ライフサイエンスコーパス: prandial

1 30 min of eating (approximately 300 pmol/l, "prandial").

2 /- 0.15 vs. 1.32 +/- 0.19 mol/l per 6 h) and prandial (0.56 +/- 0.14 vs. 0.56 +/- 0.10 mol/l per 6 h)

3 .7 +/- 0.3 vs. -3.1 +/- 0.2 micromol/kg) and prandial (-3.1 +/- 0.4 vs. -3.0 +/- 0.6 pmol/kg) insulin

4 ilar for patients receiving biphasic (7.1%), prandial (6.8%), and basal (6.9%) insulin-based regimens

5 Furthermore, the post-prandial absorption of sapotexanthin to human plasma was

6 B28), Pro(B29)-insulin ("lispro") as a model prandial analog that is less thermodynamically stable an

7 HGF mice are relatively hypoglycemic in post-prandial and fasting states compared with their normal l

8 conducted the first quantitative analysis of prandial behavior in Drosophila melanogaster.

9 e reduced despite hyperinsulinemia, and post-prandial changes in triglyceride levels are markedly sup

10 ith RE gavage exhibited largely reduced post-prandial circulating RE content, indicating that LAL is

11 sign of rapid-acting insulin analogs for the prandial control of glycemia.

12 at mealtimes, thus providing both basal and prandial coverage.

13 In chronic HCV patients, post prandial distention syndrome (PDS) subtype was the predo

14 Post-prandial dysmetabolism is an independent predictor of fu

15 This state, called post-prandial dysmetabolism, induces immediate oxidant stress

16 ate-dose alcohol each positively impact post-prandial dysmetabolism.

17 and immediate favorable changes in the post-prandial dysmetabolism.

18 The prandial effect on portal venous blood flow is only marg

19 ns of the brain the physiological signals of prandial GLP-1 secreted by intestinal L-cells.

20 itors also exhibited the ability to suppress prandial glucose elevations after an oral glucose challe

21 mic response above baseline during identical prandial glucose infusions was greater (1,411 +/- 94 vs.

22 0.93; 95% CI, 0.14-1.72; P = 0.02) and post-prandial glucose levels (beta = 3.0; 95% CI, 0.5-5.5; P

23 of AHIREM and AHINREM with fasting and post-prandial glucose levels and HOMA-IR.

24 were associated with fasting glycemia, post-prandial glucose levels, and HOMA-IR in models that adju

25 he Cip4-null mice displayed lower early post-prandial glucose levels.

26 controlled glucose output and restoring post-prandial glucose uptake and storage as glycogen.

27 n its current clinical use in improving post-prandial glycaemic control in type 2 diabetics.

28 ss in the biphasic group (31.9%) than in the prandial group (44.7%, P=0.006) or in the basal group (4

29 the biphasic group (3.0), and highest in the prandial group (5.7) (P<0.001 for the overall comparison

30 similar in the biphasic group (7.3%) and the prandial group (7.2%) (P=0.08) but higher in the basal g

31 The mean weight gain was higher in the prandial group than in either the biphasic group or the

32 ing starch digestion in order to reduce post-prandial hyperglycemia.

33 In conclusion, prandial hypertriglyceridemia in men with MetS was due t

34 ormones, could potentially contribute a post-prandial incretin effect.

35 Used as prandial insulin (for example, insulin lispro, insulin a

36 , including the concept of physiologic basal-prandial insulin and the availability of insulin analogu

37 The addition of biphasic or prandial insulin aspart reduced levels more than the add

38 receive biphasic insulin aspart twice daily, prandial insulin aspart three times daily, or basal insu

39 receive biphasic insulin aspart twice daily, prandial insulin aspart three times daily, or basal insu

40 topping sulfonylureas) initially, and later, prandial insulin can be added in a stepwise fashion.

41 rol algorithm directed insulin delivery, and prandial insulin delivery was calculated with a standard

42 ably suppressed in IFG and NFG groups during prandial insulin infusion, indicating that hepatic insul

43 During both the basal and prandial insulin infusions, glucose disappearance prompt

44 Stepwise prandial insulin intensification provides glycaemic cont

45 that of insulin glargine, both combined with prandial insulin lispro, in patients with type 2 diabete

46 l levels (n = 6) or varied so as to create a prandial insulin profile (n = 6).

47 re advanced in development, and they improve prandial insulin secretion, reduce excess glucagon produ

48 sing bedtime insulin with oral agents, basal-prandial insulin strategies, and the new insulin analogu

49 Patients who added a basal or prandial insulin-based regimen to oral therapy had bette

50 But currently available prandial insulins are suboptimal: The onset of action is

51 sulin replacement in diabetes often requires prandial intervention to reach hemoglobin A(c) (HbA(c))

52 n association between oxidative stress, post-prandial lipaemia and endothelial dysfunction in non-dia

53 e diabetic dyslipidaemia, in particular post-prandial lipaemia, and of oxidative stress on the action

54 ensity lipoprotein and abnormalities of post-prandial lipaemia.

55 ids will therefore affect the course of post-prandial lipid oxidation.

56 s led to reductions in both fasting and post-prandial plasma glucose levels with concomitant reductio

57 Subjects who were fed had lower post-prandial ratings on hunger scales and higher ratings on

58 easing peptide antagonist inhibited the post-prandial rise in plasma gastrin in control rats, but had

59 displayed marked blunting of the usual post-prandial rise in plasma triglycerides.

60 that the Y2R plays an important role in post-prandial satiety and provide further insight into the me

61 myriad functions, including roles as a post-prandial satiety factor and lipid antioxidant.

62 conditions that mimics many aspects of post-prandial sleep in mammals.

63 leads to exaggerated supraphysiological post-prandial spikes in blood glucose and lipids.

64 o examine the effect of follicular phase and prandial state on brain activation (food > nonfood contr

65 ndividual hormones and the importance of the prandial state remain unknown.

66 curacy independent of triglyceride level and prandial state, non-HDL-C proves to be the better marker

67 ee fatty acid levels, especially in the post-prandial state.

68 blood glucose levels in the fasted and post-prandial states, indicating a role for p300 in maintaini

69 to on-screen measurements and the subject's prandial status.

70 e aimed to assess the efficacy and safety of prandial Technosphere inhaled insulin compared with twic

71 1 ratio to receive 52 weeks' treatment with: prandial Technosphere inhaled insulin powder plus bedtim

72 m)technetium-mebrofenin scintigraphy or post-prandial variations in gallbladder volume; gallbladder c