Erythromycin has therapeutic efficacy on muscle fatigue acting specifically on orosomucoid to increase muscle bioenergetics and physiological parameters of endurance.


Journal

Pharmacological research
ISSN: 1096-1186
Titre abrégé: Pharmacol Res
Pays: Netherlands
ID NLM: 8907422

Informations de publication

Date de publication:
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

105118

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Jingjing Wan (J)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.

Zhen Qin (Z)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.

Hong Lei (H)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.

Pengyuan Wang (P)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.

Yu Zhang (Y)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.

Jiayi Feng (J)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.

Jie Wei (J)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.

Yang Sun (Y)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China. Electronic address: DawnySun@126.com.

Xia Liu (X)

Department of Clinical Pharmacy, School of Pharmacy, Second Military Medical University, Shanghai, 200433, China. Electronic address: lxflying@aliyun.com.

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Classifications MeSH