Literature DB >> 21443508

Anabolic androgenic steroids abuse and liver toxicity.

M Neri1, S Bello, A Bonsignore, S Cantatore, I Riezzo, E Turillazzi, V Fineschi.   

Abstract

In the athletes the wide use of Anabolic Androgenic Steroids (AAS) cause series damage in various organs, in particular, analyzing the liver, elevation on the levels of liver enzymes, cholestatic jaundice, liver tumors, both benign and malignant, and peliosis hepatis are described. A prolonged AAS administration provokes an increase in the activities of liver lysosomal hydrolases and a decrease in some components of the microsomal drug-metabolizing system and in the activity of the mitochondrial respiratory chain complexes without modifying classical serum indicators of hepatic function. Liver is a key organ actively involved in numerous metabolic and detoxifying functions. As a consequence, it is continuously exposed to high levels of endogenous and exogenous oxidants that are by-products of many biochemical pathways and, in fact, it has been demonstrated that intracellular oxidant production is more active in liver than in tissues, like the increase of inflammatory cytokines, apoptosis and the inhibitors of apoptosis NF- κB and Heat Shock Proteins.

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Year:  2011        PMID: 21443508     DOI: 10.2174/138955711795445916

Source DB:  PubMed          Journal:  Mini Rev Med Chem        ISSN: 1389-5575            Impact factor:   3.862


  18 in total

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7.  Boldenone Undecylenate-Mediated Hepatorenal Impairment by Oxidative Damage and Dysregulation of Heat Shock Protein 90 and Androgen Receptors Expressions: Vitamin C Preventive Role.

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Review 8.  Neurotoxicity by synthetic androgen steroids: oxidative stress, apoptosis, and neuropathology: A review.

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9.  Anabolic steroids abuse and male infertility.

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10.  The anabolic androgenic steroid nandrolone decanoate disrupts redox homeostasis in liver, heart and kidney of male Wistar rats.

Authors:  Stephan P Frankenfeld; Leonardo P Oliveira; Victor H Ortenzi; Igor C C Rego-Monteiro; Elen A Chaves; Andrea C Ferreira; Alvaro C Leitão; Denise P Carvalho; Rodrigo S Fortunato
Journal:  PLoS One       Date:  2014-09-16       Impact factor: 3.240

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