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1.
Nutr Diabetes ; 4: e141, 2014 Oct 20.
Artigo em Inglês | MEDLINE | ID: mdl-25329603

RESUMO

OBJECTIVE: Recent studies indicate that sphingolipids, sphingomyelin (SM) and ceramide (Cer) are associated with the development of metabolic syndrome. However, detailed profiles of serum sphingolipids in the pathogenesis of this syndrome are lacking. Here we have investigated the relationship between the molecular species of sphingolipids in serum and the clinical features of metabolic syndrome, such as obesity, insulin resistance, fatty liver disease and atherogenic dyslipidemia. SUBJECTS: We collected serum from obese (body mass index, BMI⩾35, n=12) and control (BMI=20-22, n=11) volunteers (18-27 years old), measured the levels of molecular species of SM and Cer in the serum by liquid chromatography-mass spectrometry and analyzed the parameters for insulin resistance, liver function and lipid metabolism by biochemical blood test. RESULTS: The SM C18:0 and C24:0 levels were higher, and the C20:0 and C22:0 levels tended to be higher in the obese group than in the control group. SM C18:0, C20:0, C22:0 and C24:0 significantly correlated with the parameters for obesity, insulin resistance, liver function and lipid metabolism, respectively. In addition, some Cer species tended to correlate with these parameters. However, SM species containing unsaturated acyl chains and most of the Cer species were not associated with these parameters. CONCLUSIONS: The present results demonstrate that the high levels of serum SM species with distinct saturated acyl chains (C18:0, C20:0, C22:0 and C24:0) closely correlate with the parameters of obesity, insulin resistance, liver function and lipid metabolism, suggesting that these SM species are associated with the development of metabolic syndrome and serve as novel biomarkers of metabolic syndrome and its associated diseases.

2.
Neurosci Lett ; 309(3): 169-72, 2001 Aug 31.
Artigo em Inglês | MEDLINE | ID: mdl-11514068

RESUMO

We have previously reported that a nitric oxide (NO)-donor, (+/-)-(E)-4-ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide (NOR3) induced cell death even at a low concentration in undifferentiated PC12 cells. In the present study, we found that PC12 cells which were cultured long-term for over 80 passages acquired resistance to the NOR3-induced cell toxicity. After 24 h exposure to 10-100 microM NOR3, a concentration-dependent cell death was observed in short-term cultured PC12 cells (8-30 passages), but not in long-term cultured cells (over 80 passages). In the cells cultured short-term, the cell death was accompanied by nuclear condensation and fragmentation. We further examined the alterations in total glutathione (GSH) levels, and activities of antioxidant enzymes, superoxide dismutase (SOD) and catalase in the short- and long-term cultured PC12 cells. SOD activity decreased in the long-term cultured cells, while catalase activity did not change. The GSH content significantly increased in the cells cultured long-term. Furthermore, the long-term but not the short-term cultured cells, expressed neuronal NO synthase (nNOS), but neither endothelial nor inducible NOS. These findings suggest that the PC12 cells acquire resistance to the NO-induced toxicity, accompanied by an increase in the GSH level and the expression of nNOS after long-term culture.


Assuntos
Óxido Nítrico Sintase/biossíntese , Óxido Nítrico/toxicidade , Animais , Catalase/metabolismo , Técnicas de Cultura de Células/métodos , Morte Celular/efeitos dos fármacos , Morte Celular/fisiologia , Células Cultivadas , Relação Dose-Resposta a Droga , Resistência a Medicamentos/fisiologia , Glutationa/metabolismo , Óxido Nítrico Sintase/metabolismo , Óxido Nítrico Sintase Tipo I , Óxido Nítrico Sintase Tipo II , Óxido Nítrico Sintase Tipo III , Nitrocompostos/toxicidade , Células PC12 , Ratos , Superóxido Dismutase/metabolismo , Fatores de Tempo
3.
Eur J Pharmacol ; 397(1): 25-33, 2000 May 26.
Artigo em Inglês | MEDLINE | ID: mdl-10844095

