Abstract
As the beta3-adrenergic receptor (beta3-AR) mediates a negative inotropic effect, upregulation of this receptor in patients with heart failure is considered to be harmful and associated with disease progression. The development of beta3-AR antagonists has therefore been proposed as a potential therapeutic option for heart failure. However, as increased intracellular myocyte Na+ levels represent a key adverse pathophysiological feature of heart failure, and the beta3-AR mediates the stimulation of the only export route for Na+ - the Na+-K+ pump - the upregulation of this receptor may also represent a useful compensatory mechanism. Data from animal studies and circumstantial observations from clinical trials suggest that beta3-AR activation is beneficial in severe heart failure, and that beta3-AR agonists are a promising therapeutic option for the treatment of this disease.
| Original language | English |
|---|---|
| Journal | Current Opinion in Investigational Drugs |
| Volume | 10 |
| Issue number | 9 |
| Pages (from-to) | 955-62 |
| Number of pages | 8 |
| ISSN | 0967-8298 |
| Publication status | Published - Sept 2009 |
| Externally published | Yes |
Keywords
- Adrenergic beta-Agonists/metabolism
- Animals
- Clinical Trials as Topic
- Heart Failure/drug therapy
- Humans
- Myocardial Contraction/drug effects
- Receptors, Adrenergic, beta-3/genetics
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