Research Article
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Exercise and Caloric Restriction Improves Liver Damage in Metabolic Syndrome Model

Year 2021, Volume: 80 Issue: 1, 15 - 21, 15.06.2021

Abstract

Objective: Detecting the level of antioxidant and tissue damage that can occur in liver tissue induced metabolic syndrome by a high fructose diet in rats and the changes after exercise and/or caloric restriction.

Materials and Methods: Sprague-Dawley male rats were divided into five groups: control (C), metabolic syndrome (M), metabolic syndrome with exercise (ME), metabolic syndrome with caloric restriction (MCR), and metabolic syndrome with exercise and caloric restriction (MECR). To induce metabolic syndrome, a 10% fructose solution was given to rats in drinking water for 3 months. Exercise and caloric restriction were applied to the related groups for 6 weeks after the induction of metabolic syndrome. Glucose in the blood, lipid peroxidation (LPO), sialic acid (SA), hexosamine, mucin, fucose, glutathione (GSH) levels, alkaline phosphatase (ALP), tissue factor (TF), superoxide dismutase (SOD), catalase (CAT), and glutathione-Stransferase (GST) activities were measured in rat liver homogenates.

Results: In the liver, LPO levels increased and TF activities decreased in the M group compared to the C group and increased in the MCR and MECR groups compared to M group. GSH levels, SOD, and CAT activities decreased in M compared to C group and increased more significantly in MECR group compared to M group. SA levels increased in MCR and MECR groups compared with M group. Fucose levels also increased in MECR compared with the all others.

Conclusion: Liver tissue damage that occurs after a fructose diet and decreased antioxidant levels was shown to improve best in combined exercise and caloric restriction treatment (MECR group).

