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Activation of the CRF 2 receptor modulates skeletal muscle mass under physiological and pathological conditions
- Source :
- American Journal of Physiology-Endocrinology and Metabolism. 285:E889-E898
- Publication Year :
- 2003
- Publisher :
- American Physiological Society, 2003.
-
Abstract
- Two receptors activated by the corticotropin-releasing factor (CRF) family of peptides have been identified, the CRF 1 receptor (CRF1R) and the CRF 2 receptor (CRF2R). Of these, the CRF2R is expressed in skeletal muscle. To understand the role of the CRF2R in skeletal muscle, we utilized CRFR knockout mice and CRF2R-selective agonists to modulate nerve damage and corticosteroid- and disuse-induced skeletal muscle atrophy in mice. These analyses demonstrated that activation of the CRF2R decreased nerve damage and corticosteroid- and disuse-induced skeletal muscle mass and function loss. In addition, selective activation of the CRF2R increased nonatrophy skeletal muscle mass. Thus we describe for the first time a novel activity of the CRF2R, modulation of skeletal muscle mass.
- Subjects :
- Male
medicine.medical_specialty
Physiology
Peptide Hormones
Endocrinology, Diabetes and Metabolism
Biology
Receptors, Corticotropin-Releasing Hormone
Amphibian Proteins
Dexamethasone
Muscle hypertrophy
Rats, Sprague-Dawley
Mice
Atrophy
Physiology (medical)
Internal medicine
medicine
Animals
Muscle, Skeletal
Receptor
Insulin-like growth factor 1 receptor
Denervation
Skeletal muscle
Organ Size
medicine.disease
Sciatic Nerve
Muscular Disorders, Atrophic
Hindlimb
Rats
Mice, Inbred C57BL
Muscular Atrophy
medicine.anatomical_structure
Endocrinology
Female
Stress, Mechanical
medicine.symptom
Peptides
ITGA7
hormones, hormone substitutes, and hormone antagonists
Muscle Contraction
Muscle contraction
Subjects
Details
- ISSN :
- 15221555 and 01931849
- Volume :
- 285
- Database :
- OpenAIRE
- Journal :
- American Journal of Physiology-Endocrinology and Metabolism
- Accession number :
- edsair.doi.dedup.....4ba074f43444c9afb1d59e347adc404d
- Full Text :
- https://doi.org/10.1152/ajpendo.00081.2003