Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Mais filtros

País/Região como assunto
Tipo de documento
Intervalo de ano de publicação
1.
Arch Microbiol ; 206(7): 300, 2024 Jun 11.
Artigo em Inglês | MEDLINE | ID: mdl-38861201

RESUMO

Microorganisms produce diverse classes of metabolites under various physiological conditions. Many bacterial strains have been reported to carry out the process of desulfurization in a cost-effective manner by converting dibenzothiophene (DBT) into 2-hydroxybiphenyl (2-HBP) and then using the 2-HBP as a carbon source for growth and development. Key rate-limiting factors and an increased concentration of 2HBP (400 µM) affect the biodesulfurization activity of bacteria through the produced metabolites. Thus, this study was designed to explore the nature of the metabolites produced by Rhodococcus erythropolis in the presence of DBT and 2HBP supplemented with a culture medium. A total of 330 metabolites were detected, and the key metabolites identified were 11Z-eicosaenoyl-EA, 1-carboxyethylisoleucine, 1(3)-glyceryl-PGF2alpha, taurine, 2-hydroxynicotinic acid, 4,4-dimethyl-14alpha-hydroxymethyl-5alpha-cholest-8-en-3beta-ol, and 10-nitrooleic acid. The supplementation of DBT and DBT-2HBP resulted in the differential regulation of these metabolites, either through downregulation or overexpression. Furthermore, at high concentrations of 2-HBP, 1-carboxyethylisoleucine, taurine, 2-hydroxynicotinic acid, and nicotinic acid were upregulated. This work proposes that the identified metabolites may play a role in bacteria-mediated desulphurization and could be beneficial in developing a cost-effective method of desulphurization for refining petroleum.


Assuntos
Compostos de Bifenilo , Petróleo , Rhodococcus , Tiofenos , Rhodococcus/metabolismo , Rhodococcus/crescimento & desenvolvimento , Petróleo/metabolismo , Compostos de Bifenilo/metabolismo , Tiofenos/metabolismo , Biodegradação Ambiental , Meios de Cultura/química , Meios de Cultura/metabolismo , Enxofre/metabolismo
2.
Commun Biol ; 7(1): 668, 2024 May 30.
Artigo em Inglês | MEDLINE | ID: mdl-38816577

RESUMO

Parkinson's disease is managed using levodopa; however, as Parkinson's disease progresses, patients require increased doses of levodopa, which can cause undesirable side effects. Additionally, the oral bioavailability of levodopa decreases in Parkinson's disease patients due to the increased metabolism of levodopa to dopamine by gut bacteria, Enterococcus faecalis, resulting in decreased neuronal uptake and dopamine formation. Parkinson's disease patients have varying levels of these bacteria. Thus, decreasing bacterial metabolism is a promising therapeutic approach to enhance the bioavailability of levodopa in the brain. In this work, we show that Mito-ortho-HNK, formed by modification of a naturally occurring molecule, honokiol, conjugated to a triphenylphosphonium moiety, mitigates the metabolism of levodopa-alone or combined with carbidopa-to dopamine. Mito-ortho-HNK suppresses the growth of E. faecalis, decreases dopamine levels in the gut, and increases dopamine levels in the brain. Mitigating the gut bacterial metabolism of levodopa as shown here could enhance its efficacy.


Assuntos
Encéfalo , Dopamina , Enterococcus faecalis , Microbioma Gastrointestinal , Levodopa , Doença de Parkinson , Levodopa/metabolismo , Levodopa/administração & dosagem , Microbioma Gastrointestinal/efeitos dos fármacos , Dopamina/metabolismo , Doença de Parkinson/tratamento farmacológico , Doença de Parkinson/metabolismo , Doença de Parkinson/microbiologia , Encéfalo/metabolismo , Encéfalo/efeitos dos fármacos , Animais , Enterococcus faecalis/metabolismo , Enterococcus faecalis/efeitos dos fármacos , Masculino , Antiparkinsonianos/metabolismo , Antiparkinsonianos/administração & dosagem , Antiparkinsonianos/farmacologia , Carbidopa , Humanos , Compostos de Bifenilo/metabolismo , Camundongos , Compostos Organofosforados/metabolismo , Camundongos Endogâmicos C57BL
3.
Braz. j. biol ; 78(2): 248-254, May-Aug. 2018. tab, graf
Artigo em Inglês | LILACS | ID: biblio-888871

