Adrenergic antagonists Flashcards
Adrenergic Antagonists AKA?
adrenergic blockers or sympatholytics
Adrenergic Antagonists Reversibly or irreversibly bind to receptor but do NOT trigger the usual effects of the endogenous ______
catecholamines
how are Adrenergic Antagonists classified?
Classified, like the agonists, according to their affinity for alpha or beta receptors
Non-selective drugs in this class can profoundly affect BP
Alpha-adrenergic Receptor Antagonists
in Alpha-adrenergic Receptor Antagonists, Blockade of α receptors reduces sympathetic tone of blood vessels resulting in decreased ________
peripheral vascular resistance
Blockade of α receptors reduces sympathetic tone of blood vessels resulting in decreased peripheral vascular resistance. This induces a reflex tachycardia and the magnitude of the response depends on the_____of the individual.
sympathetic tone
Blockade of α receptors reduces sympathetic tone of blood vessels resulting in decreased peripheral vascular resistance. This induces a reflex tachycardia and the magnitude of the response depends on the sympathetic tone of the individual.
Effects are more profound in an individual who is standing versus supine
_____patients will also have a more marked response
Hypovolemic
CV Drugs that block α1-receptors
Doxazosin (Cardura)
Prazosin (Minipress)
Terazosin (Hytrin)
BPH Drugs that block α1-receptors
Alfuzosin (Uroxatral)
Silodosin (Rapaflo)
Tamsulosin (Flomax)
Alpha-adrenergic Receptor Antagonists Misc- special uses?
Phenoxybenzamine (Dibenzyline) - pheochromocytoma
Phentolamine (OraVerse) – pheochromocytoma and NE extravasation
Prazosin, terazosin, and doxazosin are what class of drugs?
Alpha-adrenergic Receptor Antagonists
Alpha-adrenergic Receptor Antagonists CV effects:
Relaxation of arterial and venous smooth muscle
Can cause profound orthostatic hypotension with first-dose
- Need to reduce first dose and dose at bedtime
Alpha-adrenergic Receptor Antagonists ADRs
Dizziness Fatigue Nasal congestion HA Orthostatic hypotension Sexual dysfunction
Beta-adrenergic Receptor Antagonists can be distinguished by the following properties:
- Relative affinity for β1 and β2 receptors
- Intrinsic sympathomimetic activity
- Blockade of α receptors
- Differences in lipid solubility
- Capacity to induce vasodilation
- Pharmacokinetic parameters
these block both β1 and β2 receptors
Nonselective: block both β1 and β2 receptors