2011
DOI: 10.1016/j.foodchem.2010.08.020
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The inhibitory effects of ethanol extracts from sorghum, foxtail millet and proso millet on α-glucosidase and α-amylase activities

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Cited by 193 publications
(132 citation statements)
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“…(37)(38)(39)(40)(41) These interactions inhibit carbohydrate-hydrolyzing enzymes, such as α-glucosidase and α-amylase, thereby lowering starch digestibility. (42) The presence of the protein matrix has also been associated with reduced starch gelatinization during cooking resulting in partially-gelatinized sorghum starch granules that may resist enzymatic degradation in vivo. (27) Sorghum starch has amongst the highest gelatinization temperatures, ranging from 66-81 °C, depending upon cultivars, and is higher than that of maize, wheat and barley.…”
Section: Starchesmentioning
confidence: 99%
“…(37)(38)(39)(40)(41) These interactions inhibit carbohydrate-hydrolyzing enzymes, such as α-glucosidase and α-amylase, thereby lowering starch digestibility. (42) The presence of the protein matrix has also been associated with reduced starch gelatinization during cooking resulting in partially-gelatinized sorghum starch granules that may resist enzymatic degradation in vivo. (27) Sorghum starch has amongst the highest gelatinization temperatures, ranging from 66-81 °C, depending upon cultivars, and is higher than that of maize, wheat and barley.…”
Section: Starchesmentioning
confidence: 99%
“…stearothermophilus α-glucosidase inhibition assay was performed as described previously 15 . α-glucosidase (50 µl, 0.5 U/ml) and 0.2 M K 3 PO 4 buffer (pH 6.8, 50 µl) were mixed with 50 µl of the test sample.…”
Section: α-Glucosidase Inhibitory Effectmentioning
confidence: 99%
“…Nutritional studies concerning the application of cereal grain diets rich in inhibitors of ␣ -amylases proved that their biological activity significantly influences the metabolism of starch of the studied organisms. The proteins consumed in food are resistant to digestion by pepsin and they are transported in their unchanged form to the duodenum, where they inactivate porcine pancreas amylase ( 16 ). Inhibitors of ␣ -amylases can play a significant function in diet therapy for metabolic syndrome, because they hinder absorption of saccharides into the alimentary tract, which lowers the glycemic index of consumable food ( 15 , 17 ).…”
mentioning
confidence: 99%