Supporting Institution

Marmara University Scientific Research Projects Commission

Project Number

SAG-C-YLP-041213-0449

References

  • 1. Sener TE, Cevik O, Çetinel Ş, Şener G. (2020). Oxidative stress and urinary system damage in fructose-induced rat model of metabolic syndrome: Effect of calorie restriction and exercise. J Res Pharm 2020; 24 (3): 318-325.
  • 2. Bouzas C, Bibiloni MDM, Garcia S, Mateos D, Martínez-González M.Á, Salas-Salvadó J, et al. Dietary quality changes according to the preceding maximum weight: A longitudinal analysis in the predimed-plus randomized trial. Nutrients, 2020; 12(10), 3023.
  • 3. Yilmaz Demirtas C, Bircan FS, Pasaoglu OT, Turkozkan N. The effects of resveratrol on hepatic oxidative stress in metabolic syndrome model induced by high fructose diet. Bratisl Lek Listy 2018; 119(1):36-40.
  • 4. Martinez-Gonzalez MA, Martinez JA, Hu FB, Gibney MJ, Kearney J. Physical inactivity, sedentary lifestyle and obesity in the European Union. Int J Obes Relat Metab Disord 1999; 23: 1192–201.
  • 5. Balton VH, Korita I, Bulo A. How is metabolic syndrome related to dyslipidemia? Biochem Med 2008; 18: 14–24.
  • 6. Panickar KS. Beneficial Effects of Herbs, Spices and Medicinal Plants on the Metabolic Syndrome, Brain and Cognitive Function. Cent Nerv Syst Agents Med Chem 2013; 13: 13-29.
  • 7. Basciano H, Federico L, Adeli K. Fructose, insulin resistance and metabolic dyslipidemia. Nutr Metab 2005; 2(1):5.
  • 8. Kannappan S, Palanisamy N, Anuradha CV. Suppression of hepatic oxidative events and regulation of eNOS expression in the liver by naringenin in fructose-administered rats. Eur J Pharmacol 2010; 645: 177-184.
  • 9. Caponi PW, Lehnen AM, Pinto GH, Borges J, Markoski M, Machado UF, et al. Aerobic exercise training inducesmetabolic benefits in rats with metabolic syndrome independent of dietary changes. Clinics 2013; 68(7): 1010-1017.
  • 10. Williamson DF, Pamuk E, Thun M, Flanders D, Byers T, Heath C. Prospective study of intentional weight loss and mortality in never-smoking overweight US white women aged 40–64 years. Am J Epidemiol 1995; 141(12): 1128–1141.
  • 11. Williamson DF, Thompson JT, Thun M, Flanders D, Pamuk E, Byers E. Intentional weight loss and mortality among overweight individuals with diabetes. Diabetes Care 2000; 23(10); 1499–1504.
  • 12. Kurosaka Y, Machida S, Shiroya Y, Yamauchi H, & Minato K. Protective Effects of Voluntary Exercise on Hepatic Fat Accumulation Induced by Dietary Restriction in Zucker Fatty Rats. Int J Mol Sci 2021; 22(4), 2014.
  • 13. Pereira RM, Botezelli JD, da Cruz Rodrigues KC, Mekary RA, Cintra DE, Pauli JR, et al. Fructose consumption in the development of obesity and the effects of different protocols of physical exercise on the hepatic metabolism. Nutrients 2017; 9(4), 405.
  • 14 . Pósa A, Szabó R, Kupai K, Csonka A, Szalai Z, Veszelka M, et al. Exercise training and calorie restriction influence the metabolic parameters in ovariectomized female rats. Oxid Med Cell Longev 2015; 787063.
  • 15. Weindruch R, Walford RL. The Retardation of Aging and Disease by Dietary Restriction. Springfield, Illinois: Charles C. Thomas; 1988.
  • 16. Beutler E. Glutathione. In: Red blood cell metabolism: A Manual of Biochemical Methods. 2nd ed. New York: Grune and Stratton; 1975, 112–114.
  • 17. Ledwozyw A, Michalak J, Stepien A, Kadziolka A. The relationship between plasma triglycerides, cholesterol, total lipids and lipid peroxidation products during human atherosclerosis. Clin Chim Acta 1986, 155(3):275-283.
  • 18. Warren L. The thiobarbituric acid assay of sialic acids. J Biol Chem 1959; 234: 1971-1975.
  • 19. Winzler RJ. Determination of serum glycoproteins. Glick D, editors. Methods of Biochemical Analysis. New York: Interscience Publishers Inc. 1955; 2: 279-311.
  • 20. Dische Z, Shettles LB. A specific color reaction of methylpentoses and a spectrophotometric micromethod for their determination. J Biol Chem 1948; 175; 595-603.
  • 21. Shakeerabanu M, Sjahta K, Praveen R.C, Manimaran A. The defensive effect of quercetinon indomethacin induced gastric damage in rats. Adv Biol Res 2011; 5(1); 64-70.
