CC BY-NC-ND 4.0 · Journal of Morphological Sciences 2015; 32(01): 033-036
DOI: 10.4322/jms.071614
Original Article
Thieme Revinter Publicações Ltda Rio de Janeiro, Brazil

Morphometric analysis of mice's ventricular myocardium submitted to androgenic anabolizing steroids use

D. M. Alves
1   Departamento de Anatomia, Universidade Federal de Alfenas - Unifal, Rua Gabriel Monteiro da Silva, 700, Centro, CEP 37130-000, Alfenas, MG, Brazil
,
M. S. O. Silva
1   Departamento de Anatomia, Universidade Federal de Alfenas - Unifal, Rua Gabriel Monteiro da Silva, 700, Centro, CEP 37130-000, Alfenas, MG, Brazil
,
B. Zavan
1   Departamento de Anatomia, Universidade Federal de Alfenas - Unifal, Rua Gabriel Monteiro da Silva, 700, Centro, CEP 37130-000, Alfenas, MG, Brazil
,
D. A. Nogueira
1   Departamento de Anatomia, Universidade Federal de Alfenas - Unifal, Rua Gabriel Monteiro da Silva, 700, Centro, CEP 37130-000, Alfenas, MG, Brazil
,
G. J. M. Fernandes
1   Departamento de Anatomia, Universidade Federal de Alfenas - Unifal, Rua Gabriel Monteiro da Silva, 700, Centro, CEP 37130-000, Alfenas, MG, Brazil
,
W. C. Rossi Junior
1   Departamento de Anatomia, Universidade Federal de Alfenas - Unifal, Rua Gabriel Monteiro da Silva, 700, Centro, CEP 37130-000, Alfenas, MG, Brazil
,
A. Esteves
1   Departamento de Anatomia, Universidade Federal de Alfenas - Unifal, Rua Gabriel Monteiro da Silva, 700, Centro, CEP 37130-000, Alfenas, MG, Brazil
› Author Affiliations
Further Information

Publication History

14 April 2014

09 July 2015

Publication Date:
08 October 2018 (online)

Abstract

Introduction: Androgenic anabolizing steroids (AAS) are a group of natural and synthetic compounds deriving from testosterone or one of its sub-products which are more and more used by young people for improving physical performance or for aesthetic reason. Complications, such as arteriosclerosis and acute myocardium infarction (AMI), have been reported in AAS' users, but the records about the ventricular anatomical structure of those users are few. Because of that, this study aimed to verify morphologic and quantitative morphometric possible alterations on mice's left ventricular myocardium submitted to their use. Materials and Methods: Thirty mice were divided into three 10-animals groups (group 1: received Deca-Durabolin®; group 2: received Potenay®; and group 3: received saline solution), each one of them composed by five males and five females, treated once a week and put to swimming thrice a week during one month. Results: Results revealed that there were no significant alterations in the quantity of muscle fibers in the animals treated with AAS but there were significant differences when comparing male-to-female mice and left ventricular area (μm2). It was observed that mice in group 1 (Deca-Durabolin®) presented a lesser left ventricular area when compared to those in group 3 (control) but, when analyzing cardiac muscle ibers morphologically, it was veriied that the myocardium was looser and softer in drug-submitted animals, especially those in group 1 (Deca-Durabolin®). Conclusion: There are effective signiicant differences when a morphologic and quantitative morphometric analysis is done concerning mice's left ventricular myocardium submitted to AAS.