Exam 2 - Alpha/Beta Antagonists Flashcards
Describe and compare the effects of an α blocker on the blood pressure and heart rate.
α blockers cause vasodilation by blocking α1 receptors on vascular smooth muscle, leading to a decrease in blood pressure. Reflexively, this can cause a compensatory increase in heart rate (reflex tachycardia) due to baroreceptor activation
List the alpha and beta blockers described in class, and their clinical uses.
α blockers: Prazosin: Used for hypertension and benign prostatic hyperplasia (BPH).
Phentolamine: Used for pheochromocytoma and to reverse vasoconstriction.
β blockers: Propranolol (non-selective): Used for hypertension, arrhythmias, and angina.
Metoprolol (β1 selective): Used for heart failure, hypertension, and arrhythmias
Differentiate the effects of a blocker in the presence or absence of an agonist.
In the PRESENCE of an agonist (like epinephrine), α blockers prevent vasoconstriction, reducing blood pressure.
In the ABSENCE of an agonist, α blockers primarily cause baseline vasodilation, but their effect on BP is less pronounced since no vasoconstrictive stimuli are present
Explain the following sentence: Phentolamine converts a pressor (epinephrine) into a depressor.
Phentolamine blocks α receptors, preventing the vasoconstrictive effects of epinephrine (a pressor). With α receptors blocked, epinephrine’s β2-mediated vasodilation dominates, causing a drop in blood pressure (depressor effect)
Define the difference between selective and non-selective beta-blockers.
Selective: Target only β1 receptors (e.g., metoprolol), affecting primarily the heart (lowering heart rate and contractility).
Non-selective: Block both β1 and β2 receptors (e.g., propranolol), affecting the heart as well as the lungs and vascular smooth muscle (potential for bronchoconstriction)
Describe the clinical indications and toxicities of typical α and β blockers
α Blockers:
Indications: Hypertension, BPH.
Toxicities: Orthostatic hypotension, reflex tachycardia.
β Blockers:
Indications: Hypertension, arrhythmias, heart failure, angina.
Toxicities: Bradycardia, bronchoconstriction (non-selective), fatigue