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Efectos de la suplementación con selenio sobre la activación de la vía de señalización de insulina PI3K/Akt/GLUT-4: una revisión sistemática con metanálisis de modelos animales de diabetes
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Palabras clave

Insulin
Selênio
Suplementos Dieteticos
Genómica

Cómo citar

Efectos de la suplementación con selenio sobre la activación de la vía de señalización de insulina PI3K/Akt/GLUT-4: una revisión sistemática con metanálisis de modelos animales de diabetes. (2026). Revista Eletrônica Acervo Saúde, 26(3), e22857. https://doi.org/10.25248/reas.e22857.2026

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Resumen

Objetivo: Nos propusimos dilucidar, a través de una revisión sistemática y un metaanálisis, cómo la exposición al selenio puede influir en la activación de la vía de señalización PI3K/Akt/GLUT-4 en modelos animales de diabetes. Métodos: Se realizó una búsqueda en las bases de datos PubMed/Medline, Cochrane Library, LILACS, Web of Science y Scopus, sin límite de tiempo, con foco en estudios realizados en modelos animales de diabetes. Resultados: Se incluyeron 13 artículos en esta revisión. Los hallazgos muestran que la suplementación con selenio resultó en una mayor expresión de la proteína GLUT-4, así como una mejoría de la glucosa en ayunas, la insulina en ayunas y el HOMA-IR en el modelo animal, ignorando estudios realizados en humanos que muestran un efecto diabetogénico de este mineral en muchos estudios realizados. De igual manera, este metaanálisis muestra resultados controvertidos con respecto a la modulación de la vía PI3K/Akt/GLUT-4 y el metabolismo de la glucosa en diferentes modelos animales. Consideraciones finales: La relación entre el selenio y la señalización de insulina es compleja y depende de la dosis, el compuesto y el tejido, es importante interpretar estos resultados con cuidado.

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Referencias

ALHARITHY M, ALAFIF N. Association of Selenium Intake and Selenium Concentrations with Risk of Type 2 Diabetes in Adults: A Narrative Review. Metabolites, 2023; 13: 767.

ABDULMALEK AS, BALBAA M. Synergistic effect of nano-selenium and metformin on type 2 diabetic rat model: Diabetic complications alleviation through insulin sensitivity, oxidative mediators and inflammatory markers. PLoS One, 2019; 14: e0220779.

AL-QURAISHY S, et al. Anti-hyperglycemic activity of selenium nanoparticles in streptozotocin-induced diabetic rats. International Journal of Nanomedicine, 2015; 10: 6741–6756.

BARAKAT GM, et al. Effects of Selenium and Exendin-4 on Glucagon-Like Peptide-1 Receptor, IRS-1, and Raf-1 in the Liver of Diabetic Rats. Biochemical Genetits, 2012; 50: 922–935.

BARAKAT G, et al. Effects of exendin-4 and selenium on the expression of GLP-1R, IRS-1, and preproinsulin in the pancreas of diabetic rats. Journal of Physiology Biochemistry, 2017; 73: 387-394.

CAI X, et al. Dosage-effect of selenium supplementation on blood glucose and oxidative stress in type 2 diabetes mellitus and normal mice. Journal of Trace Elements in Medicine and Biology, 2024; 3: 127410.

DUBEY P, et al. Role of Minerals and Trace Elements in Diabetes and Insulin Resistance. Nutrients, 2020; 12: 1864.

FARROKHIAN A, et al. Selenium Supplementation Affects Insulin Resistance and Serum hs-CRP in Patients with Type 2 Diabetes and Coronary Heart Disease. Hormone and Metabolic Research, 2016; 48: 263-268.

HASSAN RM, et al. Mitigating effect of single or combined administration of nanoparticles of zinc oxide, chromium oxide, and selenium on genotoxicity and metabolic insult in fructose/streptozotocin diabetic rat model. Environmental Science and Pollution Research, 2021; 28: 48517-48534.

HE J, et al. Nano-selenium modulates glucose metabolism and reduces insulin resistance through activation of the PI3K/Akt pathway in diabetic mice. Journal of Trace Element in Medicine and Biology, 2019; 81: 127130.

HEI YJ, et al. Stimulation of MAP kinase and S6 kinase by vanadium and selenium in rat adipocytes. Molecular and Cellular Biochemistry, 1998; 178: 367-375.

HWANG D, et al. Selenium acts as an insulin-like molecule for the down-regulation of diabetic symptoms via endoplasmic reticulum stress and insulin signalling proteins in diabetes-induced non-obese diabetic mice. Journal of Biosciences, 2007; 32: 723–735.

JABŁOŃSKA E, RESZKA E. Selenium and Epigenetics in Cancer: Focus on DNA Methylation. Advances in Cancer Research, 2017; 136 :193-234.

KIM SS, et al. Exercise training and selenium or a combined treatment ameliorates aberrant expression of glucose and lactate metabolic proteins in skeletal muscle in a rodent model of diabetes. Nutrition Research and Practice, 2011; 5: 205-213.

