Abstract | BACKGROUND: OBJECTIVE: DESIGN: Ten type 2 diabetic patients [mean (+/-SEM) age: 62 +/- 2 y; body mass index (kg/m(2)): 27 +/- 1] and 9 healthy control subjects (age: 58 +/- 1 y; body mass index: 27 +/- 1) participated in 2 trials in which the plasma insulin response was measured after the ingestion of 0.7 g carbohydrate . kg(-1) . h(-1) with or without 0.35 g . kg(-1) . h(-1) of a mixture that contained a protein hydrolysate, leucine, and phenylalanine. Continuous infusions with [6,6-(2)H(2)] glucose were then given to investigate plasma glucose disposal. RESULTS: Plasma insulin responses were higher by 299 +/- 64% and 132 +/- 63% in the CHO+PRO trial than in the CHO trial in the diabetic patients and the matched control subjects, respectively (P < 0.001). The subsequent plasma glucose responses were reduced by 28 +/- 6% and 33 +/- 3% in the CHO+PRO trial than in the CHO trial in the diabetic patients and the matched control subjects, respectively (P < 0.001). The reduced plasma glucose response in the diabetic patients was attributed to a 13 +/- 3% increase in glucose disposal (P < 0.01). CONCLUSIONS:
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Authors | Ralph J F Manders, Anton J M Wagenmakers, René Koopman, Antoine H G Zorenc, Paul P C A Menheere, Nicolaas C Schaper, Wim H M Saris, Luc J C van Loon |
Journal | The American journal of clinical nutrition
(Am J Clin Nutr)
Vol. 82
Issue 1
Pg. 76-83
(Jul 2005)
ISSN: 0002-9165 [Print] United States |
PMID | 16002803
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Blood Glucose
- Dietary Carbohydrates
- Insulin
- Protein Hydrolysates
- Phenylalanine
- Leucine
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Topics |
- Blood Glucose
(drug effects)
- Case-Control Studies
- Diabetes Mellitus, Type 2
(diet therapy, metabolism)
- Dietary Carbohydrates
(administration & dosage)
- Drug Interactions
- Humans
- Insulin
(metabolism)
- Insulin Secretion
- Leucine
(administration & dosage, pharmacology)
- Male
- Middle Aged
- Phenylalanine
(administration & dosage, therapeutic use)
- Protein Hydrolysates
(administration & dosage, therapeutic use)
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