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The effect of beta-blockers on bone metabolism as potential drugs under investigation for osteoporosis and fracture healing.
- Source :
-
Expert opinion on investigational drugs [Expert Opin Investig Drugs] 2008 Sep; Vol. 17 (9), pp. 1281-99. - Publication Year :
- 2008
-
Abstract
- Background: beta-Adrenergic receptor antagonists (beta-blockers) have a well-recognised antihypertensive action that is mediated through a reduction in cardiac output and in the release of renin from the kidneys and inhibition of the action of endogenous catecholamines on beta-adrenergic receptors. This class of drugs has been shown to reduce the incidence of cardiovascular disease. Recent evidence suggests that beta-blockers may also have an effect on bone structure, metabolism and fracture healing.<br />Objective: This paper reviews in vitro and in vivo data that suggest beta-blockers have primarily an anabolic effect on bone metabolism.<br />Results: The sympathetic nervous system has a catabolic effect on bone, and in vitro studies have shown that adrenergic agonists stimulate bone resorption. The beta-blocker propranolol has been shown to increase bone formation in ovariectomised female rats. Also, recent observational clinical studies provide evidence to show that beta-blockers are associated with reduction in fracture risk in both men and women.<br />Conclusion: Although there are some controversial studies, most research concludes that beta-blockers show promise in the treatment of osteoporosis and fracture healing.
- Subjects :
- Adrenergic beta-Antagonists pharmacokinetics
Animals
Drug Evaluation, Preclinical
Humans
Sympathetic Nervous System drug effects
Sympathetic Nervous System metabolism
Adrenergic beta-Antagonists therapeutic use
Fracture Healing drug effects
Osteoporosis drug therapy
Osteoporosis metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1744-7658
- Volume :
- 17
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Expert opinion on investigational drugs
- Publication Type :
- Academic Journal
- Accession number :
- 18694363
- Full Text :
- https://doi.org/10.1517/13543784.17.9.1281