2006, Number 1
<< Back Next >>
Inv Salud 2006; 8 (1)
Diabetes, oxidative stress and antioxidants
Ramos IML, Batista GCM, Gómez MBC, Zamora PAL
Language: Spanish
References: 64
Page: 7-15
PDF size: 475.98 Kb.
ABSTRACT
Diabetes mellitus is a group of metabolic diseases characterized by high blood glucose levels. Over time, diabetes can lead to blindness, kidney failure, nerve damage and atherosclerosis, what make it one of the main causes of morbidity and mortality. Nowadays some evidences show that such complications, due mainly to a biochemical imbalance are produced by the excessive production of free radicals (FR), which causes oxidative damage to the bio-molecules and that cannot be counteract by the antioxidant systems. Fortunately, this damage can be avoided or diminished with the administration of adequate doses of exogenous antioxidants (high-quality supplements), which could permit to the diabetic patients to have a better quality of life, because it is to expect that the micro and macro vascular complications caused mainly by the excessive production of FR diminish with the administration of antioxidant compounds.
REFERENCES
LeRoit D, Taylor SI, Olefssky JM. Diabetes Mellitus. Texto básico y clínico. 2ª ed. Ed. Mc-Graw Hill, Interamericana. México, D.F. 2003: 1331 pág.
www.cica.es/aliens/samfyc/introduc.htm 2005.
www.sobrentrenamiento.com/PubliCE/articulo.asp?Ida=558&tp=s 2005.
Taylor SI. Diabetes mellitus. The metabolic and molecular bases of inherited diseases. 7th ed. Ed. McGrawHill, USA. 1995: 843 pág.
Khan A, Lasker SS, Chowdhury TA. Are spouses of patients with type 2 diabetes at increased risk of developing diabetes? Diabetes Care, 2003;26:710-712.
Wolff SP. Diabetes mellitus and free radicals. Free radicals, transition metals and oxidative stress in the aetiology of diabetes mellitus and complications. Br Med Bull, 1993;49:642-652.
www.entornomedico.org/noticias/print.php?sid=2077 2005.
Benjamin SM, Valdez R, Geiss LS, Rolka DB, Narayan KM. Estimated number of adults with prediabetes in the US in 2000: Opportunities for prevention. Diabetes Care, 2003;26:645-649.
Pavia C, Ferrer I, Valls C, Artuch R, Colomé C, Vilaseca MA. Total homocysteine in patients with type 1 diabetes. Diabetes Care, 2000;23:84-87.
Jara Albarrán A. Endocrinología. Ed. Médica Panamericana; Madrid, España. 2001: 920 pág.
Gracy RW, Talent JM, Kong Y, Conrad CC. Reactive oxygen species: the unavoidable environmental insult? Mutat Res, 1999;428:17-22.
Rodríguez Capote K, Céspedes Miranda E. Estrés oxidativo y envejecimiento. Rev Cubana Invest Biomed, 1999;18:67-76.
Rodríguez Perón JM, Menéndez López JR, Trujillo López Y. Radicales libres en la biomedicina y estrés oxidativo. Rev Cubana Med Milit, 2001;30:36-44.
Liu Y, Gutterman DD. Oxidative stress and potassium channel function. Clin Exp Pharmacol Physiol, 2002;29:305-311.
Dorado Martínez C, Rugerio Vargas C, Rivas Arancibia S. Estrés oxidativo y neurodegeneración. Rev Fac Med UNAM, 2003;46:229-235.
Irie M, Asami S, Ikeda M, Kassai H. Depressive state relates to female oxidative DNA damage via neutrophil activation. Biochem Biophys Res Commun, 2003;311:1014-1018.
Pitozzi V, Giovannelli L, Bardini G, Rotella CM, Dolara P. Oxidative DNA damage in peripheral blood cells in type 2 diabetes mellitus: higher vulnerability of polymorphonuclear leucocytes. Mutat Res, 2003;529:129-133.
Sánchez-Rodríguez M, Santiago-Osorio E, Vargas LA, Mendoza-Nuñez VM. Propuesta de un constructo para evaluar integralmente el estrés oxidativo. Bioquimia, 2004;29:81-90.
Astaneie F, Afshari M, Mojtahedi A, Mostafalou S, Zamani MJ, Larijani B, Abdollahi M. Total antioxidant capacity and levels of epidermal growth factor and nitric oxide in blood and saliva of insulin-dependent diabetic patients. Arch Med Res, 2005;36:376-381.
www.neogym-online.com/nutest.htm 2005.
www.labnutricion.cl/estres.htm 2005.
www.efdeportes.com/efd66/oxid.htm 2005.
Batista-González C, Corona-Rivera JR, Gómez-Meda BC, Zamora-Perez AL, Ramos-Ibarra ML, Zúñiga-González G. Micronucleated erythrocytes in preterm newborns in relation to maternal pathology. Rev Biomed, 2006;17:(en prensa).
