Erythromycin has therapeutic efficacy on muscle fatigue acting specifically on orosomucoid to increase muscle bioenergetics and physiological parameters of endurance.
AMP-Activated Protein Kinases
/ metabolism
Adenosine Triphosphate
/ metabolism
Animals
Cell Line
Energy Metabolism
/ drug effects
Erythromycin
/ pharmacology
Gene Expression Regulation
Glycogen
/ metabolism
Humans
Male
Mice, Inbred C57BL
Mitochondria, Muscle
/ drug effects
Muscle Fatigue
/ drug effects
Muscle, Skeletal
/ drug effects
Orosomucoid
/ genetics
Physical Endurance
/ drug effects
Receptors, CCR5
/ metabolism
Running
Signal Transduction
Swimming
Time Factors
AMPK
C-C motif chemokine receptor 5 (CCR5)
erythromycin
glycogen
muscle endurance
orosomucoid (ORM)
Journal
Pharmacological research
ISSN: 1096-1186
Titre abrégé: Pharmacol Res
Pays: Netherlands
ID NLM: 8907422
Informations de publication
Date de publication:
11 2020
11 2020
Historique:
received:
15
01
2020
revised:
12
07
2020
accepted:
31
07
2020
pubmed:
11
8
2020
medline:
2
9
2021
entrez:
11
8
2020
Statut:
ppublish
Résumé
At present, there are still no official or semi-official recommendations for the treatment of muscle fatigue. We previously reported that acute phase protein orosomucoid (ORM) can enhance muscle endurance and exert anti-fatigue effect. In attempting to seek anti-fatigue drugs that target ORM, we found macrolide antibiotics, particularly erythromycin, were effective. Erythromycin can significantly prolong the time of mice forced-swimming and treadmill running, increase muscle fatigue index, alleviate fatigue-induced tissue damage, and elevate glycogen content, mitochondria function and ATP level in the muscle. Also, erythromycin increases ORM protein expression in a dose- and time- dependent manner both in vitro and in vivo. Further studies found that erythromycin could increase the activity of ORM promoter and the stability of ORM mRNA, which might both be responsible for the ORM up-regulation. ORM knockdown or knockout could abolish the promoting effect of erythromycin in mice forced-swimming time, muscle fatigue index and glycogen level. Furthermore, those effects were also abolished in mice with C-C motif chemokine receptor 5 (CCR5) antagonist administration or AMPKα2 deficiency. Therefore, erythromycin could enhance muscle glycogen and endurance via up-regulating the level of ORM and activating CCR5-AMPK pathway, indicating it might act as a potential drug to treat muscle fatigue.
Identifiants
pubmed: 32777256
pii: S1043-6618(20)31426-2
doi: 10.1016/j.phrs.2020.105118
pii:
doi:
Substances chimiques
CCR5 protein, mouse
0
Orosomucoid
0
Receptors, CCR5
0
Erythromycin
63937KV33D
Adenosine Triphosphate
8L70Q75FXE
Glycogen
9005-79-2
AMP-Activated Protein Kinases
EC 2.7.11.31
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
105118Informations de copyright
Copyright © 2020 Elsevier Ltd. All rights reserved.