ライフサイエンスコーパス: diet supplement

1 rmination of the actual forms of selenium in diet supplements.

2 successfully applied to water, black tea and diet supplements.

3 Hens were fed diets supplemented (2.8% wt:wt) with corn oil (CO; n-6)

4 hesize that more vitamin D exposure (through diet, supplements, and sunlight) and higher intake of ca

5 .12, which is recently being widely used for diet supplements, beverages, or drug medicines due to it

6 vel of evidence that a hypercaloric fructose diet (supplemented by pure fructose) increases liver fat

7 ced in Sprague-Dawley rats by a high adenine diet supplemented by high P and Ca for 28 days that led

8 anaphylaxis after eating a jelly product for diet supplement containing erythritol as a major compone

9 wk normal (n = 10) or HC diet (n = 8), or HC diet supplemented daily with antioxidant vitamins C (1 g

10 7) or high cholesterol (HC) (n = 7) diet, HC diet supplemented daily with antioxidant vitamins E (100

11 or 12 weeks pigs were fed a normal, HC or HC diet supplemented daily with antioxidants (HC + AO, 100

12 In the SHRSP fed a normal NaCl diet, supplementing dietary K+ with KCl exacerbated hype

13 6), obese (OB, n = 7) or obese fed a complex diet supplement for 12 weeks (OBD, n = 6).

14 Obese mares fed the complex diet supplement had better insulin sensivity, greater ce

15 that Caenorhabditis elegans fed a bacterial diet supplemented high glucose at day 5 of adulthood (HG

16 We need a better understanding of diet and diet supplement intake during pregnancy and lactation an

17 d a standard diet, a high fat diet, or these diets supplemented isocalorically with nervonic acid.

18 bese (OB, n = 7, BCS 7.7 +/- 0.2), and Obese Diet Supplemented (OBD, n = 7, BCS 7.7 +/- 0.2), and fed

19 Total intakes (diet+supplements) of vitamin C and vitamin E, but not di

20 ere treated with 0.5% alpha-lipoic acid as a diet supplement or with hydroxyethyl starch deferoxamine

21 h fat/high sucrose (HF/HS) diet or a regular diet supplemented or not with indomethacin (+/-INDO) for

22 the higher intake of calcium is attained by diet, supplements, or both.

23 om a wide array of matrices, including food, diet supplements, tissues, and plasma.

24 tabolic rate compared to vehicle-treated and diet-supplemented uremic mice, which lost both lean body

25 ng (home age, water source, filter use), and diet (supplement use; 24-h calorie, fat, protein, micron

26 ed a nutritionally complete amino acid-based diet supplemented with (+)-catechin (0-8 mmol/kg diet) o

27 A diet supplemented with (R)-lipoic acid, a mitochondrial

28 nd then fed an essentially sphingolipid-free diet supplemented with 0 to 0.1% (w/w) sphingomyelin (SM

29 ts received normal powdered diet or powdered diet supplemented with 0.02% or 0.1% Zx soon after induc

30 parenchymal cells of Fischer 344 rats fed a diet supplemented with 0.03% N-2-acetylaminofluorene (AA

31 WT) and TRPC5 knock-out (KO) mice were fed a diet supplemented with 0.5% cholic acid (CA) for 21 days

32 (WT) littermates were fed standard chow or a diet supplemented with 0.5% cholic acid for 2 weeks.

33 d by feeding the animals a choline-deficient diet supplemented with 0.5% ethionine for 24 hrs and the

34 8 weeks of age, mdx mice were fed a standard diet supplemented with 1% soybean oil alone or in combin

35 et with 0.5% K(+) (HFD; n = 7) to a high-fat diet supplemented with 1.5% K(+) (HFD+K; n = 6).

36 ) on either a low-fat, high-fat, or high-fat diet supplemented with 1.5X branched chain amino acids (

37 de response of naive B cells from mice fed a diet supplemented with 1000 ppm of celecoxib.

38 ed a control diet with those that were fed a diet supplemented with 2000 ppm I3C.

