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      Influence of gallic acid on α-amylase and α-glucosidase inhibitory properties of acarbose

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          Abstract

          Acarbose is an antidiabetic drug which acts by inhibiting α-amylase and α-glucosidase activities but with deleterious side effects. Gallic acid (GA) is a phenolic acid that is widespread in plant foods. We therefore investigated the influence of GA on α-amylase and α-glucosidase inhibitory properties of acarbose ( in vitro). Aqueous solutions of acarbose and GA were prepared to a final concentration of 25μM each. Thereafter, mixtures of the samples (50% acarbose + 50% GA; 75% acarbose + 25% GA; and 25% acarbose + 75% GA) were prepared. The results revealed that the combination of 50% acarbose and 50% GA showed the highest α-glucosidase inhibitory effect, while 75% acarbose + 25% GA showed the highest α-amylase inhibitory effect. Furthermore, all the samples caused the inhibition of Fe 2+-induced lipid peroxidation ( in vitro) in rat pancreatic tissue homogenate, with the combination of 50% acarbose and 50% GA causing the highest inhibition. All the samples also showed antioxidant properties (reducing property, 2,2′-azino-bis (-3-ethylbenzthiazoline-6-sulphonate [ABTS*] and 1,1-diphenyl-2-picrylhydrazyl [DPPH] free radicals scavenging abilities, and Fe 2+ chelating ability). Therefore, combinations of GA with acarbose could be employed as antidiabetic therapy, with a possible reduction of side effects of acarbose; nevertheless, the combination of 50% acarbose and 50% GA seems the best.

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          Antioxidant activity applying an improved ABTS radical cation decolorization assay.

          A method for the screening of antioxidant activity is reported as a decolorization assay applicable to both lipophilic and hydrophilic antioxidants, including flavonoids, hydroxycinnamates, carotenoids, and plasma antioxidants. The pre-formed radical monocation of 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS*+) is generated by oxidation of ABTS with potassium persulfate and is reduced in the presence of such hydrogen-donating antioxidants. The influences of both the concentration of antioxidant and duration of reaction on the inhibition of the radical cation absorption are taken into account when determining the antioxidant activity. This assay clearly improves the original TEAC assay (the ferryl myoglobin/ABTS assay) for the determination of antioxidant activity in a number of ways. First, the chemistry involves the direct generation of the ABTS radical monocation with no involvement of an intermediary radical. Second, it is a decolorization assay; thus the radical cation is pre-formed prior to addition of antioxidant test systems, rather than the generation of the radical taking place continually in the presence of the antioxidant. Hence the results obtained with the improved system may not always be directly comparable with those obtained using the original TEAC assay. Third, it is applicable to both aqueous and lipophilic systems.
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            Biostatistical Analysis

            Populations and samples. Measures of central tendency. Measures of dispersion and variability. Testing of goodness of fit. Contingency tables. The normal distribuition. One-sample hypotheses. Two-sample hypotheses; Paired-sample hypotheses. Multisample hypotheses. Multisample hypotheses. The analysis of variance. Multiple comparasion. Two factor analysis of variance. Data transformations. Multiway factorial analysis of variance. Nested (hierarchial) analysis of variance. Simple linear regression. Comparing simple linear regression equations. Simple linear correlation. Polynomial regression. The binomial distribution. The posion distribution and randomness. Circular distributions. Descriptive statistics. Circula4 distribution. Hypotheses testing.
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              Antioxidant activity of dietary polyphenols as determined by a modified ferric reducing/antioxidant power assay.

              Most nonenzymatic antioxidant activity (scavenging of free radicals, inhibition of lipid peroxidation, etc.) is mediated by redox reactions. The antioxidant (AO) activity of polyphenols (PPs), as ferric-reducing power, was determined for the first time using a modified FRAP (ferric reducing/antioxidant power) assay. Reaction was followed for 30 min, and both Fe(II) standards and samples were dissolved in the same solvent to allow comparison. Selected representative PPs included flavonoids (quercetin, rutin, and catechin), resveratrol, tannic acid, and phenolic acids (gallic, caffeic, and ferulic). Carotenoids (beta-carotene and zeaxanthine), ascorbic acid, Trolox, and BHA were included for comparison. Equivalent concentration 1 (EC(1)), as the concentration of AO with a reducing effect equivalent to 1 mmol/L Fe(II), was used to compare AO efficiency. PPs had lower EC(1) values, and therefore higher reducing power, than ascorbic acid and Trolox. Tannic acid and quercetin had the highest AO capacity followed by gallic and caffeic acids. Resveratrol showed the lowest reducing effect. Carotenoids had no ferric reducing ability. Polyphenol's AO efficiency seemed to depend on the extent of hydroxylation and conjugation.
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                Author and article information

                Journal
                J Food Drug Anal
                J Food Drug Anal
                Journal of Food and Drug Analysis
                Taiwan Food and Drug Administration
                1021-9498
                2224-6614
                2016
                11 April 2016
                : 24
                : 3
                : 627-634
                Affiliations
                [a ]Department of Biochemistry, Federal University of Technology Akure, Akure, Nigeria
                [b ]Department of Biochemistry, Federal University Oye, Oye-Ekiti, Nigeria
                Author notes
                [* ]Corresponding author. Department of Biochemistry, Federal University of Technology, Private Mail Bag 704, Akure 340001, Nigeria. E-mail addresses: goboh2001@ 123456yahoo.com , goboh@ 123456futa.edu.ng (G. Oboh).
                Article
                jfda-24-03-627
                10.1016/j.jfda.2016.03.003
                9336674
                28911570
                bd400daa-a549-4d1a-a366-187c63b298fe
                © 2016 Taiwan Food and Drug Administration

                This is an open access article under the CC-BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 20 October 2015
                : 08 March 2016
                : 15 March 2016
                Categories
                Original Article

                acarbose,antidiabetic,combination therapy,gallic acid,plant foods

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