The effects of antioxidant dietary supplements on oxidative stress and its implications in Metabolic Syndrome: a review

Autores

Palavras-chave:

Metabolic Syndrome X, Dietary supplements, Antioxidant, Oxidative stress

Resumo

The aim was to perform a review in order to elucidate the actions and efficacy of different antioxidant supplements used on Metabolic Syndrome. The articles were searched during October of 2015 to December of 2018, using the databases PubMed and Web of Knowledge. The keywords used were: “Metabolic Syndrome” AND “dietary supplements” OR “antioxidant”. The included articles were published from 2010 and in English. It was applied for articles selection inclusion and exclusion criteria. The articles that fulfilled criteria were analyzed through a full-text reading. Search results in 368 articles (PubMed: 198; Web of Knowledge: 170). After eliminating duplicated data and applying criteria, 16 articles were included to the review. The antioxidant supplements used on the studies included eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), nigella sativa (NS) and garlic, superoxide dismutase (SOD), cholecalciferol, Coenzyme Q10 (CoQ10), quercetin dehydrate, glycine, α-lipoic acid (ALA), glutathione precursor (F1), taurine, phenolic acids, red yeast rice-olive extract, curcumin, goji berry and arginine. Findings demonstrate a decrease in oxidative stress by increasing antioxidant enzyme activity, G6DH, Nrf2 with a consequently positive effect on insulin sensitivity, glucose tolerance, improvement in lipid profile, decrease on inflammatory and endothelium dysfunction markers with antioxidant supplements. Therefore, we could conclude that supplementation with antioxidant potential is able to ameliorate parameters of Metabolic Syndrome.

Downloads

Não há dados estatísticos.

Biografia do Autor

Giuseppe Potrick Stefani, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA)

Possui Graduação em Nutrição pela Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Mestrado em Ciências da Saúde com ênfase em Fisiologia e Fisiopatogênese (UFCSPA) e Especialização em Nutrição Clínica e Esportiva pelo Instituto de Pesquisas e Gestão em Saúde (iPGS). Atualmente é docente dos cursos de Pós-Graduação em Nutrição Esportiva e Treinamento Físico pela UNISINOS, Pós-Graduação em Nutrição Clínica e Esportiva pelo iPGS. Tem experiência na área de Nutrição Esportiva com ênfase em Fisiologia do Exercício, Fisiologia Cardiovascular atuando principalmente nos seguintes temas: suplementação, treinamento de força, estresse oxidativo e insuficiência cardíaca. Possui qualificação internacional concedida pela Sociedade Internacional para Avanço da Cineantropometria (ISAK), sendo cineantropometrista nível II.

Bruna Marmett, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA)

Possui Graduação em Nutrição pela Universidade Federal de Ciências da Saúde de Porto Alegre (2014) e Mestrado em Ciências da Saúde (UFCSPA) (2017). Atualmente é aluna de Doutorado em Ciências da Saúde (UFCSPA), atuando em pesquisas no Laboratório de Poluição Atmosférica nas áreas de poluição atmosférica, monitoramento ambiental, exercício físico, suplementação, estresse oxidativo e dano em DNA.

Cláudia Ramos Rhoden, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA)

possui graduação em Farmácia pela Universidade Federal do Rio Grande do Sul (1986), especialização em Análises Clínicas pela Universidade Federal do Rio Grande do Sul (1987), mestrado em Farmacologia pela Fundação Faculdade Federal de Ciências Médicas de Porto Alegre (1991), doutorado em Ciências Biológicas (Fisiologia) pela Universidade Federal do Rio Grande do Sul (2000) e pós-doutorado no Programa de Fisiologia com ênfase em Ciência Ambiental na Harvard University (2002). Atualmente é professora da Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), criada em janeiro de 2008 a partir da transformação da Fundação Faculdade Federal de Ciências Médicas de Porto Alegre; e coordenadora do Laboratório de Poluição Atmosférica na UFCSPA. Também é Pesquisadora Associada junto ao Departamento de Patologia da Faculdade de Medicina da Universidade de São Paulo.

