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Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage

Year 2022, Volume: 12 Issue: 4, 817 - 823, 30.12.2022
https://doi.org/10.33808/clinexphealthsci.1027516

Abstract

Objective: The aim of this study was to evaluate the ameliorative effects of swimming training on renal and bladder damage caused by a highfat diet (HFD) using morphological and biochemical measurements.
Methods: Sprague Dawley rats were fed either standard chow (CONT, 6% fat) or HFD (45% fat) for 18 weeks, these rats were divided into two subgroups at the last 6 weeks of the experiment. The exercise groups (CONT+EXC, HFD+EXC) were trained daily swimming sessions (1 h per day for 5 days/week) during the last 6 weeks. Kidney and bladder samples were prepared for light and electron microscopic examination at the end of experiment. Malondialdehyde, glutathione, interleukin-6, and tumor necrosis factor-α were measured by biochemically.
Results: Regular morphology of the renal cortex and bladder mucosa was observed in the CONT and CONT +EXC groups. Degenerated renal corpuscles and proximal tubules in the kidney and degenerated urothelium with leaky tight junctions and mast cell increase in the bladder mucosa were observed in the HFD group. Ameliorated renal cortex and bladder mucosa were observed in the HFD+EXC group. In addition, malondialdehyde, glutathione, interleukin-6, and tumor necrosis factor-α levels were also consistent with the histological findings.
Conclusion: HFD-induced renal and bladder damage may be related to increased oxidative damage. It was observed that the histological damage and altered oxidative stress parameters could be reversed by swimming training, and it is thought that moderate swimming exercise may play a role in regulating oxidative stress.

Supporting Institution

Marmara University Scientific Research Project Committee

Project Number

SAG-B-110117-0003

Thanks

The authors would like to thank to the medical students Sevde Arıkan, Yeşim Gezer, Yeşim Özbabalık and Alperen Akbaba for their support to the histological tissue processing.

