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1.
Can J Physiol Pharmacol ; 90(5): 537-45, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22510071

RESUMO

Chronic intake of high-carbohydrate or high-lipid diets is a well-known insulin resistance inducer. This study investigates the immediate effect (1-6 h) of a carbohydrate- or lipid-enriched meal on insulin sensitivity. Fasted rats were refed with standard, carbohydrate-enriched (C), or lipid-enriched (L) meal. Plasma insulin, glucose, and non-esterified fatty acids (NEFA) were measured at 1, 2, 4, and 6 h of refeeding. The glucose-insulin index showed that either carbohydrates or lipids decreased insulin sensitivity at 2 h of refeeding. At this time point, insulin tolerance tests (ITTs) and glucose tolerance tests (GTTs) detected insulin resistance in C rats, while GTT confirmed it in L rats. Reduced glycogen and phosphorylated AKT and GSK3 content revealed hepatic insulin resistance in C rats. Reduced glucose uptake in skeletal muscle subjected to the fatty acid concentration that mimics the high NEFA level of L rats suggests insulin resistance in these animals is mainly in muscle. In conclusion, carbohydrate- or lipid-enriched meals acutely disrupt glycemic homeostasis, inducing a transient insulin resistance, which seems to involve liver and skeletal muscle, respectively. Thus, the insulin resistance observed when those types of diets are chronically consumed may be an evolution of repeated episodes of this transient insulin resistance.


Assuntos
Carboidratos da Dieta/administração & dosagem , Gorduras na Dieta/administração & dosagem , Resistência à Insulina/fisiologia , Insulina/sangue , Insulina/metabolismo , Animais , Glicemia/metabolismo , Proteínas de Ligação a DNA/metabolismo , Desoxiglucose/metabolismo , Dieta Hiperlipídica , Carboidratos da Dieta/metabolismo , Gorduras na Dieta/metabolismo , Jejum/sangue , Jejum/metabolismo , Ácidos Graxos não Esterificados/sangue , Teste de Tolerância a Glucose/métodos , Índice Glicêmico , Glicogênio/metabolismo , Quinase 3 da Glicogênio Sintase/metabolismo , Homeostase , Fígado/metabolismo , Masculino , Músculo Esquelético/metabolismo , Proteínas Proto-Oncogênicas c-akt/metabolismo , Ratos , Ratos Wistar , Fatores de Transcrição/metabolismo
2.
Muscle Nerve ; 40(5): 847-54, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19722251

RESUMO

Glucose transporter 4 (GLUT4) expression in adipose tissue decreases during fasting. In skeletal muscle, we hypothesized that GLUT4 expression might be maintained in a beta-adrenergic-dependent way to ensure energy disposal for contractile function. Herein we investigate beta-blockade or beta-stimulation effects on GLUT4 expression in oxidative (soleus) and glycolytic [extensor digitorum longus (EDL)] muscles of fasted rats. Fasting increased GLUT4 mRNA in soleus (24%) and EDL (40%), but the protein content increased only in soleus (30%). beta1-beta2-, and beta1-beta2-beta3-blockade decreased (20-30%) GLUT4 mRNA content in both muscles, although GLUT4 protein decreased only in EDL. When mRNA and GLUT4 protein regulations were discrepant, changes in the mRNA poly(A) tail length were detected, indicating a posttranscriptional modulation of gene expression. These results show that beta-adrenergic activity regulates GLUT4 gene expression in skeletal muscle during fasting, highlighting its participation in preservation of GLUT4 protein in glycolytic muscle.


Assuntos
Jejum/metabolismo , Expressão Gênica , Transportador de Glucose Tipo 4/biossíntese , Glicólise/fisiologia , Fibras Musculares Esqueléticas/metabolismo , Receptores Adrenérgicos beta/metabolismo , Agonistas Adrenérgicos beta/farmacologia , Antagonistas Adrenérgicos beta/farmacologia , Animais , Glicólise/efeitos dos fármacos , Masculino , Fibras Musculares Esqueléticas/efeitos dos fármacos , RNA Mensageiro/biossíntese , Ratos , Ratos Wistar
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