The involvement of Transforming Growth Factors in regulation of cellular function in male diabetic rats’ testes is less understood. Adult male Sprague-Dawley rats (120 – 140gm) were divided into 3 groups. Control group (n = 7); fed on normal rat pellets. Streptozotocin diabetic group (n = 7); received a single IP injection of streptozotocin 45 mg/kg BW (Guneli et al., 2008) in Na+ citrate buffer pH 4.5. Insulin resistant group (n = 7); fed ad libitum on special diet containing 25% fructose W/W for 12 weeks (Arikawe et al., 2006; Arikawe et al., 2012). Following hyperglycaemia confirmation, blood samples were collected under light anaesthesia (IM ketamine, 10mg/kg) for serum activin and inhibin (Transforming Growth Factor β) Concentrations. Animals were perfused with 4% Paraformaldehyde (PFA). Testes were isolated and fixed in 4% PFA overnight and embedded in paraffin. 5µm thick sections were made and mounted on poly-L-lysine coated slides. Immunohistochemical analysis was assessed using Androgen receptor (C-19) and Sox-9 antibodies (Santa Cruz Biotechnology, USA) through light microscopy. Serum inhibin was significantly lower (P < 0.05) in the insulin resistant group compared to the control and streptozotocin groups. There was no significant difference in serum activin concentrations amongst the three groups. C-19 and Sox-9 indexes were significantly lower (P < 0.05) in both experimental groups compared to control group. The results of the study indicate that streptozotocin and insulin resistance affect Leydig and Sertoli cell function.
37th Congress of IUPS (Birmingham, UK) (2013) Proc 37th IUPS, PCB287
Poster Communications: Serum transforming growth factor ╬▓ concentrations and primary antibodies immunostaining effects on Leydig and Sertoli Cells in streptozotocin-induced and insulin resistant diabetic adult male rat
A. P. Arikawe1, K. A. Dada2, A. O. Ogunsola3, D. Osiagwu4, B. O. Iranloye5
1. Department of Physiology, College of Medicine of the University of Lagos, Lagos, Lagos, Nigeria. 2. Department of Physiology, College of Medicine of the University of Lagos, Lagos, Lagos, Nigeria. 3. Department of Physiology, College of Medicine of the University of Lagos, Lagos, Lagos, Nigeria. 4. Department of Anatomic and Molecular Pathology, College of Medicine of the University of Lagos, Lagos, Lagos, Nigeria. 5. Department of Physiology, College of Medicine of the University of Lagos, Lagos, Lagos, Nigeria.
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Where applicable, experiments conform with Society ethical requirements.