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










Base de dados
Intervalo de ano de publicação
1.
Int J Biol Macromol ; 107(Pt A): 254-260, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28890369

RESUMO

The application of nanotechnology has created high impact in diagnosis and prognosis of various disorders including cardiovascular diseases. In the present study, we investigated the beneficial effect of selenium incorporated guar gum nanoparticles (SGG) compared to nascent selenium (Se) and guar gum nanoparticles (GGN) against ischemiareperfusion (IR) induced alterations in oxidative phosphorylation and energy metabolism in H9c2 cardiac cells. Ischemia and reperfusion were induced for 1h. The alterations in activities of various complexes (complex 1, II, III and IV) of mitochondrial electron transport chain (ETC), aconitase activity, oxygen consumption rate, and the ATP content were seen. The role of heat shock protein, hypoxia inducible factor-1α and atrial natriuretic factor (ANP) were also analyzed. Then the beneficial properties of various particles like Se, GGN and SGG were evaluated. Among these, SGG treatment (1 and 5ng) was found to be more beneficial compared to other particles. Overall results reveal that SGG nanoparticles are effective in protecting H9c2 cardiac cells from IR injury via improving the efficiency of ETC in H9c2 cells.


Assuntos
Galactanos/administração & dosagem , Mananas/administração & dosagem , Mitocôndrias/efeitos dos fármacos , Nanopartículas/administração & dosagem , Gomas Vegetais/administração & dosagem , Traumatismo por Reperfusão/tratamento farmacológico , Animais , Antioxidantes/administração & dosagem , Antioxidantes/química , Antioxidantes/metabolismo , Metabolismo Energético , Galactanos/síntese química , Galactanos/química , Coração/efeitos dos fármacos , Coração/fisiopatologia , Humanos , Mananas/síntese química , Mananas/química , Mitocôndrias/metabolismo , Mioblastos/efeitos dos fármacos , Mioblastos/metabolismo , Mioblastos/patologia , Nanopartículas/química , Gomas Vegetais/síntese química , Gomas Vegetais/química , Ratos , Espécies Reativas de Oxigênio/metabolismo , Traumatismo por Reperfusão/metabolismo , Traumatismo por Reperfusão/patologia , Selênio/química
2.
Eur J Pharmacol ; 812: 73-81, 2017 Oct 05.
Artigo em Inglês | MEDLINE | ID: mdl-28684236

RESUMO

The role of phytochemicals in general well-being has been recognized. Curcumin is an ideal example. Hypoxia in adipose tissue is a major cause of inflammation and insulin resistance in obesity. Herein we mainly explored inflammation, insulin resistance and angiogenesis in 3T3-L1 adipocytes and possible reversal with the curcumin during hypoxia. Hypoxia for 24h significantly increased (P ≤ 0.05) the secretion of monocyte chemotactic protein-1 (4.59 fold), leptin (2.96 fold) and reduced adiponectin (2.93 fold). mRNA level of resistin (6.8 fold) and toll-like receptor-4 (TLR-4) (8.8 fold) was upregulated. Increased serine phosphorylation of insulin receptor substrate 1 (IRS-1) (1.9 fold) and decreased expression of insulin receptor substrate 2 (IRS-2) (0.53 fold) in hypoxic group were observed. Hypoxia significantly increased (P ≤ 0.05) basal glucose uptake (3.3 fold), GLUT-1 expression and angiogenic factors but down regulated GLUT-4. Curcumin protected adipocytes from hypoxia induced inflammation and insulin resistance via reducing inflammatory adipokine, nuclear factor-κB (NF-κB)/c-jun N-terminal kinase (JNK) and serine phosphorylation of IRS-1 receptors and improving adiponectin secretion.


Assuntos
Adipócitos/citologia , Adipócitos/efeitos dos fármacos , Curcumina/farmacologia , Resistência à Insulina , Células 3T3-L1 , Transporte Ativo do Núcleo Celular/efeitos dos fármacos , Adipócitos/metabolismo , Animais , Biomarcadores/metabolismo , Hipóxia Celular/efeitos dos fármacos , Núcleo Celular/efeitos dos fármacos , Núcleo Celular/metabolismo , Citocinas/metabolismo , Ativação Enzimática/efeitos dos fármacos , Regulação da Expressão Gênica/efeitos dos fármacos , Transportador de Glucose Tipo 1/metabolismo , Proteínas Quinases JNK Ativadas por Mitógeno/metabolismo , Camundongos , Receptor 4 Toll-Like/metabolismo , Fator de Transcrição RelA/metabolismo
3.
Nat Prod Res ; 28(18): 1480-4, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24735436

RESUMO

This study evaluated the inhibitory potential of ethyl acetate extract of Parmotrema tinctorum (PTEE), an edible lichen, against aldose reductase (AR) and carbohydrate digestive enzymes such as α-glucosidase and α-amylase. It was also screened for antioxidant activities by using DPPH, ABTS, superoxide and hydroxyl radical-scavenging assays. PTEE exhibited α-glucosidase, α-amylase and AR inhibition along with significant antiglycation potential with an estimated IC50 value of 58.45 ± 1.24, 587.74 ± 3.27, 139.28 ± 2.6 and 285.78 ± 1.287 µg/mL, respectively. Antioxidant activity of PTEE against DPPH (IC50 396.83 ± 2.98 µg/mL), ABTS (151.34 ± 1.79 µg/mL), superoxide (30.29 ± 1.17 µg/mL) and hydroxyl (35.42 ± 1.22 µg/mL) radicals suggests the antioxidant potential of P. tinctorum. Significant antioxidant activity and inhibitory potential against carbohydrate digestive enzymes and AR suggest that P. tinctorum can be developed as functional food/nutraceuticals for diabetes after detailed study.


Assuntos
Aldeído Redutase/antagonistas & inibidores , Líquens/química , alfa-Amilases/efeitos dos fármacos , alfa-Glucosidases/efeitos dos fármacos , Antioxidantes/farmacologia , Compostos de Bifenilo/farmacologia , Inibidores Enzimáticos/farmacologia , Humanos , Concentração Inibidora 50 , Picratos/farmacologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...