RESUMO

Abstract This study was carried out to assess the antibacterial, cytotoxic and antioxidant activities of extracts of Morus nigra L. HPLC was used to determine the fingerprint chromatogram of the crude ethanolic extract (Mn-EtOH). The antibacterial effect was assessed through the method of microdilution. The cytotoxicity was tested against human tumour cell lines using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. The total phenolic and flavonoid contents were also assessed through the Folin-Ciocalteu and aluminum chloride methods, respectively. Antioxidant activities of the extracts were evaluated by using 2,2-diphenyl-1-picrylhydrazil (DPPH) radical scavenging and β-carotene-linoleic acid bleaching methods. The presence of phenolic compounds in Mn-EtOH was confirmed using HPLC. The extracts showed activity against most microorganisms tested. The extracts did not show any expressive antiproliferative effect in the assessment of cytotoxicity. The most significant total phenolic content was 153.00 ± 11.34 mg of gallic acid equivalent/g to the ethyl acetate extract (AcOEt). The total flavonoid content was 292.50 ± 70.34 mg of catechin equivalent/g to the AcOEt extract, which presented the best antioxidant activity (IC50 50.40 ± 1.16 μg/mL) for DPPH scavenging. We can conclude that this species shows strong antibacterial and antioxidant activities, as well as weak cytotoxic effects.


Resumo Este estudo foi realizado para avaliar as atividades antibacteriana, citotóxica e antioxidante de extratos de Morus nigra L. HPLC foi utilizado para determinar o perfil de compostos fenólicos do extrato etanólico bruto (Mn-EtOH). O efeito antibacteriano foi avaliado através do método de microdiluição. A citotoxicidade foi testada contra linhagens celulares de tumores humanos utilizando o ensaio do brometo de 3-(4,5-dimetil-2-tiazolil)-2,5-difenil-2H-tetrazólio (MTT). O conteúdo total de compostos fenólicos e flavonoides também foi avaliado por meio dos métodos de Folin-Ciocalteu e cloreto de alumínio, respectivamente. A atividade antioxidante dos extratos foi avaliada por meio do sequestro do radical livre 2,2-difenil-1-picrilhidrazil (DPPH) e co-oxidação do sistema β-caroteno-ácido linoleico. A presença de compostos fenólicos em Mn-EtOH foi confirmada utilizando HPLC. Os extratos mostraram atividade contra a maioria dos microrganismos testados. Os extratos não mostraram qualquer efeito antiproliferativo expressivo na avaliação da citotoxicidade. O conteúdo fenólico total mais significativo foi de 153,00 ± 11,34 mg de equivalente de ácido gálico/g para o extrato acetato de etila (AcOEt). O conteúdo de flavonoides totais foi de 292,50 ± 70,34 mg de equivalente de catequina/g para o extrato AcOEt, que apresentou a melhor atividade antioxidante (IC50 50,40 ± 1,16 mg/mL) para o sequestro do DPPH. Podemos concluir que esta espécie apresenta forte atividade antibacteriana e antioxidante, bem como fraca atividade citotóxica.


