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From Wikipedia, the free encyclopedia

Alpha-1 blockers (also called alpha-adrenergic blocking agents) constitute a variety of drugs which block α1-adrenergic receptors in arteries and smooth muscles.



Reduce arteriolar resistance and increase venous capacitance causing reflex tachycardia.Depending on plasma concentration they may cause postural hypotension.Alpha-1 blockers may decrease LDL and triglycerides and increase HDL.


These drugs may be used to treat:

Examples of alpha blockers

Selective Alpha-1 blockers
Blocker Use Common Brand Name
Doxazosin[2] Hypertension and benign prostatic hyperplasia (BPH) (Cardura)
Silodosin Benign prostatic hyperplasia (Rapaflo)
Prazosin Hypertension (Minipress)
Tamsulosin Benign prostatic hyperplasia (Flomax)
Alfuzosin Benign prostatic hyperplasia (Uroxatral)
Terazosin Hypertension and BPH (Hytrin)

Others include:

Non-selective Adrenergic blockers:

Silodosin shows high affinity and selectivity for α1A adrenergic receptors found in the prostate which ensures that it works quickly and effectively to relieve the symptoms of BPH. Silodosin's low affinity for α1B receptors in the blood vessels is thought to be reflected in its low incidene of orthostatic and vasodilatory side effects.[3]

Tamsulosin is relatively selective for α1a-adrenergic receptors, which are mainly present in the prostate. Hence, it may have a more selective action in BPH with minimal effects on blood pressure.

Adverse effects and interactions

By reducing α1-adrenergic activity of the blood vessels, these drugs may cause hypotension (low blood pressure) and interrupt the baroreflex response. In doing so, they may cause dizziness, lightheadedness, or fainting when rising from a lying or sitting posture (known as orthostatic hypotension or postural hypotension). For this reason, it is generally recommended that alpha blockers should be taken at bedtime. Additionally, the risk of first dose phenomenon may be reduced by starting at a low dose and titrating upwards as needed.

Because these medications may cause orthostatic hypotension, as well as hypotension in general, these agents may interact with other medications that increase risk for hypotension, such as other antihypertensives and vasodilators.

As discussed above, tamsulosin may have less risk for hypotension and orthostatic hypotension due to its selectivity for α1a-adrenergic receptors. On the other hand, the drug (a) elevates risk for floppy iris syndrome, and (b) might show ADRs characteristic of the sulfa related drugs.


  1. ^ Höfner K (December 1999). "alpha(1)-Blocker therapy in the nineties: focus on the disease". Prostate Cancer Prostatic Dis. 2 (S4): S9–S15. doi:10.1038/sj.pcan.4500368. PMID 12496768. 
  2. ^ Yilmaz E, Batislam E, Basar MM, Tuglu D, Ferhat M, Basar H (June 2005). "The comparison and efficacy of 3 different alpha1-adrenergic blockers for distal ureteral stones". J. Urol. 173 (6): 2010–2. doi:10.1097/01.ju.0000158453.60029.0a. PMID 15879806. 
  3. ^ Nomiya M, Yamaguchi O. A quantitative analysis of mRNA expression of alpha 1 and beta-adrenoceptor subtypes and their functional roles in human normal and obstructed bladders. J Urol. 2003;170(2 Pt 1):649-653.

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