  • 22. Mylorie AA, Collins H, Umbles C, Kyle J. Erythrocyte superoxide dismutase activity and other parameters of copper status in rats ingesting lead acetate. Toxicol Appl Pharmacol 1986; 82(3): 512-520.
  • 23. Aebi H. Catalase in vitro. Methods Enzymol. 1984, 105:121-126.
  • 24. Habig WH, Jacoby WB. Assays for differentiation of glutathione S- transferases. Methods in Enzymol. 1981; 77: 398-405.
  • 25. Walter K, Schült C. Acid and alkaline phosphatase in serum: two point method. In: Methods of Enzymatic Analysis. 2nd ed. Bergmeyer HU, editors. Verlag Chemie: Academic Press, Inc. New York and London; 1974. 2: 856-886.
  • 26. Ingram GIC, Hills M. Reference method for the one-stage prothrombin time test on human blood. Thromb Haemost 1976; 36(1): 237-238.
  • 27. Dalle-Donne I, Aldini G, Carini M, Colombo R, Rossi R, Milzani A. Protein carbonylation, cellular dysfunction and disease progression. J Cell Mol Med 2006; 10(2): 389-406.
  • 28. Rutledge AC, Adele K. Fructose and the metabolic syndrome: Pathophysiology and molecular mechanisms. Nutr Rev 2007; 65: 13-23.
  • 29. Abdullah MM, Riediger NN, Chen Q, Zhao Z, Azordegan N, Xu Z, et al. Effects of long-term consumption of a high fructose diet on conventional cardiovascular risk factors in Sprague-Dawley rats. Mol Cell Biochem 2009; 327 (1-2): 247-256.
  • 30. Paśko P, Bartoń H, Zagrodzki P, Gorinstein S. Effect of amaranth seeds (Amaranthus cruentus) in the diet on some biochemical parameters and essential trace elements in blood of high fructose-fed rats. Nat Prod Res 2011; 25: 844-849.
  • 31. Babacanoğlu C, Yıldırım N, Sadi G, Pektas MB, Akar F. Resveratrol prevents high-fructose corn syrup-induced vascular insulin resistance and dysfunction in rats. Food Chem Toxicol 2013; 60; 160-167.
  • 32. Masterjohn C, Park Y, Lee J, Noh SK, Koo SI, Bruno RS. Dietary Fructose Feeding Increases Adipose Methylglyoxal Accumulation in Rats in Association with Low Expression and Activity of Glyoxalase-2. Nutrients 2013; 5: 3311-3328.
  • 33. Zhao CX, Xu X, Cui Y, Wang P, Wei X, Yang S, et al. Increased endothelial nitric-oxide synthase expression reduces hypertension and hyperinsulinemia in fructose-treated rats. J Pharmacol Exp Ther 2009; 328(2): 610–620.
  • 34. Giani JF, Mayer MA, Munoz MC, Silberman EA, Hocht C, Taira CA, et al. Chronic infusion of angiotensin-(1-7) improves insulin resistance and hypertension induced by a high-fructose diet in rats. Am J Physiol Endocrinol Metab 2009; 296(2): E262-E271.
  • 35. Wang DD, Sievenpiper JL, De Souza RJ, Cozma AI, Chiavaroli L, Ha V, et al.Effect of fructose on postprandial triglycerides: a systematic review and meta-analysis of controlled feeding trials. Atherosclerosis 2014; 232(1):125–133.
  • 36. Steinberg HO, Chaker H, Leaming R, Johnson A, Brechtel G, Baron AD. Obesity/Insulin Resistance is Associated with Endothelial Dysfunction. Implications for the Syndrome of Insulin Resistance. J Clin Invest 1996; 97(11): 2610-2601.
  • 37. Delbosc S, Paizanis E, Magous R, Araiz C, Dimo T, Cristol JP, et al. Involvement of oxidative stress and NADPH oxidase activation in the development of cardiovascular complications in a model of insulin resistance, the fructose-fed rat. Atherosclerosis. 2005; 179(1):43-9.
  • 38. Singh I, Singh PK, Bhansali S, Shafiq N, Malhotra S, Pandhi P, et al. Effects of three different doses of a fruit extract of Terminalia chebula on metabolic components of metabolic syndrome, in a rat model. Phytother Res 2010; 24:107-112.
  • 39 . Castro-Barquero S, Ruiz-León AM, Sierra-Pérez M, Estruch R, Casas, R. Dietary strategies for metabolic syndrome: a comprehensive review. Nutrients 2020; 12(10): 2983.
  • 40. Venditti P, Gomez-Cabrera MC, Zhang Y, Radak, Z. Oxidant antioxidants and adaptive responses to exercise. Oxid Med Cell Longev 2015; 290190.
  • 41. Vincent HK, Powers SK, Demirel HA, Coombes JS, Naito H. Exercise training protects against contraction-induced lipid peroxidation in the diaphragm. Eur J Appl Physiol 1999; 79, 268-273.
