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1.
J Nutr Biochem ; 24(3): 544-9, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22784432

RESUMO

Rapeseeds are naturally rich in cardioprotective micronutrients but refining leads to substantial losses or the production of undesirable compounds. The Optim'Oils European project proposed innovative refining conditions to produce an optimized rapeseed oil enriched in micronutrients and low in trans linolenic acid. We aimed to investigate cardioprotective properties of this Optimized oil. In a randomized, double-blind, controlled, cross-over study, 59 healthy normolipidaemic men consumed either Optimized or Standard rapeseed oils (20 g/d) and margarines (22 g/d) for 3 weeks. The Optimized oil reduced the trans FA concentration (p=0.009) and increased the contents of alpha-tocopherol (p=0.022) and coenzyme Q10 (p<0.001) in comparison with the Standard oil. Over the 3-week trial, Total-/HDL-cholesterol and LDL-/HDL-cholesterol were increased by 4% (p<0.05) with the Standard oil consumption whereas none of them rose with the Optimized rapeseed oil which increased the HDL-cholesterol and ApoA1 plasma content (+2%, NS and +3%, p<0.05 respectively). The effects observed on the plasma HDL-cholesterol levels (p=0.059), the Total-/HDL-cholesterol ratio (p=0.092), and on the ApoA1 concentrations (p=0.060) suggest an improvement of the cholesterol profile with the Optimized rapeseed oil. Finally, the Optimized oil reduced the plasma content of LDLox (-6%, NS), this effect being significantly different from the Standard oil (p=0.050). In conclusion, reasonable intake of an Optimized rapeseed oil resulting from innovative refining processes and enriched in cardioprotective micronutrients represent a relevant nutritional approach to prevent the risk of cardiovascular diseases by improving the cholesterol profile and reducing LDL oxidation.


Assuntos
Doenças Cardiovasculares/prevenção & controle , Alimentos Fortificados/análise , Micronutrientes/administração & dosagem , Óleos de Plantas/química , Ácido alfa-Linolênico/administração & dosagem , Adulto , Idoso , Apolipoproteínas/sangue , Biomarcadores/sangue , Índice de Massa Corporal , Brassica rapa/química , Colesterol/sangue , Estudos Cross-Over , Método Duplo-Cego , Ácidos Graxos Monoinsaturados , Humanos , Masculino , Margarina/análise , Micronutrientes/sangue , Pessoa de Meia-Idade , Estresse Oxidativo/efeitos dos fármacos , Fitosteróis/sangue , Óleo de Brassica napus , Triglicerídeos/sangue , Ubiquinona/análogos & derivados , Ubiquinona/sangue , Vitamina E/sangue , Ácido alfa-Linolênico/sangue
2.
J Agric Food Chem ; 59(9): 4483-8, 2011 May 11.
Artigo em Inglês | MEDLINE | ID: mdl-21417278

RESUMO

The main proposal of this study was to evaluate in vivo whether micronutrient-enriched rapeseed oils obtained using different crushing and refining procedures and characterized by different quantities and qualities of micronutrients (optimized oils) could have any beneficial effect on the antioxidant status of the brain. Sprague-Dawley rats were fed a high-fat diet for 4 weeks. The lipid source consisted of 20% optimized rapeseed oils with different quantities and qualities of micronutrients. The control group received traditional refined rapeseed oil. The experimental optimized oils decreased lipid peroxidation and increased endogenous antioxidant status in parallel with the enhancement of micronutrients. No alteration in acetylcholinesterase activity was induced by the high-fat diet in any experimental group. These results indicate that a regular intake of optimized rapeseed oils can prevent oxidative stress, providing evidence that optimized rapeseed oils could be a functional food with potentially important neuroprotective properties.


Assuntos
Antioxidantes/metabolismo , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Micronutrientes/farmacologia , Oxidantes/metabolismo , Extratos Vegetais/farmacologia , Óleos de Plantas/química , Substâncias Protetoras/farmacologia , Animais , Gorduras na Dieta/administração & dosagem , Ácidos Graxos Monoinsaturados , Feminino , Humanos , Masculino , Estresse Oxidativo/efeitos dos fármacos , Óleo de Brassica napus , Ratos , Ratos Sprague-Dawley
3.
Atherosclerosis ; 213(2): 422-8, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20678771

RESUMO

Many epidemiological studies have demonstrated that vegetable food consumption is associated with a reduced risk of cardiovascular diseases. The beneficial effects have been attributed to the content of bioactive molecules present in large quantities in plant food. The main proposal of this study was to evaluate in vivo whether micronutrient-enriched rapeseed oils (optimised oils) obtained using different crushing and refining procedures and characterised by different quantities and qualities of micronutrients, could have any beneficial effect on lipid profile and antioxidant status of plasma and liver. Sprague-Dawley rats were fed a high-fat diet for 4 weeks. The lipid source consisted of 20% optimised rapeseed oils with different quantities and qualities of micronutrients. The control group received traditional refined rapeseed oil. The experimental optimised oils all had a hypolipidaemic effect. In the group fed the highest levels of micronutrients, the reduction in plasma and hepatic triglycerides reached 25% and 17%, respectively, that of cholesterol 20% and 14%, respectively. In plasma, the ferric antioxidant capacity, superoxide dismutase, glutathione peroxidase and reduced glutathione significantly increased and lipid peroxidation decreased in parallel with the enhancement of micronutrients. The same trend was observed in the liver, except for glutathione peroxidase which was not affected by optimised oils. These results indicate that a regular intake of optimised rapeseed oils can help to improve lipid status and prevent oxidative stress, providing evidence that optimised oils could be a functional food with potentially important cardioprotective properties.


