Casein Hydrolysate with Glycemic Control Properties: Evidence from Cells, Animal Models, and Humans
Evidence exists to support the role of dairy derived proteins whey and casein in glycemic management. The objective of the present study was to use a cell screening method to identify a suitable casein hydrolysate and to examine its ability to impact glycemia related parameters in an animal model an...
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Published in | Journal of agricultural and food chemistry Vol. 66; no. 17; pp. 4352 - 4363 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
American Chemical Society
02.05.2018
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Abstract | Evidence exists to support the role of dairy derived proteins whey and casein in glycemic management. The objective of the present study was to use a cell screening method to identify a suitable casein hydrolysate and to examine its ability to impact glycemia related parameters in an animal model and in humans. Following screening for the ability to stimulate insulin secretion in pancreatic beta cells, a casein hydrolysate was selected and further studied in the ob/ob mouse model. An acute postprandial study was performed in 62 overweight and obese adults. Acute and long-term supplementation with the casein hydrolysate in in vivo studies in mice revealed a glucose lowering effect and a lipid reducing effect of the hydrolysate (43% reduction in overall liver fat). The postprandial human study revealed a significant increase in insulin secretion (p = 0.04) concomitant with a reduction in glucose (p = 0.03). The area under the curve for the change in glucose decreased from 181.84 ± 14.6 to 153.87 ± 13.02 (p = 0.009). Overall, the data supports further work on the hydrolysate to develop into a functional food product. |
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AbstractList | Evidence exists to support the role of dairy derived proteins whey and casein in glycemic management. The objective of the present study was to use a cell screening method to identify a suitable casein hydrolysate and to examine its ability to impact glycemia related parameters in an animal model and in humans. Following screening for the ability to stimulate insulin secretion in pancreatic beta cells, a casein hydrolysate was selected and further studied in the ob/ob mouse model. An acute postprandial study was performed in 62 overweight and obese adults. Acute and long-term supplementation with the casein hydrolysate in in vivo studies in mice revealed a glucose lowering effect and a lipid reducing effect of the hydrolysate (43% reduction in overall liver fat). The postprandial human study revealed a significant increase in insulin secretion (p = 0.04) concomitant with a reduction in glucose (p = 0.03). The area under the curve for the change in glucose decreased from 181.84 ± 14.6 to 153.87 ± 13.02 (p = 0.009). Overall, the data supports further work on the hydrolysate to develop into a functional food product. |
Author | Gibney, Eileen R Whelan, Helena Gaudel, Celine Cagney, Gerard Robinson, Aisling Nongonierma, Alice B FitzGerald, Richard J Brennan, Lorraine Egan, Thelma Holton, Thérèse A Drummond, Elaine Noronha, Nessa Jacquier, Jean-Christophe Newsholme, Philip Shields, Denis C Flynn, Sarah |
AuthorAffiliation | University of Limerick School of Biomolecular and Biomedical Sciences, Food for Health Ireland (FHI) and UCD Conway Institute of Biomolecular and Biomedical Research Department of Biological Sciences School of Agriculture and Food Science, Institute of Food and Health and Food for Health Ireland (FHI) School of Medicine, Food for Health Ireland (FHI) and UCD Conway Institute of Biomolecular and Biomedical Research Food for Health Ireland (FHI) |
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SubjectTerms | 3T3-L1 Cells Adult Aged Animals Blood Glucose - analysis Blood Glucose - drug effects Caseins - administration & dosage Cell Line Dietary Supplements Female Humans Insulin - metabolism Insulin Secretion Insulin-Secreting Cells Male Mice Mice, Inbred C57BL Mice, Obese Middle Aged Models, Animal Obesity Overweight Postprandial Period |
Title | Casein Hydrolysate with Glycemic Control Properties: Evidence from Cells, Animal Models, and Humans |
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