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Reducing Beta-Glucan Solubility in Oat Bran Muffins by Freeze-Thaw Treatment Attenuates Its Hypoglycemic Effect

September 2007 Volume 84 Number 5
Pages 512 — 517
Xiaomiao Lan-Pidhainy,1 Yolanda Brummer,2 Susan M. Tosh,2,3 Thomas M. Wolever,1 and Peter J. Wood2

University of Toronto, Department of Nutritional Sciences, Toronto, ON. Agriculture and Agri-Food Canada, Food Research Program, Guelph. Corresponding author. E-mail: toshs@agr.gc.ca


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Accepted May 22, 2007.
ABSTRACT

The viscosity of soluble fibers such as β-glucan depends on their concentration in solution and molecular weight (MW) distribution. We investigated whether freezing treatment of oat bran muffins affected the physicochemical properties of β-glucan, and its physiological effectiveness in lowering postprandial blood glucose response. A controlled range of β-glucan solubility was achieved by subjecting oat bran muffins containing two levels of β-glucan to repeated freeze-thaw temperature cycling. β-Glucan solubilized by in vitro digestion extraction was measured by flow-injection analysis. MW distributions of β-glucan were analyzed using size-exclusion chromatography. β-Glucan solubility decreased as the number of freeze-thaw cycles increased, while MW distribution of β-glucan decreased slightly. Peak blood glucose rise (PBGR) after fresh muffins (8 and 12 g of β-glucan/serving) was significantly lower than that after muffins (8 and 12 g of β-glucan/serving) treated with four freeze-thaw (FT) cycles (1.84 ± 0.2 vs. 2.31 ± 0.1 mmol/L, P = 0.007). Compared with the control whole wheat muffins, the reduction in incremental area under the glucose response curve (AUC) after fresh muffins (8 and 12 g of β-glucan/serving) was nearly twice that after 4 FT cycles (43.3 ± 4.4% vs. 27.0 ± 5.4%, P = 0.016). A significant inverse linear relationship was found between the log [concentration] of extractable β-glucan and PBGR (r2 = 0.85, P = 0.01), and AUC (r2 = 0.71, P = 0.03). The results show that reduction of β-glucan solubility in foods attenuates its physiological effectiveness in lowering postprandial glycemia.



© 2007 AACC International, Inc.