Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage

Detalhes bibliográficos
Autor(a) principal: Infante, Nick Alexandre
Data de Publicação: 2025
Outros Autores: Faria, Vinicius Silva, Cornachione, Anabelle Silva, Barros Manchado-Gobatto, Fúlvia, Zagatto, Alessandro Moura [UNESP], Beck, Wladimir Rafael
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s11332-025-01363-4
https://hdl.handle.net/11449/299798
Resumo: Introduction: Exercise-induced muscle damage (EIMD) triggers several events that will initiate the repair process of this tissue through the activation of satellite cells (SC). The transcription factor PAX7 is used as a SC marker, being expressed during the quiescence, activation, and proliferation of these cells. The literature presents some therapeutic resources aimed at reducing damage or accelerating the muscle repair, acting on inflammation or oxidative stress. Among such therapeutic resources, we can find the melatonin administration, a hormone with anti-inflammatory, antiapoptotic, and antioxidant actions. Purpose: This study aims to analyze the effects of melatonin on PAX7 after EIMD. Methods: Sixty-five male Wistar rats were divided into seven groups: control (CTG), which received vehicle solution (ethanol and NaCl) and were euthanized at 98 days old, and six groups that received melatonin (EMG) or not (EG) immediately after the skeletal muscle damage induction protocol (SMDIP) through swimming exercise, being euthanized 24, 48, or 72 h after the SMDIP, denominated EG24, EG48, EG72, EMG24, EMG48, and EMG72. Results: There was an effect of time showing higher serum creatine kinase 48 h after SMDIP (F = 3.27; p < 0.05) compared to 24 or 72 h after. However, the group EMG48 showed a significant reduction (p = 0.010) in the concentration of this enzyme in relation to EG48. There was a reduction in PAX7 in animals that received melatonin in comparison with those that received vehicle solution (F = 13.90; p = 0.001). Conclusion: Melatonin reduced muscle damage, demonstrated by the decrease of CK-MM and PAX7.
id UNSP_4661611bcb43e0df35aa5ec7091d2dfb
oai_identifier_str oai:repositorio.unesp.br:11449/299798
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damageMuscle repairN-Acetyl-5-methoxytryptamineRatsSatellite cell markerSwimmingIntroduction: Exercise-induced muscle damage (EIMD) triggers several events that will initiate the repair process of this tissue through the activation of satellite cells (SC). The transcription factor PAX7 is used as a SC marker, being expressed during the quiescence, activation, and proliferation of these cells. The literature presents some therapeutic resources aimed at reducing damage or accelerating the muscle repair, acting on inflammation or oxidative stress. Among such therapeutic resources, we can find the melatonin administration, a hormone with anti-inflammatory, antiapoptotic, and antioxidant actions. Purpose: This study aims to analyze the effects of melatonin on PAX7 after EIMD. Methods: Sixty-five male Wistar rats were divided into seven groups: control (CTG), which received vehicle solution (ethanol and NaCl) and were euthanized at 98 days old, and six groups that received melatonin (EMG) or not (EG) immediately after the skeletal muscle damage induction protocol (SMDIP) through swimming exercise, being euthanized 24, 48, or 72 h after the SMDIP, denominated EG24, EG48, EG72, EMG24, EMG48, and EMG72. Results: There was an effect of time showing higher serum creatine kinase 48 h after SMDIP (F = 3.27; p < 0.05) compared to 24 or 72 h after. However, the group EMG48 showed a significant reduction (p = 0.010) in the concentration of this enzyme in relation to EG48. There was a reduction in PAX7 in animals that received melatonin in comparison with those that received vehicle solution (F = 13.90; p = 0.001). Conclusion: Melatonin reduced muscle damage, demonstrated by the decrease of CK-MM and PAX7.Laboratory of Endocrine Physiology and Physical Exercise Department of Physiological Sciences Federal University of São Carlos - UFSCarSchool of Health and Human Performance Dublin City UniversityMuscle Physiology and Biophysics Laboratory Department of Physiological Sciences Federal University of São Carlos - UFSCarLaboratory of Applied Sport Physiology School of Applied Sciences University of Campinas - UNICAMPLaboratory of Physiology and Sports Performance Department of Physical Education School of Science - Bauru Campus São Paulo State University – UNESPLaboratory of Physiology and Sports Performance Department of Physical Education School of Science - Bauru