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Food Nutr Res. 2012;56. doi: 10.3402/fnr.v56i0.7989. Epub 2012 Apr 13.

The effect of α- or β-casein addition to waxy maize starch on postprandial levels of glucose, insulin, and incretin hormones in pigs as a model for humans.

Food & nutrition research

Anthony P Kett, Christine M Bruen, Fiona O'Halloran, Valérie Chaurin, Peadar G Lawlor, James A O'Mahony, Linda Giblin, Mark A Fenelon

Affiliations

  1. Teagasc Food Research Centre, Moorepark, Fermoy, Co. Cork, Ireland.

PMID: 22509144 PMCID: PMC3327470 DOI: 10.3402/fnr.v56i0.7989

Abstract

BACKGROUND: Starch is a main source of glucose and energy in the human diet. The extent to which it is digested in the gastrointestinal tract plays a major role in variations in postprandial blood glucose levels. Interactions with other biopolymers, such as dairy proteins, during processing can influence both the duration and extent of this postprandial surge.

OBJECTIVE: To evaluate the effect of the addition of bovine α- or β-casein to waxy maize starch on changes in postprandial blood glucose, insulin, and incretin hormones [glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide 1 (GLP-1)] in 30 kg pigs used as an animal model for humans.

DESIGN: Gelatinised starch, starch gelatinised with α-casein, and starch gelatinised with β-casein were orally administered to trained pigs (n = 8) at a level of 60 g of available carbohydrate. Pre- and postprandial glucose measurements were taken every 15 min for the first hour and every 30 min thereafter up to 180 min. Insulin, GIP, and GLP-1 levels were measured in plasma samples up to 90 min postprandial.

RESULTS: Starch gelatinised with α-casein had a significantly (p < 0.05) lower peak viscosity on pasting and resulted in significantly lower glucose release at 15, 30, and 90 min postprandial compared to starch gelatinised with β-casein. During the first 45-min postprandial, the area under the glucose curve (AUC) for starch gelatinised with α-casein was significantly (p < 0.05) lower than that for starch gelatinised with β-casein. There was also a significant (p < 0.05) difference at T30 in GIP levels in response to the control compared to starch gelatinised with α- or β-casein. Significant (p < 0.05) increases in several free amino acid concentrations were observed on ingestion of either α- or β-casein gelatinised with starch at 30 and 90 min postprandial compared to starch alone. In addition, plasma levels of six individual amino acids were increased on ingestion of starch gelatinised with α-casein compared to ingestion of starch gelatinised with β-casein.

CONCLUSION: The presence of casein fractions (α- or β-casein) in gelatinised waxy maize starch affects swelling characteristics, viscosity, and subsequent in vivo digestion as determined by glucose levels in blood postprandial.

Keywords: digestion; glucose and insulin; incretin hormones; waxy maize starch

References

  1. J Clin Invest. 1966 Sep;45(9):1487-502 - PubMed
  2. Am J Clin Nutr. 1967 Jan;20(1):24-33 - PubMed
  3. J Clin Invest. 1966 Sep;45(9):1479-86 - PubMed
  4. Eur J Clin Nutr. 2002 Nov;56(11):1049-71 - PubMed
  5. J Clin Invest. 1999 Apr;103(7):931-43 - PubMed
  6. J Nutr. 2008 Feb;138(2):397-402 - PubMed
  7. Physiol Rev. 2001 Jul;81(3):1031-64 - PubMed
  8. Am J Clin Nutr. 1997 Nov;66(5):1264-76 - PubMed
  9. Am J Clin Nutr. 2000 Jul;72(1):96-105 - PubMed
  10. Diabetes Care. 1999 Jan;22(1):10-8 - PubMed
  11. Nutr Metab (Lond). 2008 Apr 08;5:9 - PubMed
  12. Am J Clin Nutr. 2004 Nov;80(5):1246-53 - PubMed
  13. Gastroenterology. 2007 May;132(6):2131-57 - PubMed
  14. Jpn J Vet Res. 1985 Apr;33(1-2):1-9 - PubMed
  15. Eur J Clin Nutr. 1999 Dec;53(12):959-65 - PubMed
  16. Am J Clin Nutr. 2005 Jul;82(1):76-83 - PubMed
  17. Eur J Clin Invest. 1998 Sep;28 Suppl 2:8-13 - PubMed
  18. Br J Nutr. 2000 Mar;83 Suppl 1:S149-55 - PubMed
  19. Ann N Y Acad Sci. 2006 Jul;1070:10-26 - PubMed
  20. Diabetes Care. 1991 Feb;14(2):95-101 - PubMed
  21. Clin Nutr. 2004 Aug;23(4):641-6 - PubMed
  22. Diabetes Care. 1991 Sep;14(9):824-38 - PubMed
  23. Am J Clin Nutr. 1981 Mar;34(3):362-6 - PubMed
  24. J Am Coll Nutr. 1985;4(4):437-50 - PubMed

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