Durum wheat particle size affects starch and protein digestion in vitro

Eur J Nutr. 2018 Feb;57(1):319-325. doi: 10.1007/s00394-016-1321-y. Epub 2016 Oct 26.

Abstract

Purpose: The term bioaccessibility refers to the proportion of a nutrient released from a complex food matrix during digestion and, therefore, becoming potentially available for absorption in the gastrointestinal tract. In the present study, we assessed the starch and protein bioaccessibility from a range of wheat endosperm products differing in particle size.

Methods: Five porridge meals (size A, flour, mean particle size 0.11 mm, size B, small, mean particle size 0.38 mm, size C, semolina, mean particle size 1.01 mm, size D, medium, mean particle size 1.44 mm, size E, large, mean particle size 1.95 mm) with theoretically different postprandial glycaemic responses were subjected to oral processing in vitro, followed by simulated gastric and duodenal digestion.

Results: A significant increase (P < 0.001) in starch degradation was observed in size A (52%) compared with size E (25%). Both sizes C and D gave less, although not significantly, digestible starch (32 and 28%, respectively). The glucose release significantly decreased as the particle size of the meal increased (92.16% detected for size A vs 47.39% for size E). In agreement with starch degradation and glucose release, size A gave the most digestible protein.

Conclusions: This data provide further evidence that, by decreasing the size of wheat endosperm, starch release and glycaemic response are enhanced. We also showed that protein bioaccessibility followed a similar trend as for starch digestion. Finally, these results support the hypothesis that different degrees of starch encapsulation elicit different blood glucose responses.

Keywords: Glycaemic response; In vitro models; Starch digestion; Wheat endosperm.

MeSH terms

  • Amylases / metabolism
  • Bile / metabolism
  • Biological Availability
  • Blood Glucose / metabolism
  • Digestion*
  • Duodenum / metabolism
  • Edible Grain / chemistry*
  • Gastric Mucosa / enzymology
  • Glucose / metabolism
  • Humans
  • Lipase / metabolism
  • Pancreas / enzymology
  • Particle Size*
  • Pepsin A / metabolism
  • Plant Proteins / metabolism*
  • Saliva / immunology
  • Starch / metabolism*
  • Starch / pharmacokinetics
  • Triticum*

Substances

  • Blood Glucose
  • Plant Proteins
  • Starch
  • Lipase
  • Amylases
  • Pepsin A
  • Glucose