCTs) and alpha-tocopherol have anti-inflammatory properties.

198 After a single dose injection of all-rac-alpha-tocopherol, highest maximal daily increase (S(max)

199 justment for BMI and serum concentrations of alpha-tocopherol (HR: 1.16; 95% CI: 0.88, 1.51).

200 he main minor compounds of virgin olive oil (alpha-tocopherol, hydroxytyrosol, tyrosol and oleuropein

201 ately 0.59mg/mL) than commercially available alpha-tocopherol (IC50 0.63mg/mL).

202 These findings suggest benefit of alpha tocopherol in mild to moderate AD by slowing funct

203 activity of gallic acid, methyl gallate, and alpha-tocopherol in a bulk Kilka fish oil and its oil-in

204 peroxyl radicals much more efficiently than alpha-tocopherol in a chlorobenzene/water two-phase syst

205 more effective antioxidant than palm TRF and alpha-tocopherol in both food systems at 0.02% and 0.05%

206 nges of lipids, fatty acids, phytosterol and alpha-tocopherol in New Zealand brown macroalgae, Undari

207 The effect of adding alpha-tocopherol in proportions ranging from 0.002 to 5%

208 O and on the antioxidative activity of 40muM alpha-tocopherol in SSO (55 degrees C).

209 O) and on the antioxidative effectiveness of alpha-tocopherol in SSO.

210 extract components in the water-phase and of alpha-tocopherol in the lipid-phase.

211 mg/kg of butylated hydroxytoluene (BHT) and alpha-tocopherol in the Rancimat test at 50-70 degrees C

212 lected nutrients (beta-carotene, lutein, and alpha-tocopherol) in the freeze-dried CRF material was m

213 Compared with the highest quintile of alpha-tocopherol intake in ULSAM (follow-up: 12 y), lowe

214 The objective was to determine whether alpha-tocopherol intake or serum concentrations are asso

215 his study demonstrated that incorporation of alpha-tocopherol into liposomes contributes a significan

216 xperiment as a tool to explore incorporating alpha-tocopherol into self-emulsified systems containing

217 y occurring members of the vitamin E family, alpha-tocopherol is the most biologically active species

218 ontents were expressed as mass equivalent of alpha-tocopherol known as the most active form of this l

219 thin and/or canthaxanthin) combined with two alpha-tocopherol levels (normal and high: 500 and 1000 m

220 t carotenoid-types/mixtures and increased of alpha-tocopherol levels from normal to high, respectivel

221 alpha-Tocopherol levels increased progressively at incre

222 The aim of this study was to prepare alpha-tocopherol loaded nanoliposomes as carriers of DHA

223 alpha-Tocopherol-loaded niosome was developed using modi

224 The rate of beta-carotene, lutein and alpha-tocopherol loss displayed first order reaction kin

225 assess ORs of miscarriage in women with low alpha-tocopherol (<12.0 mumol/L) and gamma-tocopherol (<

226 h seaweed extracts than antioxidants BHT and alpha-tocopherol (<5h and <17, respectively).

227 aw < 0.001), oleic acid (P-raw = 0.003), and alpha-tocopherol (margarine and vegetable oil) (P-raw <

228 25(OH)D (mean: +26.7%; 95% CI: 23.2, 30.3%), alpha-tocopherol (mean: +8.7%; 95% CI: 3.6, 13.7%), zinc

229 r delta-tocotrienol and higher than those of alpha-tocopherol metabolites.

230 oxidant interactions of gamma-terpinene with alpha-tocopherol mimic 2,2,5,7,8-pentamethyl-6-chromanol

231 dismutase (SOD2), and chemical antioxidants alpha-tocopherol, MitoTEMPO, and MitoQ restored neurite

232 th MetS had lower (P < 0.05) baseline plasma alpha-tocopherol (mumol/mmol lipid) and greater oxidized

233 Participants received either 2000 IU/d of alpha tocopherol (n = 152), 20 mg/d of memantine (n = 15

234 dant films based on methylcellulose (MC) and alpha-tocopherol nanocapsule suspension (NCs) were devel

235 prepare co-surfactant free, olive-oil based alpha tocopherol nanoemulsions, using a food grade non-i

236 roved that, except in the lowest proportion, alpha-tocopherol not only exerts a prooxidant effect on

237 amount of ascorbic acid and had no effect on alpha-tocopherol or total phenolic concentrations.

238 0.72; 95% CI: 0.56, 0.93; P-raw = 0.013) and alpha-tocopherol (OR: 0.71; 95% CI: 0.51, 0.98; P-raw =

239 d metabolic syndrome (MetS) health status on alpha-tocopherol pharmacokinetics in plasma and lipoprot

240 ficantly affected the contents of vitamin C, alpha-tocopherol, phytoene, and beta-carotene in fruits;

241 Besides having higher alpha-tocopherol protection from oxidative phenomena, EV

242 Paradoxically, alpha-tocopherol remained in circulation longer in parti

243 These findings support higher dietary alpha-tocopherol requirements for MetS adults.

244 ardiometabolic risk who fail to meet dietary alpha-tocopherol requirements.

245 cable data found in the literature regarding alpha-tocopherol's (aToc's) behavior in dimyristoyl phos

246 Little is known about alpha-tocopherol's bioavailability as a constituent of f

247 alpha-Tocopherol and alpha-tocopherol/selenium combination is able to acceler

248 The alpha-tocopherol/selenium combination significantly enha

249 n both cell types at 24, 48, and 72 hours by alpha-tocopherol/selenium combination.

