Acrylamide reduces plasma antioxidant vitamin levels in rats due to increased oxidative damage
Palavras-chave:
Acrylamide, Malondialdehyde, Retinoic acid, Sialic acid, α-tocopherolResumo
Objective
Acrylamide is a potentially neurotoxic and carcinogenic chemical and naturally creates during the heating process of carbohydrate-rich foods, such as potato chips and breakfast cereals. Acrylamide might be ingested by people via consuming food that contains it. Therefore, we investigated the effect of acrylamide given orally to male and female rats on plasma retinoic acid and α-tocopherol and serum sialic acid and malondialdehyde levels.
Method
A total of 50 Wistar rats were used (25 female and 25 male, three-four weeks old). The rats of each sex were given 2 and 5mg/kg/day acrylamide via drinking water for 90 days. At the end of the treatment, the animals were euthanized by cervical dislocation. Blood specimens were collected through cardiac puncture, and serum and plasma samples were analysed using the high-performance liquid chromatography technique with a Ultraviolet detector.
Results
The analysis of the plasma and serum samples revealed that serum sialic acid and malondialdehyde levels in both sexes given 5mg/kg/day acrylamide were significantly increased, and the serum sialic acid levels were higher in female rats given 2mg/kg/day acrylamide. The plasma retinoic acid and α-tocopherol levels significantly decreased in both sexes given only the highest dose.
Conclusion
The results show that acrylamide causes an increase in oxidative stress and leads to a decrease in the levels of retinoic acid and α-tocopherol which play a role in the defense mechanism against this stress.
Referências
Stadler RH, Blank L, Vorga N, Robert F, Hav J, Guy, PA, et al. Acrylamide from Maillard reaction products. Nature. 2002;419(6906):449-50. http://dx.doi.org/10.1038/419449a
Tareke E, Rydberg P, Karlsson P. Analysis of acrylamide, a carcinogen formed in heated foodstuffs. J Agric Food Chem. 2000;50:4998-5006.
Virk-Baker MK, Nagy TR, Barnes S, Groopman J. Dietary acrylamide and human cancer: a systematic review of literature. Nutr Cancer. 2014;66:774-90.
El-Sayyad HI, El-Gammal HL, Habak LA, Abdel-Galil HM, Fernando A, Gaur RL, et al. Structural and ultrastructural evidence of neurotoxic effects of fried potato chips on rat postnatal development. Nutrition. 2011;27:1066-75.
Singh T, Kushwah AS. Acrylamide: a possible risk factor for cardiac health. Asian J Pharm Clin Res. 2018;11(10):39-48.
Pelucchi C, La VC, Bosetti C, Boyle P, Boffetta P. Exposure to acrylamide and human cancer: a review and meta-analysis of epidemiologic studies. Ann Oncol. 2011;7:1487-99.
European Food Safety Authority. Scientific opinion on acrylamide in food. EFSA J. 2015;13(6):4104.
Tran NL, Barraj LM, Collinge S. Reduction in dietary acrylamide exposure-impact of potatoes with low acrylamide potential. Risk Anal. 2017;37(9):1754-67.
Kopp EK, Dekant W. Toxicokinetics of acrylamide in rats and humans following single oral administration of low doses. Toxicol Appl Pharmacol. 2009;235:135-42.
Ankaiah R, Kurrey NK, Krishnan MH. The positive intervention effects of resveratrol on acrylamide -induced cyto-/Genotoxicity in primary lymphocytes of rat. Phcog Mag. 2018;14:643-8.
Kumar D, Rızvı SI. Erythrocyte membrane bound and plasma sialic acid during aging. Biologia. 2013;68(4):762-5.
Tucker JM, Townsend DM. Alpha-tocopherol: roles in prevention and teraphy of human disease. Biomed Pharmacother. 2005;59:380-7.
Hajibabaei K. Antioxidant properties of vitamin E. Ann Res Antioxid. 2016;1(2):e22.
Cañete A, Cano E, Muñoz-Chápuli R, Carmona R. Role of vitamin A/retinoic acid in regulation of embryonic and adult hematopaiesis. Nutrients. 2017;9(2):159. http://dx.doi.org/10.3390/nu9020159
Guimarães IG, Lim C, Yildirim-Aksoy M, Li MH, Klesius PH. Effects of dietary levels of vitamin A on growth, hematology, immune response and resistance of Nile tilapia (Oreochromis niloticus) to Streptococcus iniae. Anim Feed Sci Thecnol. 2014;188:126-36.
Hall JA, Grainger JR, Spencer SP, Belkaid Y. The role of retinoic acid in tolerance and immunity. Immunity. 2011;35:13-22.
Grotto D, Maria LS, Valentini J. Importance of the lipid peroxidation biomarkers and methodological aspects for malondialdehyde quantification. Quim Nova. 2009;32:169-74.
Khoubnasabjafari M, Ansarin K, Jouyban A. Reliability of malondialdehyde as a biomarker of oxidative stress in psychological disorders. Bioimpacts. 2015;5:123-7.
