White and Brown Crystal Sugar dietary: a high consumption effect in D. Melanogater
DOI:
https://doi.org/10.5902/2179460X74331Keywords:
Sugar intake, Oxidative stress, Male and female flies, Enzyme activity, Sucrose, IronAbstract
The high consumption of sugars in their different forms has been of concern to the International Health organization (WHO). In this study, D. melanogater (born in the dietary medium - Generation F1) male and females were submitted to a white (WS) and brown (BS) Cristal Sugars rich diet. Results obtained indicate an increase in oxidative stress with an increase in the consumption of sugar in the diet, as observed in the increase in the enzymatic activity of SOD, CAT and GPx. These results are corroborated by analyzes of lipid peroxidation (TBARS), carbonyl content and ROS (DCFH), which clearly demonstrate an increase in the formation of reactive oxygen species with the increase in the consumption of sugars both white and brown crystal sugars. Another effect observed by the increase in sugar consumption was the augmentation in glucose levels (white and brown sugars) and in iron levels (brown sugar). In this sense, the high consumption of iron in brown sugar has contributed more strongly to the formation of ROS in D. melanogaster, mainly in females.
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Aaseth, J., Dusek, P. & Roos, P.M. (2018). Prevention of progression in Parkinson’s disease. Biometals, 31:737–747. https://doi.org/10.1007/s10534-018-0131-5. DOI: https://doi.org/10.1007/s10534-018-0131-5
Aebi, H. (1984). Catalase in vitro, Method Enzymol. 105, 121–126. DOI: https://doi.org/10.1016/S0076-6879(84)05016-3
Barbosa, K. B. F. et al. (2010) Estresse oxidativo: conceito, implicações e fatores modulatórios. Revista de Nutrição, 23(4), 629–643, aug. DOI: https://doi.org/10.1590/S1415-52732010000400013
Bornfeldt, K. E. (2016). Does elevated glucose promote atherosclerosis? Pros and Cons. Circ Res. July, 8, 119(2): 190–193. doi:10.1161/CIRCRESAHA.116.308873. DOI: https://doi.org/10.1161/CIRCRESAHA.116.308873
Brookheart, R.T., Swearingen, A.R., Collins, C.A., Cline, L.M., & Duncan, J.G. (2017). High-sucrose-induced maternal obesity disrupts ovarian function and decreases fertility in Drosophila melanogaster. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 863(6), June, 1255-1263. DOI: https://doi.org/10.1016/j.bbadis.2017.03.014
Brown, I. J., Stamler, J., & Van Horn, L. (2011). International Study of Macro/Micronutrients and Blood Pressure Research Group. Sugar-sweetened beverage, sugar intake of individuals, and their blood pressure: international study of macro/micronutrients and blood pressure. Hypertension, 57(4):695–701. DOI: https://doi.org/10.1161/HYPERTENSIONAHA.110.165456
Calap-Quintana, P., González-Fernández, J., Sebastiá-Ortega, N., Llorens, J.V.,& Moltó, M.D. (2017) Review Drosophila melanogaster Models of Metal-Related Human Diseases and Metal Toxicity, Int. J. Mol. Sci., 18, 1456, doi: https:// doi.org/10.3390/ijms18071456. DOI: https://doi.org/10.3390/ijms18071456
Chandegra, B., Tang, J.L.Y, Chi, H., & Alic, N. (2017). Sexually dimorphic effects of dietary sugar on lifespan, feeding and starvation resistance in Drosophila. Aging (Albany NY). Dec, 9(12): 2521–2528. DOI: https://doi.org/10.18632/aging.101335
