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1.
J Oleo Sci ; 59(8): 407-14, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20625232

RESUMO

Docosahexaenoic acid (DHA) regulates the lipid metabolism and inflammation that is closely associated with oxidative stress. The present study investigated the effects of DHA on the development of nonalcoholic steatohepatitis (NASH). To induce fatty liver, rats were fed choline-deficient high-fat diets (CDHF). The rats were then divided into 4 groups treated over the subsequent 6 weeks as follows: control, CDHF, CDHF+oxidative stress (NASH), and NASH+DHA (1.0 g/kg, p.o.). Rats of the control group were fed MF chow diet only. NASH rats showed severe steatohepatitis and liver fibrosis. Treatment with DHA significantly decreased the n-6/n-3 ratio in the livers and increased plasma SOD like activity compared with NASH rats. In addition, DHA attenuated the liver fibrosis during NASH development. Therefore, a higher DHA ratio in the liver of NASH rats might regulate the inflammatory response through a low n-6 ratio and diminished oxidative stress, effectively inhibiting liver fibrosis during NASH progression. These results suggested that DHA is a novel functional food for the prevention of NASH.


Assuntos
Modelos Animais de Doenças , Ácidos Docosa-Hexaenoicos/farmacologia , Fígado Gorduroso/patologia , Animais , Deficiência de Colina/complicações , Deficiência de Colina/metabolismo , Deficiência de Colina/patologia , Dieta , Gorduras na Dieta/efeitos adversos , Gorduras na Dieta/farmacologia , Progressão da Doença , Ácidos Docosa-Hexaenoicos/uso terapêutico , Avaliação Pré-Clínica de Medicamentos , Fígado Gorduroso/etiologia , Fígado Gorduroso/metabolismo , Fígado Gorduroso/prevenção & controle , Metabolismo dos Lipídeos/efeitos dos fármacos , Peroxidação de Lipídeos/efeitos dos fármacos , Peróxidos Lipídicos/sangue , Peróxidos Lipídicos/metabolismo , Fígado/efeitos dos fármacos , Fígado/metabolismo , Fígado/patologia , Masculino , Ratos , Ratos Wistar , Superóxido Dismutase/sangue , Superóxido Dismutase/metabolismo , Superóxido Dismutase-1
2.
J Agric Food Chem ; 53(24): 9472-7, 2005 Nov 30.
Artigo em Inglês | MEDLINE | ID: mdl-16302764

RESUMO

Two major anthocyanins were isolated from the acidified methanolic extract of eggplant (Solanum melongena L.) by column chromatography and preparative high-performance liquid chromatography. These anthocyanins were interconvertible under room light illumination condition. By means of tandem time-of-flight mass spectrometry and nuclear magnetic resonance spectroscopy, their structures were identified and elucidated as delphinidin 3-[4-(cis-p-coumaroyl)-l-rhamnosyl(1-->6)glucopyranoside]-5-glucopyranoside (compound 1) and delphinidin 3-[4-(trans-p-coumaroyl)-l-rhamnosyl-(1-->6)glucopyranoside]-5-glucopyranoside (compound 2), respectively. The results indicated that nasunin comprised cis and trans isomers of the p-coumaric acid moiety in its structure.


Assuntos
Antocianinas/análise , Solanum melongena/química , Antocianinas/química , Cromatografia Líquida de Alta Pressão , Ácidos Cumáricos/análise , Ácidos Cumáricos/química , Frutas/química , Espectroscopia de Ressonância Magnética , Espectrometria de Massas , Propionatos
3.
J Agric Food Chem ; 53(16): 6272-5, 2005 Aug 10.
Artigo em Inglês | MEDLINE | ID: mdl-16076105

RESUMO

Nasunin, delphinidin-3-(p-coumaroylrutinoside)-5-glucoside, an antioxidant anthocyanin isolated from eggplant peels, was demonstrated as an angiogenesis inhibitor. Nasunin at higher 10 microM suppressed microvessel outgrowth in an ex vivo angiogenesis assay using a rat aortic ring. The effect of nasunin was examined in various in vitro angiogenesis models using human umbilical vein endothelial cells (HUVECs). Nasunin suppressed HUVEC proliferation in a dose-dependent manner (50-200 microM); however, it had no significant effect on HUVEC chemotaxis in a Boyden chamber assay and HUVEC tube formation on a reconstituted basement membrane. These results imply that nasunin with both antioxidant and antiangiogenic activities might be useful to prevent angiogenesis-related diseases.