References

  • Palmer NO, Bakos HW, Owens JA, Setchell BP, Lane M. Diet and exercise in an obese mouse fed a high-fat diet improve metabolic health and reverse perturbed sperm function. Am J Physiol Endocrinol Metab. 2012;302(7):768-80.
  • Barretti DL, Magalhães Fde C, Fernandes T, do Carmo EC, Rosa KT, Irigoyen MC, et al. Effects of aerobic exercise training on cardiac renin-angiotensin system in an obese Zucker rat strain. PloS one. 2012;7(10):46114.
  • Emami SR, Jafari M, Haghshenas R, Ravasi A. Impact of eight weeks endurance training on biochemical parameters and obesity-induced oxidative stress in high fat diet-fed rats. J Exerc Nutrition Biochem. 2016;20(1):29-35.
  • Luo H, Wang X, Chen C, Wang J, Zou X, Li C, et al. Oxidative stress causes imbalance of renal renin angiotensin system (RAS) components and hypertension in obese Zucker rats. J Am Heart Assoc. 2015;4:001559.
  • Oberbach A, Jehmlich N, Schlichting N, Heinrich M, Lehmann S, Wirth H, et al. Molecular fingerprint of high fat diet induced urinary bladder metabolic dysfunction in a rat model. PloS one. 2013;8(6):66636.
  • Oberbach A, Schlichting N, Heinrich M, Lehmann S, Till H, Mohr FW, et al. Weight loss surgery improves the metabolic status in an obese rat model but does not affect bladder fibrosis associated with high fat diet feeding. Int J Obes. 2014;38(8):1061-7.
  • Sanford MT, Yeh JC, Mao JJ, Guo Y, Wang Z, Zhang R, et al. Voluntary exercise improves voiding function and bladder hyperalgesia in an animal model of stress-induced visceral hypersensitivity: A multidisciplinary approach to the study of urologic chronic pelvic pain syndrome research network study. Neurourol Urodyn. 2020;39(2):603-12.
  • Lee WC, Chien CT, Yu HJ, Lee SW. Bladder dysfunction in rats with metabolic syndrome induced by long-term fructose feeding. J Urol. 2008;179(6):2470-6.
  • Linden MA, Pincu Y, Martin SA, Woods JA, Baynard T. Moderate exercise training provides modest protection against adipose tissue inflammatory gene expression in response to high-fat feeding. Physiol Rep. 2014;2(7).
  • Lee S, Kuk JL, Davidson LE, Hudson R, Kilpatrick K, Graham TE, et al. Exercise without weight loss is an effective strategy for obesity reduction in obese individuals with and without Type 2 diabetes. J Appl Physiol. 2005;99(3):1220-5.
  • Leite Nde C, Ferreira TR, Rickli S, Borck PC, Mathias PC, Emilio HR, et al. Glycolytic and mitochondrial metabolism in pancreatic islets from MSG-treated obese rats subjected to swimming training. Cell Physiol Biochem. 2013;31(2-3):242-56.
  • Friedman JE, Ishizuka T, Liu S, Farrell CJ, Bedol D, Koletsky RJ, et al. Reduced insulin receptor signaling in the obese spontaneously hypertensive Koletsky rat. Am J Physiol. 1997;273(5):1014-23.
  • Pérusse L, Collier G, Gagnon J, Leon AS, Rao DC, Skinner JS, et al. Acute and chronic effects of exercise on leptin levels in humans. J Appl Physiol. 1997;83(1):5-10.
  • Dülger EÇ, Çanillioğlu YE, Çetinel Ş, Şener G, Ercan F. Protective Effects of Montelukast Against Stress-Induced Degeneration of the Urinary Bladder. Clin Exp Health Sci. 2018;8(3):211-6.
  • Beutler E. Red cell metabolism : A manual of biochemical methods. Orlando, FL: Grune & Stratton; 1984.
  • Ghorbanzadeh V, Mohammadi M, Mohaddes G, Dariushnejad H, Chodari L, Mohammadi S. Protective effect of crocin and voluntary exercise against oxidative stress in the heart of high-fat diet-induced type 2 diabetic rats. Physiol Int. 2016;103(4):459-68.
  • Kume S, Uzu T, Araki S, Sugimoto T, Isshiki K, Chin-Kanasaki M, et al. Role of altered renal lipid metabolism in the development of renal injury induced by a high-fat diet. J Am Soc Nephrol. 2007;18(10):2715-23.