39 balanced diet (control) or the same balanced diet supplemented with 3 g fructose . kg(-1) . d(-1) and

40 Pemt(-/-) mice were fed a control diet, or a diet supplemented with 3 g/kg of DHA, from gestational d

41 ere fed regular chow (control) or a high-fat diet supplemented with 30% d-fructose in drinking water

42 of 16 birds (8 male, 8 female) were fed a C- diet supplemented with 35 mg 3R,3'R-zeaxanthin for 1, 3,

43 (C- group; n = 8), or a carotenoid-deficient diet supplemented with 35 mg 3R,3'R-zeaxanthin per kilog

44 ntrol (vehicle-supplemented) diet or control diet supplemented with 4-HPR beginning 1 day after carci

45 for aging and half of each group received a diet supplemented with 40-ppm (w/w) melatonin for 9.3 we

46 zinc supplement for one 90-d period, and the diet supplemented with 50 mg Zn/d for another 90-d perio

47 ow-flavonol diet and for 2 weeks on the same diet supplemented with 76-110 mg of flavonols (mostly qu

48 In addition, an artificial diet supplemented with 9,10-KODA arrested fall armyworm

49 a an action at the hypothalamic level, and a diet supplemented with a low dose of the element is capa

50 Remarkably, females on a high-sugar diet supplemented with a separate source of water have m

51 mg per rat per day) or were fed the purified diet supplemented with a source of retinol (100 units of

52 In this study, we fed IRP2(-/-) mice a diet supplemented with a stable nitroxide, Tempol, and s

53 mated with wild-type females that received a diet supplemented with alpha-tocopherol or a control die

54 Feeding these mice for 5 months with a diet supplemented with antioxidants (vitamins C and E, s

55 d not increase in monkeys fed an atherogenic diet supplemented with B vitamins (3.8+/-0.3 micromol/L)

56 and efficacy assessment of a hypocaloric HP-diet supplemented with beta-cryptoxanthin in NAFLD.

57 A hypocaloric HP-diet supplemented with beta-cryptoxanthin safely and eff

58 Mice fed a chow diet supplemented with bile acid showed increased hepati

59 is needed to confirm the adequacy of a vegan diet supplemented with calcium and vitamin D with respec

60 mice received either regular chow or a chow diet supplemented with canola oil for 6 months.

61 Feeding a diet supplemented with carbonyl iron resulted in a more

62 re significantly reduced when the rats fed a diet supplemented with cholestin.

63 Here, we demonstrate that mice fed a diet supplemented with cholic acid have reduced fertilit

64 ale and female rats whose mothers were fed a diet supplemented with choline (SUP; 5 mg/kg choline chl

65 /6 mice received a either standard diet or a diet supplemented with CoQ10 (200 mg/kg/day) for five we

66 n litters from dams fed the folate-deficient diet supplemented with deoxyuridine.

67 female Sprague-Dawley rates were fed AIN-76A diet supplemented with DHEA alone (800 or 400 mg/kg diet

68 x other experimental groups (fed atherogenic diet supplemented with different doses of P. nigrum, P.

69 serotonin of mice fed for 9 wk on a high-fat diet supplemented with different sources of fiber (rye b

70 nduced with caerulein or a choline-deficient diet supplemented with DL-ethionine) and control mice.

71 We have previously shown that a diet supplemented with dried plum powder (DP) prevented

72 alpha-Syn-transgenic mice raised on a diet supplemented with eicosanoyl-5-hydroxytryptamide, a

73 high-cholesterol diet, or a high-cholesterol diet supplemented with either carvedilol or propranolol.

74 type and Pparalpha(-/-) null mice a high fat diet supplemented with either fenofibrate or Wy14643, a

75 or in cynomolgus macaques fed an atherogenic diet supplemented with either fish oil (1.6 g n-3 fatty

76 compared the lipid effects of a natural food diet supplemented with either MCTs, palm oil, or high ol

77 In this study, mice were fed a diet supplemented with either monounsaturated fatty acid

78 on tetrachloride (CCl(4)), choline-deficient diet supplemented with ethionine, or 3,5-diethoxycarbony

79 (95% CI, 0.43 to 0.85) for the Mediterranean diet supplemented with EVOO and 0.82 (CI, 0.61 to 1.10)

80 es of diabetes occurred in the Mediterranean diet supplemented with EVOO, Mediterranean diet suppleme

81 ticipants were randomized to a Mediterranean diet supplemented with extra virgin olive oil, a Mediter

82 tatus to receive 1 of 3 diets: Mediterranean diet supplemented with extra-virgin olive oil (EVOO), Me

83 at high cardiovascular risk, a Mediterranean diet supplemented with extra-virgin olive oil or nuts re

84 ment, to one of three diets: a Mediterranean diet supplemented with extra-virgin olive oil, a Mediter

85 omly assigned to 1 of 3 diets: Mediterranean diet supplemented with extravirgin olive oil, Mediterran

86 ctomy) rats maintained on a 1.02% phosphorus diet supplemented with ferric salts (formulated to 0.95%

87 diet (59.2% kcal) alone or an isocaloric HF diet supplemented with fish oil (HF-FO) for 12 weeks.

