ライフサイエンスコーパス: alpha-tocopherol

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

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

3 receiving memantine alone or memantine plus alpha tocopherol.

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

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

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

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

8 ascorbic acid, butylated hydroxylanisole and alpha-tocopherol.

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

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

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

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

13 red with the individual activities of CE and alpha-tocopherol.

14 ol was higher than the corresponding loss of alpha-tocopherol.

15 ns on all fractions were higher than that on alpha-tocopherol.

16 ty of Mito-Bodipy-TOH is on par with that of alpha-tocopherol.

17 ned ability of the mutants to bind and carry alpha-tocopherol.

18 tios, fatty acids, beta-carotene, lutein and alpha-tocopherol.

19 have also been produced as an alternative to alpha-tocopherol.

20 tructures predicted a decreased affinity for alpha-tocopherol.

21 r every 1-mg (2.3-mumol) increase in dietary alpha-tocopherol.

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

23 influence the radical scavenging activity of alpha-tocopherol.

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

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

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

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

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

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

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

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

32 s assigned to 1 of 4 intervention groups: 1) alpha-tocopherol, 2) beta-carotene, 3) both, or 4) place

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

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

35 4-87.43% of Recommended Daily Intake (RDI)), alpha-tocopherol (38.90-51.87% RDI), manganese (>100% RD

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

37 or substantially longer time (>410 min) than alpha-tocopherol (87 min).

38 It has been shown that in the presence of alpha-tocopherol, a strong antioxidant, the damage cause

39 30 +/- 11 h), and the minimum estimated (2)H-alpha-tocopherol absorbed (24% +/- 16%) did not vary bet

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

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

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

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

44 The alpha-tocopherol acetate form is often used in foods and

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

46 The conversion of alpha-tocopherol acetate to alpha-tocopherol after in vi

47 Oil-in-water emulsions containing alpha-tocopherol acetate were prepared using quillaja sa

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

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

50 0 and 37% decreased risk of incident asthma (alpha-tocopherol: adjusted odds ratio = 0.52; 95% confid

51 he conversion of alpha-tocopherol acetate to alpha-tocopherol after in vitro digestion was also consi

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

53 alpha-Tocopherol alone significantly increased the heali

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

55 ined the effects of Palm vitamin E (PVE) and alpha-tocopherol (alpha-TF) supplementations on adrenali

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

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

58 genous antioxidant system of muscle tissues, alpha-tocopherol (alpha-TOH) and ascorbic acid (AA).

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

60 A series of naphthyridinol analogs of alpha-tocopherol (alpha-TOH, right) with varying sidecha

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

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

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

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

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

66 ,2,5,7,8-pentamethyl-6-hydroxy-chromanol, an alpha-tocopherol analogue lacking the phytyl tail).

67 but borderline inverse associations between alpha tocopherol and wheezing without cold (OR 0.45, 95%

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

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

70 alpha-Tocopherol and alpha-tocopherol/selenium combinati

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 een high oleic sunflower oil containing only alpha-tocopherol and the sample containing a mixture of

95 tabolites influenced by cropping period were alpha-tocopherol and the unsaturated lipid fraction in N

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

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

98 used antioxidants in the food industry, BHT, alpha-tocopherol, and dodecyl gallate.

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

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

101 (calcium carbonate, inulin, rutin, carnosol, alpha-tocopherol, and trisodium pyrophosphate) were adde

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

103 s phospholipid formulations that incorporate alpha-tocopherol as a stabilizing agent but there are fe

104 () scavenging capacity were calculated using alpha-tocopherol as reference compound.

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

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

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

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

109 n and most active form of natural vitamin E. alpha-Tocopherol-associated protein (TAP) was found to b

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

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

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

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

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

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

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

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

118 ence of hepatobiliary cancers in the Finnish Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC)

119 not receive beta-carotene supplements in the Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC)

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

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

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

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

124 otein (TAP) was found to be one of the major alpha-tocopherol binding proteins in human serum and in

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

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

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

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

129 er inhibition of lipid oxidation compared to alpha-tocopherol, butylated hydroxytoluene and crude app

130 by a colorimetric method and carotenoids and alpha-tocopherol by a HPLC method.

131 and can be explained by the regeneration of alpha-tocopherol by CE despite the interaction effect of

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

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

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

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

136 he types of interactions exhibited by CE and alpha-tocopherol combined at different ratios were measu

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

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

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

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

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

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

143 Unlabeled alpha-tocopherol concentrations were higher in older adu

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

145 alpha-Tocopherol-containing supplement use was associate

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

147 The alpha-tocopherol content decreased in all treatments at

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

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

150 alpha-casein, beta-casein, kappa-casein and alpha-tocopherol contents, and unfavourable traits, such

151 was estimated to be at an intake of 12.8 mg alpha-tocopherol/d.

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

153 C57BL/6 mice (n = 10) were also fed alpha-tocopherol-deficient and -enriched diets for 14 d.

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

155 gher activity than the reference antioxidant alpha-tocopherol, depending on geometrical constrains in

156 he RRR-stereoisomer together with gamma- and alpha-tocopherol determination can be considered as a po

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

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

159 Maternal alpha-tocopherol dietary supplementation prevented NTD a

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

161 This was also reflected in decay of alpha-tocopherol during storage being similar in MCT and

162 25-hydroxyvitamin D2, 25-hydroxyvitamin D3, alpha-tocopherol (E), gamma-tocopherol (E), and phylloqu

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

164 inate (alpha-TOS), a synthetic derivative of alpha-tocopherol, enhanced the cells' sensitivity to dox

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

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

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

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

169 relative increase in omega-3 fatty acids and alpha-tocopherol, from winter to summer, was greater in

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

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

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

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

174 alpha-tocopherol, gamma-tocopherol, delta-tocopherol, be

175 0.92 to 5.39; adjusted P = .03) less in the alpha tocopherol group compared with the placebo group.