Schmid W. The micronucleus test. Mutat Res, 1975;31:9-15.
Ceriello A, Mercuri F, Quagliaro L, Assaloni R, Motz E, Tonutti L, Taboga C. Detection of nitrotyrosine in the diabetic plasma: evidence of oxidative stress. Diabetologia, 2001;44:834-838.
Šardaš S, Yilmaz M, Öztok U, Çakir N, Karakaya AE. Assessment of DNA strand breakage by comet assay in diabetic patients and the role of antioxidant supplementation. Mutat Res, 2001;490:123-129.
El-Missiry MA, Othman AI, Amer MA. L-Arginine ameliorates oxidative stress in alloxan-induced experimental diabetes mellitus. J Appl Toxicol, 2004;24:93-97.
Hunter-Lavin C, Hudson PR, Mukherjee S, Davies GK, Williams CP, Harvey JN, Child DF, Williams JH. Folate supplementation reduces serum hsp70 levels in patients with type 2 diabetes. Cell Stress Chaperones, 2004;9:344-349.
Davi G, Falco A, Patrono C. Lipid peroxidation in diabetes mellitus. Antioxid Redox Signal, 2005;7:256-268.
Gunes A, Ceylan A, Sarioglu Y, Stefek M, Bauer V, Karasu C. The Antioxidants in Diabetes-induced Complications (ADIC) Study Group. Reactive oxygen species mediate abnormal contractile response to sympathetic nerve stimulation and noradrenaline in the vas deferens of chronically diabetic rats: effects of in vivo treatment with antioxidants. Fundam Clin Pharmacol, 2005;19:73-79.
Kalogerakis G, Baker AM, Christov S, Rowley KG, Dwyer K, Winterbourn C, Best JD, Jenkins AJ. Oxidative stress and high –density lipoprotein function in type 1 diabetes and end-stage renal disease. Clin Sci, (Lond) 2005;108:497-506.
Okutan H, Ozcelik N, Yilmaz HR, Uz E.Effects of caffeic acid phenethyl ester on lipid peroxidation and antioxidant enzymes in diabetic rat heart. Clin Biochem, 2005;38:191-196.
www.fuedin.org/info congresos/04_02/congreso.htm 2006.
Sakamaki H, Akazawa S, Ishibashi M, Izumino K, Takino H, Yamasaki H, Yamaguchi Y, Goto S, Urata Y, Kondo T, Nagataki S. Significance of glutathione-dependent antioxidant system in diabetes-induced embryonic malformations. Diabetes, 1999;48:1138-1144.
Schraufstatter IU, Hyslop PA, Hinshaw DB, Spragg RG, Sklar LA, Cochrane CG. Hydrogen peroxide-induced injury of cells and its prevention by inhibitors of poly (ADP-ribose) polymerase. Proc Natl Acad Sci, USA. 1986;83:4908-4912.
Lafleur MV, Retel J. Contrasting effects of SH-compounds on oxidative DNA damage: repair and increase of damage. Mutat Res, 1993;295:1-10.
Yoshie Y, Ohshima H. Synergistic induction of DNA strand breakage by cigarette tar and nitric oxide. Carcinogenesis, 1997;18:1359-1363.
Migliore L, Bevilacqua C, Scarpato R.Cytogenetic study and FISH analysis in lymphocytes of systemic lupus erythematosus (SLE) and systemic sclerosis (SS) patients. Mutagenesis, 1999;14:227-31.
Ortiz GG, Reiter RJ, Zúñiga G, Melchiorri D, Sewerynek E, Pablos MI, Oh ChS, García JJ, Bitzer-Quintero OK. Genotoxicity of paraquat: micronuclei induced in bone marrow and peripheral blood are inhibited by melatonin. Mutat Res, 2000;464:239-245.
Ramos-Remus C, Dorazco-Barragan G, Aceves-Avila FJ, Alcaraz- Lopez F, Fuentes-Ramirez F, Michel-Diaz J, Torres-Bugarin O, Ventura-Aguilar A, Zúñiga-Gonzalez G. Genotoxicity assessment using micronuclei assay in rheumatoid arthritis patients. Clin Exp Rheumatol, 2002;20:208-212.
Torres-Bugarín O, Ventura-Aguilar A, Zamora-Perez A, Gómez-Meda BC, Ramos-Ibarra ML, Morga-Villela G, Gutierrez-Franco A, Zúñiga- González G. Evaluation of cisplatin + 5-FU, carboplatin + 5-FU, and ifosfamide + epirubicine regimens using the micronuclei test and nuclear abnormalities in the buccal mucosa. Mutat Res, 2004;565:91-101.