Chatterjee, S., Khunti, K. & Davies, M. J. (2017). Type 2 diabetes. Lancet, 389: 2239–51, http://dx.doi.org/10.1016/S0140-6736(17)30058-2. DOI: https://doi.org/10.1016/S0140-6736(17)30058-2
Danielsen, E.T., Moeller, M.E., & Rewitz, K.F. (2013). Sinalização de nutrientes e tempo de desenvolvimento da maturação. Curr. Topo. Dev. Biol., 105, 37 – 67. DOI: https://doi.org/10.1016/B978-0-12-396968-2.00002-6
Ecker, A et al. High-sucrose diet induces diabetic-like phenotypes and oxidative stress in Drosophila melanogaster: Protective role of Syzygium cumini and Bauhinia forficata. Biomedicine & Pharmacotherapy. Volume 89, May 2017, Pages 605-616. DOI: https://doi.org/10.1016/j.biopha.2017.02.076
Espositoa, K., Maiorinoa, M.I., Ceriellob, A.,& Giugliano, D. (2010) Prevention and control of type 2 diabetes by mediterranean diet: a systematic review. Diabetes Res. Clin. Pract., 89, 97-102. DOI: https://doi.org/10.1016/j.diabres.2010.04.019
Finelli, A., Kelkar, A., Song, H.J., Yang, H., & Konsolaki, M. (2004). A model for studying Alzheimer's Abeta42-induced toxicity in Drosophila melanogaster. Mol. Cell Neurosci.2004, 26 (3), 365-375. DOI: https://doi.org/10.1016/j.mcn.2004.03.001
Folmer, V., Soares, J. C. M., & Rocha, J.B.T. (2002). Oxidative stress in mice is dependent on the free glucose content of the diet. The International Journal of Biochemistry & Cell Biology, 34(10), October, 1279-1285, https://doi.org/10.1016/S1357-2725(02)00065-1. DOI: https://doi.org/10.1016/S1357-2725(02)00065-1
Galarisa, D., Barboutib, A., & Pantopoulosc, K. (2019). Iron homeostasis and oxidative stress: An intimate relationship, BBA - Molecular Cell Research, 1866, 118535, https://doi.org/10.1016/j.bbamcr.2019.118535. DOI: https://doi.org/10.1016/j.bbamcr.2019.118535
Ighodaro, O. M., & Akinloye, A. O. (2018). First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): Their fundamental role in the entire antioxidant defence grid, Alexandria Journal of Medicine, 54, 287–293, https://doi.org/10.1016/j.ajme.2017.09.001. DOI: https://doi.org/10.1016/j.ajme.2017.09.001
Jeibmann, A., & Paulus, W. (2009) Drosophila melanogaster as a Model Organism of Brain Diseases. Int. J. Mol. Sci., 10, 407-440, doi: https:// doi.org/10.3390/ijms10020407. DOI: https://doi.org/10.3390/ijms10020407
Khatun, S., Mandi, M., Rajak, P. & Roy, S. (2018). Interplay of ROS and behavioral pattern in fluoride exposed Drosophila melanogaster. Chemosphere 209, 220e231. DOI: https://doi.org/10.1016/j.chemosphere.2018.06.074
Lang, S., Hilsabeck, T.A., Wilson, K. A., Sharma, A., Bose, N., … & Brackman, D.J. (2019). A conserved role of the insulin-like signaling pathway in dietdependent uric acid pathologies in Drosophila melanogaster. PLoS Genet, 15(8): e1008318. https://doi.org/10.1371/journal.pgen.1008318. DOI: https://doi.org/10.1371/journal.pgen.1008318
Levine, R.L., Garland, D., Oliver, C. N., Amici, A., Climent, I., Lenz, A. G., Alm, B., Shaltiel, S., & Stadman, E.R. (1990). Damage to proteins and lipids tissues under oxidative stress. Methods in Enzymology, 186:464. DOI: https://doi.org/10.1016/0076-6879(90)86141-H
Malik, V.S., Popkin, B.M., Bray, G.A., Després, J.P., & Hu, F.B. (2010). Sugar-sweetened beverages, obesity, type 2 diabetes mellitus, and cardiovascular disease risk. Circulation, 121(11):1356–1364. DOI: https://doi.org/10.1161/CIRCULATIONAHA.109.876185