Assuntos
Humanos , Extratos Vegetais/farmacologia , Morus/química , Antibacterianos/farmacologia , Antioxidantes/farmacologia , Fenóis/análise , Picratos/metabolismo , Flavonoides/análise , Compostos de Bifenilo/metabolismo , Extratos Vegetais/toxicidade , Extratos Vegetais/química , Sobrevivência Celular/efeitos dos fármacos , Linhagem Celular Tumoral , Antibacterianos/toxicidade , Antibacterianos/química , Antioxidantes/toxicidade , Antioxidantes/química
4.
Braz. j. microbiol ; 46(3): 769-776, July-Sept. 2015. tab, ilus
Artigo em Inglês | LILACS | ID: lil-755829

RESUMO

The white button mushroom, Agaricus bisporus, is the most commonly grown mushroom in Iran; however, there is a significant shortage of research on its antioxidant activity and other medicinal properties. The aim of this study was to evaluate antioxidant capacity of the methanolic extracts from four cultivated strains and four Internal Transcribed Spacer (ITS)-identified, Iranian wild isolates of A. bisporus. Evaluations were made for total phenols, flavonoids and anthocyanins, and 2, 2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity. Overall, results showed that all the wild isolates exhibited significantly lower DPPH-derived EC50, compared to the cultivated strains (p < 0.05). A relatively high relationship was observed between total phenols and flavonoids or anthocyanins (r2 > 0.60). However, these constituents could not statistically differentiate the group of wild samples from the cultivated ones, and there was low correlation with the DPPH-derived EC50s (r2 < 0.40). In conclusion, comparisons showed that wild isolate 4 and cultivated strains A15 and H1 had higher antioxidant capacity than the others (p < 0.05). This result identifies these mushrooms as good candidates for further investigation.

.


Assuntos
Humanos , Agaricus/metabolismo , Antocianinas/metabolismo , Antioxidantes/metabolismo , Compostos de Bifenilo/metabolismo , Flavonoides/metabolismo , Fenóis/metabolismo , Picratos/metabolismo , Agaricus/genética , DNA Intergênico/genética , Irã (Geográfico) , Oxirredução , Espécies Reativas de Oxigênio/metabolismo
5.
Biol. Res ; 48: 1-17, 2015. graf, tab
Artigo em Inglês | LILACS | ID: biblio-950779

RESUMO

BACKGROUND: Excessive production of free radicals causes direct damage to biological molecules such as DNA, proteins, lipids, carbohydrates leading to tumor development and progression. Natural antioxidant molecules from phytochemicals of plant origin may directly inhibit either their production or limit their propagation or destroy them to protect the system. In the present study, Monodora myristica a non-timber forest product consumed in Cameroon as spice was screened for its free radical scavenging properties, antioxidant and enzymes protective activities. Its phenolic compound profile was also realized by HPLC. RESULTS: This study demonstrated that M. myristica has scavenging properties against DPPH',OH',NO', and ABTS'radicals which vary in a dose depending manner. It also showed an antioxidant potential that was comparable with that of Butylated Hydroxytoluene (BHT) and vitamin C used as standard. The aqueous ethanol extract of M. myristica barks (AEH); showed a significantly higher content in polyphenolic compounds (21.44 ± 0.24 mg caffeic acid/g dried extract) and flavonoid (5.69 ± 0.07 quercetin equivalent mg/g of dried weight) as compared to the other studied extracts. The HPLC analysis of the barks and leaves revealed the presence of several polyphenols. The acids (3,4-OH-benzoic, caffeic, gallic, O- and P- coumaric, syringic, vanillic), alcohols (tyrosol and OH-tyrosol), theobromine, quercetin, rutin, catechine and apigenin were the identified and quantified polyphenols. All the tested extracts demonstrated a high protective potential on the superoxide dismutase (SOD), catalase and peroxidase activities. CONCLUSION: Finally, the different extracts from M. myristica and specifically the aqueous ethanol extract reveal several properties such as higher free radical scavenging properties, significant antioxidant capacities and protective potential effects on liver enzymes.


