Aluísio M. Fonseca
Federal University of Ceará
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Featured researches published by Aluísio M. Fonseca.
Revista Brasileira De Farmacognosia-brazilian Journal of Pharmacognosy | 2009
Aluísio M. Fonseca; Ayla M.C. Bizerra; João Sammy N. Souza; Francisco José Queiroz Monte; Maria da Conceição F. de Oliveira; Marcos Carlos de Mattos; Geoffrey A. Cordell; Raimundo Braz-Filho; Telma L. G. Lemos
Uma analise dos componentes da agua-de-coco (Cocos nucifera L.) de duas variedades da fruta (verde e amarelo) por hidrodestilacao e extracao com solvente, mostrou a presenca de alcoois, cetonas, tiois, acidos carboxilicos, fenois, e esteres. Significativa atividade antioxidante foi observada, usando o metodo DPPH, para as amostras obtidas por hidrodestilacao e extracao de eter de petroleo para ambas as variedades do coco.
Archives of Toxicology | 2010
Marne C. Vasconcellos; Dinara Jaqueline Moura; Renato Moreira Rosa; Miriana da Silva Machado; Temenouga N. Guecheva; Izabel Vianna Villela; Bruna F. Immich; Raquel Carvalho Montenegro; Aluísio M. Fonseca; Telma L. G. Lemos; Maria Elisabete Amaral de Moraes; Jenifer Saffi; Letícia V. Costa-Lotufo; Manoel Odorico de Moraes; João Antonio Pêgas Henriques
Biflorin is a natural quinone isolated from Capraria biflora L. Previous studies demonstrated that biflorin inhibits in vitro and in vivo tumor cell growth and presents potent antioxidant activity. In this paper, we report concentration-dependent cytotoxic, genotoxic, antimutagenic, and protective effects of biflorin on Salmonella tiphymurium, yeast Saccharomyces cerevisiae, and V79 mammalian cells, using different approaches. In the Salmonella/microsome assay, biflorin was not mutagenic to TA97a TA98, TA100, and TA102 strains. However, biflorin was able to induce cytotoxicity in haploid S. cerevisiae cells in stationary and exponential phase growth. In diploid yeast cells, biflorin did not induce significant mutagenic and recombinogenic effects at the employed concentration range. In addition, the pre-treatment with biflorin prevented the mutagenic and recombinogenic events induced by hydrogen peroxide (H2O2) in S. cerevisiae. In V79 mammalian cells, biflorin was cytotoxic at higher concentrations. Moreover, at low concentrations biflorin pre-treatment protected against H2O2-induced oxidative damage by reducing lipid peroxidation and DNA damage as evaluated by normal and modified comet assay using DNA glycosylases. Our results suggest that biflorin cellular effects are concentration dependent. At lower concentrations, biflorin has significant antioxidant and protective effects against the cytotoxicity, genotoxicity, mutagenicity, and intracellular lipid peroxidation induced by H2O2 in yeast and mammalian cells, which can be attributed to its hydroxyl radical-scavenging property. However, at higher concentrations, biflorin is cytotoxic and genotoxic.
Zeitschrift für Naturforschung C | 2005
Marne C. Vasconcellos; Raquel Carvalho Montenegro; Gardenia C.G. Militão; Aluísio M. Fonseca; Otília Deusdênia L. Pessoa; Telma L. G. Lemos; Cláudia Pessoa; Manoel Odorico de Moraes; Letícia V. Costa-Lotufo
Capraria biflora L. (Scrophulariaceae) is a perennial shrub widely distributed in several countries of tropical America. The present work verified the cytotoxic and antioxidant potential of biflorin, an o-naphthoquinone isolated from C. biflora collected in the northeast region of Brazil. The cytotoxicity was tested on three different animal cell models: mouse erythrocytes, sea urchin embryos and tumor cells, while the antioxidant activity was assayed by the thiocyanate method. Biflorin lacked activity on mouse erythrocytes as well as on the development of sea urchin eggs, but strongly inhibited the growth of all five tested tumor cell lines, especially the skin, breast and colon cancer cells with IC50 of 0.40, 0.43 and 0.88 μg/ml for B16, MCF-7 and HCT-8, respectively. Biflorin also showed potent antioxidant activity against autoxidation of oleic acid in a water/alcohol system.
