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1 nfused for 9 h with L-[1-13C]leucine, in the postabsorptive (0-3 h) and postprandial (3-9 h) states a
2 tty acids are a crucial energy source in the postabsorptive and fasted states when glucose supply is
3 ic capacity of GR-deficient adipocytes under postabsorptive and fasting conditions, resulting from im
4 NP-43, were found to have decreased rates of postabsorptive and insulin-stimulated glucose turnover t
5 serial muscle biopsies was used to determine postabsorptive and postprandial (20 g milk protein) MyoP
6                         Body composition and postabsorptive and postprandial muscle protein synthesis
7 e and the bed-rest phase, and rates of acute postabsorptive and postprandial MyoPS (aMyoPS) at the en
8 of endogenous glucose production in both the postabsorptive and postprandial states.
9  a 16-h fast, seven dogs were studied in the postabsorptive basal state and during a tolbutamide (0.2
10 nces of genetics, ethnicity-race, and sex as postabsorptive bioavailability modifiers; and 3) discuss
11         However, Dgat1(-/-) mice had reduced postabsorptive chylomicronemia (1 h after a high fat cha
12  apo E3/3 group but remained 51% higher than postabsorptive concentrations in the apo E4/3 group; thi
13                                          The postabsorptive concentrations of plasma triglycerides an
14 ch in polyunsaturated fat for 15-29 d, their postabsorptive concentrations of TRL triglycerides, apo
15 0.01) and a trend toward increased MPB under postabsorptive conditions (P = 0.09).
16 fore and after supplementation during basal, postabsorptive conditions and during a hyperaminoacidemi
17 ceived a [(2) H5 ]Phe tracer infusion during postabsorptive conditions and during a hyperinsulinaemic
18 njunction with muscle biopsies during basal, postabsorptive conditions and during combined amino acid
19 n the rate of muscle protein synthesis under postabsorptive conditions in the elderly and may explain
20                                        Under postabsorptive conditions, MPS and LPB were equivalent b
21                                              Postabsorptive elimination of the various forms of vitam
22      The extent of the renal contribution to postabsorptive endogenous glucose production (EGP) in hu
23           The contribution of the kidneys to postabsorptive endogenous glucose production is a matter
24 ociated gene expression were assessed in the postabsorptive (fasted) and postprandial (fed; 480 kcal,
25  hepatic glucose production (P = 0.004), and postabsorptive fat oxidation (P = 0.03) improved equally
26  exercise combined with weight loss enhances postabsorptive fat oxidation, which appears to be a key
27                                     Rates of postabsorptive FFA (palmitate) storage into upper-body s
28                                              Postabsorptive FFA flux and splanchnic FFA delivery were
29 ncentrations compared with saline, with mean postabsorptive glucose concentrations (2400-0800) of 5.6
30   These data document that glucagon supports postabsorptive glucose concentrations in humans.
31                                              Postabsorptive glucose production was appropriately supp
32                                        Eight postabsorptive healthy men ( approximately 21 y of age)
33 hway in determining body fat distribution in postabsorptive humans and whether adipocyte lipogenic pr
34 s) by adipocytes occurs in vivo in overnight postabsorptive humans and, if so, whether there are regi
35 ge pathway, which had remained undetected in postabsorptive humans until recently, can have considera
36  during infusion of 14C-labeled glutamine in postabsorptive humans.
37                         We hypothesized that postabsorptive hyperglucagonemia represents a gut-depend
38  (MPS) and leg protein breakdown (LPB) under postabsorptive (hypoinsulinemic-euglycemic clamp) and po
39 he low-dose insulin infusion, which achieved postabsorptive insulin levels, the muscle mitochondrial
40 plexity of the relationships between pre and postabsorptive mechanisms underlying Trp's appetite-inhi
41  using the modified methods in normal-weight postabsorptive men and women.
42 stinal mucosa, but the extent and site(s) of postabsorptive metabolism in the human is unknown.
43                                              Postabsorptive MitoPS rates were significantly lower in
44                           Bed rest decreased postabsorptive MPS by 30% +/- 9% (CON group) and by 10%
45                                     Although postabsorptive MPS was unaffected, catabolic changes wit
46                                              Postabsorptive MyoPS rates did not differ between legs o
47 rial and hepatic venous blood was sampled in postabsorptive (n = 6; study A) and postprandial (n = 5;
48 table isotope tracers were infused to assess postabsorptive netPB [postabsorptive PB - protein synthe
49 t important gluconeogenic amino acids, in 14 postabsorptive NIDDM subjects and 18 nondiabetic volunte
50                                          Six postabsorptive nondiabetic subjects who were scheduled f
51                         These data show that postabsorptive nonhepatic glucose production in humans m
52 sma AA availability during hemodialysis in a postabsorptive or postprandial state.
53 ax Encore 29n (SensorMedix) was performed in postabsorptive (overnight fast >8 h) healthy subjects (n
54                    Based on the premise that postabsorptive patients with type 1 diabetes receiving i
55 were infused to assess postabsorptive netPB [postabsorptive PB - protein synthesis (PS)] and the anab
56                                              Postabsorptive PB was lower after 4 wk of the high dose
57 id not differ between groups during both the postabsorptive period and the amino acid infusion, while
58 ervations, no significant differences in the postabsorptive phenylalanine net balance were observed b
59                                  We measured postabsorptive plasma amino acid profile and glucose, fo
60 s of variance for repeated measures) lowered postabsorptive plasma concentrations of tHcy by -11.7% +
61 cagon, in concert with insulin, supports the postabsorptive plasma glucose concentration in humans.
