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1.
J Ethnopharmacol ; 100(3): 323-32, 2005 Sep 14.
Artigo em Inglês | MEDLINE | ID: mdl-15941635

RESUMO

Geum quellyon Sweet, a perennial herb of the Rosaceae family, has been used in the traditional medicine of the Mapuche Amerindians of Chile to treat tooth neuralgia, gastric inflammation, prostatitis and to regulate menstruation, and for its diuretic and aphrodisiac properties. Although many benefits have been claimed for this plant, few scientific studies are available in the literature. In this study, we investigated the antioxidant activity of a methanolic extract of Geum quellyon roots. We also examined the anticancer action of this plant on Caco-2 (colon adenocarcinoma cells), DU-145 (androgen-insensitive prostate cancer cells) and KB (oral squamous carcinoma cells) human tumor cell lines. Our data showed that Geum quellyon extract, containing tannins, exhibits interesting antioxidant properties, expressed by its capacity to scavenge 1,1-diphenyl-2-picryl-hydrazyl radical (DPPH) and superoxide anion (O(2)*-), to inhibit xanthine oxidase activity, to chelate metals, and to protect plasmid DNA from cleavage induced by hydroxyl radicals (*OH) and nitric oxide (NO). These results may explain, at least in part, its use in Mapuche traditional medicine for gastric inflammation and prostatitis. The assays on human tumor cell lines demonstrated that this natural product exhibits a inhibitory effect on all human cancer cells examined, and seem to indicate that necrosis cell death is triggered in KB cells and Caco-2, while apoptotic cell demise appears to be induced in DU-145. The effect evidenced in Caco-2 cells can be in part correlated to a modulation of redox-sensitive mechanisms.


Assuntos
Antineoplásicos Fitogênicos/farmacologia , Antioxidantes/farmacologia , Geum/química , Compostos de Bifenilo/química , Células CACO-2 , Linhagem Celular Tumoral , Quelantes/química , Quelantes/farmacologia , Chile , Ensaio Cometa , DNA de Neoplasias/biossíntese , DNA de Neoplasias/efeitos dos fármacos , Ensaios de Seleção de Medicamentos Antitumorais , Inibidores Enzimáticos/farmacologia , Sequestradores de Radicais Livres/farmacologia , Humanos , Hidrazinas/química , Peróxido de Hidrogênio/química , Células KB , L-Lactato Desidrogenase/metabolismo , Masculino , Medicina Tradicional , Picratos , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Raízes de Plantas/química , Neoplasias da Próstata/tratamento farmacológico , Neoplasias da Próstata/metabolismo , Espécies Reativas de Oxigênio/metabolismo , Taninos/química , Taninos/isolamento & purificação , Taninos/farmacologia , Sais de Tetrazólio , Tiazóis , Raios Ultravioleta , Xantina Oxidase/antagonistas & inibidores
2.
Nat Prod Commun ; 7(5): 603-6, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22799086

RESUMO

Two depsides and five depsidones, isolated from lichens, were tested to determine their in vivo protective effects on tobacco leaves challenged with tobacco mosaic virus (TMV). The results indicate that most of these compounds are able to reduce either the number and/or the size of necrotic lesions following virus infection. Pannarin, 1'-chloro-pannarin and stictic acid provided the more effective protective results, reducing by at least 45% the number and size of lesions. Real Time PCR assays were used to explore the target of action against TMV by examining the response behavior of genes involved in the plant defense mechanism. The application of the lichen substances did not lead to changes in the transcriptional levels of pathogen-related (PR1a), allene oxide synthase 2 (AOS2) or oxophytodienoate reductase (OPR3) genes. Thus, the protection observed in the tobacco leaves treated with the lichen compounds may be mediated by a mechanism which does not involved the SA- or JA-mediated defensive plant response. A possible structure-activity relationship is presented.


Assuntos
Depsídeos/farmacologia , Lactonas/farmacologia , Líquens/química , Nicotiana/microbiologia , Doenças das Plantas/terapia , Vírus do Mosaico do Tabaco/efeitos dos fármacos , Folhas de Planta/microbiologia , Relação Estrutura-Atividade
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