Assuntos
Inibidores da Angiogênese/farmacologia , Antocianinas/farmacologia , Solanum melongena/química , Animais , Antocianinas/isolamento & purificação , Antioxidantes , Aorta/efeitos dos fármacos , Divisão Celular/efeitos dos fármacos , Células Endoteliais/efeitos dos fármacos , Humanos , Masculino , Neovascularização Fisiológica/efeitos dos fármacos , Ratos , Ratos Wistar , Veias Umbilicais/efeitos dos fármacos
4.
J Agric Food Chem ; 50(1): 166-71, 2002 Jan 02.
Artigo em Inglês | MEDLINE | ID: mdl-11754562

RESUMO

Antioxidant activities of freeze-dried preparations of a 70% acetone extract of pomegranate (Punica granatum L.) and its three major anthocyanidins (delphinidin, cyanidin, and pelargonidin) were evaluated. Free radical scavenging activities were examined using an ESR technique with spin trapping; DMPO for hydroxyl (.OH) and superoxide (O(2)(.-) ) radicals; and [(MGD)(2)Fe(2+)] for nitric oxide (NO). Inhibitory effects on lipid peroxidation were estimated by the levels of malonaldehyde and 4-hydroxyalkenals in rat brain homogenates. Pomegranate extract exhibited scavenging activity against.OH and O(2)(.-). Anthocyanidins inhibited a Fenton reagent.OH generating system possibly by chelating with ferrous ion. Anthocyanidins scavenged O(2)(.)- in a dose-dependent manner. The ID(50) values of delphinidin, cyanidin, and pelargonidin were 2.4, 22, and 456 microM, respectively. In contrast, anthocyanidins did not effectively scavenge NO. Anthocyanidins inhibited H(2)O(2)-induced lipid peroxidation in the rat brain homogenates. The ID(50) values of delphinidin, cyanidin, and pelargonidin for them were 0.7, 3.5, and 85 microM, respectively. These findings suggest that the above anthocyanidins contribute to the antioxidant activity of pomegranate fruits.


Assuntos
Antocianinas/metabolismo , Antioxidantes/metabolismo , Sequestradores de Radicais Livres/metabolismo , Frutas/química , Onagraceae/química , Antocianinas/farmacologia , Antioxidantes/farmacologia , Relação Dose-Resposta a Droga , Espectroscopia de Ressonância de Spin Eletrônica , Radical Hidroxila/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Extratos Vegetais/química , Superóxidos/metabolismo
5.
J Nutr Sci Vitaminol (Tokyo) ; 48(5): 359-64, 2002 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-12656208

RESUMO

Acetyl-CoA synthetase (AceCS), which catalyzes the activation of acetate to produce acetyl-CoA, was found to have a much greater Km value for acetate in liver mitochondria than that in the heart mitochondria of rats, indicating that two different types of AceCS are located in the liver and heart mitochodria. Recently, Fujino et al. reported that mouse heart mitochondrial AceCS, designated AceCS2, was expressed in a wide range of tissues, however, it was apparently absent from the liver. In this study, liver mitochondrial AceCS activity, but not heart AceCS2, was greatly induced in di(2-ethylhexyl)phthalate (DEHP)-treated rats. We purified and characterized the rat liver mitochondrial AceCS. The molecular mass of the enzyme estimated by SDS-PAGE was -58 kDa, which was quite different from that of the heart mitochondrial enzyme, AceCS2. The calculated Km value for the acetate of the partially purified liver enzyme was much greater, being about 100 times that of heart enzyme, AceCS2.


Assuntos
Acetato-CoA Ligase/isolamento & purificação , Mitocôndrias Hepáticas/enzimologia , Acetato-CoA Ligase/efeitos dos fármacos , Animais , Dietilexilftalato/administração & dosagem , Eletroforese em Gel de Poliacrilamida , Masculino , Mitocôndrias Cardíacas/enzimologia , Ratos , Ratos Sprague-Dawley
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