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Acylated and unacylated ghrelin impair skeletal muscle atrophy in mice.

Authors :
Porporato PE
Filigheddu N
Reano S
Ferrara M
Angelino E
Gnocchi VF
Prodam F
Ronchi G
Fagoonee S
Fornaro M
Chianale F
Baldanzi G
Surico N
Sinigaglia F
Perroteau I
Smith RG
Sun Y
Geuna S
Graziani A
Source :
The Journal of clinical investigation [J Clin Invest] 2013 Feb; Vol. 123 (2), pp. 611-22. Date of Electronic Publication: 2013 Jan 02.
Publication Year :
2013

Abstract

Cachexia is a wasting syndrome associated with cancer, AIDS, multiple sclerosis, and several other disease states. It is characterized by weight loss, fatigue, loss of appetite, and skeletal muscle atrophy and is associated with poor patient prognosis, making it an important treatment target. Ghrelin is a peptide hormone that stimulates growth hormone (GH) release and positive energy balance through binding to the receptor GHSR-1a. Only acylated ghrelin (AG), but not the unacylated form (UnAG), can bind GHSR-1a; however, UnAG and AG share several GHSR-1a-independent biological activities. Here we investigated whether UnAG and AG could protect against skeletal muscle atrophy in a GHSR-1a-independent manner. We found that both AG and UnAG inhibited dexamethasone-induced skeletal muscle atrophy and atrogene expression through PI3Kβ-, mTORC2-, and p38-mediated pathways in myotubes. Upregulation of circulating UnAG in mice impaired skeletal muscle atrophy induced by either fasting or denervation without stimulating muscle hypertrophy and GHSR-1a-mediated activation of the GH/IGF-1 axis. In Ghsr-deficient mice, both AG and UnAG induced phosphorylation of Akt in skeletal muscle and impaired fasting-induced atrophy. These results demonstrate that AG and UnAG act on a common, unidentified receptor to block skeletal muscle atrophy in a GH-independent manner.

Details

Language :
English
ISSN :
1558-8238
Volume :
123
Issue :
2
Database :
MEDLINE
Journal :
The Journal of clinical investigation
Publication Type :
Academic Journal
Accession number :
23281394
Full Text :
https://doi.org/10.1172/JCI39920