88 Mice fed the iso-caloric diet supplemented with fish oil exhibited significantly

89 Feeding rats a diet supplemented with fish oil suppressed hepatic SREBP

90 We studied the effects of a saturated fat diet supplemented with fish oil, trans10,cis12 conjugate

91 and 8 weeks of consuming a control diet or a diet supplemented with fish oil.

92 months for 2 years after starting a high-fat diet supplemented with fructose.

93 Burn-injury rats received the IMPACT diet supplemented with glutamine, arginine, fish oil, an

94 Mice fed a control diet supplemented with homocysteine had a 3-fold elevati

95 Whether a very low-protein diet supplemented with ketoanalogues (sVLPD), compared w

96 cholesterol diet (Chol), or high-cholesterol diet supplemented with L-arginine (Arg).

97 a low-fat, high-complex carbohydrate (LFHCC) diet supplemented with long-chain n-3 polyunsaturated fa

98 on a starch (ST) diet, sucrose (SU) diet, or diet supplemented with metformin (SU + MET).

99 Compared with mice receiving the high-fat diet supplemented with methionine and choline (controls)

100 r findings indicate that in mice, a maternal diet supplemented with methyl donors enhanced the severi

101 Finally, feeding a modified lithogenic diet supplemented with milk fat, instead of cocoa butter

102 n diet supplemented with EVOO, Mediterranean diet supplemented with mixed nuts, and control diet grou

103 with extra-virgin olive oil, a Mediterranean diet supplemented with mixed nuts, or a control diet (ad

104 ed with extravirgin olive oil, Mediterranean diet supplemented with mixed nuts, or advice to follow a

105 e oil (TMD+VOO) or traditional Mediterranean diet supplemented with nuts (TMD+Nuts)] in equal proport

106 .82 (CI, 0.61 to 1.10) for the Mediterranean diet supplemented with nuts compared with the control di

107 extra-virgin olive oil (EVOO), Mediterranean diet supplemented with nuts, or a control diet (advice o

108 with extra virgin olive oil, a Mediterranean diet supplemented with nuts, or a control diet.

109 ion of O. strigicollis fed on the artificial diet supplemented with Pantoea dispersa OS1.

110 Animals were fed a Western diet supplemented with pea fiber.

111 saturated fatty acids (1.2 g/d); or an LFHCC diet supplemented with placebo for 12 wk (control).

112 ed a fixed amount of a normal calcium (1.2%) diet supplemented with potassium citrate or potassium ch

113 The PD flies were fed diet supplemented with resveratrol (15, 30, and 60 mg/kg

114 Rats were fed an obesogenic diet supplemented with resveratrol (30mg/kg/day) or not

115 pe mice were fed a high-fat diet or high-fat diet supplemented with resveratrol for 13 weeks.

116 gene were maintained on a retinol-deficient diet supplemented with retinoic acid (-A) or on a contro

117 In vivo, a diet supplemented with SJW was found to activate intesti

118 Indeed, we show that feeding mice a diet supplemented with sodium selenite results in an MR-

119 criptions and emphasized a low-saturated fat diet supplemented with specially manufactured baked good

120 ceptor (LXR) ligands, APP23 mice were fed HF diet supplemented with synthetic LXR agonist T0901317 (T

121 When mice were fed a low-fat diet supplemented with taurocholic acid, but not with gl

122 In albino Abca4(-/-) mice receiving a diet supplemented with the antioxidant vitamin E, higher

123 epatocytes from rats fed a low-fat diet or a diet supplemented with the corresponding fat for 21 days

124 AhR ligand-free diet, or an AhR ligand-free diet supplemented with the dietary AhR ligand indole-3-c

125 Mice were fed a control diet or a diet supplemented with the FXR agonist PX20606, with or

126 st, cancer-susceptible Trp53(-/-) mice fed a diet supplemented with the high-anthocyanin tomatoes sho

127 of mice fed a high cholesterol diet or chow diet supplemented with the HMGCR inhibitor lovastatin.

128 re intercrosses were randomly allocated to a diet supplemented with the selective COX-2 inhibitor nim

129 Obese mice fed a diet supplemented with the SIRT1-activating molecule res

130 og retinol equivalents (RE)/g diet] or a CON diet supplemented with the synthetic retinoid N-(4-hydro

131 ted with metabolic syndrome in response to a diet supplemented with the trans-10, cis-12 isomer of co

132 e died within 1 week of weaning unless fed a diet supplemented with thyroid powder.