  • Yamamoto T, Takabatake Y, Takahashi A, Kimura T, Namba T, Matsuda J, et al. High-Fat Diet-Induced Lysosomal Dysfunction and Impaired Autophagic Flux Contribute to Lipotoxicity in the Kidney. J Am Soc Nephrol. 2017;28(5):1534-51.
  • Sun Y, Ge X, Li X, He J, Wei X, Du J, et al. High-fat diet promotes renal injury by inducing oxidative stress and mitochondrial dysfunction. Cell Death Dis. 2020;11(10):914.
  • Moinuddin I, Leehey DJ. A comparison of aerobic exercise and resistance training in patients with and without chronic kidney disease. Adv Chronic Kidney Dis. 2008;15(1):83-96.
  • Pechter U, Maaroos J, Mesikepp S, Veraksits A, Ots M. Regular low-intensity aquatic exercise improves cardio-respiratory functional capacity and reduces proteinuria in chronic renal failure patients. Nephrol Dial Transplant. 2003;18(3):624-5.
  • Coelho BL, Rocha LG, Scarabelot KS, Scheffer DL, Ronsani MM, Silveira PC, et al. Physical exercise prevents the exacerbation of oxidative stress parameters in chronic kidney disease. J Ren Nutr. 2010;20(3):169-75.
  • Park S, Kim CS, Lee J, Suk Kim J, Kim J. Effect of Regular Exercise on the Histochemical Changes of d-Galactose-Induced Oxidative Renal Injury in High-Fat Diet-Fed Rats. Acta Histochem Cytochem. 2013;46(4):111-9.
  • Gasbarro G, Lin DL, Vurbic D, Quisno A, Kinley B, Daneshgari F, et al. Voiding function in obese and type 2 diabetic female rats. Am J Physiol Renal Physiol. 2010;298(1):F72-7.
  • Trayhurn P, Wang B, Wood IS. Hypoxia and the endocrine and signalling role of white adipose tissue. Arch Physiol Biochem. 2008;114(4):267-76.
  • Fan EW, Chen LJ, Cheng JT, Tong YC. Changes of urinary bladder contractility in high-fat diet-fed mice: the role of tumor necrosis factor-α. Int J Urol. 2014;21(8):831-5.
  • Gharaee-Kermani M, Rodriguez-Nieves JA, Mehra R, Vezina CA, Sarma AV, Macoska JA. Obesity-induced diabetes and lower urinary tract fibrosis promote urinary voiding dysfunction in a mouse model. The Prostate. 2013;73(10):1123-33.
  • Hotamisligil GS, Shargill NS, Spiegelman BM. Adipose expression of tumor necrosis factor-alpha: direct role in obesity-linked insulin resistance. Science (New York, NY). 1993;259(5091):87-91.
  • Vadhavkar M, Golbidi S, Sea J, Longpre M, Stothers L, Laher I. Exercise improves bladder function in diabetic mice. Neurourol Urodyn. 2011;30(1):174-82.
  • Reena, Kaur T, Kaur A, Singh M, Buttar HS, Pathak D, et al. Mast cell stabilizers obviate high fat diet-induced renal dysfunction in rats. Eur J Pharmacol. 2016;777:96-103.
  • Chien CT, Yu HJ, Lin TB, Lai MK, Hsu SM. Substance P via NK1 receptor facilitates hyperactive bladder afferent signaling via action of ROS. Am J Physiol Renal Physiol. 2003;284(4):F840-51.
  • Karanth J, Kumar R, Jeevaratnam K. Response of antioxidant system in rats to dietary fat and physical activity. Indian J Physiol Pharmacol. 2004;48(4):446-52.
  • Noeman SA, Hamooda HE, Baalash AA. Biochemical study of oxidative stress markers in the liver, kidney and heart of high fat diet induced obesity in rats. Diabetol Metab Syndr. 2011;3(1):17.
  • Acikel Elmas M, Cakici SE, Dur IR, Kozluca I, Arinc M, Binbuga B, et al. Protective effects of exercise on heart and aorta in highfat diet-induced obese rats. Tissue Cell. 2019;57:57 65.
  • Muller CR, Leite APO, Yokota R, Pereira RO, Americo ALV, Nascimento NRF, et al. Post-weaning Exposure to High-Fat Diet Induces Kidney Lipid Accumulation and Function Impairment in Adult Rats. Front Nutr. 2019;6(60).
  • Martins A, Mas S. Lipotoxicity and kidney. Port J Nephrol Hypert. 2015;29(4):306-15.
  • Bobulescu IA. Renal lipid metabolism and lipotoxicity. Curr Opin Nephrol Hypertens. 2010;19(4):393.
Year 2022, Volume: 12 Issue: 4, 817 - 823, 30.12.2022
https://doi.org/10.33808/clinexphealthsci.1027516