Referências

Souza LJd, Gicovate Neto C, Chalita FEB, Reis AFF, Bastos DA, Souto Filho JTD, et al. Prevalence of obesity and cardiovascular risk factors in Campos, RJ. Prevalência de obesidade e fatores de risco cardiovascular em Campos, Rio de Janeiro. Arquivos Brasileiros de Endocrinologia & Metabologia. 2003;47(6):669-76.

Grundy SM. Metabolic syndrome: Connecting and reconciling cardiovascular and diabetes worlds. Journal of the American College of Cardiology. 2006;47(6):1093-100.

Barbosa PJB, Lessa Í, Almeida Filho Nd, Magalhães LBNC, Araújo J. Criteria for central obesity in a Brazilian population: impact on metabolic syndrome Critério de obesidade central em população brasileira: impacto sobre a síndrome metabólica. Arquivos Brasileiros de Cardiologia. 2006;87(4):407-14.

Marquezine GF, Oliveira CM, Pereira AC, Krieger JE, Mill JG. Metabolic syndrome determinants in an urban population from Brazil: Social class and gender-specific interaction. International Journal of Cardiology. 2008;129(2):259-65.

Salaroli LB, Barbosa GC, Mill JG, Molina MCB. Prevalence of metabolic syndrome in population-based study, Vitoria, ES - Brazil. Arquivos Brasileiros De Endocrinologia E Metabologia. 2007;51(7):1143-52.

Oliveira EPd, Souza MLAd, Lima MdDAd. Prevalence of metabolic syndrome in a semi-arid rural area in Bahia. Prevalência de síndrome metabólica em uma área rural do semi-árido baiano. Arquivos Brasileiros de Endocrinologia & Metabologia. 2006;50(3):456-65.

Leão LSCdS, Barros ÉG, Koifman RJ. Prevalência de Síndrome Metabólica em Adultos Referenciados para Ambulatório de Nutrição no Rio de Janeiro, Brasil. Rev Bras Cardiol. 2010;23(2):93-100.

Fogal AS, Ribeiro AQ, Priore SE, Franceschini SdCC. Prevalência de síndrome metabólica em idosos: uma revisão sistemática Prevalence of metabolic syndrome in the elderly: a systematic review Revista da Associação Brasileira de Nutrição [Internet]. 2014; Ano 6(1):[29-35 pp.].

Qiao Q, Gao W, Zhang L, Nyamdorj R, Tuomilehto J. Metabolic syndrome and cardiovascular disease. Ann Clin Biochem. 2007;44(Pt 3):232-63.

Czernichow S, Vergnaud A-C, Galan P, Arnaud J, Favier A, Faure H, et al. Effects of long-term antioxidant supplementation and association of serum antioxidant concentrations with risk of metabolic syndrome in adults. American Journal of Clinical Nutrition. 2009;90(2):329-35.

Miranda C, Zanette G, Livolsi P, Azzano S, Villalta ML, Monselesan S, et al. Prevalence of the Metabolic Syndrome in Newly Diagnosed Type 2 Diabetes Mellitus According to the ATP III Criteria Modified by the AHA-NHLBI: Gender Differences. Diabetes. 2015;64:A681-A.

Stefani GP, Baldissera G, Nunes RB, Heck TG, Rhoden CR. Metabolic Syndrome and DNA Damage: The Interplay of Environmental and Lifestyle Factors in the Development of Metabolic Dysfunction. Open Journal of Endocrine and Metabolic Diseases. 2015;5:65-76.

Yara S, Lavoie JC, Levy E. Oxidative stress and DNA methylation regulation in the metabolic syndrome. Epigenomics. 2015;7(2):283-300.

Ceriello A, Motz E. Is oxidative stress the pathogenic mechanism underlying insulin resistance, diabetes, and cardiovascular disease? The common soil hypothesis revisited. Arteriosclerosis Thrombosis and Vascular Biology. 2004;24(5):816-23.

