ライフサイエンスコーパス: atherogenic diet

1 tery and abdominal aorta of 7 rabbits fed an atherogenic diet.

2 Ac) or (Sc) peptide before initiation of the atherogenic diet.

3 een the 3 groups on either a chow diet or an atherogenic diet.

4 s on a chow diet, and sixfold in mice fed an atherogenic diet.

5 ty lipoprotein receptor Ldlr(-/-) mice on an atherogenic diet.

6 esterase-null mice fed either control or an atherogenic diet.

7 ment in T-cell-deficient mice fed a high fat atherogenic diet.

8 ercholesterolemia induced by feeding them an atherogenic diet.

9 wine by 6 months' feeding of a hypercaloric, atherogenic diet.

10 etes, obesity, a sedentary lifestyle, and an atherogenic diet.

11 culating proatherogenic cells in mice fed an atherogenic diet.

12 mice fed either a standard rodent chow or an atherogenic diet.

13 cteristics of autoimmunity in response to an atherogenic diet.

14 G-LDL or in isolated aortae from mice fed an atherogenic diet.

15 h muscle cell content after 8 or 16 weeks of atherogenic diet.

16 e non-Tg littermates on B6 background fed an atherogenic diet.

17 n in EC-specific STAT3 knock-out mice on the atherogenic diet.

18 loss, increased physical activity, and anti-atherogenic diet.

19 plaque collagenases) after 5 and 10 weeks of atherogenic diet.

20 ontransgenic littermate controls were fed an atherogenic diet.

21 half of them deficient in TIMP-1, was fed an atherogenic diet.

22 tic lesions in LDL receptor-null mice fed an atherogenic diet.

23 tery and abdominal aorta of 7 rabbits fed an atherogenic diet.

24 001) in angiotensin II-treated animals on an atherogenic diet.

25 animals receiving either standard chow or an atherogenic diet.

26 ls were placed on either standard chow or an atherogenic diet.

27 rmation in LDL receptor-deficient mice on an atherogenic diet.

28 by C57BL/6 mice fed the bile acid-containing atherogenic diet.

29 e for 24 to 36 hours before the onset of the atherogenic diet.

30 ipids and lipid deposition in animals fed on atherogenic diets.

31 After 16 weeks of atherogenic diet (0.1% cholesterol, 10% calories from pa

32 eroma in 33 rabbits by balloon injury and an atherogenic diet (0.3% cholesterol and 4.7% coconut oil)

33 male heterozygous apoE-deficient mice fed an atherogenic diet (2 x 10(3) +/- 2.5 x 10(3) microm2 in h

34 0.5% kcal from fat) (fructose group, n = 9), atherogenic diet (20% kcal from fructose and 46% kcal fr

35 rger than C57BL/6 wild type mice when fed an atherogenic diet (37,123 +/- 3485 microm2 versus 16, 688

36 We examined the effect that an atherogenic diet (AD) high in saturated fatty acids and

37 1 transgenic mice (AGER1-tg) subjected to an atherogenic diet and arterial wire-injury.

38 atherosclerosis was induced in 18 rabbits by atherogenic diet and double balloon endothelial denudati

39 After 19 weeks on the atherogenic diet, aortae were collected for quantitative

40 ts and the animals randomized to continue an atherogenic diet (atherosclerosis progression) or resume

41 C57BL/6J and IL-6 -/- mice fed an atherogenic diet both demonstrated markedly reduced plas

42 decreased in B6 mice upon challenge with the atherogenic diet but increased in C3H, indicating that p

43 -cholesterol levels on both the chow and the atherogenic diets, but this locus did not contribute to

44 ression of vascular damage in response to an atherogenic diet by quantifying the in vivo accumulation

45 nd tempers chronic inflammatory responses to atherogenic diet by restraining proinflammatory signalin