Abstract

Project Number

SAG-B-110117-0003

References

  • Palmer NO, Bakos HW, Owens JA, Setchell BP, Lane M. Diet and exercise in an obese mouse fed a high-fat diet improve metabolic health and reverse perturbed sperm function. Am J Physiol Endocrinol Metab. 2012;302(7):768-80.
  • Barretti DL, Magalhães Fde C, Fernandes T, do Carmo EC, Rosa KT, Irigoyen MC, et al. Effects of aerobic exercise training on cardiac renin-angiotensin system in an obese Zucker rat strain. PloS one. 2012;7(10):46114.
  • Emami SR, Jafari M, Haghshenas R, Ravasi A. Impact of eight weeks endurance training on biochemical parameters and obesity-induced oxidative stress in high fat diet-fed rats. J Exerc Nutrition Biochem. 2016;20(1):29-35.
  • Luo H, Wang X, Chen C, Wang J, Zou X, Li C, et al. Oxidative stress causes imbalance of renal renin angiotensin system (RAS) components and hypertension in obese Zucker rats. J Am Heart Assoc. 2015;4:001559.
  • Oberbach A, Jehmlich N, Schlichting N, Heinrich M, Lehmann S, Wirth H, et al. Molecular fingerprint of high fat diet induced urinary bladder metabolic dysfunction in a rat model. PloS one. 2013;8(6):66636.
  • Oberbach A, Schlichting N, Heinrich M, Lehmann S, Till H, Mohr FW, et al. Weight loss surgery improves the metabolic status in an obese rat model but does not affect bladder fibrosis associated with high fat diet feeding. Int J Obes. 2014;38(8):1061-7.
  • Sanford MT, Yeh JC, Mao JJ, Guo Y, Wang Z, Zhang R, et al. Voluntary exercise improves voiding function and bladder hyperalgesia in an animal model of stress-induced visceral hypersensitivity: A multidisciplinary approach to the study of urologic chronic pelvic pain syndrome research network study. Neurourol Urodyn. 2020;39(2):603-12.
  • Lee WC, Chien CT, Yu HJ, Lee SW. Bladder dysfunction in rats with metabolic syndrome induced by long-term fructose feeding. J Urol. 2008;179(6):2470-6.
  • Linden MA, Pincu Y, Martin SA, Woods JA, Baynard T. Moderate exercise training provides modest protection against adipose tissue inflammatory gene expression in response to high-fat feeding. Physiol Rep. 2014;2(7).
  • Lee S, Kuk JL, Davidson LE, Hudson R, Kilpatrick K, Graham TE, et al. Exercise without weight loss is an effective strategy for obesity reduction in obese individuals with and without Type 2 diabetes. J Appl Physiol. 2005;99(3):1220-5.
  • Leite Nde C, Ferreira TR, Rickli S, Borck PC, Mathias PC, Emilio HR, et al. Glycolytic and mitochondrial metabolism in pancreatic islets from MSG-treated obese rats subjected to swimming training. Cell Physiol Biochem. 2013;31(2-3):242-56.
  • Friedman JE, Ishizuka T, Liu S, Farrell CJ, Bedol D, Koletsky RJ, et al. Reduced insulin receptor signaling in the obese spontaneously hypertensive Koletsky rat. Am J Physiol. 1997;273(5):1014-23.
  • Pérusse L, Collier G, Gagnon J, Leon AS, Rao DC, Skinner JS, et al. Acute and chronic effects of exercise on leptin levels in humans. J Appl Physiol. 1997;83(1):5-10.
  • Dülger EÇ, Çanillioğlu YE, Çetinel Ş, Şener G, Ercan F. Protective Effects of Montelukast Against Stress-Induced Degeneration of the Urinary Bladder. Clin Exp Health Sci. 2018;8(3):211-6.
  • Beutler E. Red cell metabolism : A manual of biochemical methods. Orlando, FL: Grune & Stratton; 1984.
  • Ghorbanzadeh V, Mohammadi M, Mohaddes G, Dariushnejad H, Chodari L, Mohammadi S. Protective effect of crocin and voluntary exercise against oxidative stress in the heart of high-fat diet-induced type 2 diabetic rats. Physiol Int. 2016;103(4):459-68.
  • Kume S, Uzu T, Araki S, Sugimoto T, Isshiki K, Chin-Kanasaki M, et al. Role of altered renal lipid metabolism in the development of renal injury induced by a high-fat diet. J Am Soc Nephrol. 2007;18(10):2715-23.
  • Yamamoto T, Takabatake Y, Takahashi A, Kimura T, Namba T, Matsuda J, et al. High-Fat Diet-Induced Lysosomal Dysfunction and Impaired Autophagic Flux Contribute to Lipotoxicity in the Kidney. J Am Soc Nephrol. 2017;28(5):1534-51.
  • Sun Y, Ge X, Li X, He J, Wei X, Du J, et al. High-fat diet promotes renal injury by inducing oxidative stress and mitochondrial dysfunction. Cell Death Dis. 2020;11(10):914.
  • Moinuddin I, Leehey DJ. A comparison of aerobic exercise and resistance training in patients with and without chronic kidney disease. Adv Chronic Kidney Dis. 2008;15(1):83-96.
  • Pechter U, Maaroos J, Mesikepp S, Veraksits A, Ots M. Regular low-intensity aquatic exercise improves cardio-respiratory functional capacity and reduces proteinuria in chronic renal failure patients. Nephrol Dial Transplant. 2003;18(3):624-5.
  • Coelho BL, Rocha LG, Scarabelot KS, Scheffer DL, Ronsani MM, Silveira PC, et al. Physical exercise prevents the exacerbation of oxidative stress parameters in chronic kidney disease. J Ren Nutr. 2010;20(3):169-75.
  • Park S, Kim CS, Lee J, Suk Kim J, Kim J. Effect of Regular Exercise on the Histochemical Changes of d-Galactose-Induced Oxidative Renal Injury in High-Fat Diet-Fed Rats. Acta Histochem Cytochem. 2013;46(4):111-9.
  • Gasbarro G, Lin DL, Vurbic D, Quisno A, Kinley B, Daneshgari F, et al. Voiding function in obese and type 2 diabetic female rats. Am J Physiol Renal Physiol. 2010;298(1):F72-7.
  • Trayhurn P, Wang B, Wood IS. Hypoxia and the endocrine and signalling role of white adipose tissue. Arch Physiol Biochem. 2008;114(4):267-76.
  • Fan EW, Chen LJ, Cheng JT, Tong YC. Changes of urinary bladder contractility in high-fat diet-fed mice: the role of tumor necrosis factor-α. Int J Urol. 2014;21(8):831-5.
  • Gharaee-Kermani M, Rodriguez-Nieves JA, Mehra R, Vezina CA, Sarma AV, Macoska JA. Obesity-induced diabetes and lower urinary tract fibrosis promote urinary voiding dysfunction in a mouse model. The Prostate. 2013;73(10):1123-33.
  • Hotamisligil GS, Shargill NS, Spiegelman BM. Adipose expression of tumor necrosis factor-alpha: direct role in obesity-linked insulin resistance. Science (New York, NY). 1993;259(5091):87-91.
  • Vadhavkar M, Golbidi S, Sea J, Longpre M, Stothers L, Laher I. Exercise improves bladder function in diabetic mice. Neurourol Urodyn. 2011;30(1):174-82.
  • Reena, Kaur T, Kaur A, Singh M, Buttar HS, Pathak D, et al. Mast cell stabilizers obviate high fat diet-induced renal dysfunction in rats. Eur J Pharmacol. 2016;777:96-103.
  • Chien CT, Yu HJ, Lin TB, Lai MK, Hsu SM. Substance P via NK1 receptor facilitates hyperactive bladder afferent signaling via action of ROS. Am J Physiol Renal Physiol. 2003;284(4):F840-51.
  • Karanth J, Kumar R, Jeevaratnam K. Response of antioxidant system in rats to dietary fat and physical activity. Indian J Physiol Pharmacol. 2004;48(4):446-52.
  • Noeman SA, Hamooda HE, Baalash AA. Biochemical study of oxidative stress markers in the liver, kidney and heart of high fat diet induced obesity in rats. Diabetol Metab Syndr. 2011;3(1):17.
  • Acikel Elmas M, Cakici SE, Dur IR, Kozluca I, Arinc M, Binbuga B, et al. Protective effects of exercise on heart and aorta in highfat diet-induced obese rats. Tissue Cell. 2019;57:57 65.
  • Muller CR, Leite APO, Yokota R, Pereira RO, Americo ALV, Nascimento NRF, et al. Post-weaning Exposure to High-Fat Diet Induces Kidney Lipid Accumulation and Function Impairment in Adult Rats. Front Nutr. 2019;6(60).
  • Martins A, Mas S. Lipotoxicity and kidney. Port J Nephrol Hypert. 2015;29(4):306-15.
  • Bobulescu IA. Renal lipid metabolism and lipotoxicity. Curr Opin Nephrol Hypertens. 2010;19(4):393.
There are 37 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Articles
Authors

