Anabolic-androgenic steroids induce apoptotic cell death in adult rat ventricular myocytes

J Cell Physiol. 2001 Apr;187(1):90-5. doi: 10.1002/1097-4652(2001)9999:9999<00::AID-JCP1057>3.0.CO;2-Y.

Abstract

We tested whether exposure to anabolic-androgenic steroids (AASs) would induce apoptosis in adult rat ventricular myocytes in vitro. Myocytes were exposed to stanozolol (STZ), testosterone enanthate (TE) and testosterone (T) (0.1 micromol/L, 1 micromol/L, 10 micromol/L, and 100 micromol/L) for 20 h. The percentage of myocytes undergoing apoptosis was determined by terminal deoxynucleotidyl transferase-mediated nick end labeling (TUNEL) and was found to be increased when compared to control myocytes at STZ 10 micromol/L 12 +/- 2% (mean +/- SD), STZ 100 micromol/L 42 +/- 3%; TE 1 micromol/L 11 +/- 2%, TE 10 micromol/L 21 +/- 3%, TE 100 micromol/L 62 +/- 2%; T 10 micromol/L 11 +/- 2%, T 100 micromol/L 40 +/- 3% (P < 0.001 vs. CTL 2 +/- 2%). The STZ-, TE- and T-induced dose-dependent apoptotic cell death was corroborated by a significantly increased DNA laddering in myocytes exposed to STZ and T > or = 10 micromol/L and TE > or = 1 micromol/L. Notably, STZ, TE, and T exposure markedly increased the expression of the pro-apoptotic oncogene Bax-alpha, as assessed by reverse transcription-polymerase chain reaction. Taken together, these results clearly show for the first time that AASs induce apoptotic cell death in a dose-dependent manner. This finding may have important implications in understanding the pathogenesis of ventricular remodeling, cardiomyopathy, and sudden cardiac death associated with AAS abuse.

MeSH terms

  • Anabolic Agents / administration & dosage
  • Anabolic Agents / pharmacology*
  • Animals
  • Apoptosis / drug effects*
  • Cell Nucleus / ultrastructure
  • Cell Survival / drug effects
  • Cells, Cultured
  • DNA Fragmentation / drug effects
  • Dose-Response Relationship, Drug
  • Heart / drug effects*
  • Heart Ventricles / cytology
  • In Situ Nick-End Labeling
  • Male
  • Myocardium / cytology
  • Myocardium / metabolism
  • Proto-Oncogene Proteins / biosynthesis
  • Proto-Oncogene Proteins c-bcl-2*
  • Rats
  • Rats, Sprague-Dawley
  • Stanozolol / administration & dosage
  • Stanozolol / pharmacology*
  • Testosterone / administration & dosage
  • Testosterone / analogs & derivatives*
  • Testosterone / pharmacology*
  • Transcriptional Activation
  • bcl-2-Associated X Protein

Substances

  • Anabolic Agents
  • Bax protein, rat
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Testosterone
  • Stanozolol
  • testosterone enanthate