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      Study of antimicrobial potential and cytotoxic of Cordia nodosa species

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          Background Increasingly infectious agents change, which is why there is a failure in the treatment of microbial infections, above all, the emergence of resistance to existing antibiotics [1]. Therefore, the search for new antimicrobial substances from natural products has increased the interest of researchers. Brazil is considered the country has one of the greatest biodiversity on the planet, where the popular use of medicinal plants has become an important source for discovery of new active compounds [2]. However, for the safe use of these plant species, popular knowledge must relate to the performance of bioassays that demonstrate the therapeutic efficacy and low toxicity. Cordia species belonging to the family Boraginaceae, are used in folk medicine to treat gastric ulcers and proven front possess antimicrobial potential Escherichia coli and Staphylococcus aureus [3]. Phytochemical studies carried out with species of this family revealed the presence of alkaloids, naphthoquinones, saponins, tannins, flavonoids, among others, responsible for this spectrum of biological activities. Cordia nodosa specie has proven antifungal activity but the work as they relate to the antibacterial activity are scarce [4]. The aim of this study was to evaluate the antimicrobial activity and toxicity of Cordia nodosa. Methods The experimental research was conducted in the Research Laboratory of Wound Care, Federal University of Alagoas. Four fractions were tested in different parts of Cordia nodosa, A, B, C and D. Antimicrobial activity was determined by microbial sensitivity tests, the method of disk diffusion (DD) and broth microdilution method for determination of minimum inhibitory concentration (MIC). The percentage inhibition of bacterial disk diffusion test was calculated by dividing the average inhibition hundred times the sample by the average zone of inhibition positive control [5]. 8 were used bacterial strains, among them Gram-positive and Gram-negative bacteria, distributed by American Type Cell Collection. The toxicity evaluation of the samples was measured by testing toxicity on Artemia salina. Results and conclusions Samples B and C were considered moderately active against the strain of Staphylococcus aureus, with a percent inhibition of 29.2% (inhibition = 8 mm) and 55.6% (inhibition = 15 mm), respectively, when compared with the mean of the positive control used Gentamicin (about 27 mm). Both samples were also moderately active against the strains of S. epidermidis, involving inhibition percentages of 33.4%. The sample C presented little active front of the line of P. aeruginosa as the percentage of inhibition was less than 25%. The results obtained with the MIC determination showed that the sample B is the fraction of better antimicrobial activity inhibiting the growth of the strain of S. epidermidis concentration of 1000 to 125 mg mL- 1. Identified the absence of toxicity in all samples, because the mortality of Artemia salina was ≤ 30%. This finding dismissed the test quantitative, and therefore the LC50 determination, because it means that the concentrations tested were below the LC50 of each sample (LC50 ≥ 1000 mg mL-1). These results represent the first evidence of safety of plant species that are performed in sequence in vivo bioassays.

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          Acute toxicity and mutagenic activity of Mexican plants used in traditional medicine.

          The present work was undertaken to determine safety parameters of selected Mexican medicinal plants chosen on the basis of their frequency of medicinal use and commercial importance. The medicinal herbs included Amphipteryngium adstringens, Hintonia standleyana, Hintonia latiflora, Piper sanctum, Haemathoxylon brasiletto, Iostephane heterophylla, Valeriana procera, Arracacia tolucensis, Brickellia veronicaefolia, Scaphyglottis livida, Exostema caribaeum, Hippocratea excelsa, Ligusticum porteri, Poliomintha longiflora and Gnaphalium sp. In the acute toxicity studies in mice performed according to the Lorke procedure, Exostema caribaeum, Hippocratea excelsa, Ligusticum porteri and Poliomintha longiflora were the most toxic with LD(50) values between 1085 and 2mg/kg. The Ames test revealed that Gnaphalium sp. and Valeriana procera extracts induced mutations of S. typhimurium TA98 with or without the S9 microsomal fraction, and TA100 in the presence of the enzymatic fraction, respectively. The tincture of Valeriana procera, however, was non-mutagenic. Finally, in the Artemia salina lethality test Brickellia veronicaefolia, Arracacia tolucensis, Poliomintha longiflora and Piper sanctum caused significant mortality of the crustacean larvae with LC(50) in the range of 37-227 microg/mL.
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            Plantas medicinais e seus constituintes bioativos: uma revisão da bioatividade e potenciais benefícios nos distúrbios da ansiedade em modelos animais

            A procura de novos agentes terapêuticos provenientes de plantas medicinais para doenças psiquiátricas tem progredido significativamente na última década. Isso reflete num grande número de preparações herbárias para as quais o potencial psicoterapêutico tem sido avaliado em diversos modelos animais. O intuito desta revisão é fornecer uma ampla visão das plantas medicinais que apresentam efeitos terapêuticos significantes em modelos animais de doenças psiquiátricas, especificamente os distúrbios da ansiedade. Um considerável número de constituintes herbários cujos efeitos comportamentais e ações farmacológicas têm sido bem caracterizados podem ser bons candidatos para futuras investigações que podem resultar em uso clínico, merecendo, portanto, uma maior atenção em estudos posteriores.
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              Author and article information

              Conference
              BMC Proc
              BMC Proc
              BMC Proceedings
              BioMed Central
              1753-6561
              2014
              1 October 2014
              : 8
              : Suppl 4
              : P69
              Affiliations
              [1 ]Laboratório de Pesquisa em Tratamento de Feridas, Universidade Federal de Alagoas, Campus A.C. Simões - Av. Lourival Melo Mota, s/n, Cidade Universitária - Maceió, Alagoas, 57072-900, Brazil
              [2 ]Instituto de Tecnologia e Pesquisa, Universidade Tiradentes - Av. Murilo Dantas, Farolândia - Aracaju, Sergipe, 49032-490, Brazil
              [3 ]Laboratório de Farmacologia e Imunidade, Universidade Federal de Alagoas, Campus A. C. Simões - Av. Lourival Melo Mota, s/n, Cidade Universitária - Maceió, Alagoas, Brasil
              Article
              1753-6561-8-S4-P69
              10.1186/1753-6561-8-S4-P69
              4204213
              a29a3ffc-769a-487b-ad3c-7bcac23386da
              Copyright © 2014 dos Santos et al.; licensee BioMed Central Ltd.

              This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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.

              5th Congress of the Brazilian Biotechnology Society (SBBIOTEC)
              Florianópolis, Brazil
              10-14 November 2013
              History
              Categories
              Poster Presentation

              Medicine
              Medicine

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