133 o, we fed L-FABP(-/-) and WT mice a high-fat diet supplemented with trans-fatty acids and fructose (T

134 ted, monounsaturated fatty acids or standard diet supplemented with tryptophan (0.4 g/(kg.d), 8 weeks

135 led-packed meat obtained from lambs fed on a diet supplemented with two different doses of a rosemary

136 lanemic phenotype was rapidly triggered by a diet supplemented with ursodeoxycholic acid.

137 tervention groups [traditional Mediterranean diet supplemented with virgin olive oil (TMD+VOO) or tra

138 By contrast, mice receiving the diet supplemented with Vitamin E at a later age did not

139 atherogenic diet (control) or an atherogenic diet supplemented with vitamin E, vitamins E and C, vita

140 d C (1000 mg; HC+vitamins, n = 5), or normal diet supplemented with vitamins (N+vitamins, n = 5).

141 ich recapitulate features of PXE, were fed a diet supplemented with warfarin and vitamin K1.

142 Gmm(Apo) larvae when their mothers are fed a diet supplemented with Wigglesworthia cell extracts.

143 mor onset were observed when mice consumed a diet supplemented with wine solids containing <0.22 mmol

144 However, groups fed a cholesterol-enriched diet supplemented with yoghurt containing B. pseudocaten

145 A diet supplemented with Zetia (ezetimibe) and lovastatin

146 S trial (n = 294) that a Mediterranean (MED) diet, supplemented with polyphenol-rich Mankai duckweed,

147 ed amount of a normal calcium and phosphorus diet, supplemented with potassium chloride (as control),

148 -/-)) mice were fed regular chow or high-fat diets supplemented with 0.075% or 1.25% cholesterol duri

149 ontrol; T100, T200, and T300 groups received diets supplemented with 100, 200, and 300 mg/kg of GML,

150 profiles in the skeletal muscle of pigs fed diets supplemented with 3.0% soybean, canola, or fish oi

151 Female Balb/c mice were fed diets supplemented with 5wt% SSO or a physical mixture o

152 reduce gilthead seabream allergenicity using diets supplemented with a calcium chelator.

153 ths of age and continuing for 8 months, with diets supplemented with a fruit or vegetable extract ide

154 Feeding with diets supplemented with arginine, glutamine, and arginin

155 tose randomly received standard diets or the diets supplemented with ascorbic acid and alpha-tocopher

156 rcholesterolemic men were fed 3 natural-food diets supplemented with behenate oil, palm oil, or high-

157 Diets supplemented with biologic oils (no supplementatio

158 nSOD and mtMnSOD) was observed in shrimp fed diets supplemented with BV-CSNP (0.1, 0.2, and 0.3 mg/kg

159 3 groups (n=8) and fed with cholesterol-rich diets supplemented with cellulose (CC, control), agave D

160 e with a truncated APC gene product were fed diets supplemented with ceramide, sphingomyelin, glucosy

161 the livers of BALB/c mice that had been fed diets supplemented with clofibrate or gemfibrozil.

162 were also monitored in the livers of mice on diets supplemented with eicosapentaenoic acid (C20:5 ome

163 Using isocaloric diets supplemented with either CaCO(3), Ca(3)(PO(4))(2)

164 verity is significantly enhanced in mice fed diets supplemented with either choline or the gut microb

165 The present paper reports that diets supplemented with either spinach, strawberries or

166 diterranea (PREDIMED), testing Mediterranean diets supplemented with extra virgin olive oil or nuts v

167 Antioxidants and diets supplemented with foods high in oxygen radical abs

168 This study reveals that diets supplemented with Ginkgo biloba extract have notab

169 igate, HFE(-/-) mice were fed iron-deficient diets supplemented with increasing amounts of iron, with

170 Diets supplemented with low-dose aspirin reduced circula

171 placebo-treated mice, soy meal diet (but not diets supplemented with low-dose or high-dose isoflavone

172 y support including high-protein and low-fat diets supplemented with medium-chain triglycerides, ther

173 Aphids feeding on artificial diets supplemented with NAM impaired stylet movement cau

174 reptozotocin-induced diabetic rats receiving diets supplemented with or without alpha-lipoic acid (40

175 Effects of diets supplemented with or without Moringa oleifera leaf

176 Here, we investigated if diets supplemented with purified PAC modulated pulmonary

177 g no added lipid (n = 5 cows); and treatment diets supplemented with SO (n = 5 cows; unrefined soybea

178 Feeding diets supplemented with triolein or tripalmitolein to th

179 When compared with control diets, diets supplemented with walnuts resulted in a significan

180 ned to one of four diets: Control (C); and C diets supplemented with: 1.2% Nannochloropsis sp. oil (O

181 Energy-balanced diets, supplemented with tomato paste, tomato powder, or