Furukawa S, Fujita T, Shimabukuro M, Iwaki M, Yamada Y, Nakajima Y, et al. Increased oxidative stress in obesity and its impact on metabolic syndrome. Journal of Clinical Investigation. 2004;114(12):1752-61.

Mahjoub S, Masrour-Roudsari J. Role of oxidative stress in pathogenesis of metabolic syndrome. Caspian J Intern Med. 2012;3(1):386-96.

Vericel E, Januel C, Carreras M, Moulin P, Lagarde M. Diabetic patients without vascular complications display enhanced basal platelet activation and decreased antioxidant status. Diabetes. 2004;53(4):1046-51.

Grundy SM, Hansen B, Smith SC, Cleeman JI, Kahn RA, Conference P. Clinical Management of Metabolic Syndrome - Report of the American heart Association/National Heart, Lung, and Blood Institute/American Diabetes Association Conference on Scientific Issues Related to Management. Circulation. 2004;109(4):551-6.

Chao P-c, Huang C-n, Hsu C-c, Yin M-c, Guo Y-r. Association of dietary AGEs with circulating AGEs, glycated LDL, IL-1 alpha and MCP-1 levels in type 2 diabetic patients. European Journal of Nutrition. 2010;49(7):429-34.

Wei J, Zeng C, Gong Q-y, Li X-x, Lei G-h, Yang T-b. Associations between Dietary Antioxidant Intake and Metabolic Syndrome. Plos One. 2015;10(6).

Al-Rasheed N, Al-Rasheed N, Bassiouni Y, Faddah L, Mohamad AM. Potential Protective Effects of Nigella Sativa and Allium Sativum Against Fructose-Induced Metabolic Syndrome in Rats. Journal of Oleo Science. 2014;63(8):839-48.

Carillon J, Knabe L, Montalban A, Stevant M, Keophiphath M, Lacan D, et al. Curative diet supplementation with a melon superoxide dismutase reduces adipose tissue in obese hamsters by improving insulin sensitivity. Molecular Nutrition & Food Research. 2014;58(4):842-50.

Molinar-Toribio E, Perez-Jimenez J, Ramos-Romero S, Romeu M, Giralt M, Taltavull N, et al. Effect of n-3 PUFA supplementation at different EPA:DHA ratios on the spontaneously hypertensive obese rat model of the metabolic syndrome. British Journal of Nutrition. 2015;113(6):878-87.

Ozdogan S, Kaman D, Simsek BC. Effects of coenzyme Q10 and alpha-lipoic acid supplementation in fructose fed rats. Journal of Clinical Biochemistry and Nutrition. 2012;50(2):145-51.

Diaz-Flores M, Cruz M, Duran-Reyes G, Munguia-Miranda C, Loza-Rodriguez H, Pulido-Casas E, et al. Oral supplementation with glycine reduces oxidative stress in patients with metabolic syndrome, improving their systolic blood pressure. Canadian Journal of Physiology and Pharmacology. 2013;91(10):855-60.

Erbas O, Solmaz V, Aksoy D, Yavasoglu A, Sagcan M, Taskiran D. Cholecalciferol (vitamin D 3) improves cognitive dysfunction and reduces inflammation in a rat fatty liver model of metabolic syndrome. Life Sciences. 2014;103(2):68-72.

Sinha-Hikim I, Sinha-Hikim AP, Shen R, Kim HJ, Kim H, French SW, et al. A novel cystine based antioxidant attenuates oxidative stress and hepatic steatosis in diet-induced obese mice. Exp Mol Pathol. 2011;91(1):419-28.

El Mesallamy HO, El-Demerdash E, Hammad LN, El Magdoub HM. Effect of taurine supplementation on hyperhomocysteinemia and markers of oxidative stress in high fructose diet induced insulin resistance. Diabetology & Metabolic Syndrome. 2010;2.

