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
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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
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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
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4
Q

Neurotransmitters Involved

A
  • Acetylcholine
  • Norepinephrine (NE)
  • Epinephrine
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5
Q

Preganglionic transmission is mediated by what neurotransmitter?

A

Acetylcholine

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6
Q

Postganglionic transmission is mediated by what neurotransmitter?

A

Norepinephrine

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7
Q

Adrenal medulla stimulation to release epinephrine is mediated by what neurotransmitter?

A

Acetylcholine

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8
Q

Four subtypes of adrenergic receptors

A

Alpha-1, Alpha-2, Beta-1, and Beta-2

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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
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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)
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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
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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
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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
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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
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15
Q

Adverse effects of Beta-2 stimulation

A
  • Hyperglycemia

- Tremor

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16
Q

Epinephrine

A
  • Nonselective adrenergic agonist
  • Stimulates all alpha and beta receptors
  • Many therapeutic uses, such as:
    - Cardiopulmonary arrest
    - Ventricular fibrillation
    - Anaphylactic shock – shock decreases blood pressure; epinephrine will increase blood pressure
    - Asthma
  • Adverse effects related to stimulation of all receptors are common
  • CNS and cardiac adverse effects are the most common and may be the most serious
17
Q

Phenylephrine

A
  • Alpha-1 stimulant (selective!)
  • Potent vasoconstrictor
  • Avoid IV extravasation
  • Pharmacotherapeutics include:
    - Vascular failure
    - Hypotension
    - Shock states
  • Topical pharmacotherapeutics:
    - Nasal decongestant – vasoconstricts
    - Patients with hypertension are at risk when taking these medications because their blood pressure will rise even more
    - Pupil dilation (mydriasis)
18
Q

Prazosin

A
  • Alpha-1 blocker
  • Used to treat hypertension
  • The first dose may cause syncope (fainting)
19
Q

Isoproterenol

A
  • Nonselective Beta-2 stimulant (may stimulate Beta-1 if Beta-2 is not available)
  • Pharmacotherapeutics include:
    - Congestive heart failure
    - Various types of shock
    - Hypoperfusion
  • Inhaled pharmacotherapeutics include:
    - Asthma
    - Bronchitis
    - Emphysema
    - COPD
  • Adverse effects are primarily related to cardiac stimulation
20
Q

Propranolol

A
  • Nonspecific beta-blocker (Beta-1 or Beta-2)
  • Used primarily for cardiovascular disorders
  • Adverse effects are due to cardiac and respiratory effects
  • Discontinue slowly to prevent rebound tachycardia leading to angina and possibly myocardial infarction
  • Cannot be abruptly discontinued