46 After 13 weeks on an atherogenic diet, C57BL/6 mice reconstituted with apoE n

47 Consistently, high cholesterol atherogenic diet-challenged Sort1 knock-out mice showed

48 ApoE-/- LCAT-/- mice fed the atherogenic diet, compared with apoE-/- mice, had higher

49 To do this, DKO mice were first fed an atherogenic diet containing 0.1% cholesterol, 10% fat fo

50 n rats as well as rabbits, fed on normal and atherogenic diet containing 10% of SL1 and SL2 (experime

51 Mice were fed an atherogenic diet containing 15% fat, 1.25% cholesterol,

52 Apo E-KO mice were fed with an atherogenic diet containing 2% (w/w) PS-DHA for 7 weeks.

53 CYP7A1 repression caused by feeding mice an atherogenic diet containing bile acids.

54 component of aortic aneurysms induced by an atherogenic diet containing cholate in mice deficient in

55 Rabbits were fed an atherogenic diet (control) or an atherogenic diet supple

56 After 12 weeks on an atherogenic diet, cystatin C deficiency yielded signific

57 ild-type and heterozygous counterparts on an atherogenic diet despite having lower levels of apolipop

58 Ossabaw pigs fed a modified atherogenic diet develop severe metabolic syndrome and a

59 CSE-knockout mice fed with atherogenic diet developed early fatty streak lesions in

60 therogenic diet group, n = 13), and modified atherogenic diet (different source of fat and higher pro

61 After 22 weeks on the atherogenic diet (early fibrous plaque stage), the diffe

62 iac, hepatic and renal antioxidant status of atherogenic diet fed hamsters.

63 ces or prevents vascular disease, we treated atherogenic diet-fed ldlr(-/-) mice with recombinant ost

64 nd fatty acid metabolism in high cholesterol atherogenic diet-fed mice.

65 e New Zealand White rabbits that were fed an atherogenic diet for 1 week before injury and until euth

66 LDLr-/- mice were generated and consumed an atherogenic diet for 12 or 26 weeks.

67 oprotein E-deficient (apoE(-/-)) mice fed an atherogenic diet for 12 weeks.

68 ide transfer protein gene, were placed on an atherogenic diet for 16 weeks, then either made diabetic

69 All mice then were fed an atherogenic diet for 16 weeks.

70 Reversa mice were fed an atherogenic diet for 16 weeks.

71 IL-8RH (the homologue of CXCR-2), and fed an atherogenic diet for 16 wk.

72 crossed into the apoE0 background and fed an atherogenic diet for 16-25 weeks.

73 Thirty-two cynomolgus monkeys were fed an atherogenic diet for 2 years (progression phase) and the

74 Feeding a bile acid-containing atherogenic diet for 3 weeks to C57BL/6 mice led to a 70

75 variectomized cynomolgus monkeys were fed an atherogenic diet for 30 months; 25 received 175 microg/d

76 variectomized cynomolgus monkeys were fed an atherogenic diet for 34 months.

77 Rabbits consumed an atherogenic diet for 4 months to produce atheroma, follo

78 Six cynomolgus monkeys were fed a high-fat atherogenic diet for 44 months and then a low-fat regres

79 Cynomolgus monkeys (n=28) were fed an atherogenic diet for 47+/-10 (mean+/-SE) months.

80 Both groups consumed an atherogenic diet for 5 (n=8) or 10 weeks (n=9).

81 ensity lipoprotein receptor that consumed an atherogenic diet for 8 and 16 weeks.

82 57BL/6 strain for 7 generations, were fed an atherogenic diet for 8 weeks.

83 The atherogenic diet group had metabolic syndrome and abnorm

84 2% cholesterol and 0.7% cholate by weight) (atherogenic diet group, n = 13), and modified atherogeni

85 Ovariectomized C57BL/6 mice fed an atherogenic diet had increased hepatic levels of active

86 ments demonstrated that B6Tg2576 mice fed an atherogenic diet had more spatial learning impairment th

87 mice were fed with either a high-cholesterol atherogenic diet (HCD) or matching normal diet (ND), res

88 in rabbits, or the rabbits were placed on an atherogenic diet, hepatic mRNA for apoJ was increased by