Orlando P, Silvestri S, Bruge F, Tiano L, Kloting I, Falcioni G, et al. High-Fat Diet-Induced Met-Hemoglobin Formation in Rats Prone (WOKW) or Resistant (DA) to the Metabolic Syndrome: Effect of CoQ(10) Supplementation. Biofactors. 2014;40(6):603-9.

Pfeuffer M, Auinger A, Bley U, Kraus-Stojanowic I, Laue C, Winkler P, et al. Effect of quercetin on traits of the metabolic syndrome, endothelial function and inflammation in men with different APOE isoforms. Nutrition Metabolism and Cardiovascular Diseases. 2013;23(5):403-9.

Oxidative aspects of metabolic syndrome and atherosclerosis [Internet]. 2015.

Urakawa H, Katsuki A, Sumida Y, Gabazza EC, Murashima S, Morioka K, et al. Oxidative stress is associated with adiposity and insulin resistance in men. Journal of Clinical Endocrinology & Metabolism. 2003;88(10):4673-6.

Maassen JA, Romijn JA, Heine RJ. Fatty acid-induced mitochondrial uncoupling in adipocytes as a key protective factor against insulin resistance and beta cell dysfunction: a new concept in the pathogenesis of obesity-associated type 2 diabetes mellitus. Diabetologia. 2007;50(10):2036-41.

D'Autreaux B, Toledano MB. ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis. Nature Reviews Molecular Cell Biology. 2007;8(10):813-24.

Filosa S, Fico A, Paglialunga F, Balestrieri M, Crooke A, Verde P, et al. Failure to increase glucose consumption through the pentose-phosphate pathway results in the death of glucose-6-phosphate dehydrogenase gene-deleted mouse embryonic stem cells subjected to oxidative stress. Biochem J. 2003;370(Pt 3):935-43.

Sekhar RV, McKay SV, Patel SG, Guthikonda AP, Reddy VT, Balasubramanyam A, et al. Glutathione synthesis is diminished in patients with uncontrolled diabetes and restored by dietary supplementation with cysteine and glycine. Diabetes Care. 2011;34(1):162-7.

Xu Y, Wang G, Li C, Zhang M, Zhao H, Sheng J, et al. Pu-erh tea reduces nitric oxide levels in rats by inhibiting inducible nitric oxide synthase expression through toll-like receptor 4. Int J Mol Sci. 2012;13(6):7174-85.

Olivieri F, Lazzarini R, Babini L, Prattichizzo F, Rippo MR, Tiano L, et al. Anti-inflammatory effect of ubiquinol-10 on young and senescent endothelial cells via miR-146a modulation. Free Radic Biol Med. 2013;63:410-20.

Egert S, Bosy-Westphal A, Seiberl J, Kuerbitz C, Settler U, Plachta-Danielzik S, et al. Quercetin reduces systolic blood pressure and plasma oxidised low-density lipoprotein concentrations in overweight subjects with a high-cardiovascular disease risk phenotype: a double-blinded, placebo-controlled cross-over study. British Journal of Nutrition. 2009;102(7):1065-74.

Zentella de Pina M, Vazquez-Meza H, Pardo JP, Rendon JL, Villalobos-Molina R, Riveros-Rosas H, et al. Signaling the signal, cyclic AMP-dependent protein kinase inhibition by insulin-formed H2O2 and reactivation by thioredoxin. Journal of Biological Chemistry. 2008;283(18):12373-86.

Agca CA, Tuzcu M, Hayirli A, Sahin K. Taurine ameliorates neuropathy via regulating NF-κB and Nrf2/HO-1 signaling cascades in diabetic rats. Food Chem Toxicol. 2014;71:116-21.

Pessin JE, Kwon H. How does high-fat diet induce adipose tissue fibrosis? J Investig Med. 2012;60(8):1147-50.

Gottlieb MGV, Cruz IBM, Schwanke CHA, Bodanese LC. Oxidative stress as an emergent cardiometabolic risk factor. Scientia Medica [Internet]. 2010; 20(3):[243-9 pp.].

