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Dexamethasone exacerbates cisplatinā€induced muscle atrophy

Authors :
Yosuke Isa
Saori Yabe
Risako Kon
Yuki Kai
Yoshihiko Chiba
Minoru Narita
Hiroyasu Sakai
Minami Kimura
Nobutomo Ikarashi
Yuka Tsukimura
Junzo Kamei
Fumiaki Sato
Source :
Clinical and Experimental Pharmacology and Physiology. 46:19-28
Publication Year :
2018
Publisher :
Wiley, 2018.

Abstract

Dexamethasone for antiemetic therapy is typically administered with anticancer drugs such as cisplatin. We previously reported that cisplatin upregulates the muscle-specific E3 ubiquitin ligase genes, namely muscle ring-finger protein 1 (MuRF1) and atrophy gene-1 (atrogin-1), and promotes muscle atrophy in mice. It is well known that dexamethasone causes upregulation of MuRF1 and Atrogin-1 expression in skeletal muscles. Although it is speculated that a combination of dexamethasone and cisplatin worsens muscle atrophy, there are no reports based on research. We thereby investigated the effects of cisplatin and dexamethasone, alone or in combination, on the expression of MuRF1 and Atrogin-1 in murine skeletal muscles and C2C12 myotubes. Mice were intraperitoneally injected with cisplatin or the vehicle control once daily for 4 days. Dexamethasone or the vehicle control was subcutaneously administered 30 minutes prior to the administration of cisplatin. Dexamethasone enhanced MuRF1 and Atrogin-1 gene expression upregulated by cisplatin in murine quadriceps muscles and C2C12 myotubes. Cisplatin-caused upregulation of myostatin and downregulation of IGF-1 gene expression were also enhanced by co-administration of dexamethasone in murine quadriceps muscles and C2C12 myotubes. This study shows that the combination treatment of cisplatin and dexamethasone exacerbated muscle atrophy in mice. Therefore, this treatment regimen might exacerbate muscle atrophy in cancer patients.

Details

ISSN :
14401681 and 03051870
Volume :
46
Database :
OpenAIRE
Journal :
Clinical and Experimental Pharmacology and Physiology
Accession number :
edsair.doi.dedup.....964c51d0d71584c80161a78d7cfe9158
Full Text :
https://doi.org/10.1111/1440-1681.13024