89 However, when maintained on an atherogenic diet high in fat and cholesterol, the HDL is

90 An atherogenic diet, high in fat and cholesterol, exacerbat

91 Pedigreed baboons (n = 251) were fed 2 atherogenic diets, high in fat and cholesterol, that dif

92 oprotein E-deficient (ApoE(-/-)) mice fed an atherogenic diet highlighted DC efficacy in effector T-c

93 ed lesion development in apoE+/- mice fed an atherogenic diet, indicating that the adverse effect is

94 Atherogenic diet induced a significant (P<0.001) increas

95 An atherogenic diet induced aortic atherosclerosis and exac

96 ssess an antioxidant protective role against atherogenic diet induced oxidative stress in cardiac, he

97 When fed an atherogenic diet, MAKO/LDLRKO mice displayed exacerbated

98 However, with the atherogenic diet, male transgenic mice exhibited signifi

99 12 weeks of being fed a cholesterol-enriched atherogenic diet, mice injected with GdCl(3) exhibited 5

100 partly contribute to the inhibitory role of atherogenic diet on lung tumorigenesis.

101 ificantly inhibited the alteration effect of atherogenic diet on the lipid profile and antioxidant en

102 ressing lipoprotein(a), even in mice not fed atherogenic diets or with overt atherosclerosis.

103 micromol/L in monkeys fed an unsupplemented atherogenic diet (P<0.01) but did not increase in monkey

104 5.2+/-1.2% in those animals maintained on an atherogenic diet (P:<0.0001).

105 After 2 months under a 1.25% cholesterol atherogenic diet, Pfn(+/-)Ldlr(-/-) (PfnHet) exhibited a

106 On an atherogenic diet, PON activity decreased by 52%, and apo

107 oteins isolated from transgenic mice fed the atherogenic diet promoted cholesterol efflux from choles

108 eficiency in LDLr-/- and apoE-/- mice fed an atherogenic diet resulted in increased aortic cholestero

109 However, when fed an atherogenic diet rich in fat, cholesterol, and cholate,

110 ant administration of allosamidin and fed an atherogenic diet showed aggravated atherosclerotic lesio

111 The atherogenic diet stimulated leukocyte rolling in the mes

112 The atherogenic diet stimulated leukocyte rolling in the mes

113 0.01) but did not increase in monkeys fed an atherogenic diet supplemented with B vitamins (3.8+/-0.3

114 ntrol and six other experimental groups (fed atherogenic diet supplemented with different doses of P.

115 netic behavior in cynomolgus macaques fed an atherogenic diet supplemented with either fish oil (1.6

116 were fed an atherogenic diet (control) or an atherogenic diet supplemented with vitamin E, vitamins E

117 Using an atherogenic diet that produces both hyperhomocysteinemia

118 On the pro-atherogenic diet the mean aortic lesion area was reduced

119 After 8 weeks on the atherogenic diet, the fatty streaks formed in the aortic

120 After 8 wk on atherogenic diet, the LDLR-/- P/E-/- mice developed fatt

121 On an atherogenic diet, there was a trend toward greater ather

122 L/6J backcross progeny fed either chow or an atherogenic diet to detect QTLs that regulate high-densi

123 /+) littermates, followed by feeding them an atherogenic diet to produce atherosclerosis.

124 les in the liver of B6By and B6J mice fed an atherogenic diet using a DNA microarray.

125 F and IPS greatly reduced in animals fed the atherogenic diet versus chow-fed controls.

126 ein null mutation (LDLR-/-) maintained on an atherogenic diet was assessed.

127 The carotid artery of minipigs fed an atherogenic diet was injured by repetitive balloon hyper

128 This differential response to the atherogenic diet was unanticipated, since chow-fed LDLr(

129 n observed in the arteries of rabbits fed on atherogenic diets was significantly reduced when structu

130 ce, which only develop atherosclerosis on an atherogenic diet, were evaluated.

131 lammatory when the mice are maintained on an atherogenic diet, when they are injected with LDL-derive

132 streptozotocin-induced diabetes consuming an atherogenic diet, without changes in gross glomerular mo