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Immunohistomorphometric and Hormonal Analysis of the Pituitary Gonadotropic Cells After Application of the Nandrolone Decanoate and Swimming Training in Adult Male Rats

Published online by Cambridge University Press:  10 June 2020

Jasmina Sretenovic
Affiliation:
Faculty of Medical Sciences, Department of Physiology, University of Kragujevac, Svetozara Markovica 69, 34000Kragujevac, Serbia
Vladimir Zivkovic
Affiliation:
Faculty of Medical Sciences, Department of Physiology, University of Kragujevac, Svetozara Markovica 69, 34000Kragujevac, Serbia
Ivan Srejovic*
Affiliation:
Faculty of Medical Sciences, Department of Physiology, University of Kragujevac, Svetozara Markovica 69, 34000Kragujevac, Serbia
Vladimir Ajdzanovic
Affiliation:
Department of Cytology, Institute for Biological Research “Sinisa Stankovic” – National Institute of Republic of Serbia, University of Belgrade, Bulevar Despota Stefana 142, 11000Belgrade, Serbia
Natasa Ristic
Affiliation:
Department of Cytology, Institute for Biological Research “Sinisa Stankovic” – National Institute of Republic of Serbia, University of Belgrade, Bulevar Despota Stefana 142, 11000Belgrade, Serbia
Miroljub Trifunovic
Affiliation:
Department of Otorhinolaryngology and Maxillofacial Surgery, General Hospital Studenica, Jug Bogdanova 110, 36000Kraljevo, Serbia
Suzana Pantovic
Affiliation:
Faculty of Medical Sciences, Department of Physiology, University of Kragujevac, Svetozara Markovica 69, 34000Kragujevac, Serbia
Slavoljub Jovic
Affiliation:
Faculty of Veterinary Medicine, Department of Physiology and Biochemistry, University of Belgrade, Bulevar oslobodjenja 18, Belgrade11000, Serbia
Vladimir Jakovljevic
Affiliation:
Faculty of Medical Sciences, Department of Physiology, University of Kragujevac, Svetozara Markovica 69, 34000Kragujevac, Serbia Department of Human Pathology, I.M. Sechenov First Moscow State Medical University, Moscow119992, Russian Federation
Sergey Bolevich
Affiliation:
Department of Human Pathology, I.M. Sechenov First Moscow State Medical University, Moscow119992, Russian Federation
Zoran Milosavljevic
Affiliation:
Faculty of Medical Science, Department of Histology and Embryology, University of Kragujevac, Svetozara Markovica 69, 34 000Kragujevac, Serbia
Verica Milosevic
Affiliation:
Department of Cytology, Institute for Biological Research “Sinisa Stankovic” – National Institute of Republic of Serbia, University of Belgrade, Bulevar Despota Stefana 142, 11000Belgrade, Serbia
*
*Author for correspondence: Ivan Srejovic, E-mail: [email protected]
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Abstract

The aim of the study was to investigate the effects of chronic nandrolone decanoate treatment and/or swimming training on immunohistomorphometric parameters on rat pituitary gonadotropic cells. Male Wistar albino rats, 10 weeks old, were classified into four groups: control (T−N−), nandrolone (T−N+), swimming training (T+N−), and swimming training with nandrolone (T+N+). The T+ groups swam for 4 weeks, 1 h/day, 5 days/week. The N+ groups received nandrolone decanoate (20 mg/kg) once per week for 4 weeks. Pituitary tissue sections were processed and stained for immunohistochemical analysis and immunofluorescence. The volume density of luteinizing hormone (LH) cells was decreased by 48% in T−N+ and for 35% in the T+N+ group. The volume density of follicle-stimulating hormone (FSH) cells was decreased by 39% in T−N+ and for 30% in T+N+ compared to the control. Nandrolone alone, or combined with swimming training, decreased the number of LH/FSH cells compared to the control. The levels of the immunofluorescent signal of LH/FSH cells were increased in all experimental groups. Nandrolone alone decreased the serum level of LH by 17%, whereas swimming training alone increased FSH levels by 11% compared to the control. Serum levels of testosterone were increased in all experimental groups. Nandrolone alone, or combined with swimming training, decreased immunohistomorphometric parameters of gonadotropic cells, whereas the levels of immunofluorescent signal were increased.

