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1.
Nutr Hosp ; 36(2): 463-469, 2019 04 10.
Artigo em Espanhol | MEDLINE | ID: mdl-30866635

RESUMO

Introduction: Mexico has reported in 2016 a combined prevalence of obesity and overweight of 33.2% in children. The objective of this work was to make a literature review of the factors associated with obesity in Mexican children, such as genetic factors, feeding patterns, sedentary lifestyle and gut microbiota. We found that in Mexican children SNP (single nucleotide polymorphism) is present in genes such as MC4R, FTO and ADRB1, associated with obesity, and that PON-1192 polymorphism increases the risk of suffering insulin resistance. On the other hand, the variant of the ADIPOR2 gene (rs11061971) protects Mexican children against obesity, as well as a greater number of copies of the AMY gene was found in children with normal weight. The evidence of the number of copies is very important, since the current diet of the Mexican population is rich in carbohydrates and fats, origin of a nutritional transition that includes sedentary activities and a high consumption of sugary drinks. The consumption of certain foods causes important changes in the gut microbiota that contribute to the development of obesity and insulin resistance. It has been found that Mexican children with obesity have a higher abundance of phylum Firmicutes and B. eggerhii bacteria. Therefore, as obesity is so diverse, it is essential to diversify the treatment in which government authorities, parents and health authorities should get involved, as well as reinforcing nutrition and healthy eating issues in primary education in the country in order to reverse the prevalence and prevent the development of other pathologies in Mexican children.


Introducción: México ha reportado en el año 2016 una prevalencia combinada de obesidad y sobrepeso del 33,2% en niños. El objetivo de este trabajo fue hacer una revisión bibliográfica de los factores asociados a la obesidad en niños mexicanos, como factores genéticos, patrones de alimentación, sedentarismo y microbiota intestinal. Se encontró que en niños mexicanos existe la presencia de SNP (single nucleotide polymorphism) en genes como MC4R, FTO y ADRB1, asociados a la obesidad, y que el polimorfismo PON1-192 incrementa el riesgo de padecer resistencia a la insulina. Por otro lado, la variante del gen ADIPOR2 (rs11061971) protege a los niños mexicanos contra la obesidad, al tiempo que un mayor número de copias del gen AMY fue encontrada en niños con peso normal. La evidencia del número de copias es de gran importancia, ya que la dieta actual del mexicano es rica en carbohidratos y grasas, origen de una transición nutricional que incluye actividades sedentarias y un alto consumo de bebidas azucaradas. El consumo de determinados alimentos provoca cambios importantes en la microbiota intestinal que contribuyen al desarrollo de la obesidad y la resistencia a la insulina. Se ha encontrado que niños mexicanos con obesidad presentan mayor abundancia de bacterias del phylum Firmicutes y de la especie B. eggerhii. Al ser tan diverso el tema de obesidad, es indispensable diversificar el tratamiento en el que se involucren autoridades gubernamentales, padres de familia e instancias sanitarias, así como reforzar temas de nutrición y alimentación saludable en la educación primaria del país para revertir las cifras y prevenir el desarrollo de otras patologías en los niños mexicanos.


Assuntos
Obesidade Infantil/epidemiologia , Adolescente , Criança , Pré-Escolar , Humanos , Lactente , Recém-Nascido , México/epidemiologia , Prevalência , Comportamento Sedentário
2.
Food Chem ; 138(4): 2250-9, 2013 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-23497883

RESUMO

We have investigated the effects of the intake of oils heated at frying temperature in order to find an oil model for deep-frying that prevents postprandial oxidative stress. Twenty obese people received four breakfasts following a randomised crossover design consisting of different oils (virgin olive oil (VOO), sunflower oil (SFO), and a mixed seed oil (SFO/canola oil) with added dimethylpolysiloxane (SOX) or natural antioxidants from olives (SOP)), which were subjected to 20 heating cycles. The intake of SFO-breakfast reduced plasma GSH levels and the GSH/GSSG ratio, increased protein carbonyl levels, and induced a higher gene expression of the different NADPH-oxidase subunits, Nrf2-Keap1 activation, gene expression of the antioxidant enzymes in peripheral blood mononuclear cells and antioxidant plasma activities than the intake of the breakfasts prepared with VOO, SOP and SOX. Oils with phenolic compounds, whether natural (VOO) or artificially added (SOP), or with artificial antioxidant (SOX), could reduce postprandial oxidative stress compared with sunflower oil.


Assuntos
Antioxidantes/metabolismo , Obesidade/dietoterapia , Obesidade/metabolismo , Estresse Oxidativo , Óleos de Plantas/metabolismo , Adulto , Idoso , Antioxidantes/química , Ácidos Graxos Monoinsaturados/química , Ácidos Graxos Monoinsaturados/metabolismo , Feminino , Aditivos Alimentares/metabolismo , Temperatura Alta , Humanos , Masculino , Pessoa de Meia-Idade , Azeite de Oliva , Oxirredução , Óleos de Plantas/química , Período Pós-Prandial , Óleo de Brassica napus , Óleo de Girassol
3.
Brain Stimul ; 6(1): 84-6, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22537865

RESUMO

Transcranial magnetic stimulation (TMS) is a non-invasive technique used recently to treat different neuropsychiatric and neurodegenerative disorders. Despite its proven value, the mechanisms through which TMS exerts its beneficial action on neuronal function remain unclear. Recent studies have shown that its beneficial effects may be at least partly due to a neuroprotective effect on oxidative and cell damage. This study shows that TMS can modulate the Nrf2 transcriptor factor in a Huntington's disease-like rat model induced by 3-nitropropionic acid (3-NP). Western blot analysis demonstrated that 3-NP caused a reduction in Nrf2 in both cytoplasm and nucleus, while TMS applied to 3-NP-treated rats triggered an increase in cytoplasm and nucleus Nrf2 levels. It was therefore concluded that TMS modulates Nrf2 expression and translocation and that these mechanisms may partly explain the neuroprotective effect of TMS, as well as its antioxidant and cell protection capacity.


Assuntos
Antioxidantes/metabolismo , Doença de Huntington/metabolismo , Fator 2 Relacionado a NF-E2/metabolismo , Estimulação Magnética Transcraniana , Animais , Western Blotting , Modelos Animais de Doenças , Masculino , Ratos , Ratos Wistar
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