Assuntos
Extratos Vegetais/farmacologia , Sequestradores de Radicais Livres/farmacologia , Especiarias , Annonaceae/química , Polifenóis/química , Antioxidantes/farmacologia , Peroxidases/efeitos dos fármacos , Picratos/metabolismo , Ácidos Sulfônicos/metabolismo , Superóxido Dismutase/efeitos dos fármacos , Flavonoides/análise , Compostos de Bifenilo/metabolismo , Técnicas In Vitro , Camarões , Extratos Vegetais/química , Catalase/efeitos dos fármacos , Florestas , Cromatografia Líquida de Alta Pressão , Radical Hidroxila/metabolismo , Folhas de Planta/química , Casca de Planta/química , Benzotiazóis/metabolismo , Óxido Nítrico/metabolismo
6.
Biol. Res ; 47: 1-10, 2014. graf, tab
Artigo em Inglês | LILACS | ID: biblio-950772

RESUMO

BACKGROUND: Based on the ethnomedicinal uses and the effective outcomes of natural products in various diseases, this study was designed to evaluate Isodon rugosus as possible remedy in oxidative stress, alzheimer's and other neurodegenerative diseases. Acetylecholinestrase (AChE) and butyrylcholinesterase (BChE) inhibitory activities of crude methanolic extract (Ir.Cr), resultant fractions (n-hexane (Ir.Hex), chloroform (Ir.Cf), ethyl acetate (Ir.EtAc), aqueous (Ir.Aq)), flavonoids (Ir.Flv) and crude saponins (Ir.Sp) of I. rugosus were investigated using Ellman's spectrophotometric method. Antioxidant potential of I. rugosus was determined using DPPH, H2O2 and ABTS free radicals scavenging assays. Total phenolic and flavonoids contents of plant extracts were determined and expressed in mg GAE/g dry weight and mg RTE/g of dry sample respectively. RESULTS: Among different fractions Ir.Flv and Ir.Cf exhibited highest inhibitory activity against AChE (87.44 ± 0.51, 83.73 ± 0.64%) and BChE (82.53 ± 0.71, 88.55 ± 0.77%) enzymes at 1 mg/ml with IC50 values of 45, 50 for AChE and 40, 70 µg/ml for BChE respectively. Activity of these fractions were comparable to galanthamine causing 96.00 ± 0.30 and 88.61 ± 0.43% inhibition of AChE and BChE at 1 mg/ml concentration with IC50 values of 20 and 47 µg/ml respectively. In antioxidant assays, Ir.Flv, Ir.Cf, and Ir.EtAc demonstrated highest radicals scavenging activities in DPPH and H2O2 assays which were comparable to ascorbic acid. Ir.Flv was found most potent with IC50 of 19 and 24 µg/ml against DPPH and H2O2 radicals respectively. Whereas antioxidant activates of plant samples against ABTS free radicals was moderate. Ir.Cf, Ir.EtAc and Ir.Cr showed high phenolic and flavonoid contents and concentrations of these compounds in different fractions correlated well to their antioxidant and anticholinestrase activities. CONCLUSION: It may be inferred from the current investigations that the Ir.Sp, Ir.Flv and various fractions of I. rugosus are good sources of anticholinesterase and antioxidant compounds. Different fractions can be subjected to activity guided isolation of bioactive compounds effective in neurological disorders.


Assuntos
Saponinas/análise , Flavonoides/análise , Extratos Vegetais/química , Inibidores da Colinesterase/análise , Isodon/química , Antioxidantes/análise , Picratos/metabolismo , Acetilcolinesterase/efeitos dos fármacos , Saponinas/isolamento & purificação , Espectrofotometria/métodos , Ácidos Sulfônicos/metabolismo , Flavonoides/isolamento & purificação , Compostos de Bifenilo/metabolismo , Butirilcolinesterase/efeitos dos fármacos , Clorofórmio , Sequestradores de Radicais Livres/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Concentração Inibidora 50 , Isodon/classificação , Isodon/enzimologia , Componentes Aéreos da Planta/química , Misturas Complexas , Metanol , Benzotiazóis/metabolismo , Radicais Livres/análise , Hexanos , Peróxido de Hidrogênio/metabolismo , Medicina Tradicional , Acetatos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA