α-blockers
Also known as
Key examples
- Doxazosin
- Tamsulosin
- Alfuzosin
Common indications
- As a first-line medical option to improve symptoms in benign prostatic hyperplasia.
- As an add-on treatment in resistant hypertension, when other medicines (e.g. calcium channel blockers, ACE inhibitors, thiazide diuretics) are insufficient.
Mechanisms of action
- Although often described using the broad term ‘α-blocker,’ most drugs in this class (including doxazosin, tamsulosin and alfuzosin) are highly selective for the α1-adrenoceptor.
- Alpha1-adrenoceptors
are found mainly in smooth muscle, including in blood vessels and the
urinary tract (the bladder neck and prostate in particular).
- Stimulation
induces contraction; blockade induces relaxation.
- Alpha1-blockers therefore cause vasodilatation and a fall in blood pressure, and reduced resistance to bladder outflow.
Important adverse effects
- Predictably from their effects on vascular tone, α-blockers can cause postural hypotension, dizziness and syncope. This is particularly prominent after the first dose (rather like with ACE inhibitors and angiotensin receptor blockers).
Warnings
- Alpha-blockers should not be used in patients with existing postural hypotension.
Important interactions
- In general, combining antihypertensive drugs results in additive blood pressure lowering effects (this may well be the therapeutic aim). To avoid pronounced first-dose hypotension, it may be prudent to omit doses of one or more existing antihypertensive drugs on the day the α-blocker is started. This is particularly the case for β-blockers, which inhibit the reflex tachycardia that forms part of the compensatory response to vasodilatation.
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