Cargando…

Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?

Skeletal muscle is a tissue that has recently been recognized for its ability to produce androgens under physiological conditions. The steroidogenesis process is known to be negatively influenced by reactive oxygen species (ROS) in reproductive Leydig and ovary cells, while their effect on muscle st...

Descripción completa

Detalles Bibliográficos
Autores principales: Antinozzi, Cristina, Duranti, Guglielmo, Ceci, Roberta, Lista, Marco, Sabatini, Stefania, Caporossi, Daniela, Di Luigi, Luigi, Sgrò, Paolo, Dimauro, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223901/
https://www.ncbi.nlm.nih.gov/pubmed/35743011
http://dx.doi.org/10.3390/ijms23126566
_version_ 1784733238704472064
author Antinozzi, Cristina
Duranti, Guglielmo
Ceci, Roberta
Lista, Marco
Sabatini, Stefania
Caporossi, Daniela
Di Luigi, Luigi
Sgrò, Paolo
Dimauro, Ivan
author_facet Antinozzi, Cristina
Duranti, Guglielmo
Ceci, Roberta
Lista, Marco
Sabatini, Stefania
Caporossi, Daniela
Di Luigi, Luigi
Sgrò, Paolo
Dimauro, Ivan
author_sort Antinozzi, Cristina
collection PubMed
description Skeletal muscle is a tissue that has recently been recognized for its ability to produce androgens under physiological conditions. The steroidogenesis process is known to be negatively influenced by reactive oxygen species (ROS) in reproductive Leydig and ovary cells, while their effect on muscle steroidogenesis is still an unexplored field. Muscle cells are continuously exposed to ROS, resulting from both their metabolic activity and the surrounding environment. Interestingly, the regulation of signaling pathways, induced by mild ROS levels, plays an important role in muscle fiber adaptation to exercise, in a process that also elicits a significant modulation in the hormonal response. The aim of the present study was to investigate whether ROS could influence steroidogenesis in skeletal muscle cells by evaluating the release of testosterone (T) and dihydrotestosterone (DHT), as well as the evaluation of the relative expression of the key steroidogenic enzymes 5α-reductase, 3β-hydroxysteroid dehydrogenase (HSD), 17β-HSD, and aromatase. C2C12 mouse myotubes were exposed to a non-cytotoxic concentration of hydrogen peroxide (H(2)O(2)), a condition intended to reproduce, in vitro, one of the main stimuli linked to the process of homeostasis and adaptation induced by exercise in skeletal muscle. Moreover, the influence of tadalafil (TAD), a phosphodiesterase 5 inhibitor (PDE5i) originally used to treat erectile dysfunction but often misused among athletes as a “performance-enhancing” drug, was evaluated in a single treatment or in combination with H(2)O(2). Our data showed that a mild hydrogen peroxide exposure induced the release of DHT, but not T, and modulated the expression of the enzymes involved in steroidogenesis, while TAD treatment significantly reduced the H(2)O(2)-induced DHT release. This study adds a new piece of information about the adaptive skeletal muscle cell response to an oxidative environment, revealing that hydrogen peroxide plays an important role in activating muscle steroidogenesis.
format Online
Article
Text
id pubmed-9223901
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-92239012022-06-24 Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis? Antinozzi, Cristina Duranti, Guglielmo Ceci, Roberta Lista, Marco Sabatini, Stefania Caporossi, Daniela Di Luigi, Luigi Sgrò, Paolo Dimauro, Ivan Int J Mol Sci Article Skeletal muscle is a tissue that has recently been recognized for its ability to produce androgens under physiological conditions. The steroidogenesis process is known to be negatively influenced by reactive oxygen species (ROS) in reproductive Leydig and ovary cells, while their effect on muscle steroidogenesis is still an unexplored field. Muscle cells are continuously exposed to ROS, resulting from both their metabolic activity and the surrounding environment. Interestingly, the regulation of signaling pathways, induced by mild ROS levels, plays an important role in muscle fiber adaptation to exercise, in a process that also elicits a significant modulation in the hormonal response. The aim of the present study was to investigate whether ROS could influence steroidogenesis in skeletal muscle cells by evaluating the release of testosterone (T) and dihydrotestosterone (DHT), as well as the evaluation of the relative expression of the key steroidogenic enzymes 5α-reductase, 3β-hydroxysteroid dehydrogenase (HSD), 17β-HSD, and aromatase. C2C12 mouse myotubes were exposed to a non-cytotoxic concentration of hydrogen peroxide (H(2)O(2)), a condition intended to reproduce, in vitro, one of the main stimuli linked to the process of homeostasis and adaptation induced by exercise in skeletal muscle. Moreover, the influence of tadalafil (TAD), a phosphodiesterase 5 inhibitor (PDE5i) originally used to treat erectile dysfunction but often misused among athletes as a “performance-enhancing” drug, was evaluated in a single treatment or in combination with H(2)O(2). Our data showed that a mild hydrogen peroxide exposure induced the release of DHT, but not T, and modulated the expression of the enzymes involved in steroidogenesis, while TAD treatment significantly reduced the H(2)O(2)-induced DHT release. This study adds a new piece of information about the adaptive skeletal muscle cell response to an oxidative environment, revealing that hydrogen peroxide plays an important role in activating muscle steroidogenesis. MDPI 2022-06-12 /pmc/articles/PMC9223901/ /pubmed/35743011 http://dx.doi.org/10.3390/ijms23126566 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Antinozzi, Cristina
Duranti, Guglielmo
Ceci, Roberta
Lista, Marco
Sabatini, Stefania
Caporossi, Daniela
Di Luigi, Luigi
Sgrò, Paolo
Dimauro, Ivan
Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?
title Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?
title_full Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?
title_fullStr Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?
title_full_unstemmed Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?
title_short Hydrogen Peroxide Stimulates Dihydrotestosterone Release in C2C12 Myotubes: A New Perspective for Exercise-Related Muscle Steroidogenesis?
title_sort hydrogen peroxide stimulates dihydrotestosterone release in c2c12 myotubes: a new perspective for exercise-related muscle steroidogenesis?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223901/
https://www.ncbi.nlm.nih.gov/pubmed/35743011
http://dx.doi.org/10.3390/ijms23126566
work_keys_str_mv AT antinozzicristina hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis
AT durantiguglielmo hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis
AT ceciroberta hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis
AT listamarco hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis
AT sabatinistefania hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis
AT caporossidaniela hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis
AT diluigiluigi hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis
AT sgropaolo hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis
AT dimauroivan hydrogenperoxidestimulatesdihydrotestosteronereleaseinc2c12myotubesanewperspectiveforexerciserelatedmusclesteroidogenesis