Merve Açıkel Elmas 0000-0002-5992-8191

Özlem Bingöl Özakpınar 0000-0003-0287-5639

Meltem Kolgazi 0000-0003-4820-1904

Göksel Şener 0000-0001-7444-6193

Feriha Ercan 0000-0003-2339-5669

Project Number SAG-B-110117-0003
Publication Date December 30, 2022
Submission Date November 23, 2021
Published in Issue Year 2022 Volume: 12 Issue: 4

Cite

APA Açıkel Elmas, M., Bingöl Özakpınar, Ö., Kolgazi, M., Şener, G., et al. (2022). Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage. Clinical and Experimental Health Sciences, 12(4), 817-823. https://doi.org/10.33808/clinexphealthsci.1027516
AMA Açıkel Elmas M, Bingöl Özakpınar Ö, Kolgazi M, Şener G, Ercan F. Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage. Clinical and Experimental Health Sciences. December 2022;12(4):817-823. doi:10.33808/clinexphealthsci.1027516
Chicago Açıkel Elmas, Merve, Özlem Bingöl Özakpınar, Meltem Kolgazi, Göksel Şener, and Feriha Ercan. “Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage”. Clinical and Experimental Health Sciences 12, no. 4 (December 2022): 817-23. https://doi.org/10.33808/clinexphealthsci.1027516.
EndNote Açıkel Elmas M, Bingöl Özakpınar Ö, Kolgazi M, Şener G, Ercan F (December 1, 2022) Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage. Clinical and Experimental Health Sciences 12 4 817–823.
IEEE M. Açıkel Elmas, Ö. Bingöl Özakpınar, M. Kolgazi, G. Şener, and F. Ercan, “Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage”, Clinical and Experimental Health Sciences, vol. 12, no. 4, pp. 817–823, 2022, doi: 10.33808/clinexphealthsci.1027516.
ISNAD Açıkel Elmas, Merve et al. “Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage”. Clinical and Experimental Health Sciences 12/4 (December 2022), 817-823. https://doi.org/10.33808/clinexphealthsci.1027516.
JAMA Açıkel Elmas M, Bingöl Özakpınar Ö, Kolgazi M, Şener G, Ercan F. Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage. Clinical and Experimental Health Sciences. 2022;12:817–823.
MLA Açıkel Elmas, Merve et al. “Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage”. Clinical and Experimental Health Sciences, vol. 12, no. 4, 2022, pp. 817-23, doi:10.33808/clinexphealthsci.1027516.
Vancouver Açıkel Elmas M, Bingöl Özakpınar Ö, Kolgazi M, Şener G, Ercan F. Morphological and Biochemical Investigation of the Healing Effects of Exercise on High Fat Diet Induced Kidney and Bladder Damage. Clinical and Experimental Health Sciences. 2022;12(4):817-23.

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