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1.
Cell Physiol Biochem ; 22(5-6): 539-48, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-19088436

RESUMEN

Muscle resistance to insulin plays a key role in the metabolic dysregulation associated to obesity. A pro-inflammatory and pro-oxidant status has been proposed to be the link between dietary obesity and insulin resistance. Given the gender differences previously found in mitochondrial function and oxidative stress, the aim of the present study was to investigate whether this gender dimorphism leads to differences in the development of high-fat-diet-induced insulin resistance in rat skeletal muscle. Male and female rats of 15 months of age were fed with a high-fat-diet (32% fat) for 14 weeks. Control male rats showed a more marked insulin resistance status compared to females, as indicated by the glucose tolerance curve profile and the serum insulin, resistin and adiponectin levels. High-fat-diet feeding induced an excess of body weight of 16.2% in males and 38.4% in females, an increase in both muscle mitochondrial hydrogen peroxide production and in oxidative damage, together with a decrease in the Mn-superoxide dismutase activity in both genders. However, high-fat-diet fed female rats showed a less marked insulin resistance profile than males, higher mitochondrial oxygen consumption and cytochrome c oxidase activity, and a better capacity to counteract the oxidative-stress-dependent insulin resistance through an overexpression of both muscle UCP3 and GLUT4 proteins. These results point to a gender dimorphism in the insulin resistance status and in the response of skeletal muscle to high-fat-diet feeding which could be related to a more detrimental effect of age in male rats.


Asunto(s)
Envejecimiento/efectos de los fármacos , Envejecimiento/fisiología , Grasas de la Dieta/farmacología , Resistencia a la Insulina/fisiología , Músculo Esquelético/efectos de los fármacos , Músculo Esquelético/fisiología , Caracteres Sexuales , Adipoquinas/sangre , Animales , Antioxidantes/metabolismo , Glucemia/metabolismo , Peso Corporal/efectos de los fármacos , Complejo IV de Transporte de Electrones/metabolismo , Metabolismo Energético/efectos de los fármacos , Femenino , Prueba de Tolerancia a la Glucosa , Transportador de Glucosa de Tipo 4/metabolismo , Peróxido de Hidrógeno/metabolismo , Insulina/sangre , Canales Iónicos/metabolismo , Peróxidos Lipídicos/metabolismo , Masculino , Mitocondrias/efectos de los fármacos , Mitocondrias/enzimología , Proteínas Mitocondriales/metabolismo , Consumo de Oxígeno/efectos de los fármacos , Carbonilación Proteica/efectos de los fármacos , Ratas , Ratas Wistar , Proteína Desacopladora 3 , Aumento de Peso/efectos de los fármacos
2.
Cell Physiol Biochem ; 22(1-4): 327-36, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18769060

RESUMEN

High fat diets (HFD) usually lead to hyperphagia and body weight gain. However, macronutrient proportions in the diet can modulate energy intake and body fat deposition. The aim of the study was to investigate muscle and liver oxidative metabolism in response to an isocaloric intake of a HFD and to elucidate the possible gender-dependent response. Eight week-old male and female rats were fed either standard chow or HFD for 14 weeks. Energy intake, body weight and whole animal oxygen consumption were determined periodically. Mitochondrial oxygen consumption, hydrogen peroxide production, TBARS levels, Cytochrome-c-oxidase, Citrate synthase and antioxidant enzyme activities were measured in muscle and liver. UCP1 and UCP3 protein levels were analyzed in brown adipose tissue and muscle, respectively. Male rats showed higher energy efficiency, enhanced adiposity, greater hydrogen peroxide production and less effective antioxidant machinery compared to females. HFD feeding increased energy expenditure but did not modify either tissue oxidative metabolism or oxidative damage in either gender. HFD animals over-expressed uncoupling proteins in order to maintain energy balance (brown adipose tissue UCP1) and to avoid oxidative stress (skeletal muscle UCP3), thus counteracting the alterations induced by the modification of the proportion of macronutrients in the diet.


Asunto(s)
Grasas de la Dieta/farmacología , Conducta Alimentaria/efectos de los fármacos , Hígado/metabolismo , Músculo Esquelético/metabolismo , Caracteres Sexuales , Tejido Adiposo Pardo/metabolismo , Animales , Antioxidantes/metabolismo , Metabolismo Energético/efectos de los fármacos , Femenino , Peróxido de Hidrógeno/metabolismo , Canales Iónicos/metabolismo , Hígado/anatomía & histología , Hígado/enzimología , Masculino , Mitocondrias/efectos de los fármacos , Mitocondrias/metabolismo , Proteínas Mitocondriales/metabolismo , Músculo Esquelético/anatomía & histología , Músculo Esquelético/enzimología , Tamaño de los Órganos , Oxidación-Reducción/efectos de los fármacos , Consumo de Oxígeno/efectos de los fármacos , Ratas , Ratas Wistar , Sustancias Reactivas al Ácido Tiobarbitúrico/metabolismo , Proteína Desacopladora 1
3.
Cell Physiol Biochem ; 15(5): 203-10, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15956783

RESUMEN

Brown adipose tissue (BAT) thermogenesis is inhibited during late-pregnancy and lactation in the rat. However, scarce information concerning BAT functionality during mid-pregnancy is available. The aim of this work was to investigate uncoupling proteins and leptin expression during placentation in rat BAT as well as other key parameters in the thermogenic function of the tissue. BAT mitochondrial content was found to be reduced 50% in 11 and 13 day pregnant rats as compared to nonpregnant controls, although uncoupling protein 1 (UCP1) content was not modified. Furthermore, UCP3 mRNA levels were found to be highly increased during this period. beta3-adrenergic receptor (beta3-AR) decreased expression resulted in a higher alpha2/beta3 ratio. Finally, leptin mRNA levels in BAT were found to be 3-fold up-regulated in pregnant animals. In conclusion, we show the existence of profound changes in thermogenic features in BAT during gestational days 11 and 13, pointing to the importance of this tissue during mid-pregnancy.


Asunto(s)
Tejido Adiposo Pardo/metabolismo , Proteínas Portadoras/metabolismo , Leptina/metabolismo , Proteínas de la Membrana/metabolismo , Embarazo/metabolismo , Termogénesis/fisiología , Animales , Proteínas Portadoras/genética , Femenino , Regulación de la Expresión Génica , Canales Iónicos , Leptina/genética , Proteínas de la Membrana/genética , Mitocondrias/metabolismo , Proteínas Mitocondriales , Placentación/genética , Placentación/fisiología , ARN Mensajero/análisis , ARN Mensajero/metabolismo , Ratas , Ratas Wistar , Receptores Adrenérgicos beta 3/genética , Receptores Adrenérgicos beta 3/metabolismo , Termogénesis/genética , Proteína Desacopladora 1 , Proteína Desacopladora 3
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