High yield Flashcards

1
Q

Label the agents for A-C

A

A) Norepinephrine

B) Epinephrine

C) Isoproterenol

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2
Q

What are the effects of epinephrine on skeletal muscle, mediated by which receptors?

A
  • Causes muscle tremor (β2)
  • Increases K+ uptake by skeletal muscle (β2) = promotes HYPOkalemia and decreased K+ excretion by kidneys
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3
Q

What are the effects of epinephrine on blood glucose, fatty acid levels and renin?

A
  • Elevates blood glucose levels –> enhances liver glycogenolysis and gluconeogenesis (β2)
  • Increases free fatty levels in blood
  • Increases renin release (β1)
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4
Q

What are the major effects of norepinephrine?

A
  • Potent cardiac stimulant BUT reduces HR
  • Potent vasoconstrictor
  • Increases peripheral vascular resistance and BP; decreases pulse rate
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5
Q

What are the adrenergic receptor types found in the vascular beds of the skin vessels/mucous membranes, skeletal muscle, renal, and cerebral?

A
  • Skin vessels and mucous membranes (α1)
  • Skeletal muscle (α1 and β2)
  • Renal, cerebral (D1 and α1)
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6
Q

Clonidine acts on which receptors and produces what effects?

A
  • SELECTIVE α2 agonist
  • Central effect on α2 receptors in the lower brainstem area –> decrease sympathetic outflow, reduction in BP, BRADYCARDIA

*Guy holding claw weapons w/ 2 lit candles!

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7
Q

Which adrenergic receptors are activated at low doses vs. high doses of Dopamine?

What are the effects?

A
  • At low doses β1 receptors are activated (cardiac activation)
  • At high doses α1 receptors are activated (pressor effects)

*Remember D-B-A*

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8
Q

Tyramine is found where?

What is the MOA when administered parenterally and how is it metabolized?

A
  • Found in cheese, cured meats, and smoked/pickled fish
  • Releases stored NE from presynaptic adrenergic terminals (if administered parenterally)
  • Metabolized by MAO in liver (may lead to increased BP in pt’s taking MAO inhibitors)
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9
Q

What is the MOA of Metyrosine?

A

Inhibits tyrosine hydroxylase; prevents conversion of tyrosine –> L-DOPA

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10
Q

What is the MOA of Guanethidine?

A

Prevents storage, depletes NE

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11
Q

Which 2 drugs are used in the treatment of chronic urinary retention associated with BPH?

Which receptor do they target?

A
  • Tamsulosin and Silodosin (α1 selective antagonists)
  • Greater selectivity for α1A = most important α receptor subtype mediating prostate smooth muscle contraction
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12
Q

How does the (-) isomer of Dobutamine differ from the (+) isomer in its effects on α1 receptors?

A
  • Dobutamine is a selective β1 agonist
  • Has some α1 activity: the (-) isomer is an agonist at these receptors and the (+) isomer is an α1 antagonist
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