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      Constituents and Pharmacological Activities of Myrcia (Myrtaceae): A Review of an Aromatic and Medicinal Group of Plants

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          Abstract

          Myrcia is one of the largest genera of the economically important family Myrtaceae. Some of the species are used in folk medicine, such as a group known as “pedra-hume-caá” or “pedra-ume-caá” or “insulina vegetal” (insulin plant) that it is used for the treatment of diabetes. The species are an important source of essential oils, and most of the chemical studies on Myrcia describe the chemical composition of the essential oils, in which mono- and sesquiterpenes are predominant. The non-volatile compounds isolated from Myrcia are usually flavonoids, tannins, acetophenone derivatives and triterpenes. Anti-inflammatory, antinociceptive, antioxidant, antimicrobial activities have been described to Myrcia essential oils, while hypoglycemic, anti-hemorrhagic and antioxidant activities were attributed to the extracts. Flavonoid glucosides and acetophenone derivatives showed aldose reductase and α-glucosidase inhibition, and could explain the traditional use of Myrcia species to treat diabetes. Antimicrobial and anti-inflammatory are some of the activities observed for other isolated compounds from Myrcia.

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          The major volatile organic compound emitted from Arabidopsis thaliana flowers, the sesquiterpene (E)-β-caryophyllene, is a defense against a bacterial pathogen.

          Flowers have a high risk of pathogen attack because of their rich nutrient and moisture content, and high frequency of insect visitors. We investigated the role of (E)-β-caryophyllene in floral defense against a microbial pathogen. This sesquiterpene is a common volatile compound emitted from flowers, and is a major volatile released from the stigma of Arabidopsis thaliana flowers. Arabidopsis thaliana lines lacking a functional (E)-β-caryophyllene synthase or constitutively overexpressing this gene were challenged with Pseudomonas syringae pv. tomato DC3000, which is a bacterial pathogen of brassicaceous plants. Flowers of plant lines lacking (E)-β-caryophyllene emission showed greater bacterial growth on their stigmas than did wild-type flowers, and their seeds were lighter and misshapen. By contrast, plant lines with ectopic (E)-β-caryophyllene emission from vegetative parts were more resistant than wild-type plants to pathogen infection of leaves, and showed reduced cell damage and higher seed production. Based on in vitro experiments, (E)-β-caryophyllene seems to act by direct inhibition of bacterial growth, rather than by triggering defense signaling pathways. (E)-β-Caryophyllene thus appears to serve as a defense against pathogens that invade floral tissues and, like other floral volatiles, may play multiple roles in defense and pollinator attraction. © 2011 The Authors. New Phytologist © 2011 New Phytologist Trust.
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            A review on recent research results (2008-2010) on essential oils as antimicrobials and antifungals. A review.

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              Analgesic and anti-inflammatory activity of Caryophyllene oxide from Annona squamosa L. bark.

              Caryophyllene oxide was isolated from an unsaponified petroleum ether extract of the bark of Annona squamosa and studied for its analgesic and anti-inflammatory activity. Caryophyllene oxide at the doses of 12.5 and 25mg/kg body wt. and unsaponified petroleum ether extract at a dose of 50mg/kg body wt. showed significant central as well as peripheral analgesic, along with anti-inflammatory, activity. These activities of caryophyllene oxide were comparable with the standard drug used in the respective experiments. Copyright 2009 Elsevier GmbH. All rights reserved.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                09 October 2015
                October 2015
                : 16
                : 10
                : 23881-23904
                Affiliations
                [1 ]Programa de Pós-graduação em Química, Universidade Federal do Pará, Belém 66075-110, PA, Brazil; E-Mails: cascaesmm@ 123456gmail.com (M.M.C.); eloisandrade@ 123456ufpa.br (E.H.A.A.); lss@ 123456ufpa.br (L.S.S.)
                [2 ]Museu Paraense Emílio Goeldi, Belém 66040-170, PA, Brazil; E-Mail: gracazoghbi@ 123456gmail.com
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: giselle@ 123456ufpa.br ; Tel.: +5591-3201-8099; Fax: +5591-3201-7635.
                Article
                ijms-16-23881
                10.3390/ijms161023881
                4632730
                26473832
                70847250-766b-4ec5-842b-1c49045134b9
                © 2015 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/4.0/).

                History
                : 13 August 2015
                : 25 September 2015
                Categories
                Review

                Molecular biology
                myrcia,volatiles,non-volatiles,biological activities
                Molecular biology
                myrcia, volatiles, non-volatiles, biological activities

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