ライフサイエンスコーパス: adrenalectomize

1 Adrenalectomized 7B2 null animals survived past the usua

2 Interestingly, adrenalectomized 7B2 nulls also developed unexpectedly s

3 The adrenalectomized A-ZIP/F-1 mice displayed a marked impro

4 Adrenalectomized, acutely diabetic mice given a physiolo

5 nRNA) expression in rats that were intact or adrenalectomized (ADX) and replaced with corticosterone

6 le was administered daily to gonadectomized, adrenalectomized (ADX) male (experiment 1) and female (e

7 We found that adrenalectomized (ADX) mice of all three strains had inc

8 , ENaC expression and activity are robust in adrenalectomized (Adx) mice.

9 nduced c-fos expression was characterized in adrenalectomized (ADX) or adrenalectomized and corticost

10 ases in duration of inhibitory action in the adrenalectomized (adx) rat after intravenous injection,

11 e effects of two adrenal steroid agonists on adrenalectomized (ADX) rats' performance on the Y-maze.

12 s characterized in adrenalectomized (ADX) or adrenalectomized and corticosterone replaced (ADX/B) mal

13 Rats implanted with telemetry probes were adrenalectomized and given low-corticosterone pellets or

14 Rats were adrenalectomized and given normal saline for 14 d, after

15 is of thrombotic microangiopathy, SHRSP were adrenalectomized and infused with vehicle, Ang II, or AL

16 ne expression in male C57BL/6 mice that were adrenalectomized and replaced with defined levels of cor

17 stimulation, and carbachol were compared in adrenalectomized and sham-operated halothane-anesthetize

18 hypothalamo-pituitary-adrenal axis, as both adrenalectomized and sham-operated mice exhibited simila

19 n IL-1beta protein 2 h after IS, but only in adrenalectomized (and basal corticosterone replaced) sub

20 eceded the onset of anorexia, and dehydrated adrenalectomized animals (which also develop anorexia) h

21 Most adrenalectomized animals bearing transplanted cells surv

22 type I adrenal steroid receptor agonist) to adrenalectomized animals did not have a significant effe

23 hydration because PVH CRH mRNA in dehydrated adrenalectomized animals is unchanged from euhydrated ad

24 62 (a specific type II receptor agonist), to adrenalectomized animals produced changes in leukocyte d

25 Expression changes were measured in adrenalectomized animals that underwent food restriction

26 Supplementing adrenalectomized animals with corticosterone did not rei

27 , in the presence of constant B (B-replaced, adrenalectomized animals), cold stress led to increased

28 This effect of stress was not observed in adrenalectomized animals, and was reproduced in nonstres

29 omized (with saline supplementation) or sham adrenalectomized at 2 months of age.

30 Mice adrenalectomized before social defeat showed enhanced be

31 stered intraperitoneally to sham-operated or adrenalectomized/castrated (ADX/CX) male rats dose-depen

32 tomized animals is unchanged from euhydrated adrenalectomized controls.

33 ed decrements in PPG mRNA were attenuated in adrenalectomized-corticosterone-replaced rats, suggestin

34 ACTH secretion to its expected high level in adrenalectomized CRH KO mice.

35 hetic nervous system, we compared unilateral adrenalectomized, desynchronized rats that had undergone

36 atory hormones in overnight-fasted conscious adrenalectomized dogs that were given somatostatin and i

37 the formation of partner preferences, while adrenalectomized females form preferences more quickly t

38 alcohol also blocked the proestrous surge in adrenalectomized females.

39 The enBACs were transplanted into adrenalectomized, immunodeficient, and immunocompetent r

40 onitoring explants taken from rats that were adrenalectomized, intact, or treated with corticosterone

41 l corticosteroid receptor gene expression in adrenalectomized male C57BL/6 mice with fixed glucocorti

42 le was administered daily to gonadectomized, adrenalectomized male Long-Evans rats.

43 binding in the brain and pituitary of adult adrenalectomized male rats.

44 When adrenalectomized mice were transplanted with denervated

45 ne dependent, as evidenced by its absence in adrenalectomized mice, in which plasma corticosterone le

46 and spleen atrophy, which was attenuated in adrenalectomized mice.