  • 42. Duarte J, Pérez-Palencia R, Vargas F, Ocete MA, Pérez-Vizcaino F, Zarzuelo A, Tamargo J. Antihypertensive effects of the flavonoid quercetin in spontaneously hypertensive rats. Br J Pharmacol 2001; 133:117-24.
  • 43. Alipour M, Salehi I, Soufi FG. Effect of Exercise on Diabetes-Induced Oxidative Stress in the Rat Hippocampus. Iran Red Crescent Med J 2012; 14(4); 222-228.
  • 44. Lima TI, Monteiro IC, Valença S, Leal-Cardoso JH, Fortunato RS, Carvalho DP, Teodoro BG, Ceccatto VM. Effect of exercise training on liver antioxidant enzymes in STZ-diabetic rats. Life Sci 2015; 128; 64–71.
  • 45 Hagopian K. Krebs cycle enzymes from livers of old mice are differantially regulated by caloric restriction. Physiol and Behavior 2005; 85: 581-592.
  • 46. Speakman JR, Mitchell SE. Caloric restriction. Mol Aspects Med 2011; 32(3):159–221.
  • 47. He XY, Zhao XL, Gu Q, Shen JP, Hu Y, Hu RM. Calorie restriction from a young age preserves the functions of pancreatic β cells in aging rats. Tohoku J Exp Med 2012; 227(4): 245–252.
  • 48. Horrillo D, Gallardo N, Lauzurica N, Barrus MT, San Frutos MG, Andres A, et al. Development of liver fibrosis during aging: effects of caloric restriction. J Biol Regul Homeost Agents. 2013; 27(2); 377–388.
  • 49. Mohammadi M, Ghaznavi R, Keyhanmanesh R, Sadeghipour HR, Naderi R, Mohammadi H. Caloric restriction prevents lead-induced oxidative stress and inflammation in rat liver. Scientific World J 2014; 20; 821524.
  • 50. Mackman N. Tissue-specific hemostasis in mice. Arterioscler Thromb Vasc Biol 2005; 25: 2273–2281.
  • 51. Nemerson Y. Tissue factor: then and now. Thromb Haemost 1995; 74(1): 180-184.
  • 52. Emekli-Alturfan E, Basar I, Malali E, Elemek E, Oktay S, Ayan F, et al. Plasma tissue factor and tissue factor activities of periodontitis patients with cardiovascular diseases. Pathophysiol Haemost Thromb 2010; 37: 77–81.
  • 53. Yarat A, Tunali T, Pisiriciler R, Akyuz S, Ipbuker A, Emekli N. Salivary thromboplastic activity in diabetics and healthy controls. Clin Oral Investig 2004; 8: 36–39.
  • 54. Aktop S, Emekli-Alturfan E, Ozer C, Gonul O, Garip H, Yarat A, et al. Effects of ankaferd blood stopper and celox on the tissue factor activities of warfarin-treated rats. Clin Appl Thromb Hemost 2014; 20: 16–21.
  • 55. Emekli-Alturfan E, Kasikci E and Yarat A. Tissue factor activities of streptozotocin induced diabetic rat tissues and the effect of peanut consumption. Diabetes Metab Res Rev 2007; 23: 653–658.
  • 56. Mehmetoğlu İ. Klinik Biyokimya El Kitabı. Konya: Nobel Tıp Kitabevleri; 2013. s. 155-156.
  • 57. Koçyiğit Y, Aksak MC, Atamer Y, Aktaş A. Futbolcu ve basketbolcularda akut egzersiz ve C vitamininin karaciğer enzimleri ve plazma lipid düzeylerine etkisi. J Clin Exp Invest 2011; 2 (1): 62-68.
  • 58. Emekli N, Yarat A, Akbay TT, Koç LÖ, Alturfan EI. Tükürük Biyokimyası. İçinde: Tükürük Histolojisi, Fizyolojisi, Mikrobiyolojisi ve Biyokimyası. Emekli N, Yarat A, editors. İstanbul: Nobel Tip Kitapevleri Ltd. Şti; 2008. s.328-331.
  • 59 Ünübol Aypak S, Uysal H. Glikoproteinlerin Yapısı ve Fonksiyonları. FÜ Sağ Bil Vet Derg 2010; 24;2;107-114.
  • 60. Crook MA, Tutt P, Pickup JC. Elevated serum sialic acid concentration in NIDDM and its relationship to blood pressure and retinopathy. Diabetes Care 1993; 16 (1): 57-60.
  • 61. Porter-Turner MM, Sidmore JC, Khokher MA, Singh BM, Rea CA. Relationship between erythrocyte GLUT1 function and membrane glycation in type 2 diabetes. Br J Biomed Sci 2011; 68(4):203-207.
  • 62. Sacan O, Ertik O, Ipci Y, Kabasaka L, Sener G , Yanardag R. Protective effect of chard extract on glycoprotein compounds and enzyme activities in streptozotocin-induced hyperglycemic rat lungs. Bulg Chem Commun 2018; 50(1):119-123.
  • 63. Mittal N, Kaur J, Mahmood A. Changes in tubular membrane glycosylation in diabetic, insulin and thyroxin treated rat kidneys. Indian J Exp Biol 1996; 34(8):782-785.
  • 64. Spiro RG, SpiroMJ, Effect of diabetes on the biosynthesis of the renal glomerular basement membrane. Studies on the glucosyltransferase. Diabetes 1971; 20(10):641-648.
Year 2021, Volume: 80 Issue: 1, 15 - 21, 15.06.2021

Abstract

Project Number

SAG-C-YLP-041213-0449

References

  • 1. Sener TE, Cevik O, Çetinel Ş, Şener G. (2020). Oxidative stress and urinary system damage in fructose-induced rat model of metabolic syndrome: Effect of calorie restriction and exercise. J Res Pharm 2020; 24 (3): 318-325.
  • 2. Bouzas C, Bibiloni MDM, Garcia S, Mateos D, Martínez-González M.Á, Salas-Salvadó J, et al. Dietary quality changes according to the preceding maximum weight: A longitudinal analysis in the predimed-plus randomized trial. Nutrients, 2020; 12(10), 3023.
  • 3. Yilmaz Demirtas C, Bircan FS, Pasaoglu OT, Turkozkan N. The effects of resveratrol on hepatic oxidative stress in metabolic syndrome model induced by high fructose diet. Bratisl Lek Listy 2018; 119(1):36-40.
  • 4. Martinez-Gonzalez MA, Martinez JA, Hu FB, Gibney MJ, Kearney J. Physical inactivity, sedentary lifestyle and obesity in the European Union. Int J Obes Relat Metab Disord 1999; 23: 1192–201.
  • 5. Balton VH, Korita I, Bulo A. How is metabolic syndrome related to dyslipidemia? Biochem Med 2008; 18: 14–24.
  • 6. Panickar KS. Beneficial Effects of Herbs, Spices and Medicinal Plants on the Metabolic Syndrome, Brain and Cognitive Function. Cent Nerv Syst Agents Med Chem 2013; 13: 13-29.
  • 7. Basciano H, Federico L, Adeli K. Fructose, insulin resistance and metabolic dyslipidemia. Nutr Metab 2005; 2(1):5.
  • 8. Kannappan S, Palanisamy N, Anuradha CV. Suppression of hepatic oxidative events and regulation of eNOS expression in the liver by naringenin in fructose-administered rats. Eur J Pharmacol 2010; 645: 177-184.
  • 9. Caponi PW, Lehnen AM, Pinto GH, Borges J, Markoski M, Machado UF, et al. Aerobic exercise training inducesmetabolic benefits in rats with metabolic syndrome independent of dietary changes. Clinics 2013; 68(7): 1010-1017.
  • 10. Williamson DF, Pamuk E, Thun M, Flanders D, Byers T, Heath C. Prospective study of intentional weight loss and mortality in never-smoking overweight US white women aged 40–64 years. Am J Epidemiol 1995; 141(12): 1128–1141.
  • 11. Williamson DF, Thompson JT, Thun M, Flanders D, Pamuk E, Byers E. Intentional weight loss and mortality among overweight individuals with diabetes. Diabetes Care 2000; 23(10); 1499–1504.
  • 12. Kurosaka Y, Machida S, Shiroya Y, Yamauchi H, & Minato K. Protective Effects of Voluntary Exercise on Hepatic Fat Accumulation Induced by Dietary Restriction in Zucker Fatty Rats. Int J Mol Sci 2021; 22(4), 2014.
  • 13. Pereira RM, Botezelli JD, da Cruz Rodrigues KC, Mekary RA, Cintra DE, Pauli JR, et al. Fructose consumption in the development of obesity and the effects of different protocols of physical exercise on the hepatic metabolism. Nutrients 2017; 9(4), 405.
  • 14 . Pósa A, Szabó R, Kupai K, Csonka A, Szalai Z, Veszelka M, et al. Exercise training and calorie restriction influence the metabolic parameters in ovariectomized female rats. Oxid Med Cell Longev 2015; 787063.
  • 15. Weindruch R, Walford RL. The Retardation of Aging and Disease by Dietary Restriction. Springfield, Illinois: Charles C. Thomas; 1988.
  • 16. Beutler E. Glutathione. In: Red blood cell metabolism: A Manual of Biochemical Methods. 2nd ed. New York: Grune and Stratton; 1975, 112–114.
  • 17. Ledwozyw A, Michalak J, Stepien A, Kadziolka A. The relationship between plasma triglycerides, cholesterol, total lipids and lipid peroxidation products during human atherosclerosis. Clin Chim Acta 1986, 155(3):275-283.
  • 18. Warren L. The thiobarbituric acid assay of sialic acids. J Biol Chem 1959; 234: 1971-1975.
  • 19. Winzler RJ. Determination of serum glycoproteins. Glick D, editors. Methods of Biochemical Analysis. New York: Interscience Publishers Inc. 1955; 2: 279-311.
  • 20. Dische Z, Shettles LB. A specific color reaction of methylpentoses and a spectrophotometric micromethod for their determination. J Biol Chem 1948; 175; 595-603.
  • 21. Shakeerabanu M, Sjahta K, Praveen R.C, Manimaran A. The defensive effect of quercetinon indomethacin induced gastric damage in rats. Adv Biol Res 2011; 5(1); 64-70.
  • 22. Mylorie AA, Collins H, Umbles C, Kyle J. Erythrocyte superoxide dismutase activity and other parameters of copper status in rats ingesting lead acetate. Toxicol Appl Pharmacol 1986; 82(3): 512-520.
  • 23. Aebi H. Catalase in vitro. Methods Enzymol. 1984, 105:121-126.
  • 24. Habig WH, Jacoby WB. Assays for differentiation of glutathione S- transferases. Methods in Enzymol. 1981; 77: 398-405.
  • 25. Walter K, Schült C. Acid and alkaline phosphatase in serum: two point method. In: Methods of Enzymatic Analysis. 2nd ed. Bergmeyer HU, editors. Verlag Chemie: Academic Press, Inc. New York and London; 1974. 2: 856-886.
  • 26. Ingram GIC, Hills M. Reference method for the one-stage prothrombin time test on human blood. Thromb Haemost 1976; 36(1): 237-238.
  • 27. Dalle-Donne I, Aldini G, Carini M, Colombo R, Rossi R, Milzani A. Protein carbonylation, cellular dysfunction and disease progression. J Cell Mol Med 2006; 10(2): 389-406.
  • 28. Rutledge AC, Adele K. Fructose and the metabolic syndrome: Pathophysiology and molecular mechanisms. Nutr Rev 2007; 65: 13-23.
  • 29. Abdullah MM, Riediger NN, Chen Q, Zhao Z, Azordegan N, Xu Z, et al. Effects of long-term consumption of a high fructose diet on conventional cardiovascular risk factors in Sprague-Dawley rats. Mol Cell Biochem 2009; 327 (1-2): 247-256.
  • 30. Paśko P, Bartoń H, Zagrodzki P, Gorinstein S. Effect of amaranth seeds (Amaranthus cruentus) in the diet on some biochemical parameters and essential trace elements in blood of high fructose-fed rats. Nat Prod Res 2011; 25: 844-849.
  • 31. Babacanoğlu C, Yıldırım N, Sadi G, Pektas MB, Akar F. Resveratrol prevents high-fructose corn syrup-induced vascular insulin resistance and dysfunction in rats. Food Chem Toxicol 2013; 60; 160-167.
  • 32. Masterjohn C, Park Y, Lee J, Noh SK, Koo SI, Bruno RS. Dietary Fructose Feeding Increases Adipose Methylglyoxal Accumulation in Rats in Association with Low Expression and Activity of Glyoxalase-2. Nutrients 2013; 5: 3311-3328.
  • 33. Zhao CX, Xu X, Cui Y, Wang P, Wei X, Yang S, et al. Increased endothelial nitric-oxide synthase expression reduces hypertension and hyperinsulinemia in fructose-treated rats. J Pharmacol Exp Ther 2009; 328(2): 610–620.
  • 34. Giani JF, Mayer MA, Munoz MC, Silberman EA, Hocht C, Taira CA, et al. Chronic infusion of angiotensin-(1-7) improves insulin resistance and hypertension induced by a high-fructose diet in rats. Am J Physiol Endocrinol Metab 2009; 296(2): E262-E271.
  • 35. Wang DD, Sievenpiper JL, De Souza RJ, Cozma AI, Chiavaroli L, Ha V, et al.Effect of fructose on postprandial triglycerides: a systematic review and meta-analysis of controlled feeding trials. Atherosclerosis 2014; 232(1):125–133.
  • 36. Steinberg HO, Chaker H, Leaming R, Johnson A, Brechtel G, Baron AD. Obesity/Insulin Resistance is Associated with Endothelial Dysfunction. Implications for the Syndrome of Insulin Resistance. J Clin Invest 1996; 97(11): 2610-2601.
  • 37. Delbosc S, Paizanis E, Magous R, Araiz C, Dimo T, Cristol JP, et al. Involvement of oxidative stress and NADPH oxidase activation in the development of cardiovascular complications in a model of insulin resistance, the fructose-fed rat. Atherosclerosis. 2005; 179(1):43-9.
  • 38. Singh I, Singh PK, Bhansali S, Shafiq N, Malhotra S, Pandhi P, et al. Effects of three different doses of a fruit extract of Terminalia chebula on metabolic components of metabolic syndrome, in a rat model. Phytother Res 2010; 24:107-112.
  • 39 . Castro-Barquero S, Ruiz-León AM, Sierra-Pérez M, Estruch R, Casas, R. Dietary strategies for metabolic syndrome: a comprehensive review. Nutrients 2020; 12(10): 2983.
  • 40. Venditti P, Gomez-Cabrera MC, Zhang Y, Radak, Z. Oxidant antioxidants and adaptive responses to exercise. Oxid Med Cell Longev 2015; 290190.
  • 41. Vincent HK, Powers SK, Demirel HA, Coombes JS, Naito H. Exercise training protects against contraction-induced lipid peroxidation in the diaphragm. Eur J Appl Physiol 1999; 79, 268-273.
  • 42. Duarte J, Pérez-Palencia R, Vargas F, Ocete MA, Pérez-Vizcaino F, Zarzuelo A, Tamargo J. Antihypertensive effects of the flavonoid quercetin in spontaneously hypertensive rats. Br J Pharmacol 2001; 133:117-24.
  • 43. Alipour M, Salehi I, Soufi FG. Effect of Exercise on Diabetes-Induced Oxidative Stress in the Rat Hippocampus. Iran Red Crescent Med J 2012; 14(4); 222-228.
  • 44. Lima TI, Monteiro IC, Valença S, Leal-Cardoso JH, Fortunato RS, Carvalho DP, Teodoro BG, Ceccatto VM. Effect of exercise training on liver antioxidant enzymes in STZ-diabetic rats. Life Sci 2015; 128; 64–71.
  • 45 Hagopian K. Krebs cycle enzymes from livers of old mice are differantially regulated by caloric restriction. Physiol and Behavior 2005; 85: 581-592.
  • 46. Speakman JR, Mitchell SE. Caloric restriction. Mol Aspects Med 2011; 32(3):159–221.
  • 47. He XY, Zhao XL, Gu Q, Shen JP, Hu Y, Hu RM. Calorie restriction from a young age preserves the functions of pancreatic β cells in aging rats. Tohoku J Exp Med 2012; 227(4): 245–252.
  • 48. Horrillo D, Gallardo N, Lauzurica N, Barrus MT, San Frutos MG, Andres A, et al. Development of liver fibrosis during aging: effects of caloric restriction. J Biol Regul Homeost Agents. 2013; 27(2); 377–388.
  • 49. Mohammadi M, Ghaznavi R, Keyhanmanesh R, Sadeghipour HR, Naderi R, Mohammadi H. Caloric restriction prevents lead-induced oxidative stress and inflammation in rat liver. Scientific World J 2014; 20; 821524.
  • 50. Mackman N. Tissue-specific hemostasis in mice. Arterioscler Thromb Vasc Biol 2005; 25: 2273–2281.
  • 51. Nemerson Y. Tissue factor: then and now. Thromb Haemost 1995; 74(1): 180-184.
  • 52. Emekli-Alturfan E, Basar I, Malali E, Elemek E, Oktay S, Ayan F, et al. Plasma tissue factor and tissue factor activities of periodontitis patients with cardiovascular diseases. Pathophysiol Haemost Thromb 2010; 37: 77–81.
  • 53. Yarat A, Tunali T, Pisiriciler R, Akyuz S, Ipbuker A, Emekli N. Salivary thromboplastic activity in diabetics and healthy controls. Clin Oral Investig 2004; 8: 36–39.
  • 54. Aktop S, Emekli-Alturfan E, Ozer C, Gonul O, Garip H, Yarat A, et al. Effects of ankaferd blood stopper and celox on the tissue factor activities of warfarin-treated rats. Clin Appl Thromb Hemost 2014; 20: 16–21.
  • 55. Emekli-Alturfan E, Kasikci E and Yarat A. Tissue factor activities of streptozotocin induced diabetic rat tissues and the effect of peanut consumption. Diabetes Metab Res Rev 2007; 23: 653–658.
  • 56. Mehmetoğlu İ. Klinik Biyokimya El Kitabı. Konya: Nobel Tıp Kitabevleri; 2013. s. 155-156.
  • 57. Koçyiğit Y, Aksak MC, Atamer Y, Aktaş A. Futbolcu ve basketbolcularda akut egzersiz ve C vitamininin karaciğer enzimleri ve plazma lipid düzeylerine etkisi. J Clin Exp Invest 2011; 2 (1): 62-68.
  • 58. Emekli N, Yarat A, Akbay TT, Koç LÖ, Alturfan EI. Tükürük Biyokimyası. İçinde: Tükürük Histolojisi, Fizyolojisi, Mikrobiyolojisi ve Biyokimyası. Emekli N, Yarat A, editors. İstanbul: Nobel Tip Kitapevleri Ltd. Şti; 2008. s.328-331.
  • 59 Ünübol Aypak S, Uysal H. Glikoproteinlerin Yapısı ve Fonksiyonları. FÜ Sağ Bil Vet Derg 2010; 24;2;107-114.
  • 60. Crook MA, Tutt P, Pickup JC. Elevated serum sialic acid concentration in NIDDM and its relationship to blood pressure and retinopathy. Diabetes Care 1993; 16 (1): 57-60.
  • 61. Porter-Turner MM, Sidmore JC, Khokher MA, Singh BM, Rea CA. Relationship between erythrocyte GLUT1 function and membrane glycation in type 2 diabetes. Br J Biomed Sci 2011; 68(4):203-207.
  • 62. Sacan O, Ertik O, Ipci Y, Kabasaka L, Sener G , Yanardag R. Protective effect of chard extract on glycoprotein compounds and enzyme activities in streptozotocin-induced hyperglycemic rat lungs. Bulg Chem Commun 2018; 50(1):119-123.
  • 63. Mittal N, Kaur J, Mahmood A. Changes in tubular membrane glycosylation in diabetic, insulin and thyroxin treated rat kidneys. Indian J Exp Biol 1996; 34(8):782-785.
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There are 64 citations in total.

Details

Primary Language English
Journal Section Research Articles
Authors

Nevin Genc-kahraman This is me 0000-0003-2143-0088

Burcin Alev Tuzuner This is me 0000-0001-5122-4977

Hazal Ipekci This is me 0000-0003-1193-168X

Unsal Veli Ustundag This is me 0000-0003-0804-1475

Tugba Tunalı-akbay This is me 0000-0002-2091-9298

Ebru Emekli-alturfan This is me 0000-0003-2419-8587

Goksel Sener This is me 0000-0001-7444-6193

Ayşen Yarat 0000-0002-8258-6118

Project Number SAG-C-YLP-041213-0449
Publication Date June 15, 2021
Submission Date April 9, 2021
Published in Issue Year 2021 Volume: 80 Issue: 1

Cite

AMA Genc-kahraman N, Tuzuner BA, Ipekci H, Ustundag UV, Tunalı-akbay T, Emekli-alturfan E, Sener G, Yarat A. Exercise and Caloric Restriction Improves Liver Damage in Metabolic Syndrome Model. Eur J Biol. June 2021;80(1):15-21.