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Effect of premeal consumption of whey protein and its hydrolysate on food intake and postmeal glycemia and insulin responses in young adults
Oleh:
Akhavan, Tina
;
Luhovyy, Bohdan L.
;
Brown, Peter H
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
The American Journal of Clinical Nutrition vol. 91 no. 04 (Apr. 2010)
,
page 966-975.
Topik:
HEALTH AND NUTRITION
;
energy and metabolism
Ketersediaan
Perpustakaan FK
Nomor Panggil:
A07.K
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Background: Dairy protein ingestion before a meal reduces food intake and, when consumed with carbohydrate, reduces blood glucose. Objective: The objective was to describe the effect of whey protein (WP) or its hydrolysate (WPH) when consumed before a meal on food intake, pre- and postmeal satiety, and concentrations of blood glucose and insulin in healthy young adults. Design: Two randomized crossover studies were conducted. WP (10–40 g) in 300 mL water was provided in experiment 1, and WP (5–40 g) and WPH (10 g) in 300 mL water were provided in experiment 2. At 30 min after consumption, the subjects were fed an ad libitum pizza meal (experiment 1) or a preset pizza meal (12 kcal/kg, experiment 2). Satiety, blood glucose, and insulin were measured at baseline and at intervals both before and after the meals. Results: In experiment 1, 20–40 g WP suppressed food intake (P < 0.0001) and 10–40 g WP reduced postmeal blood glucose concentrations and the area under the curve (AUC) (P < 0.05). In experiment 2, 10–40 g WP, but not WPH, reduced postmeal blood glucose AUC and insulin AUC in a dose-dependent manner (P < 0.05). The ratio of cumulative blood glucose to insulin AUCs (0–170 min) was reduced by 10 g WP but not by 10 g WPH. Conclusions: WP consumed before a meal reduces food intake, postmeal blood glucose and insulin, and the ratio of cumulative blood glucose to insulin AUCs in a dose-dependent manner. Intact WP, but not WPH, contributes to blood glucose control by both insulin-dependent and insulin-independent mechanisms.
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