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In Vitro Starch Digestibility and In Vivo Glycemic Response of Starch Inclusion Complexes Produced With Different Methods and Hydrothermal Treatments

OBJECTIVES: Type 2 diabetes (T2D) has become a major health-threatening problem worldwide. Slowly digested or indigestible carbohydrates such as resistant starch (RS) are associated with a low glycemic index (GI) and decreased risk of developing T2D. Recently, starch inclusion complexes (ICs) have r...

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Detalles Bibliográficos
Autores principales: Guo, Jiayue, Zhang, Yanqi, Kong, Lingyan, Tan, Libo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9193797/
http://dx.doi.org/10.1093/cdn/nzac057.008
Descripción
Sumario:OBJECTIVES: Type 2 diabetes (T2D) has become a major health-threatening problem worldwide. Slowly digested or indigestible carbohydrates such as resistant starch (RS) are associated with a low glycemic index (GI) and decreased risk of developing T2D. Recently, starch inclusion complexes (ICs) have raised attention due to their thermally stable structure and high RS content. However, results are inconsistent and few research is present regarding their GI values. The aim of this study was to investigate the in vitro digestion kinetics and in vivo glycemic response of starch ICs produced with different methods and hydrothermal treatments, and to determine their potential as a novel type of RS, i.e., RS5. METHODS: Starch-ascorbyl palmitate (AP) ICs were produced by both DMSO and the “empty” V-type method. Combined hydrothermal treatments of annealing and acid hydrolysis (ANN-ACH) were applied to enhance the RS content of the IC samples. In vitro kinetic starch digestion was performed on the treated ICs to obtain their hydrolysis patterns and estimated GI (eGI) values with white bread as a reference food. In vivo glycemic response of the IC samples was examined in C57BL6/J mice, with high amylose maize starch (HAMS, a RS2) as a comparison and pure glucose as a reference. RESULTS: The V(6h)-AP IC produced by the “empty” V-type method presented a slower and more gradual in vitro hydrolysis pattern as compared to the HAMS-AP IC produced by the DMSO method. Cooking significantly increased the eGI value of RS2, while the ANN-ACH treatment significantly decreased the eGI values of both IC samples (p < 0.05). Similarly, cooked RS2 resulted in higher postprandial glycemic response in mice as compared to raw RS2 and treated IC samples (p < 0.05). The in vivo GIs were also consistent with the eGI values obtained from the in vitro assay. Among all the tested samples, the treated V(6h)-AP IC exhibited the lowest eGI and GI values, within range of low GI foods. CONCLUSIONS: The low GI values of the ANN-ACH treated V(6h)-AP IC indicated its pronounced effect in modulating the postprandial glycemic response, marking its great potential as a novel type of RS, i.e., RS5. In addition, good consistency was reached between the in vitro and in vivo methods of evaluating GI, indicating the reliability of the in vitro assay in predicting the glycemic response. FUNDING SOURCES: The University of Alabama Graduate School Research Fund.