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Effects of chronic inhibition of Testosterone metabolism on cardiac remodeling after ischemia/reperfusion-induced myocardial damage in gonadectomized rats
Author(s) -
Octavio Maldonado,
Ángel Ramos-Ligonio,
Mario R.B. GuapilloVargas,
José María Rivera,
Ícela Palma-Lara,
Iván Rubio-Gayosso,
Israel RamírezSánchez,
Nayelli Nájera,
Guillermo Ceballos,
Enrique Méndez-Bolaina
Publication year - 2019
Publication title -
biology open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.936
H-Index - 41
ISSN - 2046-6390
DOI - 10.1242/bio.041905
Subject(s) - testosterone (patch) , biology , myocardial ischemia , ventricular remodeling , ischemia , medicine , cardiology , metabolism , reperfusion injury , endocrinology , myocardial infarction
The effects of testosterone on cardiovascular homeostasis are still not well understood. The objective of this work was to evaluate the effects of testosterone in the absence or presence of inhibition of Aromatase (4-hydroxyandrostenedione) and/or 5α reductase (Finasteride) enzymatic activities on the myocardial remodeling 30 days after ischemia/reperfusion (I/R) injury in gonadectomized rats. Results showed that testosterone administration to ORX rats resulted in decreased myocardial damaged area, inflammatory infiltrates and reduced MMP-3 and 13 expressions. Interestingly, Finasteride administration resulted in a greater decrease in scar tissue, inflammatory infiltrates, along with a significant decrease in MMP-3 and 13 expressions. In contrast, 4-hydroxyandrostenedione administrations increased all parameters. Our results suggest that testosterone does not have a direct effect since simultaneous inhibition of aromatase and 5α-reductase did not induce significant changes in I/R induced myocardial injury.

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