RESUMO

We investigated the effects of low concentrations of nitric oxide (NO) on cell viability using NO donors, (+/-)-(E)-4-methyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hex enamid e (NOR1), (+/-)-(E)-4-methyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide (NOR2), (+/-)-(E)-4-ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide (NOR3) and (+/-)-N-[(E)-4-ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1- yl]-3-pyr idine (NOR4). The half-life times of the NO release from these four NOR analogs, NOR1, NOR2, NOR3 and NOR4, were determined (6.5, 84, 105 and 340 min, respectively) by using 4,5-diaminofluorescein (DAF-2), a newly developed indicator of NO. Exposure of undifferentiated PC12 cells to low concentrations of NO donors, NOR2 or NOR3 (1-100 microM), but not NOR1 nor NOR4, resulted in cell death in a dose- and time-dependent manner, as determined from cell viability assessed by 3-(4,5-dimethyl-2-thiazolyl)-2, 5-diphenyl-2H-tetrazolium (MTT) assay. After 24 h exposure to 50 microM NOR2 or NOR3, more than 90% of PC12 cells had died. Furthermore, while the toxic effect of NOR3 was attenuated by replacing the medium at 20 min, 1 or 2 h after drug addition, it was continued by replacing the medium at 3 h or later after drug addition. The cell death was characterized by DNA degradation, nuclear condensation and fragmentation, suggesting apoptosis-like cell death. Pretreatment with an antioxidant ascorbic acid (0.1-0.5 mM) completely prevented the cell death caused by NOR3, while glutathione (0.1-0.2 mM) and cysteine (0.2-0.4 mM) provided partial protection. These findings suggest that the cell toxicity induced by NO at low concentrations strongly depends upon the duration of expose to NO from NO donors, and these toxic effects are effectively prevented by the antioxidant, ascorbic acid.


Assuntos
Óxido Nítrico/farmacologia , Células PC12/efeitos dos fármacos , Animais , Antioxidantes/farmacologia , Ácido Ascórbico/farmacologia , Sobrevivência Celular/efeitos dos fármacos , GMP Cíclico/análogos & derivados , GMP Cíclico/farmacologia , Cisteína/farmacologia , DNA/efeitos dos fármacos , DNA/metabolismo , Fragmentação do DNA/efeitos dos fármacos , Dibutiril GMP Cíclico/farmacologia , Relação Dose-Resposta a Droga , Glutationa/farmacologia , Meia-Vida , Cinética , Óxido Nítrico/metabolismo , Nitrocompostos/química , Nitrocompostos/metabolismo , Nitrocompostos/farmacologia , Oxidiazóis/farmacologia , Células PC12/citologia , Quinoxalinas/farmacologia , Ratos , Fatores de Tempo
4.
Acta amaz ; 18(3)1988.
Artigo em Português | LILACS-Express | LILACS, VETINDEX | ID: biblio-1454264

RESUMO

The effect of different levels of lime, with and without micronutrients, was tested on soybeans in a Central Amazonian oxisol yellow latosol under differents soil management practices: cutting and burning of primary forest; cutting of primary forest with mechanical clearing; cutting and burning of secundary forest. Treatments of different levels of lime (2, 3 and 5 ton/ha) without micronutrients did not differ statiscally from the treatment without lime. Significant increasses in yield were obtained with lime and micronutrients. Soil management 2, i. e., cutting of primary forest with mechanical clearing, presented low yields in most treatments. Nutrient availability and soil management of oxisols in the Amazon region are discussed.


O efeito de diferentes níveis de colagem na presença de micronutrientes, foram testados na cultuha da soja, em Latossolo Amarelo da Amazônia Central, sob três áreas com diferentes maneiras de preparo do solo: desmatamento seguido da queima de floresta primária; desmatamento seguido da retirada da floresta primária com aso de maquinas e desmatamento seguido da queima de vegetação de capoeira. As produções obtidas com as doses 1, 3 c 5 ton/ka, na ausência de micronutrientes, não diferiram estatísticamente da testemunha (0 ton/ha). No entanto, com a aplicação de 2 ton/calcário mais micronutrientes, o aumento de produção foi bastante pronunciado. 0s menores rendimentos foram obtidos no solo preparo com o uso de máquinas. A disponibilidade de nutrientes em Latossolo Amarelo, assim como o preparo de solo é discutido.

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