Nyambe-Silavwe, H, Villa Rodriguez, J, Ifie, I et al. (4 more authors) (2015) Inhibition of human α-amylase by dietary polyphenols. Journal of Functional Foods, 19 (Part A). 723 - 732. ISSN 1756-4646
Abstract
Functional foods offer the possibility to modulate the absorption of sugars, leading to benefits for diabetics and those with metabolic syndrome. As part of the characterisation of such foods, inhibition of α-amylase is used to assess components for their potential ability to modify the post-prandial glycaemic response. Many publications on phenolics as potential inhibitors report widely varying assay conditions leading to variable estimates of inhibition. On this basis, we have optimised the in vitro α-amylase inhibition assay and, in particular, we show the importance of removing certain polyphenols after the enzymic reaction when using 3,5-dinitrosalicylic acid since they interfere with this reagent. There was a substantial ~5-fold effect on acarbose IC50 values when working just outside optimal conditions. This shows that inappropriate assay conditions, such as excess enzyme, greatly influence IC50 values and could explain some discrepancies in the existing literature.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2015, Elsevier. This is an author produced version of a paper published in Journal of Functional Foods. Uploaded in accordance with the publisher's self-archiving policy. |
Keywords: | α-Amylase; diabetes; amylose; amylopectin; polyphenol |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Environment (Leeds) > School of Food Science and Nutrition (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 29 Oct 2015 11:08 |
Last Modified: | 01 Nov 2016 21:37 |
Published Version: | http://dx.doi.org/10.1016/j.jff.2015.10.003 |
Status: | Published |
Publisher: | Elsevier |
Identification Number: | 10.1016/j.jff.2015.10.003 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:91096 |