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

177 Caregiver time increased least in the alpha tocopherol group.

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

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

180 olic extracts of Centella asiatica (CE), and alpha-tocopherol have been studied.

181 Antioxidants, especially vitamin E (alpha-tocopherol), have been conjugated to lipophilic ca

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

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

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

185 hyl gallate (IC50=38.0 muM, log P=-0.23) and alpha-tocopherol (IC50=105.3 muM, log P=0.70).

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

187 The presence of up to 20 mol% alpha-tocopherol in 1-palmitoyl-2-oleoyl-phosphocholine

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

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

190 of linoleic acid much more efficiently than alpha-tocopherol in a two-phase peroxidation system cont

191 an order of magnitude more efficiently than alpha-tocopherol in a water/chlorobenzene two-phase syst

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

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

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

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

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

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

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

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

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

201 Inadequate levels of alpha-tocopherol interfere with cellular function and pr

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

203 As such, alpha-tocopherol is necessary for numerous physiological

204 that of all members of the vitamin E family, alpha-tocopherol is selectively enriched in human tissue

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

206 The major function of alpha-tocopherol is thought to be that of a lipid-solubl

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

208 ol levels on meat colour stability, although alpha-tocopherol levels (>4mugg(-1) meat) had a protecti

209 alpha-Tocopherol levels increased progressively at incre

210 ll, packaging type was more influential than alpha-tocopherol levels on meat colour stability, althou

211 ulated throughout the body to maintain blood alpha-tocopherol levels.

212 element, constructed, respectively, from an alpha-tocopherol-like chromanol moiety, a BODIPY fluorop

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

214 alpha-Tocopherol-loaded niosome was developed using modi

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

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

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

218 Thus, we have demonstrated that topical 5% alpha tocopherol may actually promote carcinogenesis whe

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

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

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

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

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

224 The effect of 7 mol% alpha-tocopherol on leakage was compared with phospholip

225 t but there are few studies of the effect of alpha-tocopherol on phospholipid structure and bilayer p

226 nvestigate the effects of iron chelators and alpha-tocopherol on this process.

227 Of all synergistic combinations of CE and alpha-tocopherol, only fraction 2/3 showed the synergist

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

229 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 =

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

231 ct, LD showed lower intramuscular fat (IMF), alpha-tocopherol, phenolic compounds, lipid oxidation an

232 , alpha-tocopherol succinate (alpha-TOS) and alpha-tocopherol phosphate (alpha-TOP), as potential ind

233 The extreme hydrophobicity of alpha-tocopherol poses a serious thermodynamic barrier f

234 at flour ranged from 0.10 to 0.69 mug/g, and alpha-tocopherol ranged from 0.12 to 0.83 mug/g.

235 hat pentoxifylline (PTX) in combination with alpha-tocopherol reduced manifestations of RIHD in rat m

236 d of the frying processes the percentages of alpha-tocopherol reduction were TBHQ-SOv (4.90%), TBHQ-S

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

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

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

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

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

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

243 The alpha-tocopherol/selenium combination significantly enha

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

245 BHT and alpha-tocopherol showed lower antioxidant activity than

246 , urinary alpha-CEHC is a valid biomarker of alpha-tocopherol status that can be used to set a value

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

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

249 hydrophobic anionic analogues of vitamin E, alpha-tocopherol succinate (alpha-TOS) and alpha-tocophe

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

251 In healthy control subjects, the effect of alpha-tocopherol supplementation on the production of in

252 enetic background may affect the response to alpha-tocopherol supplementation, but this has rarely be

253 pheral blood mononuclear cells (PBMCs) after alpha-tocopherol supplementation.

254 (2+) in solution, when supplemented with the alpha-tocopherol surrogate, PMHC (2,2,5,7,8-pentamethyl-

255 The presence of alpha-tocopherol tends to reduce the angle of tilt of th

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

257 have demonstrated the anticancer activity of alpha-tocopherol, the main and most active form of natur

258 ol moiety ensures reactivity akin to that of alpha-tocopherol, the most potent naturally occurring li

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

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

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

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

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

264 The ability of alpha-tocopherol to affect IL-6 production was influence

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

266 addition of calcium carbonate to the diet or alpha-tocopherol to cured meat may reduce colorectal can

267 involved complex interactions between CE and alpha-tocopherol to exhibit different degrees of interac

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

269 The relative contribution of PTX and alpha-tocopherol to these beneficial effects are not kno

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

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

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

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

274 The alpha-tocopherol transfer protein (alpha-TTP) is a liver

275 dedicated transport mechanisms involving the alpha-tocopherol transfer protein (alphaTTP).

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

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

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

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

280 alpha-TTP) is a liver protein that transfers alpha-tocopherol (vitamin E) to very-low-density lipopro

281 recycling of the lipid-soluble antioxidant, alpha-tocopherol (vitamin E).

282 cture in men for each 1-SD decrease in serum alpha-tocopherol was 1.58 (95% CI: 1.13, 2.22) and for a

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

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

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

286 alpha-Tocopherol was the most abundant tocopherol accoun

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

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

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

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

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

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

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

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

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

296 ipid antioxidant) and the redox recycling of alpha-tocopherol, whereas tocopherol production is not a

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

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

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