AccScience Publishing / GTM / Online First / DOI: 10.36922/gtm.2321
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ORIGINAL RESEARCH ARTICLE

Effects of high-calorie diet-induced visceral obesity on reproductive hormones and muscle tissues in male and female Wistar rats

Tatyana A. Mityukova1* Anastasia A. Basalai1* Olga Y. Poluliakh1 Tatyana E. Kuznetsova1
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1 Department of Laboratory of Biomedical Technologies and Medical Rehabilitation, Institute of Physiology, National Academy of Sciences of Belarus, Minsk, Republic of Belarus
Global Translational Medicine 2024, 3(1), 2321 https://doi.org/10.36922/gtm.2321
Submitted: 27 November 2023 | Accepted: 6 March 2024 | Published: 21 March 2024
© 2024 by the Author (s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by/4.0/ )
Abstract

Overweight and obesity are associated with alterations in the reproductive system, which affect the anabolic supply to peripheral muscle tissues. The study aimed to investigate the effects of a high-calorie diet (HCD) on the development of obesity, reproductive hormone levels, and morphofunctional characteristics of muscle tissues in Wistar rats (i.e., 54 sexually mature male and female Wistar rats) for 16 weeks. Male rats fed with an HCD displayed (i) visceral obesity and hypogonadism, (ii) a decrease in the mass of the musculus triceps surae, (iii) increased levels of total protein, cholesterol, glucose, lactate, lactate dehydrogenase, and malonic dialdehyde (MDA) and superoxide dismutase (SOD) activities, and (iv) stable concentrations of estradiol and testosterone in the muscle tissues. In contrast, female rats fed with HCD displayed (i) visceral obesity, (ii) alterations in reproductive hormones toward hyperandrogenism, (iii) decreased metabolism in the muscle tissues, and (iv) increased levels of estradiol and MDA (without SOD activation). The cross-sectional area of the muscle fiber was significantly reduced by 20% in male and 44% in female rats on HCD. In addition, the total muscle edema was reportedly increased by twofold in both male and female rats. In summation, obese male and female rats developed an imbalance of reproductive hormones and alterations in muscle tissue metabolism.

Keywords
Visceral obesity
High-calorie diet
Reproductive hormones
Muscle metabolism
Male and female Wistar rats
Funding
The work was supported by the State Program for Scientific Research (No.:4.1.1.5) of the National Academy of Sciences of Belarus.
Conflict of interest
The authors declare that they have no competing interests.
References
  1. WHO. Report Highlights the Dangers of Obesity. Available from: https://www.hps.scot.nhs.uk/publications/hps-weekly-report/volume-56/issue-18/who-report-highlights-the-dangers-of-obesity [Last accessed on 2023 Sep 05].

 

  1. Lainez NM, Coss D. Obesity, neuroinflammation, and reproductive function. Endocrinology. 2019;60:2719-2736. doi: 10.1210/en.2019-00487

 

  1. Brion MJA, Ness AR, Rogers I, et al. Maternal macronutrient and energy intakes in pregnancy and offspring intake at 10 y: Exploring parental comparisons and prenatal effects. Am J Clin Nutr. 2010;91:748-756. doi: 10.3945/ajcn.2009.28623

 

  1. Akalestou E, Genser L, Rutter GA. Glucocorticoid metabolism in obesity and following weight loss. Front Endocrinol (Lausanne). 2020;11:59. doi: 10.3389/fendo.2020.00059

 

  1. Tomlinson DJ, Erskine RM, Morse CI, et al. The impact of obesity on skeletal muscle strength and structure through adolescence to old age. Biogerontology. 2016;17:467-483. doi: 10.1007/s10522-015-9626-4

 

  1. Godoy-Matos AF, Silva Junior WS, Valerio CM. NAFLD as a continuum: From obesity to metabolic syndrome and diabetes. Diabetol Metab Syndr. 2020;12:60. doi: 10.1186/s1309802000570y

 

  1. Prasun P. Mitochondrial dysfunction in metabolic syndrome. Biochim Biophys Acta. 2020;1866(10):165838. doi: 10.1016/j.bbadis.2020.165838

 

  1. Aizawa K, Iemitsu M, Maeda S. Expression of steroidogenic enzymes and synthesis of sex steroid hormones from DHEA in skeletal muscle of rats. Am J Physiol Endocrinol Metab. 2007;292(2):E577-E584. doi: 10.1152/ajpendo.00367.2006

 

  1. Gancheva S, Zhelyazkova-Savova M, Galunska B, et al. Experimental models of metabolic syndrome in rats. Scr Sci Medica. 2015;47(2):14-21. doi: 10.14748/ssm.v47i2.1145

 

  1. Marcondes FK, Bianchi FJ, Tanno AP. Determination of the estrous cycle phases of rats: Some helpful considerations. Braz J Biol. 2002;62(4A):609-614. doi: 10.1590/S1519-69842002000400008

 

  1. Стальная ИД, Гаришвили ТГ. Метод определения малонового диальдегида с помощью тиобарбитуровой кислоты. Современные методы биохимии. Москва : Медицина. 1977;66-68. Stalnaya ID, Garishvili TG. Method for the determination of malondialdehyde using thiobarbituric acid. Mod Methods Biochem. Moscow : Medicine. 1977; 66-68. [In Russ].

