Drug Res (Stuttg) 2015; 65(1): 1-4
DOI: 10.1055/s-0033-1364000
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

An Intra-hippocampal Injection of Nandrolone Induces Learning and Memory Impairments in Rat

A. Karamian
1   Department of Biology, Faculty of Science, Urmia University, Urmia, Iran
,
F. G. Pakdel
2   Department of Physiology, Faculty of Medicine, Urmia University of Medical Science, Urmia, Iran
,
M. Ilkhanipoor
1   Department of Biology, Faculty of Science, Urmia University, Urmia, Iran
,
F. Farokhi
1   Department of Biology, Faculty of Science, Urmia University, Urmia, Iran
,
A. Ahmadi
3   Pharmaceutical Sciences Research Center, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran
› Author Affiliations
Further Information

Publication History

received 10 December 2013

accepted 18 December 2013

Publication Date:
22 January 2014 (online)

Abstract

This study was investigated to evaluate the effect of intra-hippocampal injection of the nandrolone on spatial learning task in rats. The drug or vehicle was manually injected into the hippocampus with a 10-µl Hamilton syringe attached via polyethylene tubing to 27-gauge stainless-steel injection cannula. After 6 days of recovery, learning behaviors were evaluated using an 8-arm radial maze. The results showed that intra-hippocampal injection of nandrolone can impair trained spatial learning at a dose of 5 µl. We also observed a dense cytoplasm and nucleus in CA1 neurons as well as signs of necrosis. Nandrolone can impair the time required to reach the baited arm as well as the frequency of successful arm entries. At the 10 µl dose of nandrolone, neural hypertrophy and increased dentate gyrus volume were also observed.

 
  • References

  • 1 Basaria S, Wahlstrom JT, Dobs AS. Anabolic-androgenic steroid therapy in the treatment of chronic diseases. Journal of Clinical Endocrinology & Metabolism 2001; 86: 5108-5117
  • 2 Lukas SE. Current perspectives on anabolic-androgenic steroid abuse. Trends in pharmacological sciences 1993; 14: 61-68
  • 3 Eklöf AC, Thurelius AM, Garle M et al. The anti-doping hot-line, a means to capture the abuse of doping agents in the Swedish society and a new service function in clinical pharmacology. European journal of clinical pharmacology 2003; 59: 571-577
  • 4 Perry PJ, Andersen KH, Yates WR. Illicit anabolic steroid use in athletes A case series analysis. The American Journal of Sports Medicine 1990; 18: 422-428
  • 5 Verroken M. Ethical aspects and the prevalence of hormone abuse in sport. Journal of endocrinology 2001; 170: 49-54
  • 6 Magnusson K, Birgner C, Bergström L et al. Nandrolone decanoate administration dose-dependently affects the density of kappa opioid peptide receptors in the rat brain determined by autoradiography. Neuropeptides 2009; 43: 105-111
  • 7 Magnusson K, Hallberg M, Bergquist J et al. Enzymatic conversion of dynorphin A in the rat brain is affected by administration of nandrolone decanoate. Peptides 2007; 28: 851
  • 8 Kouvelas D, Pourzitaki C, Papazisis G et al. Nandrolone abuse decreases anxiety and impairs memory in rats via central androgenic receptors. The International Journal of Neuropsychopharmacology 2008; 11: 925-934
  • 9 Su TP, Pagliaro M, Schmidt PJ et al. Neuropsychiatric effects of anabolic steroids in male normal volunteers. JAMA: the journal of the American Medical Association 1993; 269: 2760
  • 10 Paxinos G, Watson C. The rat brain in stereotaxic coordinates. 6th ed. Amsterdam: Elsevier; 2007
  • 11 Penatti CAA, Costine BA, Porter DM et al. Effects of chronic exposure to an anabolic androgenic steroid cocktail on α5-receptor-mediated GABAergic transmission and neural signaling in the forebrain of female mice. Neuroscience 2009; 161: 526-537
  • 12 Menard CS, Harlan RE. Up-regulation of androgen receptor immunoreactivity in the rat brain by androgenic-anabolic steroids. Brain research 1993; 622: 226-236
  • 13 McDaniel KL, Mundy WR, Tilson HA. Microinjection of dynorphin into the hippocampus impairs spatial learning in rats. Pharmacology Biochemistry and Behavior 1990; 35: 429-435
  • 14 Sandin J, Nylander I, Georgieva J et al. Hippocampal dynorphin B injections impair spatial learning in rats: a κ-opioid receptor-mediated effect. Neuroscience 1998; 85: 375-382
  • 15 Rossbach ULW, Steensland P, Nyberg F et al. Nandrolone-induced hippocampal phosphorylation of NMDA receptor subunits and ERKs. Biochemical and biophysical research communications 2007; 357: 1028-1033
  • 16 Kindlundh A, Rahman S, Lindblom J et al. Increased dopamine transporter density in the male rat brain following chronic nandrolone decanoate administration. Neuroscience letters 2004; 356: 131-134
  • 17 Kurling S, Kankaanpää A, Ellermaa S et al. The effect of sub-chronic nandrolone decanoate treatment on dopaminergic and serotonergic neuronal systems in the brains of rats. Brain research 2005; 1044: 67-75
  • 18 Thiblin I, Finn A, Ross SB et al. Increased dopaminergic and 5-hydroxytryptaminergic activities in male rat brain following long-term treatment with anabolic androgenic steroids. British journal of pharmacology 2009; 126: 1301-1306