Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros

Métodos Terapêuticos e Terapias MTCI
Base de dados
País/Região como assunto
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Environ Mol Mutagen ; 61(3): 329-337, 2020 03.
Artigo em Inglês | MEDLINE | ID: mdl-31489703

RESUMO

Medicinal plants are worldwide used as an efficient treatment of many diseases. Myracrodruon urundeuva Allemão (Anacardiaceae) is widely used Brazilian folk medicine to treat inflammations and infections of the female genital tract, conditions of the stomach and throat, and to heal wounds on the skin and mucous membranes. Several pharmacological properties of extracts and compounds isolated from M. urundeuva are found in the literature, corroborating its uses as antiulcer and gastroprotective, anti-inflammatory and analgesic, as well as antimicrobial. Despite these many uses in traditional herbal medicine, there are few reports of its toxic-genetic effect. This work aimed to investigate the genotoxic and mutagenic potential in vivo of the dry decoction of M. urundeuva leaves on somatic cells of Drosophila melanogaster, through the Comet assay and somatic mutation and recombination test (SMART). Six concentrations (0.5, 1.0, 2.0, 4.0, 8.0, and 16.0 mg/mL) were studied after feeding individuals for 24 hr in culture medium hydrated with extracts of M. urundeuva. In the Comet assay, all concentrations showed a genotoxic effect significantly higher than the negative control group, treated with distilled water. The two highest concentrations were also superior to the positive control group, treated with cyclophosphamide (1 mg/mL). In the SMART, there was a mutagenic effect at all concentrations tested, with a clear dose-dependent relationship. Both recombination and mutation account for these mutagenic effects. The set of results indicate that the dry decoction of M. urundeuva leaves is genotoxic and mutagenic for D. melanogaster under the experimental conditions of this study. Environ. Mol. Mutagen. 61:329-337, 2020. © 2019 Wiley Periodicals, Inc.


Assuntos
Anacardiaceae/toxicidade , Drosophila melanogaster/efeitos dos fármacos , Testes de Mutagenicidade , Mutagênicos/toxicidade , Extratos Vegetais/toxicidade , Animais , Anti-Inflamatórios/toxicidade , Brasil , Ensaio Cometa , Drosophila melanogaster/citologia , Drosophila melanogaster/genética , Medicina Tradicional , Mutação/efeitos dos fármacos , Folhas de Planta/toxicidade
2.
Ecotoxicol Environ Saf ; 141: 148-153, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28340370

RESUMO

Natural radiation of geological origin is a common phenomenon in Brazil, a country where radioactive agents such as uranium may be often found. As an unstable atom, uranium undergoes radioactive decay with the generation of a series of decay by-products, including radon, which may be highly genotoxic and trigger several pathological processes, among which cancer. Because it is a gas, radon may move freely between cracks and gaps in the ground, seeping upwards into the buildings and in the environment. In this study, two Drosophila melanogaster Meigen (Diptera, Drosophilidae) strains called Oregon-R and Wild (collected in a non-radioactive environment) were exposed to atmospheric radiation in the Lajes Pintadas city, in the semiarid zone of northeastern Brazil. After six days of environmental exposure, the organisms presented genetic damage significantly higher than that of the negative control group. The genotoxic effects observed reinforce the findings of other studies carried out in the same region, which warn about the environmental risks related to natural radioactivity occurrence. The results also validate the use of the Comet assay in hemocytes of D. melanogaster as a sensitive test to detect genotoxicity caused by natural radiation, and the use of a recently collected D. melanogaster strain in the environmental of radon.


Assuntos
Radiação de Fundo/efeitos adversos , Ensaio Cometa/métodos , Dano ao DNA , Drosophila melanogaster/efeitos da radiação , Exposição Ambiental , Radônio/toxicidade , Animais , Brasil , Clima Desértico , Drosophila melanogaster/genética , Hemócitos/química , Sensibilidade e Especificidade , Urânio/toxicidade
3.
Pest Manag Sci ; 70(4): 559-65, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23650150

RESUMO

BACKGROUND: Higher rates of diseases transmitted from insects to humans led to the increased use of organophosphate insecticides, proven to be harmful to human health and the environment. New, more effective chemical formulations with minimum genetic toxicity effects have become the object of intense research. These formulations include larvicides derived from plant extracts such as dillapiol, a phenylpropanoid extracted from Piper aduncum, and from microorganisms such as spinosad, formed by spinosyns A and D derived from the Saccharopolyspora spinosa fermentation process. This study investigated the genotoxicity of dillapiol and spinosad, characterising and quantifying mutation events and chromosomal and/or mitotic recombination using the somatic mutation and recombination test (SMART) in wings of Drosophila melanogaster. RESULTS: Standard cross larvae (72 days old) were treated with different dillapiol and spinosad concentrations. Both compounds presented positive genetic toxicity, mainly as mitotic recombination events. Distilled water and doxorubicin were used as negative and positive controls respectively. CONCLUSION: Spinosad was 14 times more genotoxic than dillapiol, and the effect was found to be purely recombinogenic. However, more studies on the potential risks of insecticides such as spinosad and dillapiol are necessary, based on other experimental models and methodologies, to ensure safe use.


Assuntos
Dioxóis/toxicidade , Inseticidas/toxicidade , Macrolídeos/toxicidade , Mutagênicos/toxicidade , Compostos Alílicos , Animais , Dano ao DNA , Drosophila melanogaster/efeitos dos fármacos , Drosophila melanogaster/genética , Combinação de Medicamentos , Larva/efeitos dos fármacos , Larva/genética , Testes de Mutagenicidade , Recombinação Genética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA