Journals / European Journal of Biology / 2021 / Cilt: 80 - Sayı: 1

Exercise and Caloric Restriction Improves Liver Damage in Metabolic Syndrome Model

Pages
15–21
Publication Date
2021-06-15
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

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).

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Objective & Hypothesis: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.
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Key Findings & Data:To induce metabolic syndrome, a 10% fructose solution was given to rats in drinking water for 3 months.
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Conclusion & Impact: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).
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Metabolic syndrome · exercise · caloric restriction

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).

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Cite This Article

GENC-KAHRAMAN, N., TUZUNER, B. A., IPEKCİ, H., USTUNDAG, U. V., TUNALI-AKBAY, T., EMEKLİ-ALTURFAN, E., SENER, G., YARAT, A. (2021). Exercise and Caloric Restriction Improves Liver Damage in Metabolic Syndrome Model. European Journal of Biology, Cilt: 80 - Sayı: 1, 15–21. https://ajindex.com/articles/205039

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References (13)

  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 obes