62 cagon, in concert with insulin, supports the postabsorptive plasma glucose concentration in humans.
63 tested the hypothesis that glucagon supports postabsorptive plasma glucose concentrations in humans.
64 y lipoprotein triglycerides (VLDL-TGs) under postabsorptive, postprandial, and walking conditions in
65 availability is a function of absorptive and postabsorptive processes, which in turn are influenced b
66                                       In the postabsorptive protocol, participants rested and remaine
67 al nutrition at rates that approximate usual postabsorptive rates and that avoid first-pass hepatic c
68                                              Postabsorptive rates of myofibrillar MPS and whole-body
69 is sufficient for the maximal stimulation of postabsorptive rates of myofibrillar MPS in rested and e
70  characterized the dose-response relation of postabsorptive rates of myofibrillar MPS to increasing a
71 ed muscle cells is inversely correlated with postabsorptive respiratory quotient of the muscle donors
72                Insulin concentration and the postabsorptive respiratory quotient were positively corr
73              These results indicate that the postabsorptive respiratory quotients and insulin-mediate
74                                              Postabsorptive resting metabolic rate (RMR) and postpran
75 ptake could account for approximately 40% of postabsorptive RGP and for 60% of RGP during hypoglycemi
76 fter the epinephrine infusion ended, but the postabsorptive RQ remained modestly elevated.
77 may influence hepatic glucose production and postabsorptive sleeping metabolic rate.
78 fused for 9 h with L-[1-(13)C]leucine in the postabsorptive state (0-3 h), who were fed half-hourly w
79 mino acid production, we administered in the postabsorptive state an IV stable isotope solution conta
80 ng a constant stable isotope infusion in the postabsorptive state and after essential amino acid (EAA
81  and renal vein samples were obtained in the postabsorptive state and during a 180-min hyperinsulinem
82 cine and [2-13C] leucine were studied in the postabsorptive state and during an amino acid infusion i
83 nd amino acid transport were measured in the postabsorptive state and during the intravenous infusion
84 ean +/- SEM: 31 +/- 2 y) were studied in the postabsorptive state and for 3.5 h after a bolus ingesti
85 Muscle and tendon biopsies were taken in the postabsorptive state at days 0, 10 and 21 for measuremen
86        Normal volunteers were studied in the postabsorptive state at rest and about 3 h after a heavy
87 were measured by indirect calorimetry in the postabsorptive state at the same time every morning.
88              Glucokinase is inhibited in the postabsorptive state by sequestration in the nucleus bou
89 nteers were studied on four occasions in the postabsorptive state during infusions of [1-(13)C]glucos
90 tein, or their co-ingestion in the overnight postabsorptive state elicit a similar stimulation of pos
91  70Zn or 68Zn was orally administered in the postabsorptive state on days 1 and 6, respectively; intr
92             Sedentary nutrient fluxes in the postabsorptive state were comparable for the WT and KO m
93                                       In the postabsorptive state, acute insulin deprivation has no e
94               Two groups were studied in the postabsorptive state, and 2 groups were studied in the f
95  improved glucose metabolic rates during the postabsorptive state, and restored insulin sensitivities
96                                       In the postabsorptive state, leucine flux was slower (P < 0.01)
97                                       In the postabsorptive state, LTx-5 had lower endogenous leucine
98                                       In the postabsorptive state, nearly all of the carbohydrate use
99                                       In the postabsorptive state, pancreas-transplant patients had s
100  (hs-CRP)], liver function, and glucose in a postabsorptive state.
101 ment, and controls were studied in the early postabsorptive state.
102 te differ from those usually reported in the postabsorptive state.
103 ation with healthy volunteers studied in the postabsorptive state.
104 fusion of [13C]leucine and [15N2]urea in the postabsorptive state.
105 patients and 11 controls were studied in the postabsorptive state; a bolus of 200 mg L[15N]2 arginine
106                                              Postabsorptive subjects received a primed constant [1-13
107  n = 10) control clamp experiments in normal postabsorptive subjects.
108 tabolic processes in humans and reveals that postabsorptive trans-to-cis-lycopene isomerization, and
109 glucose release and renal glucose release in postabsorptive type 2 diabetic subjects and age-weight-m
110 h HFP and LFP conditions increased MPS above postabsorptive values (P = 0.028 and P < 0.001, respecti
111 TRL apo B48 increased at 3 h but returned to postabsorptive values at 6 h only in the apo E3/3 group;
112    Postprandial aMyoPS rates increased above postabsorptive values in EX only.
113 ration of apo B48 at 6 h was 80% higher than postabsorptive values.
114 (13)C]leucine) decreased (P < 0.05) and net (postabsorptive vs. postprandial) leucine balance (P < 0.
115 men) volunteers under postprandial and under postabsorptive walking conditions, respectively.
116 omeostasis in patients with COPD by reducing postabsorptive whole-body protein breakdown (PB) and enh
117 s (FFAs) in visceral and subcutaneous fat in postabsorptive women.

 
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