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Curr Mol Med ; 19(8): 570-578, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31210105

RESUMO

BACKGROUND: This study was conducted to determine the effects of vitamin D supplementation on some of the gene expressions related to insulin and lipid metabolism in diabetic hemodialysis (HD) patients. METHODS: A double-blind, randomized, placebo-controlled clinical trial was carried out in 55 patients with diabetic HD. The current project used two groups in which each subject received vitamin D supplements (50,000 IU, n=28) or placebo (50,000 IU, n=27) every 2 weeks for 12 weeks. Gene expression analyses (RT-PCR) were included to obtain the rate of gene expression of the related insulin and lipid metabolism genes in peripheral blood mononuclear cells (PBMCs) of patients with diabetic HD. RESULTS: Our data revealed that consumption of vitamin D supplementation enables to overexpress the peroxisome proliferation-activated receptor gamma (PPAR-γ) (P=0.001), AKT (P=0.04), PI3K (P=0.02), insulin receptor substrate-1 (IRS1) (P0.008) and glucose transporter type 4 (GLUT-4) (P=0.01) and downregulate the expression of protein kinase C (PKC) (P=0.001) in patients with diabetic HD than control group following the 12-week intervention. In addition, vitamin D supplementation downregulated low-density lipoprotein receptor (LDLR) (P=0.03) expression in the subjects with diabetic HD than the control group. Vitamin D supplementation did not show any effects on the expression of pyruvate dehydrogenase kinase 1 (PDK1) (P=0.37), IRS2 (P=0.90) and lipoprotein (a) [Lp(a)] (P=0.05). CONCLUSION: Our findings confirmed that diabetic HD subjects who received the vitamin D supplementation (for 12 weeks), showed a significant overexpression in the PPAR-γ, AKT, PI3K, IRS1 and GLUT4 genes, and also showed a significant downregulation in the PKC and LDLR genes. Moreover, no effects on PDK1, IRS2 and Lp(a) expression were observed.


Assuntos
Nefropatias Diabéticas/terapia , Regulação da Expressão Gênica/efeitos dos fármacos , Insulina/metabolismo , Metabolismo dos Lipídeos/efeitos dos fármacos , Diálise Renal , Vitamina D/uso terapêutico , Proteínas Adaptadoras de Transdução de Sinal/biossíntese , Proteínas Adaptadoras de Transdução de Sinal/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Nefropatias Diabéticas/genética , Suplementos Nutricionais , Método Duplo-Cego , Indução Enzimática/efeitos dos fármacos , Feminino , Transportador de Glucose Tipo 4/biossíntese , Transportador de Glucose Tipo 4/genética , Humanos , Proteínas Substratos do Receptor de Insulina/biossíntese , Proteínas Substratos do Receptor de Insulina/genética , Lipoproteína(a)/biossíntese , Lipoproteína(a)/genética , Masculino , Pessoa de Meia-Idade , PPAR gama/biossíntese , PPAR gama/genética , Fosfatidilinositol 3-Quinases/biossíntese , Fosfatidilinositol 3-Quinases/genética , Proteína Quinase C/biossíntese , Proteína Quinase C/genética , Piruvato Desidrogenase Quinase de Transferência de Acetil/biossíntese , Piruvato Desidrogenase Quinase de Transferência de Acetil/genética , Transdução de Sinais , Vitamina D/administração & dosagem , Vitamina D/farmacologia , Adulto Jovem
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