LABUNSKYY VM, et al. Selenoproteins: molecular pathways and physiological roles. Physiological Reviews, 2014; 94: 739-777.

LE TKC, et al. Insulin signaling and its application. Frontiers in Endocrinology, 2023; 14: 1226655.

LIU T, et al. Dual role of selenium in oxidative stress and insulin signaling: dose-dependent effects in metabolic disorders. Free Radical Biology and Medicine, 2023; 207: 146–157.

MATTMILLER SA, et al. Regulation of inflammation by selenium and selenoproteins: impact on eicosanoid biosynthesis. Journal of Nutritional Science, 2013; 2: e28.

MCNEILL JH, et al. Insulinlike effects of sodium selenate in streptozocin-induced diabetic rats. Diabetes 1991; 40: 1675-1678.

MISU H, et al. Inverse correlation between serum levels of selenoprotein P and adiponectin in patients with type 2 diabetes. PLoS One, 2012; 7: e34952.

MISU H, et al. A liver-derived secretory protein, selenoprotein P, causes insulin resistance. Cell Metabolism, 2010; 12: 483-495.

MITA, Y., et al. Selenoprotein P-neutralizing antibodies improve insulin secretion and glucose sensitivity in type 2 diabetes mouse models. Nature Communications, 2017; 8: 1658.

MURANO K, et al. Role of supplementary selenium on the induction of insulin resistance and oxidative stress in NSY mice fed a high fat diet. Biolpgical & Pharmaceutical Bulletin, 2018; 41: 92-98.

NORTON L, et al. Insulin: The master regulator of glucose metabolism. Metabolism, 2022; 129: 155142.

SAITO Y. Selenoprotein P as an in vivo redox regulator: disorders related to its deficiency and excess. Journal of Clinical Biochemistry and Nutrition, 2020; 66: 1-7.

SHI Y, et al. Trace Elements, PPARs, and Metabolic Syndrome. International Journal of Molecular Sciences, 2020; 21: 2612.

SPECKMANN B, et al. Selenium increases hepatic DNA methylation and modulates one-carbon metabolism in the liver of mice. The Journal of Nutritional Biochemistry, 2017; 48: 112-119.

STAHEL P, et al. Supranutritional selenium intake from enriched milk casein impairs hepatic insulin sensitivity via attenuated IRS/PI3K/AKT signaling and decreased PGC-1α expression in male Sprague–Dawley rats. The Journal of Nutritional Biochemistry, 2017; 41: 142–150.

STAPLETON SR, et al. Selenium: potent stimulator of tyrosyl phosphorylation and activator of MAP kinase. Biochimica et Biophysica Acta, 1997; 1355: 259-269.

STRÓŻYK A, et al. Effectiveness and safety of selenium supplementation for type 2 diabetes mellitus in adults: a systematic review of randomised controlled trials. Journal of Human Nutrition and Dietetics, 2019; 32: 635-645.

WANG Q, et al. Increased Expression of PHGDH Under High-Selenium Stress In Vivo. Biological Trace Element Research, 2024; 202: 5145-5156.

WANG C, et al. Long-Term Supranutritional Supplementation with Selenate Decreases Hyperglycemia and Promotes Fatty Liver Degeneration by Inducing Hyperinsulinemia in Diabetic db/db Mice. PLoS One, 2014; 9: e101315.

WANG Z, et al. Selenium supplementation improves hepatic insulin sensitivity via NRF2 and PPARγ activation in diabetic models. Redox Biology, 2022; 224:102311.

XU, TJ, et al. The effect of insulin in combination with selenium on blood glucose and GLUT4 expression in the cardiac muscle of streptozotocin-induced diabetic rats. Fundamental & Clinical Pharmacology, 2010; 24: 199-204.

YANG J, et al. Selenium deficiency-induced thioredoxin suppression and thioredoxin knock down disbalanced insulin responsiveness in chicken cardiomyocytes through PI3K/Akt pathway inhibition. Cellular Signalling, 2017; 38: 192-200.

ZHENG D, et al. Comparative profiling of serum, urine, and feces bile acids in humans, rats, and mice. Communications Biology, 2024; 7: 641.

ZHOU X, et al. Selenium-enriched exopolysaccharides improve skeletal muscle glucose uptake of diabetic KKAy mice via AMPK pathway. Journal of Physiology and Biochemistry, 2014a; 70: 547–554.

ZHOU J, et al. Selenite exacerbates hepatic insulin resistance in mouse model of type 2 diabetes through oxidative stress-mediated JNK pathway. Toxicology and Applied Pharmacology, 2015; 289:409-418.

ZHOU J, et al. Selenite exacerbates hepatic insulin resistance in mouse model of type 2 diabetes through oxidative stress-mediated JNK pathway. Toxicol Appl Pharmacol, 2015; 289: 409-418.

ZHOU X, et al. Selenium enriched exopolysaccharides produced by Enterobacter cloacae Z0206 alleviate adipose inflammation in diabetic KKAy mice through the AMPK/SirT1 pathway. Molecular Medicine Reports, 2014b; 9: 683-688.