Preview

Experimental and Clinical Gastroenterology

Advanced search

Effect of high-fat diet in female rats on physiological, biochemical and hematological parameters in first generation offspring

https://doi.org/10.31146/1682-8658-ecg-234-2-137-145

Abstract

Objective of the study. To evaluate the effect of a high-fat diet in female rats on body weight, visceral fat deposits, biochemical and hematologic parameters in first generation offspring in an experiment. Materials and Methods. A control group of females receiving a normal fat diet (NFD) and a group receiving a high-fat diet (HFD) participated in the experiment. The diet was implemented before pregnancy, during pregnancy and during lactation. Male offspring within the group were divided into subgroups receiving the NFD and HFD. Feeding of males was continued for 2 months. Results. Mean weight (g) of HFD females 280.3±14.9, NFD 302±16.7; (p<0.05). Mean weight (g) of offspring of male offspring of NFD/HFD 201,9±28,7; NFD/NFD 198,2±28; HFD/HFD 207,8±29,1; HFD/NFD 185,9±27,3; (p>0,05). No relationship was found between male body weight dynamics and maternal diet [F (1, 79) = 0.002554, P=0.9598]. The increase in body weight of males was due to their diet [F (39, 79) = 2.282, P=0.0010]. The visceral adipose tissue mass ratio was predominantly HFD/HFD (p<0.05). The hemoglobin level of HFD/NFD was 6% higher than that of HFD/HFD (p<0.05). Statistically significant differences in cholesterol levels were determined between NFD/HFD and HFD/NFD (p<0.05). LDH levels were 47% lower in NFD/NFD than HFD/HFD (p<0.05). TNF-α level in NFD/HFD was 6 times higher than HFD/NFD (p<0.05). Statistically significant differences in glycemia levels at 120 min were determined between HFD/NFD and NFD/HFD (p<0.05). The glycemia level at 120 min averaged 5.9±0.6 mmol/L in the HFD/NFD group and 7.1±1.24 mmol/L in the NFD/HFD group. Conclusion. No changes in body weight, dynamics of feed and water consumption, and intergroup differences in glycemia levels were observed in females and offspring of first-generation males derived from females on HFD. No inflammatory or metabolic changes were detected. It is reasonable to consider a number of other alternative models of obesity

About the Authors

Yu. Yu. Borshchev
Almazov National Medical Research Centre of the Ministry of Health of the Russian Federation; National Medical Research Center of Oncology named after N.N. Petrov, Ministry of Health of Russia
Russian Federation


V. V. Komar
Almazov National Medical Research Centre of the Ministry of Health of the Russian Federation; St. Petersburg State Pediatric Medical University
Russian Federation


S. M. Minasyan
Almazov National Medical Research Centre of the Ministry of Health of the Russian Federation; Pavlov First St. Petersburg State Medical Universit
Russian Federation


V. Yu. Borshchev
Pavlov First St. Petersburg State Medical Universit
Russian Federation


D. V. Zakharov
St. Petersburg State Pediatric Medical University
Russian Federation


I. Yu. Burovenko
Almazov National Medical Research Centre of the Ministry of Health of the Russian Federation
Russian Federation


I. G. Zubkov
Almazov National Medical Research Centre of the Ministry of Health of the Russian Federation
Russian Federation


M. M. Galagudza
Almazov National Medical Research Centre of the Ministry of Health of the Russian Federation; Pavlov First St. Petersburg State Medical Universit; Institute for Analytical Instrumentation of the Russian Academy of Sciences
Russian Federation


References

1. Lima B.S., Sanches A.P., Ferreira M.S. et al. Maternal-placental axis and its impact on fetal outcomes, metabolism, and development. Biochim Biophys Acta Mol Basis Dis. 2023;1870(1):16685 doi: 10.1016/j.bbadis.2023.166855.

2. Shook L.L., James K.E., Roberts D.J. et al. Sex-specific impact of maternal obesity on fetal placental macrophages and cord blood triglycerides. Placenta. 2023;140:100-108. doi: 10.1016/j.placenta.2023.08.001.

3. Marciniak A., Patro-Małysza J., Kimber-Trojnar Ż. et al. Fetal programming of the metabolic syndrome. Taiwan J Obstet Gynecol. 2017 Apr;56(2):133-138. doi: 10.1016/j.tjog.2017.01.001.

4. Rodríguez-González G.L., Reyes-Castro L.A., Bautista C.J. et al. Maternal obesity accelerates rat offspring metabolic ageing in a sex-dependent manner. J Physiol. 2019 Dec;597(23):5549-5563. doi: 10.1113/JP278232.

5. Zheng J., Zhang L., Gao Y., Wu H., Zhang J. The dynamic effects of maternal high-calorie diet on glycolipid metabolism and gut microbiota from weaning to adulthood in offspring mice. Front Nutr. 2022 Jul 28;9:941969. doi: 10.3389/fnut.2022.941969.

6. Bariani M.V., Correa F., Domínguez Rubio A.P. et al. Maternal obesogenic diet combined with postnatal exposure to high-fat diet induces metabolic alterations in offspring. J Cell Physiol. 2020 Nov;235(11):8260-8269. doi: 10.1002/jcp.29482.

7. Hariri N., Thibault L. High-fat diet-induced obesity in animal models. Nutr Res Rev. 2010;23:270-99. doi: 10.1017/S0954422410000168.

8. Armitage J.A., Taylor P.D., Poston L. Experimental models of developmental programming: consequences of exposure to an energy rich diet during development. J Physiol. 2005;565:3-8. doi: 10.1113/jphysiol.2004.079756.