Type
Biological Applications
Copyright
Copyright © Microscopy Society of America 2020

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References

Arisha, AH & Moustafa, A (2019). Potential inhibitory effect of swimming exercise on the Kisspeptin-GnRH signaling pathway in male rats. Theriogenology 133, 8796.CrossRefGoogle ScholarPubMed
Bijlsma, JW, Duursma, SA, Thijssen, JH & Huber, O (1982). Influence of nandrolondecanoate on the pituitary-gonadal axis in males. Acta Endocrinol (Copenh) 101, 108112.CrossRefGoogle ScholarPubMed
De Piccoli, B, Giada, F, Benettin, A, Sartori, F & Piccolo, E (1991). Anabolic steroid use in body builders: An echocardiographic study of left ventricle morphology and function. Int J Sports Med 12, 408412.CrossRefGoogle ScholarPubMed
Evans, NA (2004). Current concepts in anabolic-androgenic steroids. Am J Sports Med 32, 534542.CrossRefGoogle ScholarPubMed
Fauquier, T, Lacampagne, A, Travo, P, Bauer, K & Mollard, P (2002). Hidden face of the anterior pituitary. Trends Endocrinol Metab 13, 304309.CrossRefGoogle ScholarPubMed
Ferrari, F, de Paiva Foletto, M, Franzói de Moraes, SM, Barnabé Peres, S, Segatelli, TM & Edna Mareze da Costa, S (2013). Testis morphophysiology of rats treated with nandrolone decanoate and submitted to physical training. Acta Sci 35, 161167.Google Scholar
Frankenfeld, SP, de Oliveira, LP, Ignacio, DL, Coelho, RG, Mattos, MN, Ferreira, AC, Carvalho, DP & Fortunato, RS (2014). Nandrolone decanoate inhibits gluconeogenesis and decreases fasting glucose in Wistar male rats. J Endocrinol 220, 143153.CrossRefGoogle ScholarPubMed
Gårevik, N, Börjesson, A, Choong, E, Ekström, L & Lehtihet, M (2016). Impact of single-dose nandrolone decanoate on gonadotropins, blood lipids and HMG CoA reductase in healthy men. Andrologia 48, 595600.CrossRefGoogle ScholarPubMed
Hackney, AC (2001). Endurance exercise training and reproductive endocrine dysfunction in man: Alterations in the hypothalamic-pituitary-testicular axis. Curr Pharm Des 7, 261273.CrossRefGoogle ScholarPubMed
Hackney, AC, Sinning, WE & Bruot, BC (1990). Hypothalamic-pituitary-testicular axis function in endurance trained male. Int J Sports Med 11, 298303.CrossRefGoogle Scholar
Hassan, AF & Kamal, MM (2013). Effect of exercise training and anabolic androgenic steroids on hemodynamics, glycogen content, angiogenesis and apoptosis of cardiac muscle in adult male rats. Int J Health Sci (Qassim) 7, 4760.CrossRefGoogle ScholarPubMed
Janssen, JA (2016). Impact of physical exercise on endocrine aging. Front Horm Res 47, 6881.CrossRefGoogle ScholarPubMed
Mabuchi, Y, Shirasawa, N, Sakuma, E, Hashimoto, Y, Kuno, M, Coombs, RJ, Herbert, DC & Soji, T (2004). Intercellular communication within the rat anterior pituitary: Relationship between LH-RH neurons and folliculo-stellate cells in the pars tuberalis. Cell Tissue Res 317, 7990.CrossRefGoogle ScholarPubMed
Manna, I, Jana, K & Samanta, PK (2003). Effect of intensive exercise-induced testicular gametogenic and steroidogenic disorders in mature male Wistar strain rats: A correlative approach to oxidative stress. Acta Physiol Scand 178, 3340.CrossRefGoogle ScholarPubMed
Mohamed, HM & Mohamed, MA (2015). Effects of different doses of nandrolone decanoate on lipid peroxidation, DNA fragmentation, sperm abnormality and histopathology of testes of male Wister rats. Exp Toxicol Pathol 67, 111.CrossRefGoogle ScholarPubMed
Nagata, S, Kurosawa, M, Mima, K, Nambo, Y, Fujii, Y, Watanabe, G & Taya, K (1999). Effects of anabolic steroid (19-nortestosterone) on the secretion of testicular hormones in the stallion. J Reprod Fertil 115, 373379.CrossRefGoogle ScholarPubMed