Campus São Paulo State University – UNESPUniversidade Federal de São Carlos (UFSCar)Dublin City UniversityUniversidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (UNESP)Infante, Nick AlexandreFaria, Vinicius SilvaCornachione, Anabelle SilvaBarros Manchado-Gobatto, FúlviaZagatto, Alessandro Moura [UNESP]Beck, Wladimir Rafael2025-04-29T18:43:30Z2025-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s11332-025-01363-4Sport Sciences for Health.1825-12341824-7490https://hdl.handle.net/11449/29979810.1007/s11332-025-01363-42-s2.0-105000056465Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengSport Sciences for Healthinfo:eu-repo/semantics/openAccess2025-06-24T05:42:18Zoai:repositorio.unesp.br:11449/299798Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-06-24T05:42:18Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage
title Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage
spellingShingle Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage
Infante, Nick Alexandre
Muscle repair
N-Acetyl-5-methoxytryptamine
Rats
Satellite cell marker
Swimming
title_short Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage
title_full Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage
title_fullStr Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage
title_full_unstemmed Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage
title_sort Melatonin decreases PAX7 and CK increment after exercise-induced skeletal muscle damage
author Infante, Nick Alexandre
author_facet Infante, Nick Alexandre
Faria, Vinicius Silva
Cornachione, Anabelle Silva
Barros Manchado-Gobatto, Fúlvia
Zagatto, Alessandro Moura [UNESP]
Beck, Wladimir Rafael
author_role author
author2 Faria, Vinicius Silva
Cornachione, Anabelle Silva
Barros Manchado-Gobatto, Fúlvia
Zagatto, Alessandro Moura [UNESP]
Beck, Wladimir Rafael
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Carlos (UFSCar)
Dublin City University
Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Infante, Nick Alexandre
Faria, Vinicius Silva
Cornachione, Anabelle Silva
Barros Manchado-Gobatto, Fúlvia
Zagatto, Alessandro Moura [UNESP]
Beck, Wladimir Rafael
dc.subject.por.fl_str_mv Muscle repair
N-Acetyl-5-methoxytryptamine
Rats
Satellite cell marker
Swimming
topic Muscle repair
N-Acetyl-5-methoxytryptamine
Rats
Satellite cell marker
Swimming
description Introduction: Exercise-induced muscle damage (EIMD) triggers several events that will initiate the repair process of this tissue through the activation of satellite cells (SC). The transcription factor PAX7 is used as a SC marker, being expressed during the quiescence, activation, and proliferation of these cells. The literature presents some therapeutic resources aimed at reducing damage or accelerating the muscle repair, acting on inflammation or oxidative stress. Among such therapeutic resources, we can find the melatonin administration, a hormone with anti-inflammatory, antiapoptotic, and antioxidant actions. Purpose: This study aims to analyze the effects of melatonin on PAX7 after EIMD. Methods: Sixty-five male Wistar rats were divided into seven groups: control (CTG), which received vehicle solution (ethanol and NaCl) and were euthanized at 98 days old, and six groups that received melatonin (EMG) or not (EG) immediately after the skeletal muscle damage induction protocol (SMDIP) through swimming exercise, being euthanized 24, 48, or 72 h after the SMDIP, denominated EG24, EG48, EG72, EMG24, EMG48, and EMG72. Results: There was an effect of time showing higher serum creatine kinase 48 h after SMDIP (F = 3.27; p < 0.05) compared to 24 or 72 h after. However, the group EMG48 showed a significant reduction (p = 0.010) in the concentration of this enzyme in relation to EG48. There was a reduction in PAX7 in animals that received melatonin in comparison with those that received vehicle solution (F = 13.90; p = 0.001). Conclusion: Melatonin reduced muscle damage, demonstrated by the decrease of CK-MM and PAX7.
publishDate 2025
dc.date.none.fl_str_mv 2025-04-29T18:43:30Z
2025-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s11332-025-01363-4
Sport Sciences for Health.
1825-1234
1824-7490
https://hdl.handle.net/11449/299798
10.1007/s11332-025-01363-4
2-s2.0-105000056465
url http://dx.doi.org/10.1007/s11332-025-01363-4
https://hdl.handle.net/11449/299798
identifier_str_mv Sport Sciences for Health.
1825-1234
1824-7490
10.1007/s11332-025-01363-4
2-s2.0-105000056465
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Sport Sciences for Health
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
_version_ 1851767067725791232