The The Effects Of Carbonated Soft Drink Consumption On Kidney Histopathology Changes In Male Rats (Rattus noervegicus) Sprague dawley Strain
DOI:
https://doi.org/10.53089/medula.v13i2.623Keywords:
carbonated soft drinks, kidney, histopathological changesAbstract
Carbonated soft drinks are beverages contain of carbon dioxide and other ingredients such as high fructose syrup (HFS). Excessive consumption of HFS causes various health problems involving multiple organs including the kidneys. The aim to this research is to determine the effects of carbonated soft drinks on kidney histopathological changes in rats. This research is a post test only control group experimental study using 24 male rats (Rattus norvegicus) Sprague dawley strain which divided into 4 groups, there are the control group (K) allowed to drink aquades ad libitum, P1 is given carbonated soft drinks 3 ml/day, P2 6 ml/day, and P3 12 ml/day for 30 days. The average of renal histopathological damage in group K:1.07, P1:4.53, P2:5.13, and P3:6.10. Data were tested with Shapiro-Wilk, followed b yhomogeneity test and One Way ANOVA test result in p=0,000 (p<0.05). The results of Post Hoc LSD analysis are p<0.05 between groups K with P1, P2, and P3 (p=0.000), P1 with P2 (p=0.023), and P1 with P3 (p=0.001). There is an effect of carbonated soft drinks on kidney histopathological changes of male rats (Rattus norvegicus) Sprague dawley strain
References
Vartanian, L. R., Schwartz, M. B. and Brownell, K. D. Effects of soft drink consumption on nutrition and health: A systematic review and meta-analysis. American Journal of Public Health. 2007; 97(4):667–675. doi: 10.2105/AJPH.2005.083782.
Adjene, J. O., Ezeoke, J. C. and Nwose, E. U. Histological effects of chronic consumption of soda pop drinks on kidney of adult Wister rats. North American journal of medical sciences. 2010; 2(5):215–217. doi: 10.4297/najms.2010.2215.
Nusaresearch. Report Of Soft Drink Consumption Habits In Indonesia. 2014 [diunduh 29 Juli 2019]. Tersedia dari: https://nusaresearch.net
Katzmarzyk, P. T, dkk. Relationship between soft drink consumption and obesity in 9-11 years old children in a multi-national study. Nutrients. 2016; 8(12):1–13. doi: 10.3390/nu8120770.
Walker, R. W., Dumke, K. A. and Goran, M. I. Fructose content in popular beverages made with and without high-fructose corn syrup. Nutrition. Elsevier Inc. 2014; 30(7–8):928–935. doi: 10.1016/j.nut.2014.04.003.
Pepin, A., Stanhope, K. L. and Imbeault, P. Are fruit juices healthier than sugar-sweetened beverages? A review. Nutrients. 2019;11(5):1–16. doi: 10.3390/nu11051006.
Cirillo, R. dkk. Ketohexokinase-dependent metabolism of fructose Induces proinflammatory mediators in proximal tubular cells. Journal of the American Society of Nephrology. 2009;20(3):545–553. doi: 10.1681/ASN.2008060576.
Yu MA, Sánchez-Lozada LG, Johnson RJ, K. D. Oxidative stress with an activation of the renin-angiotensin system in human vascular endothelial cells as a novel mechanism of uric acid-induced endothelial dysfunction. Journal of Hypertension. 2010;28(6):1234–1242.
Stephanie, N. dkk. Sugar Sweetened Beverages, Serum Uric Acid, and Blood Pressure in Adolescents. J Pediatr, 2009;154(6):807–813. doi: 10.1016/j.jpeds.2009.01.015.Sugar.
Andrew S., B. dkk. Sugar-sweetened soda consumption, hyperuricemia, and kidney disease. Int Society of Nephrology, 2012; 77(7):609–616. doi: 10.1038/ki.2009.500.Sugar-sweetened.
García-Arroyo, F. E. dkk. Vasopressin mediates the renal damage induced by limited fructose rehydration in recurrently dehydrated rats. International Journal of Biological Sciences. 2017;13(8);961–975. doi: 10.7150/ijbs.20074.
Milagres, T. dkk. Rehydration with fructose worsens dehydration-induced renal damage. BMC Nephrology. BMC Nephrology. 2018;19(1):1–9. doi: 10.1186/s12882-018-0963-9.