Matzkin, L. M., Johnson, S., Paight, C., & Markow, T.A. (2013). A dieta parental de Preadult afeta o desenvolvimento e o metabolismo da prole em Drosophila melanogaster. PLoS ONE, 8, p. e59530. DOI: https://doi.org/10.1371/journal.pone.0059530
Mcgurk, L., Berson, A., & Bonini, N. M. (2015). Drosophila as an In Vivo Model for Human Neurodegenerative Disease. Genetics, 201(2), 377-402. DOI: https://doi.org/10.1534/genetics.115.179457
Misra, H.P., & Fridovich, I. (1972). The role of superoxide anion in the autoxidation of epinephrine and simple assay for superoxide dismutase, J. Biol. Chem. 247 (10), 3170-3175. DOI: https://doi.org/10.1016/S0021-9258(19)45228-9
Morris, S. N. S, Coogan, C., Chamseddin, K., Fernandez-Kim, S. O., Kolli, S., Keller, J. N., & Bauer, J. H. (2012). Development of diet-induced insulin resistance in adult Drosophila melanogaster. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(8), Aug, 1230-1237. DOI: https://doi.org/10.1016/j.bbadis.2012.04.012
Musselman, L.P, Fink, J.L., Narzinski, K., Ramachandran, P.V., Hathiramani, S.S., Cagan, R.L. & Baranski, T.J. (2011). Uma dieta rica em açúcar produz obesidade e resistência à insulina em Drosophila do tipo selvagem. Dis. Modelo Mech., 4, 842 – 849, doi: https:// doi.org/10.1242/dmm.007948. DOI: https://doi.org/10.1242/dmm.007948
Musselman, L.P., Fink, J.L., & Baranski T.J. (2019). Similar effects of high-fructose and highglucose feeding in a Drosophila model of obesity and diabetes. PLoS ONE, 14(5): e0217096. https:// doi.org/10.1371/journal.pone.0217096. DOI: https://doi.org/10.1371/journal.pone.0217096
Na, J., Musselman, L.P., Pendse, J., Baranski, T.J., Bodmer, R., et al. (2013) A Drosophila Model of High Sugar Diet-Induced Cardiomyopathy. PLoS Genet, 9(1): e1003175. doi:https:// doi.org/10.1371/journal.pgen.1003175. DOI: https://doi.org/10.1371/journal.pgen.1003175
Nishizawa, T., & Bornfeldt, K.E. (2012). Diabetic vascular disease and the potential role of macrophage glucose metabolism. Ann Med. Sep, 44(6): 555–563. doi: https:// doi.org/10.3109/07853890.2011.585346. DOI: https://doi.org/10.3109/07853890.2011.585346
Ohkawa, H. et al. (1979) Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95, 351-358. DOI: https://doi.org/10.1016/0003-2697(79)90738-3
Parillo, M., & Riccardi, G. (2010). Composição da dieta e o risco de diabetes tipo 2: evidência epidemiológica e clínica. Fr. J. Nutr., 92, 7 - 19. DOI: https://doi.org/10.1079/BJN20041117
Pérez-Severiano, F., Santamaría, A., Pedraza-Chaverri, J., Medina-Campos, O.N., Ríos, C., & Segovia, J. (2004). Increased formation of reactive oxygen species, but no changes in glutathione peroxidase activity, in striata of mice transgenic for the Huntington’s disease mutation. Neurochem Res, 29:729–33. DOI: https://doi.org/10.1023/B:NERE.0000018843.83770.4b
Pickering, A. M. , Staab, T. A., Tower, J., Sieburth, D. S., & Davies, K. J. (2012). A conserved role for the 20S proteasome and Nrf2 transcription factor in oxidative-stresse adapta in mamífers, C. elegans and D. melanogaster. J. Exp. Biol., 216 (Pt 4): 543–553. DOI: https://doi.org/10.1242/jeb.074757
Pinto, R. E., & Bartley, W. (1969) The nature of the sex-linked differences in glutathione peroxidase activity and aerobic oxidation of glutathione in male and female rat liver. Biochem J 115:449-456. DOI: https://doi.org/10.1042/bj1150449