250 BHT and alpha-tocopherol showed lower antioxidant activity than

251 ity, which could be beneficial for improving alpha-tocopherol status, especially in cohorts at high c

252 manol (alpha-CMBHC) are useful biomarkers of alpha-tocopherol status.Adults (healthy or with MetS; n

253 gated the discrimination and distribution of alpha-tocopherol stereoisomers in plasma and milk as wel

254 ed by hyaluronic acid (HA) conjugated with d-alpha-tocopherol succinate (TOS) using a disulfide bond

255 omal cathepsin inhibitor E64 and antioxidant alpha-tocopherol, suggesting the involvement of LMP and

256 (2+) in solution, when supplemented with the alpha-tocopherol surrogate, PMHC (2,2,5,7,8-pentamethyl-

257 gs showed a clear discrimination between RRR-alpha-tocopherol, synthetic 2R stereoisomers and E2S ste

258 uding ascorbic acid) and tocopherols (mainly alpha-tocopherol) than wild grown F. vesca, as well as c

259 , to formulate emulsion adjuvants containing alpha-tocopherol, that have the potential to be made in

260 Determine whether serum alpha-tocopherol (the predominant form of vitamin E) is

261 ap segment consists of the chromanol ring of alpha-tocopherol, the most potent naturally occurring li

262 For alpha-tocopherol, the OR for the highest compared with t

263 the presence of the good hydrogen atom donor alpha-tocopherol, the oxysterol profile of 7-DHC peroxid

264 ortions of octadecanoic acid, oleic acid and alpha-tocopherol, the three compounds that are known to

265 ociated metabolites including ascorbic acid, alpha-tocopherol, threonic acid, beta-sitosterol, 4-hydr

266 hat describes TTP-facilitated trafficking of alpha-tocopherol through hepatocytes.

267 R848 was conjugated to alpha-tocopherol to constitute an R848-Toco prodrug, fol

268 The use of stereoisomers of alpha-tocopherol to correctly classify Iberian pig fat s

269 Mixed FO/MCT and the addition of alpha-tocopherol to FO improved the inflammatory respons

270 A burst and prolonged release of alpha-tocopherol to food simulant was also reported.

271 nary (1:1) and ternary (1:1:1) mixtures with alpha-tocopherol (TOH) and/or ascorbyl palmitate (AscPH)

272 The mechanisms by which TTP facilitates alpha-tocopherol trafficking in hepatocytes are poorly u

273 ated hepatic dysfunction that likely impairs alpha-tocopherol trafficking.

274 tocopherol absorption and/or impairs hepatic alpha-tocopherol trafficking.

275 pa encoding for the VitE regulatory protein [alpha-tocopherol transfer protein (alpha-TTP)] in zebraf

276 The hepatic alpha-tocopherol transfer protein (TTP) preferentially s

277 Upon treatment with alpha-tocopherol, TTP- and alpha-tocopherol-containing v

278 Incorporation of small amounts of alpha-tocopherol (vitamin E) in blends with the cellobio

279 alpha-Tocopherol (vitamin E) is an essential nutrient fo

280 Comparative studies with alpha-tocopherol (vitamin E) show that the negative intr

281 or cholesterol and the other tocopherol, low alpha-tocopherol was associated with an OR of 1.83 (95%

282 egnant women in rural Bangladesh, low plasma alpha-tocopherol was associated with increased risk of m

283 Serum alpha-tocopherol was measured at baseline using high-per

284 potential of the liposome formulations with alpha-tocopherol was observed at 4 degrees C after 90day

285 alpha-Tocopherol was the most abundant tocopherol accoun

286 In group E, 60 muM alpha-tocopherol was used, and in groups ES1, ES2, and E

287 The contents of alpha-tocopherol were 13, 14 and 9.6mug/g in winter, spr

288 amounts of long chain aliphatic alcohols and alpha-tocopherol were also identified.

289 of grape rachis alone or in combination with alpha-tocopherol were evaluated as antioxidants in (i) b

290 Plasma unlabeled alpha-tocopherol and (2)H-alpha-tocopherol were measured by using liquid chromatog

291 arotene, lutein plus zeaxanthin (L + Z), and alpha-tocopherol were routinely measured at baseline in

292 Sucrose, oxalic acid, and alpha-tocopherol were the only free sugar, organic acid,

293 vitamin D and E intakes (plasma 25[OH]D3 or alpha-tocopherol) were characterized at 10-12 weeks gest

294 nol, alpha-tocotrienol, beta-tocopherol, and alpha-tocopherol) were identified in wheat and tritordeu

295 allic acid, propyl gallate, resveratrol, and alpha-tocopherol) were investigated for their effects on

296 C27, C29, and C33), and alcohols (phytol and alpha-tocopherol), were necessary to classify the juice

297 ES1, ES2, and ES3, the combination of 60 muM alpha-tocopherol with 5 x 10(-9) M, 10 x 10(-9) M, and 5

298 ravenous d6-alpha-tocopherol and consumed d3-alpha-tocopherol with a 600-kcal defined liquid meal (DL

299 The antioxidants l-ascorbic acid and alpha-tocopherol, with better brain uptake, deserve furt

300 Encapsulation efficiency of alpha-tocopherol within niosomes was approximately 80% a

301 In this prospective study, alpha-tocopherol, within normal reference ranges, and PA