Baynes JW. Role of oxidative stress in development of complications in diabetes. Diabetes, 1991;40:405-412.
Dandona P, Thusu K, Cook S, Snyder B, Makowski J, Armstrong D, Nicotera T. Oxidative damage to DNA in diabetes mellitus. Lancet, 1996;347:444-445.
Julier K, Mackness MI, Dean JD, Durrington PN. Susceptibility of low- and high-density lipoproteins from diabetic subjects to in vitro oxidative modification. Diabet Med, 1999;16:415-423.
Gutierrez Maydata A. Estrés oxidativo en la gestación: ¿una nueva óptica en la atención a la embarazada? Rev Cubana Obstet Ginecol, 2005;31:1-9.
Lash LH, Hagen TM, Jones DP. Exogenous glutathione protects intestinal epithelial cells from oxidative injury. Proc Natl Acad Sci, USA. 1986;83:4641-4645.
Mukherjee A, Agarwal K, Aguilar MA, Sharma A. Anticlastogenic activity of beta-carotene against cyclophosphamide in mice in vivo. Mutat Res, 1991;263:41-46.
Arroyo PL, Hatch-Pigott V, Mower HF, Cooney RV. Mutagenicity of nitric oxide and its inhibition by antioxidants. Mutat Res, 1992;281:193-202.
Sai K, Hayashi M, Takagi A, Hasegawa R, Sofuni T, Kurokawa Y. Effects of antioxidants on induction of micronuclei in rat peripheral blood reticulocytes by potassium bromate. Mutat Res, 1992;269:113-118.
Pieri C, Marra M, Moroni F, Recchioni R, Marcheselli F. Melatonin: a peroxyl radical scavenger more effective than vitamin E. Life Sci, 1994;55:271-276.
Melchiorri D, Reiter RJ, Attia AM, Hara M, Burgos A, Nistico G. Potent protective effect of melatonin on in vivo paraquat-induced oxidative damage in rats. Life Sci, 1995;56:83-89.
Panda BB, Subhadra AV, Panda KK. Prophylaxis of antioxidants against the genotoxicity of methyl mercuric chloride and maleic hydrazide in Allium micronucleus assay. Mutat Res, 1995;343:75-84.
Vijayalaxmi, Reiter RJ, Leal BZ, Meltz ML. Effect of melatonin on mitotic and proliferation indices, and sister chromatid exchange in human blood lymphocytes. Mutat Res, 1996;351:187-192.
Rodríguez-Moran M, Guerrero-Romero JF, Parra-Quezada M, Segura-Pineda MJ, Levario-Carrillo M, Sotelo-Ham EI. Deficiencia de folatos y su asociación con defectos del cierre del tubo neural en el norte de México. Salud Pública de Mex, 1998;40:474-480.
Tang L, Reiter RJ, Li ZR, Ortiz GG, Yu BP, Garcia JJ. Melatonin reduces the increase in 8-hydroxy-deoxyguanosine levels in the brain and liver of kainic acid-treated rats. Mol Cell Biochem, 1998;178:299-303.
Vijayalaxmi KK, Venu R. In vivo anticlastogenic effects of L-ascorbic acid in mice. Mutat Res, 1999;438:47-51.
Rivas F, Davalos IP, Olivares N, Davalos NO, Perez-Medina R, Gomez-Partida G, Chakraborty R. Reproductive history in mothers of children with neural tube defects. Gynecol Obstet Invest, 2000;49:255-260.
Martínez-de Villareal LE, Limón-Benavides C, Valdez-Leal R, Sánchez- Peña MA, Villarreal-Pérez JZ. Efecto de la administración semanal de ácido fólico sobre los valores sanguíneos. Salud Pública de Mex, 2001;43:103-107.
Shahin AA, Ismail MM, Saleh AM, Moustafa HA, Aboul-Ella AA, Gabr HM. Protective effect of folinic acid an low-dose methotrexate genotoxicity. Z Rheumatol, 2001;60:63-68.
Gómez-Meda BC, Zúñiga-González GM, Zamora-Perez A, Ramos-Ibarra ML, Batista-González CM, Torres Mendoza BM. Folate supplementation of cyclophosphamide-treated mothers diminishes micronucleated erythrocytes in peripheral blood of newborn rats. Environ Mol Mutagen, 2004;44:174-178.
Soinio M, Marniemi J, Laakso M, Lehto S, Ronnemaa T. Elevated plasma homocysteine level is an independent predictor of coronary heart disease events in patients with type 2 diabetes mellitus. Ann Intern Med, 2004;140:94-100.
www.nacersano.org/centro/9388_9907.asp 2005.
www.well-connected.com/rreports/doc42S.html 2005.
ww.saludymedicinas.com.mx/articulo2.asp id=1032&bann=articulodehome&posicion=posicion2 2005.