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      Antimicrobial and antioxidant activities of triterpenoid and phenolic derivatives from two Cameroonian Melastomataceae plants: Dissotis senegambiensis and Amphiblemma monticola

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          Abstract

          Background

          Antimicrobial resistance is a serious threat against humankind and the search for new therapeutics is needed. This study aims to investigate the antimicrobial and antioxidant activities of ethanol extracts and compounds isolated from Dissotis senegambiensis and Amphiblemma monticola, two Cameroonian Melastomataceae species traditionally used for the treatment of fever, malaria and infectious diseases.

          Methods

          The plant extracts were prepared by maceration in ethanol. Standard chromatographic and spectroscopic methods were used to isolate and identify fourteen compounds from the two plant species [ 1–6 (from D. senegambiensis), 3, 4 and 7–14 (from A. monticola)]. A two-fold serial micro-dilution method was used to determine the minimum inhibitory concentration (MIC) against four bacterial strains including two resistant bacterial strains, methicillin resistant S. aureus (MRSA3) and methicillin resistant S. aureus (MRSA4) and three yeast strains.

          Results

          The fractionation of EtOH extracts afforded fourteen compounds belonging to triterpenoid and phenolic derivatives. The ethanol extracts, compounds 3, 5–8, 10 and the mixture of 10 +  12 were active against all the tested bacterial and fungal species. Compound 7 (MIC = 16–32 μg/mL) and 10 (MIC = 8–16 μg/mL) displayed the largest antibacterial and antifungal activities, respectively. Compounds 7, 10 and the mixture of 10 +  12 showed prominent antibacterial activity against methicillin- resistant S. aureus (MRSA) which is in some cases equal to that of ciprofloxacin used as reference antibacterial drug. Compound 8 also showed high radical-scavenging activities and ferric reducing power when compared with vitamin C and butylated hydroxytoluene used as reference antioxidants. The tested samples were non-toxic to normal cells highlighting their good selectivity.

          Conclusions

          The result of this investigation reveals the potential of D. senegambiensis and A. monticola as well as the most active compounds in the search for new antimicrobial and antioxidant agents. So, further investigations are needed.

          Electronic supplementary material

          The online version of this article (10.1186/s12906-018-2229-2) contains supplementary material, which is available to authorized users.

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          Most cited references38

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          Antimicrobial properties of tannins

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            Evaluation of antioxidant properties of pomegranate peel extract in comparison with pomegranate pulp extract

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              Antimicrobial and antioxidant activity of kaempferol rhamnoside derivatives from Bryophyllum pinnatum

              Background Bryophyllum pinnatum (Lank.) Oken (Crassulaceae) is a perennial succulent herb widely used in traditional medicine to treat many ailments. Its wide range of uses in folk medicine justifies its being called "life plant" or "resurrection plant", prompting researchers' interest. We describe here the isolation and structure elucidation of antimicrobial and/or antioxidant components from the EtOAc extract of B. pinnatum. Results The methanol extract displayed both antimicrobial activities with minimum inhibitory concentration (MIC) values ranging from 32 to 512 μg/ml and antioxidant property with an IC50 value of 52.48 μg/ml. Its partition enhanced the antimicrobial activity in EtOAc extract (MIC = 16-128 μg/ml) and reduced it in hexane extract (MIC = 256-1024 μg/ml). In addition, this process reduced the antioxidant activity in EtOAc and hexane extracts with IC50 values of 78.11 and 90.04 μg/ml respectively. Fractionation of EtOAc extract gave seven kaempferol rhamnosides, including; kaempferitrin (1), kaempferol 3-O-α-L-(2-acetyl)rhamnopyranoside-7-O-α-L-rhamnopyranoside (2), kaempferol 3-O-α-L-(3-acetyl)rhamnopyranoside-7-O-α-L-rhamnopyranoside (3), kaempferol 3-O-α-L-(4-acetyl)rhamnopyranoside-7-O-α-L-rhamnopyranoside (4), kaempferol 3-O-α-D- glucopyranoside-7-O-α-L-rhamnopyranoside (5), afzelin (6) and α-rhamnoisorobin (7). All these compounds, except 6 were isolated from this plant for the first time. Compound 7 was the most active, with MIC values ranging from 1 to 2 μg/ml and its antioxidant activity (IC50 = 0.71 μg/ml) was higher than that of the reference drug (IC50 = 0.96 μg/ml). Conclusion These findings demonstrate that Bryophyllum pinnatum and some of its isolated compounds have interesting antimicrobial and antioxidant properties, and therefore confirming the traditional use of B. pinnatum in the treatment of infectious and free radical damages.
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                Author and article information

                Contributors
                ntraissa69@yahoo.fr
                ndjateufabrice2015@gmail.com
                ekomsteve@yahoo.com
                arnaudmboutchom@yahoo.fr
                amauduc2@yahoo.com
                +237 677 808 420 , mtene2001@yahoo.fr
                ptane@yahoo.com
                hmorita@inm.u-toyama.ac.jp
                iqbal.choudhary@iccbs.edu
                +237 677 000 897 , jtamokou@yahoo.fr
                Journal
                BMC Complement Altern Med
                BMC Complement Altern Med
                BMC Complementary and Alternative Medicine
                BioMed Central (London )
                1472-6882
                16 May 2018
                16 May 2018
                2018
                : 18
                : 159
                Affiliations
                [1 ]ISNI 0000 0001 0657 2358, GRID grid.8201.b, Laboratory of Natural Products Chemistry, Department of Chemistry, , Faculty of Science, University of Dschang, ; P.O. Box 67, Dschang, Cameroon
                [2 ]ISNI 0000 0001 0657 2358, GRID grid.8201.b, Laboratory of Microbiology and Antimicrobial substances, Department of Biochemistry, , Faculty of Science, University of Dschang, ; P.O. Box 67, Dschang, Cameroon
                [3 ]ISNI 0000 0001 2171 836X, GRID grid.267346.2, Institute of Natural Medicine, , University of Toyama, ; 2630-Sugitani, Toyama, 930-0194 Japan
                [4 ]ISNI 0000 0001 0219 3705, GRID grid.266518.e, H.E.J Research Institute of Chemistry, , University of Karachi, ; -75270, Karachi, Pakistan
                Author information
                http://orcid.org/0000-0002-8088-463X
                Article
                2229
                10.1186/s12906-018-2229-2
                5956543
                29769064
                f9d379e9-b418-42cd-a6fe-c972e47ccdfd
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 30 January 2018
                : 4 May 2018
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Complementary & Alternative medicine
                dissotis senegambiensis,amphiblemma monticola,melastomataceae,triterpenoids,phenolics,antibacterial,antifungal,methicillin-resistant s. aureus

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