Natural Product Research | 2007
Telma L. G. Lemos; Francisco José Queiroz Monte; Allana Kellen L. Santos; Aluísio M. Fonseca; Hélcio Silva dos Santos; Mailcar F. Oliveira; Sônia Maria O. Costa; Otília Deusdênia L. Pessoa; Raimundo Braz-Filho
The present review focus in quinones found in species of Brazilian northeastern Capraria biflora, Lippia sidoides, Lippia microphylla and Tabebuia serratifolia. The review cover ethnopharmacological aspects including photography of species, chemical structure feature, NMR datea and biological properties. Chemical transformations of lapachol to form enamine derivatives and biological activities are discussed.
Anais Da Academia Brasileira De Ciencias | 2014
Gabrielle G.N.S Wisintainer; Evelyne Rolim Braun Simões; Telma L. G. Lemos; Sidnei Moura; Luciana G. S. Souza; Aluísio M. Fonseca; Manoel Ordorico Moraes; Cláudia Pessoa; Mariana Roesch-Ely; Joao Antonio Pegas Henriques
Biflorin is an o-naphthoquinone with proven cytotoxic effects on tumor cells showing antimicrobial, antitumor and antimutagenic activities. Biflorin is an isolated compound taken from the roots of the plant Capraria biflora L. (Schrophulariaceae), indigenous of the West Indies and South America, which is located in temperate or tropical areas. This compound has shown to be strongly active against grampositive and alcohol-acid-resistant bacteria. It has been efficient in inhibiting the proliferation tumor cell lines CEM, HL-60, B16, HCT-8 and MCF-7. Recently, SK-Br3 cell line was treated with biflorin showing important cytotoxic effects. In this article, information related to the first structural characterization studies are presented, as well as the latest reports concerning the biological activity of this molecule.
Journal of Essential Oil Research | 2006
Aluísio M. Fonseca; Otília Deusdênia L. Pessoa; Telma L. G. Lemos; Ronaldo Ferreira do Nascimento
Abstract The essential oil from the fresh leaves of Capraria biflora (Scrophulariaceae), obtained by hydrodistillation processs, was analyzed by GC and GC/MS. Nine compounds were characterized representing 91.1% of compounds present in the oil. The major components present were the sesquiterpenes β-caryophyllene (29.6%) and β-muurolene (32.6%).
Journal of Molecular Catalysis B-enzymatic | 2009
Aluísio M. Fonseca; Francisco José Queiroz Monte; Maria da Conceição F. de Oliveira; Marcos Carlos de Mattos; Geoffrey A. Cordell; Raimundo Braz-Filho; Telma L. G. Lemos
Biological & Pharmaceutical Bulletin | 2007
Marne C. Vasconcellos; Daniel P. Bezerra; Aluísio M. Fonseca; Márcio Roberto Pinho Pereira; Telma L. G. Lemos; Otília Deusdênia L. Pessoa; Cláudia Pessoa; Manoel Odorico de Moraes; Ana Paula Negreiros Nunes Alves; Letícia V. Costa-Lotufo
Magnetic Resonance in Chemistry | 2003
Aluísio M. Fonseca; Otília Deusdênia L. Pessoa; Edilberto R. Silveira; Francisco José Queiroz Monte; Raimundo Braz-Filho; Telma L. G. Lemos
Fitoterapia | 2006
Telma L. G. Lemos; Luciana L. Machado; João Sammy N. Souza; Aluísio M. Fonseca; Juliana L. Maia; Otília Deusdênia L. Pessoa