4.4 Article

Phaseolus vulgaris extract affects glycometabolic and appetite control in healthy human subjects

Journal

BRITISH JOURNAL OF NUTRITION
Volume 109, Issue 10, Pages 1789-1795

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0007114512003741

Keywords

Phaseolus vulgaris; Supplements; Mixed meals; Glucose metabolism; Satiety

Funding

  1. Indena S. p. A., Milan, Italy
  2. ICANS (International Center for the Assessment of Nutritional Status), Milan, Italy

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Extracts of Phaseolus vulgaris (beans) are known to reduce glycaemia and food intake in rodents and humans. The present study evaluated the effects of a new, standardised and purified P. vulgaris extract (PVE), when employed as a supplement in a mixed balanced meal (60 % carbohydrates, 25 % lipids and 15 % protein), on glycometabolic and appetite control. To this end, a randomised, double-blind, placebo-controlled study was performed in twelve volunteers. Plasma glucose, insulin, C-peptide, ghrelin and satiety sensation ratings were assessed at baseline and during 3 h after meal consumption associated with PVE (100 mg) or placebo. Compared with placebo, PVE consumption resulted in lower increments in glucose (+15.4 (SEM 5.4) v. 26.1 (SEM 7.3) %, P=0.04 at 30 min), insulin (+981 (SEM 115) v. 1325 (SEM 240) %, P=0.04 between 45 and 120 min) and C-peptide (+350 (SEM 27) v. 439 (SEM 30) %, P=0.04 between 30 and 90 min). In the first 2 h, plasma ghrelin decreased similarly in both groups but did not rebound as in placebo thereafter (P=0.04). Correspondingly, satiety sensation in the third hour was significantly reduced in the placebo but not in the PVE condition. PVE induced a lower desire to eat than placebo (P=0.02) over the 3 h. In conclusion, PVE supplementation reduced postprandial glucose, insulin and C-peptide excursions, suppressed ghrelin secretion and affected satiety sensations, inducing a lower desire to eat. These results support that further studies are needed to prove the concept of employing PVE as a supplement in mixed balanced meals in obese, glucose-intolerant and diabetic subjects.

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