 

  1. Сирота ТВ. Новый подход в исследовании процесса аутоокисления адреналина и использование его для измерения активности супероксиддисмутазы. Вопросы медицинской химии. 1999;3:263-272. Sirota TV. A new approach to the study of the process of autoxidation of adrenaline and its use to measure the activity of superoxide dismutase. Quest Med Chem. 1999;3:263-272. [In Russ].

 

  1. Liver Disorders and Gallstones. Functions of the Liver. Available from: https://uomustansiriyah.edu.iq/media/ lectures/4/4_2019_04_09!05_38_02_PM.pdf [Last accessed on 2023 Sep 07].

 

  1. Matull WR, Pereira SP, O’Donohue JW. Biochemical markers of acute pancreatitis. J Clin Pathol. 2006;59(4):340-344. doi: 10.1136/jcp.2002.002923

 

  1. Mescher AL. Junqueira’s Basic Histology: Text and Atlas. 12th ed. United States: McGraw-Hill Medical; 2010. p. 480.

 

  1. Parker R. The role of adipose tissue in fatty liver diseases. Liver Res. 2018;2(1):35-42. doi: 10.1016/j.livres.2018.02.002

 

  1. Maric I, Krieger JP, Van der Velden P, et al. Sex and species differences in the development of diet-induced obesity and metabolic disturbances in rodents. Front Nutr. 2022;9:828522. doi: 10.3389/fnut.2022.828522

 

  1. Taraschenko OD, Maisonneuve IM, Glick SD. Sex differences in high fat-induced obesity in rats: Effects of 18-methoxycoronaridine. Physiol Behav. 2011;103(3-4):308-314. doi: 10.1016/j.physbeh.2011.02.011

 

  1. Chukijrungroat N, Khamphaya T, Weerachayaphorn J, et al. Hepatic FGF21 mediates sex differences in high-fat high-fructose diet-induced fatty liver. Am J Physiol Endocrinol Metab. 2017;313(2):E203-E212. doi: 10.1152/ajpendo.00076.2017

 

  1. Leeners B, Geary N, Tobler PN, et al. Ovarian hormones and obesity. Hum Reprod Update. 2017;23(3):300-321. doi: 10.1093/humupd/dmw045

 

  1. Zhai L, Zhao J, Zhu Y, et al. Downregulation of leptin receptor and kisspeptin/GPR54 in the murine hypothalamus contributes to male hypogonadism caused by high-fat diet-induced obesity. Endocrine. 2018;62(1):195-206. doi: 10.1007/s12020-018-1646-9

 

  1. Feng J, Xu R, Li Y, et al. The effect of high-fat diet and exercise on KISS-1/GPR54 expression in testis of growing rats. Nutr Metab (Lond). 2021;18(1):1. doi: 10.1186/s12986-020-00517-0

 

  1. Zhou Q, Chen H, Yang S, et al. High-fat diet decreases the expression of Kiss1 mRNA and kisspeptin in the ovary, and increases ovulatory dysfunction in postpubertal female rats. Reprod Biol Endocrinol. 2014;12:127. doi: 10.1186/1477-7827-12-127

 

  1. Khodabandeh S, Hosseini A, Khazali H, et al. Interplay between polycystic ovary syndrome and hypothyroidism on serum testosterone, oxidative stress and StAR gene expression in female rats. Endocrinol Diabetes Metab. 2022;5(5):e359. doi: 10.1002/edm2.359

 

  1. Alrabadi N, Al-Rabadi GJ, Maraqa R, et al. Androgen effect on body weight and behaviour of male and female rats: Novel insight on the clinical value. Andrologia. 2020;52(10):e13730. doi: 10.1111/and.13730

 

  1. Memudu AE, Dongo GA. A study to demonstrate the potential of anabolic androgen steroid to activate oxidative tissue damage, nephrotoxicity and decline endogenous antioxidant system in renal tissue of Adult Wistar Rats. Toxicol Rep. 2023;10:320-326. doi: 10.1016/j.toxrep.2023.02.010

 

  1. Mengeste AM, Rustan AC, Lund J. Skeletal muscle energy metabolism in obesity. Obesity (Silver Spring). 2021;29:1582-1595. doi: 10.1002/oby.23227

 

  1. Muller FL, Song W, Liu Y, et al. Absence of CuZn superoxide dismutase leads to elevated oxidative stress and acceleration of age-dependent skeletal muscle atrophy. Free Radic Biol Med. 2006;40(11):1993-2004. doi: 10.1016/j.freeradbiomed.2006.01.036

 

  1. Aizawa K, Iemitsu M, Maeda S, et al. Acute exercise activates local bioactive androgen metabolism in skeletal muscle. Steroids. 2010;75(3):219-223. doi: 10.1016/j.steroids.2009.12.002

 

  1. Aizawa K, Iemitsu M, Maeda S, et al. Endurance exercise training enhances local sex steroidogenesis in skeletal muscle. Med Sci Sports Exerc. 2011;43(11):2072-2080. doi: 10.1249/MSS.0b013e31821e9d74
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Global Translational Medicine, Electronic ISSN: 2811-0021 Print ISSN: 3060-8600, Published by AccScience Publishing