Burek JD, Albee RR, Beyer JE, Bell TJ, Carreon RM, Morden DC, et al. Subchronic toxicity of acrylamide administered to rats in drinking water follewed by up to 144 days of recovery. J Environ Pathol Toxicol. 1980;4:157-82.
Warren L. The thiobarbituric acid assay of sialic acid. J Biol Chem. 1959;234:1971-5.
Draper HH, Hadley M. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol. 1990;186:421-31.
Schnaar RL, Gerardy-Schahn R, Hildebrandt H. Sialic acid in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regeneration. Physiol Rev. 2014;94:461-18.
Lijima R, Takahashi H, Namme R, Ikegami S, Yamazaki M. Novel biological function of sialic acid (N-acetylneuraminic acid) as a hydrogen peroxide scavenger. Febs Lett. 2004;561:163-6.
Rajendiran S, Lakshamanappa HS, Zachariah B, Nambiar S. Desialylation of plasma proteins in severe dengue infection possible role of oxidative stres. Am J Trop Med Hyg. 2008;79:372-7.
Yousef MI, El-Demerdash FM. Acrylamide-induced oxidative stres and biochemical perturbation in rats. Toxicol. 2006;219:133-41.
Yılmaz FM, Yılmaz G, Savaş Erdeye S, Dallar Y, Topkaya BC, et al. Serum sialic acid, hs-CRP and oxidetive stres parameters in obese children. J Pediatr Endocrinol Metab. 2007;20:205-10.
Mohan SK, Priyav V. Serum total sialic acid, lipid peroxidation, and glutathione reductase levels in patients with rheumatoid arthritis. Turk J Med Sci. 2010;40:537-40.
Ovist R, Ismail IS, Muniandy S, Vellasamy KM, Chinn K. Correlation of plasma C-reactive protein levels to sialic acid and lipid concentrations in the normal population. J Med Sci. 2007;7:1049-53.
Bajendiran KS, Ananthanarayanan RH, Satheesh S, Rajappa M. Elevated levels of serum sialic acid and high sensitivity C-reactive protein: markers of systematic inflammation in patients with chronic heart failure. Br J Biomed Sci. 2014;71:29-32.
Naruszewicz M, Zapolska-Downar D, Kośmider A, Nowicka G, Kozlowska-Wojciechowska M, Vikström AS, et al. Chronic intake of potato chips in humans increases the production of reactive oxygen radicals by leucocytes and increases plasma C-reactive protein: a plot study. Am J Clin Nutr. 2009;89(6):1951. http://dx.doi.org/10.3945/ajcn.2008.26647
Lyn-Cook LE, Tareke E, Word B, Starlard-Davenport A, Lyn-Cook BD, Hammons GJ. Food contaminant acrylamide increases inflammation in breast cells. Toxicol Ind Health. 2011;27:11-8.
Luo YS, Long TY, Shen LC, Huang SL, Chiang SY, Wu KY. Synthesis, characterization and analysis of the acrylamide- and glycidamide-glutathione conjugates. Chem Biol Interact. 2015;237:38-46. http://dx.doi.org/10.1016/j.cbi.2015.05.002
Li D, Wang P, Liu Y, Hu X, Chen F. Metabolism of acrylamide: interindividual and interspecies differences as well as the application as biomarkers. Curr Drug Metab. 2016;17:317-26.
Srivastava SP, Daş M, Seth PK. Enhancement of lipid peroxidation in rat liver on acut exposure to styrene and acrylamide a concequence of glutathione depletion. Chem Biol Interact. 1983;45:373-80.
Radu M, Munteanu MC, Petrashe S, Serban AI, Dinu D, Hermanean A, et al. Depletion of intracellular glutathione and increased lipid peroxidation mediate cytotoxicity of hematite nanoparticles in MRC-5 cells. Acta Biochem Pol. 2010;57:355-60.
Catalgol B, Ozhan G, Alpertunga B. Acrylamide-induced oxidative stres in human erythrocytes. Hum Exp Toxicol. 2009;28(10):611-7. http://dx.doi.org/10.1177/0960327109350664
Pan X, Wu X, Yan D, Peng C, Rao C, Yan H. Acrylamide-induced oxidative stress and inflammatory response are alleviated by N-acetylcysteine in PC12 cells: involvement of the crosstalk between Nrf2 and NF-κB pathways regulated by MAPKs. Toxicol Lett. 2018;288:56-64.
Birben E, Sahiner UM, Sackesen C, Erzurum S, Kalaycı O. Oxidative stress and antioxidant defence. World Allergy Organ J. 2012;5:9-19.
Sridevi B, Reddy KV, Reddy SL. Effect of trivalent and hexavalent chromium on antioxidant enzyme activities and lipid peroxidation in a freshwater field crab, Barytelphusa guerini. Bull Environ Contam Toxicol. 1998;61:389-90.
Downloads
Publicado
Como Citar
Edição
Seção
Licença
Copyright (c) 2022 Yeşim YENER, Fatma Hümeyra YERLİKAYA
Este trabalho está licenciado sob uma licença Creative Commons Attribution 4.0 International License.