Naraghi, MA, Abolhasani, F, Kashani, I, Anarkooli, IJ, Hemadi, M, Azami, A, Barbarestani, M, Aitken, RJ & Shokri, S (2010). Тhe effects of swimming exercise and supraphysiological doses of nandrolone decanoate on the testis in a adult male rat: A transmission electronic microscope study. Folia Morphol (Warsz) 69(3), 138–46.Google Scholar
Nieschlag, E & Vorona, E (2015). Doping with AAS: Adverse effects on non-reproductive organs and function. Rev Endocr Metab Disord 16, 199211.CrossRefGoogle Scholar
Noguchi, K, Arita, J, Nagamoto, A, Hosaka, M & Kimura, F (1996). A quantitative analysis of testosterone action on FSH secretion from individual pituitary cells using the cell immunoblot assay. J. Endocrinol 148, 427433.CrossRefGoogle ScholarPubMed
Piacentino, D, Kotzalidis, GD, Del Casale, A, Aromatario, MR, Pomara, C, Girardi, P & Sani, G (2015). Anabolic-androgenic steroids use and psychopathology in athletes. A systematic review. Curr Neuropharmacol 13, 11011121.CrossRefGoogle ScholarPubMed
Ristić, N, Ajdžanović, V, Petrović-Kosanović, D, Miler, M, Ušćebrka, G & Milošević, V (2019). Immunohistomorphometric changes of the pituitary gonadotropic cells after testosterone application in a rat model of the andropause. Mac Vet Rev 42, 513.CrossRefGoogle Scholar
Rivier, C & Vale, W (1985). Effects of corticotropin-releasing factor, neuro-hypophyseal peptides, and catecholamines on pituitary function. Fed Proc 44, 189195.Google Scholar
Rocha, FL, Carmo, EC, Roque, FR, Hashimoto, NY, Rossini, LV, Frimm, C, Aneas, I, Neagro, CE, Krieger, JE & Oliveira, EM (2007). Anabolic steroids induce cardiac renin-angiotensin system and impair the beneficial effects of aerobic training in rats. Am J Physiol Heart Circulation Physiol 293, H3575H3583.CrossRefGoogle ScholarPubMed
Sato, K & Iemitsu, M (2015). Exercise and sex steroid hormones in skeletal muscle. J Steroid Biochem Mol Biol 145, 200205.CrossRefGoogle ScholarPubMed
Selakovic, D, Joksimovic, J, Zaletel, I, Puskas, N, Matovic, M & Rosic, G (2017). The opposite effects of nandrolone decanoate and exercise on anxiety levels in rats may involve alterations in hippocampal parvalbumin-positive interneurons. PLoS ONE 12, e0189595.CrossRefGoogle ScholarPubMed
Shahraki, MR, Mirshekari, H & Shahraki, AR (2015). Chronic administration of high doses of nandrolone decanoate on the pituitary-gonadal axis in male rats. Int J High Risk Behav Addict 4(3), e24419.CrossRefGoogle ScholarPubMed
Sretenovic, J, Zivkovic, V, Srejovic, I & Milosavljevic, Z (2016). The effects of high doses of nandrolone decanoate on cardiac muscle tissue. SJECR 17, 303308.Google Scholar
Stokes, KA, Gilbert, KL, Hall, GM, Andrews, RC & Thompson, D (2013). Different responses of selected hormones to three types of exercise in young men. Eur J Appl Physiol 113, 775783.CrossRefGoogle ScholarPubMed
Sugizaki, MM, Dal Pai-Silva, M, Carvalho, RF, Padovani, CR, Bruno, A, Nascimento, AF, Aragon, FF, Novelli, E & Cicogna, AC (2006). Exercise training increases myocardial inotropic response in food restricted rats. Int J Cardiol 112, 191201.CrossRefGoogle ScholarPubMed
Takahashi, M, Tatsugi, Y & Kohno, T (2004). Endocrinological and pathological effects of anabolic-androgenic steroid in male rat. Endocr J 51, 425434.CrossRefGoogle Scholar
Tanno, AP, das Neves, VJ, Rosa, KT, Cunha, TS, Giordano, FC, Calil, CM, Guzzoni, V, Fenandes, T, de Oliveira, EM, Novaes, PD, Irigoyen, MC, Moura, MJ & Marcondes, FK (2011). Nandrolone and resistance training induce heart remodeling: Role of fetal genes and implications for cardiac pathophysiology. Life Sci 89, 631637.CrossRefGoogle ScholarPubMed
Wang, Y, Wisloff, U & Kemi, OJ (2010). Animal models in the study of exercise-induced cardiac hypertrophy. Physiol Res 59, 633644.Google Scholar
Yesalis, CE & Bahrke, MS (1995). Anabolic-androgenic steroids. Current issues. Sports Med 19, 326340.CrossRefGoogle ScholarPubMed