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      Antioxidant Properties of Polyphenolic Extracts from Quercus Laurina, Quercus Crassifolia, and Quercus Scytophylla Bark

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          Abstract

          The objective of this work was to determine the concentration of total phenols, total flavonoids, hydroxycinnamic acids, and proanthocyanidins present in crude extracts of Quercus laurina, Q. crassifolia, and Q. scytophylla bark. They were extracted by ethanol (90%) maceration and hot water. The antioxidant capacity was determined by the ability to capture OH•, O 2, ROO•, H 2O 2, NO•, and HClO. The hot water crude extract of Q. crassifolia was chosen to be concentrated and purified due to its higher extraction yield (20.04%), concentration of phenol compounds (747 mg gallic acid equivalent (GAE)/g, 25.4 mg quercetin equivalent (QE)/g, 235 mg ChAE/g, 25.7 mg chlorogenic acid equivalents (ChAE)/g), and antioxidant capacity (expressed as half maximal effective concentration (EC 50, µg/mL): OH• = 918, O2• = 80.5, ROO• = 577, H 2O 2 = 597, NO• ≥ 4000, HClO = 740). In a second stage, Q. crassifolia extracted with hot water was treated with ethyl acetate, concentrating the phenol compounds (860 mg GAE/g, 43.6 mg QE/g, 362 ChAE/g, 9.4 cyanidin chloride equivalents (CChE)/g) and improving the scavenging capacity (OH• = 467, O2• = 58.1, ROO• = 716, H 2O 2 = 22.0, NO• ≥ 4000, HClO = 108). Q. crassifolia had the highest polyphenolic concentration and the better capacity for scavenging reactive species, being a favorable candidate to be considered in the development of new products.

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          Hydroxyl radical scavenging activity of compatible solutes

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            Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea.

            An antioxidant fraction of Chinese green tea (green tea antioxidant; GTA), containing several catechins, has been previously shown to inhibit 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced tumor promotion in mouse skin. In the present study, GTA was shown to have antioxidative activity toward hydrogen peroxide (H2O2) and the superoxide radical (O2-). GTA also prevented oxygen radical and H2O2-induced cytotoxicity and inhibition of intercellular communication in cultured B6C3F1 mouse hepatocytes and human keratinocytes (NHEK cells). GTA (0.05-50 micrograms/ml) prevented the killing of hepatocytes (measured by lactate dehydrogenase release) by paraquat (1-10 mM) and glucose oxidase (0.8-40 micrograms/ml) in a concentration-dependent fashion. GTA (50 micrograms/ml) also prevented the inhibition of hepatocyte intercellular communication by paraquat (5 mM), glucose oxidase (0.8 micrograms/ml), and phenobarbital (500 micrograms/ml). In addition, GTA (50 micrograms/ml) prevented the inhibition of intercellular communication in human keratinocytes by TPA (100 ng/ml). Cytotoxicity and inhibition of intercellular communication, two possible mechanisms by which tumor promoters may produce their promoting effects were therefore prevented by GTA. The inhibition of these two effects of pro-oxidant compounds may suggest a mechanism by which GTA inhibits tumor promotion in vivo.
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              The conversion of procyanidins and prodelphinidins to cyanidin and delphinidin

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                Author and article information

                Journal
                Antioxidants (Basel)
                Antioxidants (Basel)
                antioxidants
                Antioxidants
                MDPI
                2076-3921
                26 June 2018
                July 2018
                : 7
                : 7
                : 81
                Affiliations
                [1 ]Programa Institucional de Doctorado en Ciencias Biológicas, Universidad Michoacana de San Nicolás Hidalgo, Ciudad Universitaria, Morelia, Michoacán CP 58030, Mexico; evalencia@ 123456umich.mx
                [2 ]Facultad de Químico Farmacobiología, Universidad Michoacana de San Nicolás de Hidalgo, Tzintzuntzan 173, Col. Matamoros, Morelia, Michoacán CP 58240, Mexico; margarc@ 123456live.ca
                [3 ]Facultad de Ingeniería Civil, Universidad Michoacana de San Nicolás de Hidalgo, Ciudad Universitaria, Morelia, Michoacán CP 58030, Mexico; ggarnica@ 123456umich.mx
                [4 ]Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional, Libramiento Norponiente 2000, Fraccionamiento Realde Juriquilla, Querétaro, Qro CP 76230, Mexico; jfigueroa@ 123456cinvestav.mx
                [5 ]Instituto de Investigaciones sobre Recursos Naturales, Universidad Michoacana de San Nicolás de Hidalgo, Avenida San Juanito Itzícuaro SN, Morelia, Michoacán CP 58330, Mexico; emelendez@ 123456umich.mx
                [6 ]Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Ciudad Universitaria, Morelia, Michoacán CP 58030, Mexico; rsalgado@ 123456umich.mx
                Author notes
                [* ]Correspondence: hmartinez@ 123456umich.mx ; Tel.: +52-(443)-314-2152
                Author information
                https://orcid.org/0000-0003-3969-8082
                Article
                antioxidants-07-00081
                10.3390/antiox7070081
                6071044
                29949924
                40a9c04a-8f28-4b8d-a176-11b91d0bb466
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 05 May 2018
                : 19 June 2018
                Categories
                Article

                quercus,oak bark,scavenging ability,polyphenols
                quercus, oak bark, scavenging ability, polyphenols

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