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Neurochemical consequence of steroid abuse: Stanozolol-induced monoaminergic changes
► In a rat model of AAS abuse stanozolol induces behavioural changes. ► These changes are related to the pathophysiology of major depressive disorder. ► We used the model of AAS abuse to examine monoaminergic systems. ► The monoaminergic system is a neurobiological substrate of depression. ► Our dat...
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Published in: | Steroids 2012-02, Vol.77 (3), p.269-275 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ► In a rat model of AAS abuse stanozolol induces behavioural changes. ► These changes are related to the pathophysiology of major depressive disorder. ► We used the model of AAS abuse to examine monoaminergic systems. ► The monoaminergic system is a neurobiological substrate of depression. ► Our data indicate that stanozolol affects brain monoamines involved in depression.
An extensive literature has documented adverse effects on mental health in anabolic androgenic steroids (AAS) abusers. Depression seems a common adverse reaction in AAS abusers. Recently it has been reported that in a rat model of AAS abuse stanozolol induces behavioural and biochemical changes related to the pathophysiology of major depressive disorder. In the present study, we used the model of AAS abuse to examine possible changes in the monoaminergic system, a neurobiological substrate of depression, in different brain areas of stanozolol-treated animals. Wistar rats received repeated injections of stanozolol (5
mg/kg, s.c.), or vehicle (propylene glycol, 1
ml/kg) once daily for 4
weeks. Twenty-four hours after last injection, changes of dopamine (DA) and relative metabolite levels, homovanilic acid (HVA) and 3,4-dihydroxy phenylacetic acid (DOPAC), serotonin (5-HT) and its metabolite levels, 5-hydroxy indolacetic acid (5-HIAA), and noradrenaline (NA) amount were investigated in prefrontal cortex (PFC), nucleus accumbens (NAC), striatum (STR) and hippocampus (HIPP). The analysis of data showed that after chronic stanozolol, DA levels were increased in the HIPP and decreased in the PFC. No significant changes were observed in the STR or in the NAC. 5-HT and 5-HIAA levels were decreased in all brain areas investigated after stanozolol exposure; however, the 5-HIAA/5-HT ratio was not altered. Taken together, our data indicate that chronic use of stanozolol significantly affects brain monoamines leading to neurochemical modifications possibly involved in depression and stress-related states. |
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ISSN: | 0039-128X 1878-5867 |
DOI: | 10.1016/j.steroids.2011.12.014 |