9. Birulina J.G., Ivanov V.V., Buyko E.E. et al. High-fat, high-carbohydrate diet-induced experimental model of metabolic syndrome in rats. Bulletin of Siberian Medicine. 2020;19(4):14-20. doi: 10.20538/1682-0363-2020-4-14-20.@@ Бирулина Ю.Г., Иванов В.В., Буйко Е.Е., и др. Экспериментальная модель метаболического синдрома у крыс на основе высокожировой и высокоуглеводной диеты. Бюллетень сибирской медицины. 2020;19(4):14-20. doi: 10.20538/1682-0363-2020-4-14-20.

10. Wentzel P., Eriksson U.J., Herrera E. High-fat diet in pregnant rats and adverse fetal outcome. Ups J Med Sci. 2019 Apr;124(2):125-134. doi: 10.1080/03009734.2019.1604588.

11. Henning R.J. Obesity and obesity-induced inflammatory disease contribute to atherosclerosis: a review of the pathophysiology and treatment of obesity. Am J Cardiovasc Dis. 2021; 11 (4): 504-29.

12. Gancheva S., Zhelyazkova-Savova M., Galunska B. et al. Experimental models of metabolic syndrome in rats. Scripta Scientifica Medica. 2015; 47 (2): 23-30. doi: 10.14748/ssm.v47i2.1145.

13. Moreno-Fernández S., Garcés-Rimón M., Vera G., Astier J., Landrier J.F., Miguel M. High fat/high glucose diet induces metabolic syndrome in an experimental rat model. Nutrients. 2018; 10 (10): 1502. doi: 10.3390/nu10101502.

14. Fortunato-Silva J., de Rezende L.P., Ferreira-Neto M.L., Bispo-da-Silva L.B., Balbi A.P.C.Intrauterine exposure to a high-fat diet, with different levels of lipids, and its gastrointestinal repercussions: a model of fetal programming in rats. J Dev Orig Health Dis. 2024 Dec 23;15: e33. doi: 10.1017/S2040174424000382.

15. Saben J., Lindsey F., Zhong Y. et al. Maternal obesity is associated with a lipotoxic placental environment. Placenta. 2014 Mar;35(3):171-7. doi: 10.1016/j.placenta.2014.01.003.

16. Challier J.C., Basu S., Bintein T. et al. Obesity in pregnancy stimulates macrophage accumulation and inflammation in the placenta. Placenta. 2008 Mar;29(3):274-81. doi: 10.1016/j.placenta.2007.12.010.

17. Saben J., Zhong Y., Gomez-Acevedo H. et al. Early growth response protein-1 mediates lipotoxicity-associated placental inflammation: role in maternal obesity. Am J Physiol Endocrinol Metab. 2013 Jul 1;305(1): E1-14. doi: 10.1152/ajpendo.00076.2013.

18. Mityukova T.A., Basalai A.A., Chudilovskaya K.N. et al. Decrease in Muscle Mass in Diet-Induced Visceral Obesity in Male Wistar Rats: Relationship with Hormonal and Metabolic Parameters. Rossijskij fiziologičeskij žurnal im. I.M. Sečenova. 2023;109(7):921-932. (in Russ.) doi: 10.31857/S0869813923070099.@@ Митюкова Т.А., Басалай А.А., Чудиловская Е.Н. и др. Снижение мышечной массы при диет-индуцированном висцеральном ожирении у крыс-самцов линии Вистар: связь с гормонально-метаболическими показателями. Российский физиологический журнал им. И.М. Сеченова. 2023;109(7):921-932. (in Russ.) doi: 10.31857/S0869813923070099.

19. Naryzhnaya N.V., Derkachev I.A., Kurbatov B.K. et al. Decrease in Infarct-Limiting Effect of Chronic Normobaric Hypoxia in Rats with Induced Metabolic Syndrome Is Associated with Disturbances of Carbohydrate and Lipid Metabolism. Bull Exp Biol Med. 2023 Apr;174(6):723-727. doi: 10.1007/s10517-023-05779-1.

20. Naryzhnaya N.V., Mukhomedzyanov A.V., Kurbatov B.K. et al. The infarct-limiting efficacy of deltorphin-II in old rats with diet-induced metabolic syndrome. Acta Biomedica Scientifica. 2022;7(6):281-289. (In Russ.) doi: 10.29413/ABS.2022-7.6.29.@@ Нарыжная Н.В., Мухомедзянов А.В., Курбатов Б.К. и др. Инфаркт-лимитирующая эффективность дельторфина-II при индуцированном диетой метаболическом синдроме у старых крыс. Acta biomedica scientifica. 2022; 7(6): 281-289. doi: 10.29413/ABS.2022-7.6.29.

21. Logvinov S.V., Mustafina L.R., Kurbatov B.K. et al. Influence of a high-carbohydrate high-fat diet on age-related changes in the myocardium in rats. Siberian Journal of Clinical and Experimental Medicine. 2023;38(1):90-98. (In Russ.) doi: 10.29001/2073-8552-2023-38-1-90-98.@@ Логвинов С.В., Мустафина Л.Р., Курбатов Б.К., и др. Влияние высокоуглеводной высокожировой диеты на возрастные изменения миокарда у крыс. Сибирский журнал клинической и экспериментальной медицины. 2023;38(1):90-98. doi: 10.29001/2073-8552-2023-38-1-90-98.


Review

For citations:


Borshchev Yu.Yu., Komar V.V., Minasyan S.M., Borshchev V.Yu., Zakharov D.V., Burovenko I.Yu., Zubkov I.G., Galagudza M.M. Effect of high-fat diet in female rats on physiological, biochemical and hematological parameters in first generation offspring. Experimental and Clinical Gastroenterology. 2025;(2):137-145. (In Russ.) https://doi.org/10.31146/1682-8658-ecg-234-2-137-145

Views: 18


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1682-8658 (Print)