Evaluation of indicators of carbohydrate and lipid metabolism in rats depending on the type of high-calorie diet
https://doi.org/10.14341/omet12712
Abstract
BACKGROUND: Recently, there has been an increase in the number of cardiovascular diseases and mortality rates among the population. This may be due to a violation of metabolic processes in the body, in particular lipid and carbohydrate metabolism, caused by an unbalanced high-calorie diet.
PURPOSE: To study and compare the main indicators of carbohydrate and lipid metabolism in a fructose-fortified diet and a diet with a high fat content under experimental conditions.
MATERIALS AND METHODS: The study was carried out on outbred white rats, males, which were divided into 3 groups — a control group and two experimental ones, 15 individuals in each. The rats of the first experimental group were kept on a high-fat diet, the second experimental group was assigned a fructose-enriched diet for 35 days. The control group was on a balanced diet. We studied the changes in the parameters of carbohydrate (glucose, insulin, insulin resistance indices) and lipid (cholesterol-, high- and low-density lipoproteins, triglycerides) metabolism on the 21st, 35th and 60th days of the experiment. The results were statistically processed using the Mann-Whitney test. The study design is retrospective.
RESULTS: During the experiment, an increase in the content of glucose, insulin, and lipid metabolism parameters was observed in the experimental groups. Moreover, the content of glucose and insulin in a fructose-fortified diet increased by 18.7% (p = 0,009), 22.2% (p = 0,076), 21.5% (p = 0,009) and 50% (p = 0,009), 62.5% (p = 0,009), 106.3% (p = 0,009) over the days of the experiment, respectively. The increase in lipid metabolism was more pronounced in the experimental group, which had an increased fat content in the diet, already in the first time period of the experiment: cholesterol — by 80,8% (p = 0,009), low-density lipoproteins — by 100% (p = 0,009), triglycerides — by 120% (p = 0,009), high-density lipoproteins — by 60.9% (p = 0,009).
CONCLUSION: The experimental data obtained show changes in lipid and carbohydrate metabolism due to increased consumption of fats and fructose.
About the Authors
O. G. GilevaRussian Federation
Olga G. Gileva
281 Kommunarov street, 426034 Izhevsk
E. G. Butolin
Evgeniy G. Butolin, MD, PhD, Professor
Izhevsk
M. V. Tereshchenko
Maria V. Tereshchenko
Izhevsk
V. G. Ivanov
Vadim G. Ivanov, MD, PhD
Izhevsk
References
1. Misnikova IV. Disorders of carbohydrate metabolism within the metabolic syndrome: diagnosis and treatment. Poliklinika. 2016; 2:17-20. (In Russ.).
2. Karpovets TP, Konopelnyuk VV, Galenova TI, et al. High-calorie diet as a factor in the development of prediabetes in rats. Byulleten’ eksperimental’noy biologii i meditsiny. 2013; 156(11):582-585. (In Russ.).
3. Reshetnyak MV, Khirmanov VN, Zybina NN, et al. Model of metabolic syndrome caused by fructose feeding: pathogenetic relationships of metabolic disorders. // Meditsinskiy akademicheskiy zhurnal. 2011; 11(3):23-27. (In Russ).
4. Buettner R, Parhofer KG, Woenckhaus M, et al. Defining high-fat-diet rat models: metabolic and molecular effects of different fat types. J Mol Endocrinol. 2006; 36(3):485-501. doi: https://doi.org/10.1677/jme.1.01909
5. Hsu C-L, Wu C-H, Huang S-L, Yen G-C. Phenolic Compounds Rutin and o -Coumaric Acid Ameliorate Obesity Induced by High-Fat Diet in Rats. J Agric Food Chem. 2009; 57(2):425-431. doi: https://doi.org/10.1021/jf802715t
6. Gileva OG. Biochemical markers of liver damage with a fructose-induced diet in rats. Probl Biol Med Pharm Chem. 2020; 23(9):53-59. (In Russ.). doi: https://doi.org/10.29296/25877313-2020-09-08
7. Kawasaki T, Igarashi K, Koeda T, et al. Rats Fed FructoseEnriched Diets Have Characteristics of Nonalcoholic Hepatic Steatosis. The Journal of Nutrition. 2009; 139:2067-2071. doi: https://doi.org/10.3945/jn.109.105858
8. Dolgov VV. Clinical laboratory diagnostics: National guidelines. In 2 volumes. Moscow: GEOTAR-Media; 2013. (In Russ.).
