Dose-dependent separation of the hypertrophic and myotoxic effects of the beta(2)-adrenergic receptor agonist clenbuterol in rat striated muscles.

Abstract

Muscle growth in response to large doses (milligrams per kilogram) of beta(2)-adrenergic receptor agonists has been reported consistently. However, such doses may also induce myocyte death in the heart and skeletal muscles and hence may not be safe doses for humans. We report the hypertrophic and myotoxic effects of different doses of clenbuterol. Rats were infused with clenbuterol (range, 1 microg to 1 mg.kg(-1)) for 14 days. Muscle protein content, myofiber cross-sectional area, and myocyte death were then investigated. Infusions of >or=10 microg.kg(-1).d(-1) of clenbuterol significantly (P<0.05) increased the protein content of the heart (12%-15%), soleus (12%), plantaris (18%-29%), and tibialis anterior (11%-22%) muscles, with concomitant myofiber hypertrophy. Larger doses (100 microg or 1 mg) induced significant (P<0.05) myocyte death in the soleus (peak 0.2+/-0.1% apoptosis), diaphragm (peak 0.15+/-0.1% apoptosis), and plantaris (peak 0.3+/-0.05% necrosis), and significantly increased the area fraction of collagen in the myocardium. These data show that the low dose of 10 microg.kg(-1).d(-1) can be used in rats to investigate the anabolic effects of clenbuterol in the absence of myocyte death.

• Authors: Jatin G Burniston, William A Clark, Lip-Bun Tan, David F Goldspink
• Journal: Muscle & nerve (Muscle Nerve) Vol. 33 Issue 5 Pg. 655-63 (May 2006) ISSN: 0148-639X [Print] United States
• PMID: 16411205 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Adrenergic beta-Agonists
• Muscle Proteins
• Clenbuterol

Topics

• Adrenergic beta-Agonists (adverse effects)
• Animals
• Apoptosis (drug effects)
• Clenbuterol (adverse effects)
• Dose-Response Relationship, Drug
• Hypertrophy (chemically induced)
• Male
• Muscle Fibers, Skeletal (drug effects)
• Muscle Proteins (metabolism)
• Muscle, Skeletal (drug effects, pathology)
• Myocardium (pathology)
• Necrosis (chemically induced)
• Rats
• Rats, Wistar
• Statistics, Nonparametric
• Time Factors