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1.
Food Chem ; 319: 126472, 2020 Jul 30.
Artigo em Inglês | MEDLINE | ID: mdl-32163839

RESUMO

Whey protein is one of the most relevant co-products manufactured by the dairy industry and it is a powerful environmental pollutant. Therefore, the enzymatic hydrolysis of whey protein concentrate (WPC 35) to produce antioxidant peptides is an innovative approach which can provide added value to whey. The WPC 35 hydrolysis with trypsin was carried out for 4.31 h at 41.1 °C with an enzyme/substrate ratio of 0.017. Under such hydrolysis conditions, the peptides produced have the highest radical scavenging activity and cytoprotector effect. The WPC hydrolysate and a permeate ≤3 kDa were characterized by SDS-page, RP-HPLC and MALDI-TOF-MS. Furthermore, O2•- and HO• scavenging activity and the cytoprotective effect against a stress agent in epithelial cells of the rat ileum (IEC-18) were determined. In this study, strong antioxidant and cytoprotective peptides were obtained from a low-cost dairy industry product, which could improve consumers' health when used as functional ingredients.


Assuntos
Peptídeos/metabolismo , Tripsina/metabolismo , Proteínas do Soro do Leite/metabolismo , Animais , Antioxidantes/metabolismo , Hidrólise , Ratos , Soro do Leite/química
2.
Acta Trop ; 127(1): 33-7, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23545130

RESUMO

Essential oils (EOs) are potential tools for controlling Musca domestica L. In a fumigant assay, M. domestica adults treated with Citrus sinensis EO (LC50=3.9mg/dm(3)), with (4R)(+)-limonene (95.1%) being its main component, died within 15min or less. The terpenes absorbed by the flies and their metabolites, analyzed using SPME fiber, were (4R)(+)-limonene (LC50=6.2mg/dm(3)), α-pinene (LC50=11.5mg/dm(3)), ß-pinene (LC50=6.4mg/dm(3)), and two new components, carveol (LC50=1122mg/dm(3)) and carvone (LC50=19mg/dm(3)), in a proportion of 50, 6.2, 12.5, 6.3 and 25%, respectively. Carveol and carvone were formed by oxidation of (4R)(+)-limonene mediated by cytochrome P450, as was suggested by a fumigation assay on flies previously treated with piperonyl butoxide, a P450 inhibitor. In this experiment, an increase in the toxicity of the EO and (4R)(+)-limonene was observed, as well as a lower production of carveol and carvone.


Assuntos
Citrus sinensis/química , Moscas Domésticas/efeitos dos fármacos , Inseticidas/farmacologia , Óleos Voláteis/farmacologia , Butóxido de Piperonila/farmacologia , Óleos de Plantas/farmacologia , Animais , Inibidores das Enzimas do Citocromo P-450 , Feminino , Inseticidas/química , Masculino , Estrutura Molecular , Óleos Voláteis/química , Butóxido de Piperonila/química , Óleos de Plantas/química , Terpenos/química , Terpenos/metabolismo , Terpenos/farmacologia
3.
Fitoterapia ; 83(2): 336-42, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22155595

RESUMO

Intense applications of synthetic insecticides for the control of adult Musca domestica have led to the insects developing resistance to most of them. In consequence, there is interest in new active ingredients as alternatives to conventional insecticides. Essential oils (EO) are potential tools for controlling M. domestica because of their effectiveness and their minimal environmental effects. In a fumigant assay, M. domestica adults treated with Minthostachys verticillata EO [LC(50)=0.5 mg/dm(3); majority components by SPME-GC: (4R)(+)-pulegone (67.5%), menthone (22.3%) and (4R)(+)-limonene (3.8%)], died within 15 min or less. The terpenes absorbed by the flies and their metabolites, analyzed using SPME fiber, were (4R)(+)-limonene (LC(50)=6.2 mg/dm(3)), menthone (LC(50)=1.9 mg/dm(3)), (4R)(+)-pulegone (LC(50)=1.7 mg/dm(3)) and a new component, menthofuran (LC(50)=0.3 mg/dm(3)), in a relative proportion of 12.4, 6.5, 35.9 and 44.2% respectively. Menthofuran was formed by oxidation of either (4R)(+)-pulegone or menthone mediated by cytochrome P450, as demonstrated by a fumigation assay on flies previously treated with piperonyl butoxide, a P450 inhibitor, which showed a decrease in toxicity of the EO, (4R)(+)-pulegone and of menthone, supporting the participation of the P450 oxidizing system in the formation of menthofuran. The enzymatic reaction of isolated fly microsomes with the EO or the (4R)(+)-pulegone produced menthofuran in both cases. Contrary to expectations, the insect detoxification system contributed to enhance the toxicity of the M. verticillata EO. Consequently, resistant strains overexpressing P450 genes will be more susceptible to either M. verticillata EO or (4R)(+)-pulegone and menthone.


Assuntos
Moscas Domésticas/efeitos dos fármacos , Inseticidas/farmacologia , Lamiaceae/química , Óleos Voláteis/farmacologia , Extratos Vegetais/farmacologia , Animais , Bioensaio , Sobrevivência Celular/efeitos dos fármacos , Monoterpenos Cicloexânicos , Sistema Enzimático do Citocromo P-450/genética , Sistema Enzimático do Citocromo P-450/metabolismo , Sinergismo Farmacológico , Moscas Domésticas/enzimologia , Moscas Domésticas/genética , Inseticidas/química , Inseticidas/isolamento & purificação , Dose Letal Mediana , Mentol/química , Mentol/isolamento & purificação , Mentol/farmacologia , Monoterpenos/química , Monoterpenos/isolamento & purificação , Monoterpenos/metabolismo , Monoterpenos/farmacologia , Óleos Voláteis/química , Óleos Voláteis/isolamento & purificação , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Folhas de Planta/química , Óleos de Plantas/química , Óleos de Plantas/isolamento & purificação , Óleos de Plantas/farmacologia , Terpenos/química , Terpenos/isolamento & purificação , Terpenos/farmacologia
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