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Arch. endocrinol. metab. (Online) ; 59(3): 210-214, 06/2015. tab, graf
Artículo en Inglés | LILACS | ID: lil-751317

RESUMEN

Objective The aim of this study was to evaluate the genetic expression of adipokines in the adipocytes of monosodium glutamate (MSG)-treated obese rats submitted to physical activity.Materials and methods Obesity was induced by neonatal MSG administration. Exercised rats (MSG and control) were subjected to swim training for 30 min for 10 weeks, whereas their respective controls remained sedentary. Total RNA was obtained from sections of the mesenteric adipose tissue of the rats. mRNA levels of adiponectin (Adipoq), tumor necrosis factor alpha (Tnf), peroxisome proliferator-activated receptor alpha (Ppara), and peroxisome proliferator-activated receptor gamma (Pparg) adipokines were quantified by quantitative Real-Time Polymerase Chain Reaction (qRT-PCR).Results In the exercise-trained control group, the expression of Adipoq increased compared to the sedentary control, which was not observed in the MSG-obese rats. Increased levels of Tnf in MSG-obese rats were not reversed by the swim training. The expression of Ppara was higher in sedentary MSG-obese rats compared to the sedentary control. Swimming increased this adipokine expression in the exercise-trained control rats compared to the sedentary ones. mRNA levels of Pparg were higher in the sedentary MSG-rats compared to the sedentary control; however, the exercise did not influenced its expression in the groups analyzed.Conclusions In conclusion, regular physical activity was not capable to correct the expression of proinflammatory adipokines in MSG-obese rat adipocytes.


Asunto(s)
Animales , Humanos , Adyuvantes Inmunológicos , Imitación Molecular/inmunología , Factores de Necrosis Tumoral , Vacunas Sintéticas/inmunología , Vacunas/química , Vacunas/inmunología , Adyuvantes Inmunológicos/química , /inmunología , /química , /metabolismo , Vacunas contra el Cáncer/química , Vacunas contra el Cáncer/inmunología , Vectores Genéticos/genética , Vectores Genéticos/inmunología , Inmunoterapia , Ligandos , Lentivirus/genética , Lentivirus/inmunología , Macaca mulatta , Neoplasias/inmunología , Neoplasias/terapia , Multimerización de Proteína , Ligando Inductor de Apoptosis Relacionado con TNF/química , Receptores Toll-Like/agonistas , Factores de Necrosis Tumoral/química , Vacunas Sintéticas/química , Proteínas de la Matriz Viral/inmunología
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