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      Chemical Composition and Antioxidant Properties of Juniper Berry ( Juniperus communis L.) Essential Oil. Action of the Essential Oil on the Antioxidant Protection of Saccharomyces cerevisiae Model Organism

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          Abstract

          The essential oil of juniper berries ( Juniperus communis L., Cupressaceae) is traditionally used for medicinal and flavoring purposes. As elucidated by gas chromatography/flame ionization detector (GC/FID) and gas chromatography/mass spectrometry (GC/MS methods), the juniper berry oil from Bulgaria is largely comprised of monoterpene hydrocarbons such as α-pinene (51.4%), myrcene (8.3%), sabinene (5.8%), limonene (5.1%) and β-pinene (5.0%). The antioxidant capacity of the essential oil was evaluated in vitro by 2,2-Diphenyl-1-picrylhydrazyl (DPPH) scavenging, 2,2-azino-bis-3-ethylbenzothiazoline-6 sulfonic acid (ABTS) radical cation scavenging, hydroxyl radical (ОН ) scavenging and chelating capacity, superoxide radical ( O 2 ) scavenging and xanthine oxidase inhibitory effects, hydrogen peroxide scavenging. The antioxidant activity of the oil attributable to electron transfer made juniper berry essential oil a strong antioxidant, whereas the antioxidant activity attributable to hydrogen atom transfer was lower. Lipid peroxidation inhibition by the essential oil in both stages, i.e., hydroperoxide formation and malondialdehyde formation, was less efficient than the inhibition by butylated hydroxytoluene (BHT). In vivo studies confirmed these effects of the oil which created the possibility of blocking the oxidation processes in yeast cells by increasing activity of the antioxidant enzymes superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx).

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          Screening of Brazilian plant extracts for antioxidant activity by the use of DPPH free radical method.

          Brazilian plant extracts belonging to 16 species of 5 different families (71 extracts) were tested against the stable DPPH (2,2-diphenyl-1-picryl-hydrazyl-hydrate) free-radical. The ability to scavenge DPPH radical was measured in these experiments by the discoloration of the solution. Ginkgo biloba and rutin, commonly used as antioxidants for medical purposes, were used as standards. Based on our results, we can say that as a general rule the ethanol extracts of plants belonging to the Verbenaceae family showed lower EC(50) values than the other plant extracts. Among the partitions, the more polar ones (ethyl acetate and n-butanol) are those that generally have higher antioxidant activity (AA). Copyright 2001 John Wiley & Sons, Ltd.
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            The deoxyribose method: a simple "test-tube" assay for determination of rate constants for reactions of hydroxyl radicals.

            Hydroxyl radicals, generated by reaction of an iron-EDTA complex with H2O2 in the presence of ascorbic acid, attack deoxyribose to form products that, upon heating with thiobarbituric acid at low pH, yield a pink chromogen. Added hydroxyl radical "scavengers" compete with deoxyribose for the hydroxyl radicals produced and diminish chromogen formation. A rate constant for reaction of the scavenger with hydroxyl radical can be deduced from the inhibition of color formation. For a wide range of compounds, rate constants obtained in this way are similar to those determined by pulse radiolysis. It is suggested that the deoxyribose assay is a simple and cheap alternative to pulse radiolysis for determination of rate constants for reaction of most biological molecules with hydroxyl radicals. Rate constants for reactions of ATP, ADP, and Good's buffers with hydroxyl radicals have been determined by this method.
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              Gas chromatographic retention indices of monoterpenes and sesquiterpenes on methyl silicon and Carbowax 20M phases

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                Author and article information

                Journal
                Antioxidants (Basel)
                Antioxidants (Basel)
                antioxidants
                Antioxidants
                MDPI
                2076-3921
                24 February 2014
                March 2014
                : 3
                : 1
                : 81-98
                Affiliations
                [1 ]Department of Pharmaceutical Chemistry, Division of Clinical Pharmacy and Diagnostics, University of Vienna, Vienna 1090, Austria; E-Mails: info@ 123456artandfragrance.de (E.S.); leopold.jirovetz@ 123456univie.ac.at (L.J.)
                [2 ]Department Biotechnology, University of Food Technologies, Plovdiv 4002, Bulgaria; E-Mails: wstoilowa@ 123456yahoo.com (I.S.); dora.trifonova@ 123456gmail.com (D.T.); a_krastanov@ 123456uft-plovdiv.bg (A.K.)
                [3 ]Kurt Kitzing Co., Wallerstein 86757, Germany; E-Mail: juergen.wanner@ 123456kurtkitzing.de
                [4 ]University Laboratory for Food Analyses, University of Food Technologies, Plovdiv 4002, Bulgaria; E-Mail: loutcian@ 123456abv.bg
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: martina.hoeferl@ 123456univie.ac.at ; Tel.: +43-1-4277-55555; Fax: +43-1-4277-855555.
                Article
                antioxidants-03-00081
                10.3390/antiox3010081
                4665443
                fe0fe1f5-336f-4740-b5af-961767665c56
                © 2014 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 license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 11 December 2013
                : 26 January 2014
                : 28 January 2014
                Categories
                Article

                juniper essential oil,juniperus communis,gc/ms,antioxidant,saccharomyces cerevisiae,antioxidant enzymes

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