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1.
Microbiol Res ; 214: 74-82, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-30031483

RESUMO

The indiscriminate use of antibiotics is causing an increase in bacterial resistance, complicating therapeutic planning. In this context, natural products have emerged as major providers of bioactive compounds. This work performs a bioguided study of Brazilian red propolis to identify compounds with antibacterial potential and to evaluate their cytotoxicity against non-tumour cells. Using bioguided fractionation performed with the hydroalcoholic extract of red propolis from Alagoas, it was possible to obtain subfractions with remarkable bacteriostatic activity compared with the precursor fractions. The SC2 subfraction was highlighted and showed the best results with minimal inhibitory concentrations (MICs) of 56.75, 28.37, 454.00, and 227.00 µg mL-1 against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa, respectively. However, this study also revealed a cytotoxic effect against the non-tumour Vero cell line. Furthermore, through chemical analyses using high resolution mass spectrometry, high performance liquid chromatography with UV detection, and gas chromatography coupled to mass spectrometry, we verified the presence of important marker compounds in the fractions and extracts, including formononetin (m/z 267.0663), biochanin A (m/z 283.0601), and liquiritigenin (m/z 255.0655). The results obtained in this study suggest an important antibacterial potential of red propolis subfractions. In this context, the bioguided fractionation has been a useful process, due to its ability to isolate and concentrate active compounds in a logical and rational way.


Assuntos
Antibacterianos/isolamento & purificação , Antibacterianos/farmacologia , Bactérias/efeitos dos fármacos , Produtos Biológicos/isolamento & purificação , Produtos Biológicos/farmacologia , Própole/química , Animais , Antibacterianos/toxicidade , Bactérias/crescimento & desenvolvimento , Produtos Biológicos/toxicidade , Brasil , Sobrevivência Celular/efeitos dos fármacos , Fracionamento Químico , Chlorocebus aethiops , Cromatografia Líquida de Alta Pressão , Células Epiteliais/efeitos dos fármacos , Células Epiteliais/fisiologia , Espectrometria de Massas , Testes de Sensibilidade Microbiana , Células Vero
2.
Biomed Pharmacother ; 91: 951-963, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28514834

RESUMO

Continuous increases in the rates of tumor diseases have highlighted the need for identification of novel and inexpensive antitumor agents from natural sources. In this study, we investigated the effects of enriched fraction from hydroalcoholic Brazilian red propolis extract against Hep-2 cancer cell line. Initially 201 fractions were arranged in 12 groups according to their chromatographic characteristics (A-L). After an in vitro cell viability screening, J and L were further selected as promising enriched fractions for this study. The chemical characterization was performed and Biochanin A, Formononetin, and Liquiritigenin compounds were quantified. Through MTT viability assay and morphological changes observed by Giemsa and DAPI staining, the results showed that red propolis inhibited cancer cells growth. Flow cytometry results indicated effects that were partly mediated through programmed cell death as confirmed by externalization of phosphatidylserine, DNA cleaved assay, increase at SUB G1-G0 phase in cell cycle analysis and loss of mitochondrial membrane potential. In conclusion, our results demonstrated that red propolis enriched fractions promoted apoptotic effects in human cancer cells through the mechanisms involving mitochondrial perturbation. Therefore, red propolis fractions contain candidate agents for adjuvant cancer treatment, which further studies should elucidate the comprehensive mechanistic pathways.


Assuntos
Antineoplásicos/farmacologia , Neoplasias/tratamento farmacológico , Própole/farmacologia , Apoptose/efeitos dos fármacos , Brasil , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Flavanonas/farmacologia , Fase G1/efeitos dos fármacos , Genisteína/farmacologia , Humanos , Isoflavonas/farmacologia , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Fase de Repouso do Ciclo Celular/efeitos dos fármacos
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