Prasad, K., & Dhar, I. (2014). Oxidative stress as a mechanism of added sugar-induced cardiovascular disease. Int J Angiol., 23(4):217-226. doi: https:// doi.org/10.1055/s-0034-1387169. DOI: https://doi.org/10.1055/s-0034-1387169
Ramirez, B. L., Jimenez-Del-Rio, M., & Velez-Pardo, C. (2011). Acute and chronic metal exposure impairs locomotion activity in Drosophila melanogaster: a model to study Parkinsonism. Biometals, 24(6), 1045-1057. DOI: https://doi.org/10.1007/s10534-011-9463-0
Rovenko, B. M. et al. (2015) High sucrose consumption promotes obesity whereas its low consumption induces oxidative stress in Drosophila melanogaster. Journal of insect physiology, 79, 42-54. DOI: https://doi.org/10.1016/j.jinsphys.2015.05.007
Rovenko, B.M., Kubrak, O.I., Gospodaryov, D.V., Yurkevych, I.S., Sanz, A., Lushchak, O.V., & Lushchak, V.I.(2015). Restriction of glucose and fructose causes mild oxidative stress independently of mitochondrial activity and reactive oxygen species in Drosophila Melanogaster. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 187, Sep, 27-39, https://doi.org/10.1016/j.cbpa.2015.04.012. PMID: 25941153. DOI: https://doi.org/10.1016/j.cbpa.2015.04.012
Schipanski, A., Yarali, A., Niewalda, T., & Gerber, B.(2008). Behavioral Analyses of Sugar Processing in Choice, Feeding, and Learning in Larval Drosophila. Chemical Senses, 33(6), July, 563–573, https://doi.org/10.1093/chemse/bjn024. DOI: https://doi.org/10.1093/chemse/bjn024
Soares, J.J., Gonçalves, M.B., Gayer, M.C., Bianchini, M.C., Caurio, A. C., Soares, S.J., Puntel, R.L., Roehrs, R., & Denardin, E.L.G. (2017). Continuous liquid feeding: New method to study pesticides toxicity in Drosophila melanogaster. Analytical Biochemistry, 537, 60-62. DOI: https://doi.org/10.1016/j.ab.2017.08.016
Sohal, R.S., Agarwal, A., Agarwal, S., & Orr, W.C. (1995). Simultaneous Overexpression of Copper – and Zinc-containing Superoxide Dismutase and catalase Retards Age-related Oxidative Damage and Increases metabolic Potential in Drosophila Melanogaster, The journal of Biological Che, istry, 270(26), Issue of june 30, 15671-15674, 1995. DOI: https://doi.org/10.1074/jbc.270.26.15671
Stanhope, K.L., Schwarz, J.M., Keim, N.L., Griffen, S.C., Bremer, A.A., Graham, J.L., et al. Consuming fructose sweetened, not glucose-sweetened, beverages increases visceral adiposity and lipids and decreases insulin sensitivity in overweight/obese humans. J Clin Invest. 2009, 119: 1322–34. https://doi.org/10.1172/JCI37385 PMID: 19381015. DOI: https://doi.org/10.1172/JCI37385
Tower, J., Pomatto, L.C.D., & Davies, K.J.A. Sex differences in the response to oxidative and proteolytic stress. Redox Biol. 2020 Apr, 31: 101488. DOI: https://doi.org/10.1016/j.redox.2020.101488
Veja Saúde (2021). O esforço nacional pela redução no consumo de açúcar. Retrieved from: https://saude.abril.com.br/coluna/com-a-palavra/o-esforco-nacional-pela-reducao-no-consumo-de-acucar/.
(World Health Organization - WHO) Guideline: Sugars intake for adults and children. Geneva: World Health Organization, 2015.
Yu, S., Zhang, G. & JIN, L. H. (2018). A high-sugar diet affects cellular and humoral immune responses in Drosophila. Experimental Cell Research. 368(2), 15 July, 215-224. DOI: https://doi.org/10.1016/j.yexcr.2018.04.032
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