47 Exploiting an adrenalectomized mouse model with depleted endogenous gl

48 To test this possibility rats were adrenalectomized or given sham surgery, with half of the

49 AFC in beta(2)AR overexpressing lungs from adrenalectomized or propranolol-treated rats revealed cl

50 activation, whereas corticosterone-depleted (adrenalectomized) paired odor-shock pups showed odor-pre

51 in branched-chain amino acid catabolism, in adrenalectomized rat skeletal muscle and liver, the two

52 nhibition of ACTH secretion at 25 micrograms/adrenalectomized rat).

53 terminal IMCD was significantly increased in adrenalectomized rats and reduced in dexamethasone-treat

54 When Astressin C 2 was administered to adrenalectomized rats at 1.0 mg subcutaneously, it inhib

55 RNA levels were not altered significantly in adrenalectomized rats before and after cortisone treatme

56 ve challenge increased LC discharge rates of adrenalectomized rats by a magnitude greater than that p

57 However, when CORT was restored in adrenalectomized rats by injection, the delayed anxiogen

58 ed at 4 hr after peripheral LPS injection in adrenalectomized rats compared with sham-operated rats.

59 dent of circulating glucocorticoids, because adrenalectomized rats displayed an identical pattern.

60 nt glucoprivic feeding were also examined in adrenalectomized rats in which the source of endogenous

61 immediate precursor of 3alpha,5alpha-THP, to adrenalectomized rats not only restored the ethanol-indu

62 icosteroid-regulated proteins in livers from adrenalectomized rats over 11 time points after drug dos

63 ized or given sham surgery, with half of the adrenalectomized rats receiving corticosterone replaceme

64 In muscle of acidotic adrenalectomized rats receiving dexamethasone, basal and

65 aint stress were examined in both intact and adrenalectomized rats receiving glucocorticoid replaceme

66 Adrenalectomized rats showed reduced contextual-fear con

67 onic CRF secretion in the LC is increased in adrenalectomized rats suggest that activity of certain C

68 F antagonist decreased LC discharge rates of adrenalectomized rats to rates comparable with those obs

69 hrough a different receptor, three groups of adrenalectomized rats were prepared: (1) vehicle, (2) ad

70 In adrenalectomized rats with basal GC replacement, additio

71 Contextual-fear conditioning in adrenalectomized rats with corticosterone replacement du

72 Treatment of adrenalectomized rats with either corticosterone, RU-283

73 In adrenalectomized rats, acidosis does not increase whole-

74 nse curve was shifted in a complex manner in adrenalectomized rats, suggesting that a proportion of C

75 al allodynia after CCI also was prevented in adrenalectomized rats, whereas the GR agonist dexamethas

76 e anxiogenic effect of stress in bilaterally adrenalectomized rats.

77 c-pituitary adrenal (HPA) axis activation in adrenalectomized rats.

78 dance increase in the inner medullary tip of adrenalectomized rats.

79 CI-induced neuropathic pain behaviors in the adrenalectomized rats.

80 This treatment was also effective in adrenalectomized rats.

81 g cocaine- and food-reinforced responding in adrenalectomized rats.

82 le fractions from the inner medullary tip of adrenalectomized rats.

83 physial ACTH secretion in intact stressed or adrenalectomized rats.

84 oto rat (WKY, 69.6+/-6.5 mm Hg; P<0.0001) or adrenalectomized SHR (73.5+/-2.1 mm Hg; P=0.0009) at the

85 e increases in brain IL-1beta protein in the adrenalectomized subjects 2 hr after stress, whether bas

86 one in an amount that led to blood levels in adrenalectomized subjects that match those produced by I

87 e hypothalamus and in other brain regions in adrenalectomized subjects, and no longer present 24 h la

88 reased blood levels of IL-1beta, but only in adrenalectomized subjects.

89 the pituitary, and did so in both intact and adrenalectomized subjects.

90 Similarly, adrenalectomized type 1 diabetic (T1D) rats exhibited de

91 LC spontaneous discharge was higher in adrenalectomized versus sham-operated rats.

92 increase corticosterone production, because adrenalectomized wild-type mice had similar disease cour

93 pression, male wild-type and ob/ob mice were adrenalectomized (with saline supplementation) or sham a