Assuntos
Doenças Cardiovasculares/prevenção & controle , Gorduras na Dieta/farmacologia , Lipídeos/sangue , Micronutrientes/farmacologia , Óleos de Plantas/uso terapêutico , Animais , Antioxidantes/metabolismo , Colesterol/metabolismo , Ácidos Graxos Monoinsaturados , Manipulação de Alimentos , Glutationa/metabolismo , Glutationa Peroxidase/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Fígado/metabolismo , Óleo de Brassica napus , Ratos , Ratos Sprague-Dawley , Superóxido Dismutase/metabolismo , Triglicerídeos/sangue , Triglicerídeos/metabolismo
4.
Free Radic Res ; 41(7): 748-56, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17577735

RESUMO

In view of the promising use of n-3 polyunsaturated fatty acids (PUFAs) in the prevention and treatment of neurological diseases, it is necessary to ascertain the lack of detrimental oxidative effects. We evaluated short- and long-term effects of 25, 50 and 75 muM docosahexaenoic acid (DHA) supplementation on the oxidative status of C6 glial cells. DHA was incorporated into cells dose and time dependently without any cytotoxic effect. Reactive oxygen species (ROS) level was related to DHA dose and supplementation time. At the lowest dose no significant increase in ROS values was observed at hour 24. Low doses of DHA strengthened the cellular antioxidant defence system as highlighted by a raise in both GPX and catalase activity, and the decreased levels of lipid peroxidation. This effect was pronounced at 24 h of supplementation, almost disappeared at hour 48, while after 72 h an opposite effect was observed: lipid peroxidation increased concomitantly with DHA doses. Therefore, the final effect of DHA on cellular redox status is dependent on dose and time supplementation.


Assuntos
Ácidos Docosa-Hexaenoicos/farmacologia , Animais , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Ácidos Docosa-Hexaenoicos/metabolismo , Ácidos Graxos/metabolismo , Citometria de Fluxo , Glioblastoma , Glutationa/metabolismo , Cinética , Lipídeos/isolamento & purificação , Ratos , Superóxidos/metabolismo , Substâncias Reativas com Ácido Tiobarbitúrico/análise
5.
Free Radic Res ; 39(8): 865-74, 2005 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16036367

RESUMO

n-3 polyunsaturated fatty acids (PUFAs) have been described to have beneficial effects on brain development and in the prevention and treatment of brain damage. C6 glioma cells were incubated with 100 microM of either C20:4n-6 (ARA), or C20:5n-3 (EPA), or C22:6n-3 (DHA) for different time periods to assess whether these acids altered the cellular oxidative state. The ARA and EPA were promptly metabolised to C22:4n-6 and C22:5n-3, respectively, whereas DHA treatment simply increased the amount of DHA in the cells. Cell viability was not affected by ARA, while a cytotoxic effect was observed 72 h after n-3 PUFAs supplementation. The levels of reactive oxygen species and thiobarbituric acid-reactive substances were significantly higher in DHA-treated cells than in EPA- and ARA-treated groups. This modification in the oxidative cellular status was also highlighted by a significant increase in catalase activity and a decrease in glutathione content in DHA-supplemented cells. Glucose-6-phosphate dehydrogenase activity, an enzyme involved in redox regulation, and O2*- release were significantly increased both in EPA and DHA groups. The effect of DHA was more severe than that of EPA. No significant changes were observed in the ARA group with respect to untreated cells. These data show that EPA and DHA induce alterations in the oxidative status that could affect the glial function.


Assuntos
Ácido Araquidônico/farmacologia , Ácidos Docosa-Hexaenoicos/farmacologia , Ácidos Graxos Insaturados/farmacologia , Neuroglia/efeitos dos fármacos , Animais , Ácido Araquidônico/toxicidade , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Ácidos Docosa-Hexaenoicos/toxicidade , Ácido Eicosapentaenoico , Ácidos Graxos Insaturados/toxicidade , Citometria de Fluxo , Glioblastoma , Glucosefosfato Desidrogenase/biossíntese , Glutationa/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Neuroglia/metabolismo , Oxirredução/efeitos dos fármacos , Estresse Oxidativo/efeitos dos fármacos , Ratos , Superóxido Dismutase , Tiobarbitúricos/metabolismo
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