9. Iizuka K. The Role of Carbohydrate Response Element Binding Protein in Intestinal and Hepat-ic Fructose Metabolism. Nutrients. 2017; 9(2):181. doi: https://doi.org/10.3390/nu9020181
10. Drapkina OM. Galectin-3 is a biomarker of fibrosis in patients with metabolic syndrome. Rossiyskiy kardiologicheskiy zhurnal. 2015; 125(9):96-100. (In Russ.). doi: https://doi.org/10.15829/1560-4071-2015-09-96-102
11. Pavlova ZSh. Biochemical mechanisms of development of non-alcoholic fatty liver disease under the influence of fructose. Tekhnologii zhivykh sistem. 2018; 4:18-27. (In Russ.). doi: https://doi.org/10.18127/j20700997-201804-02
12. Leshchenko DV. Diet-induced animal models of metabolic syndrome. Verkhnevolzhskiy meditsinskiy zhurnal. 2015; 2:34-39. (In Russ.).
13. Hwang IS, Ho H, Hoffman BB, Reaven GM. Fructose-induced insulin resistance and hypertension in rats. Hypertension. 1987; 10(5):512-516. doi: https://doi.org/10.1161/01.HYP.10.5.512
14. Reshetnyak MV, Khirmanov VN, Zybina NN. Fructoseinduced metabolic syndrome model: pathogenetic relationships of metabolic disorders. Meditsinskiy akademicheskiy zhurnal. 2011; 11(3):23-27. (In Russ.). doi: https://doi.org/10.17816/MAJ11323-27
15. de Castro UGM, dos Santos Rasas, Silva ME, et al. Age-dependent effect of high-fructose and high-fat diets on lipid metabolism and lipid accumulation in liver and kidney of rats. Lipids Health Dis. 2013; 12(1):136. doi: https://doi.org/10.1186/1476-511X-12-136
16. Kaydash OA, Ivanov VV, Vengerovsky AI, et al. An experimental model of type 2 diabetes mellitus in rats induced by a diet high in fat and low dose streptozotocin. Bulletin of Siberian Medicine. 2020; 19(2):41-47. (In Russ.). doi: https://doi.org/10.20538/1682-0363-2020-2-41-47
17. Skaletskaya GN, Skaletskiy NN, Volkova EA, Sevastyanov VI. Streptozotocin model of stable diabetes mellitus. Russian Journal of Transplantology and Artificial Organs. 2018; 20(4):83-88. (In Russ.). doi: https://doi.org/10.15825/1995-1191-2018-4-83-88
18. Obergan TYu, Lyapina MG, Grigorieva ME, Lyapina LA. Features of the pharmacodynamics of glyproline peptides in terms of the parameters of fat metabolism and thromboelastogram against the background of the development of metabolic syndrome in rats. Biomedicina. 2019, 15(4):58-66. (In Russ.)]. doi: https://doi.org/10.33647/2074-5982-15-4-58-66
Supplementary files
Review
For citations:
Gileva O.G., Butolin E.G., Tereshchenko M.V., Ivanov V.G. Evaluation of indicators of carbohydrate and lipid metabolism in rats depending on the type of high-calorie diet. Obesity and metabolism. 2022;19(1):47-52. (In Russ.) https://doi.org/10.14341/omet12712

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND 4.0).