Drugs Affecting Adrenergic Function Flashcards
1
Q
Functions of the Autonomic Nervous System
A
- Involuntary system
- Responsible for:
- Control of smooth muscle (e.g. bronchi, blood vessels, GI tract)
- Cardiac muscle
- Exocrine glands (e.g. gastric, sweat, salivary)
- Monitored by both the sympathetic and parasympathetic nervous systems
2
Q
Balanced Antagonism
A
- The ANS works by antagonism between the sympathetic and parasympathetic nervous systems
- To effect an action, a neurotransmitter needs to bind with an appropriate receptor site on the effector organ or tissue
- This is accomplished by synaptic transmission
3
Q
Synaptic Transmission
A
- Involves the synthesis of neurotransmitters in the nerve terminal
- Includes storage of the neurotransmitter awaiting an action potential
- Involves release of the specific neurotransmitter
- After release, the neurotransmitter diffuses across the synaptic gap and reversibly binds to a receptor on the postsynaptic cell
- After binding and exerting an effect, the neurotransmitter is dissociated from its binding site by a variety of mechanisms
- The neurotransmitter is now degraded or “re-uptaked” for reuse
4
Q
Neurotransmitters Involved
A
- Acetylcholine
- Norepinephrine (NE)
- Epinephrine
5
Q
Preganglionic transmission is mediated by what neurotransmitter?
A
Acetylcholine
6
Q
Postganglionic transmission is mediated by what neurotransmitter?
A
Norepinephrine
7
Q
Adrenal medulla stimulation to release epinephrine is mediated by what neurotransmitter?
A
Acetylcholine
8
Q
Four subtypes of adrenergic receptors
A
Alpha-1, Alpha-2, Beta-1, and Beta-2
9
Q
Stimulation of Alpha-1 receptors
A
- Stimulation causes:
- Vasoconstriction/Hemostasis
- Increased peripheral resistance
- Increased blood pressure (BP) – hypertensive patent would benefit from an Alpha-1 antagonist
- Pupil dilation (mydriasis)
- Closure of the internal sphincter of the bladder – a patient with urinary incontinence would benefit from an Alpha-1 agonist
- Blocking causes the opposite effects
10
Q
Adverse effects of Alpha-1 activation
A
- Hypertension – secondary to widespread vasoconstriction
- Necrosis – IV infiltration can result in extravasation (tissue damage)
- Bradycardia – secondary to reflex slowing of the heart (vasoconstriction triggers baroreceptor reflex which decreases HR)
11
Q
Stimulation of Alpha-2 receptors
A
- Activation inhibits norepinephrine release
- There are no therapeutic applications related to activation of peripheral Alpha-2 receptors. There is significance to activation of Alpha-2 receptors in the CNS
12
Q
Activation of Alpha-2 receptors
A
- Activation of Central Alpha-2 receptors
- Reduction of sympathetic outflow from brain to heart and blood vessels
- Relief of severe pain
- Blocking causes the opposite effects
13
Q
Stimulation of Beta-1 receptors
A
- Clinical Uses – cardiac arrest, heart failure, shock, heart block
- Causes:
- Tachycardia
- Increased myocardial contractility
- Increased lipolysis - Blocking causes the opposite effects
14
Q
Stimulation of Beta-2 receptors
A
- Therapeutic applications limited to the lungs and uterus
- Used to treat: asthma, delay preterm labor
- Causes:
- Bronchodilation
- Vasodilation
- Slightly decreased peripheral resistance
- Increased muscle and liver glycolysis
- Increased release of glucagon
- Relaxation of uterine smooth muscle - Blocking causes the opposite effects
15
Q
Adverse effects of Beta-2 stimulation
A
- Hyperglycemia
- Tremor