Fishel MA, Watson S, Montine TJ, Wang Q, Green PS, Kulstad JJ, et al. Hyperinsulinemia provokes synchronous increases in central inflammation and beta-amyloid in normal adults. Archives of Neurology. 2005;62(10):1539-44.

Devaraj S, Leonard S, Traber MG, Jialal I. gamma-tocopherol supplementation alone and in combination with alpha-tocopherol alters biomarkers of oxidative stress and inflammation in subjects with metabolic syndrome. Free Radical Biology and Medicine. 2008;44(6):1203-8.

DeMarco VG, Scumpia PO, Bosanquet JP, Skimming JW. alpha-Lipoic acid inhibits endotoxin-stimulated expression of iNOS and nitric oxide independent of the heat shock response in RAW 264.7 cells. Free Radical Research. 2004;38(7):675-82.

Zhang BB, Zhou G, Li C. AMPK: an emerging drug target for diabetes and the metabolic syndrome. Cell Metab. 2009;9(5):407-16.

Thirunavukkarasu V, Anitha Nandhini AT, Anuradha CV. Effect of alpha-lipoic acid on lipid profile in rats fed a high-fructose diet. Exp Diabesity Res. 2004;5(3):195-200.

Blachier F, Lancha AH, Jr., Boutry C, Tome D. Alimentary proteins, amino acids and cholesterolemia. Amino Acids. 2010;38(1):15-22.

Ibitoye OB, Ajiboye TO. Dietary phenolic acids reverse insulin resistance, hyperglycaemia, dyslipidaemia, inflammation and oxidative stress in high-fructose diet-induced metabolic syndrome rats. Arch Physiol Biochem. 2018;124(5):410-417.

Hermans N, Van der Auwera A, Breynaert A, Verlaet A, De Bruyne T, Van Gaal L, et al. A red yeast rice-olive extract supplement reduces biomarkers of oxidative stress, OxLDL and Lp-PLA2, in subjects with metabolic syndrome: a randomised, double-blind, placebo-controlled trial. Trials. 2017;18(1):302.

Ghazimoradi M, Saberi-Karimian M, Mohammadi F, Sahebkar A, Tavallaie S, Safarian H, et al. The Effects of Curcumin and Curcumin-Phospholipid Complex on the Serum Pro-oxidant-Antioxidant Balance in Subjects with Metabolic Syndrome. Phytother Res. 2017;31(11):1715-1721.

de Souza Zanchet MZ, Nardi GM, de Oliveira Souza Bratti L, Filippin-Monteiro FB, Locatelli C. Lycium barbarum Reduces Abdominal Fat and Improves Lipid Profile and Antioxidant Status in Patients with Metabolic Syndrome. Oxid Med Cell Longev. 2017; 9763210.

Medeiros RF, Gaique TG, Bento-Bernardes T, Kindlovits R, Gomes TMB, Motta NAV, et al. Arginine and aerobic training prevent endothelial and metabolic alterations in rats at high risk for the development of the metabolic syndrome. Br J Nutr. 2017; 118(1):1-10.

Mohammadi A, Sadeghnia HR, Saberi-Karimian M, Safarian H, Ferns GA, Ghayour-Mobarhan M, et al. Effects of Curcumin on Serum Vitamin E Concentrations in Individuals with Metabolic Syndrome. Phytother Res. 2017; 31(4):657-662.

Downloads

Publicado

2019-09-05

Como Citar

Stefani, G. P., Marmett, B., & Rhoden, C. R. (2019). The effects of antioxidant dietary supplements on oxidative stress and its implications in Metabolic Syndrome: a review. Revista Da Associação Brasileira De Nutrição - RASBRAN, 10(1), 117–127. Recuperado de https://rasbran.com.br/rasbran/article/view/469

Edição

Seção

Artigos de Revisão Sistemática

Artigos Semelhantes

1 2 3 4 > >> 

Você também pode iniciar uma pesquisa avançada por similaridade para este artigo.