Notoatmodjo S. Metodologi Penelitian Kesehatan. Edisi ke-2. Rineka Cipta. Jakarta. 2012
Laurence DR, AL Bacharach. Evaluation of drug activities pharmacometrics. cit: Ngatidjan, 1990, Metode Laboratorium dalam Toksikologi, reviewer: Hakim, L., Pusat Antar Universitas Bioteknologi Universitas Gadjah Mada, Yogyakarta. 1964
Ngatidjan. Petunjuk Laboratorium: Metode Laboratorium Dalam Toksikologi. Yogyakarta: FK UGM. 1991
El-tahan, N. R. and Ahmed, R. A. Histological and Biological Effects of Some Soft Drinks on Male Albino Rats. JBAAR, 2015;1(6):335–342.
Windarti, I., Widayana, I. G. E. and Muhartono. Effect Paraquat Dichloride Herbicides Orally on the Stage of Esophagus Damage in Male Rats. Juke Unila. 2015;5(9), pp. 9–12.
Muhartono dkk. Risiko Herbisida Paraquat Diklorida terhadap Ginjal Tikus Putih Spraque Dawley The Risk of Paraquat Dichloride Herbicide to Spraque Dawley Rat’s Kidney. Juke Unila. 2014;29(1):43–46.
Pichler, R. H. dkk. Pathogenesis of cyclosporine nephropathy: Roles of angiotensin II and osteopontin. Journal of the American Society of Nephrology. 1995;6(4): 1186–1196.
Zhang, Q. F. Ulinastatin inhibits renal tubular epithelial apoptosis and interstitial fibrosis in rats with unilateral ureteral obstruction. Molecular Medicine Reports. 2017;16(6):8916–8922. doi: 10.3892/mmr.2017.7692.
Tobar, A. dkk. Proximal Tubular Hypertrophy and Enlarged Glomerular and Proximal Tubular Urinary Space in Obese Subjects with Proteinuria. PLoS ONE. 2013 8(9):1–9. doi: 10.1371/journal.pone.0075547.
Corwin JE. Buku Saku Patofisiologi. Penerbit Buku Kedokteran. Jakarta: EGC. 2001
Cao, G. dkk. Beneficial effect of moderate exercise in kidney of rat after chronic consumption of cola drinks. PLoS ONE. 2016;11(3):1–16. doi: 10.1371/journal.pone.0152461.
Fahim, A., Ilyas, M. S. and Jafari, F. H. Histologic Effects of Carbonated Drinks on Rat Kidney. Journal of Rawalpindi Medical College (JRMC). 2015;19(2):165–167.
Alkhedaide, A. dkk. Chronic effects of soft drink consumption on the health state of Wistar rats: A biochemical, genetic and histopathological study. Molecular Medicine Reports. 2016;13(6):5109–5117. doi: 10.3892/mmr.2016.5199.
Dhingra, R. dkk. Soft drink consumption and risk of developing cardiometabolic risk factors and the metabolic syndrome in middle-aged adults in the community. Circulation, 2007;116(5):480–488. doi: 10.1161/CIRCULATIONAHA.107.689935.
Vermunt, S. H. F. dkk. Effects of sugar intake on body weight: A review. Obesity Reviews, 2003;4(2):91–99. doi: 10.1046/j.1467-789X.2003.00102.x.
Bray, G. A., Nielsen, S. J. and Popkin, B. M. Consumption of high-fructose corn syrup in beverages may play a role in the epidemic of obesity. American Journal of Clinical Nutrition. 2004;79(4):537–543. doi: 10.1093/ajcn/79.4.537.
Elfhag, K., Tynelius, P. and Rasmussen, F. Sugar-sweetened and artificially sweetened soft drinks in association to restrained, external and emotional eating. Physiology and Behavior. 2007;91(2–3): 191–195. doi: 10.1016/j.physbeh.2007.02.005.
Johnson, R. J., Sanchez-Lozada, L. G. and Nakagawa, T. The effect of fructose on renal biology and disease. Journal of the American Society of Nephrology. 2010;21(12):2036–2039. doi: 10.1681/ASN.2010050506.
Kanellis, J. dkk. Uric acid stimulates monocyte chemoattractant protein-1 production in vascular smooth muscle cells via mitogen-activated protein kinase and cyclooxygenase-2. Hypertension. 2003;41(6):1287–1293. doi: 10.1161/01.HYP.0000072820.07472.3B.
Convento, M. S. dkk. Pro-inflammatory and oxidative effects of noncrystalline uric acid in human mesangial cells: Contribution to hyperuricemic glomerular damage. Urological Research. 2011;39(1):21–27. doi: 10.1007/s00240-010-0282-5.
Berghe, G. Van Den. INBORN ERRORS OF Given intravenously. Annual Review of Nutrition, 1004;14(1):41–58.
Wada, J. and Makino, H. Inflammation and the pathogenesis of diabetic nephropathy. Clinical Science, 2013;124(3):139–152. doi: 10.1042/CS20120198.
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