RCS 10 - Adrenergic Agonists & Antagonists 2 Flashcards

1
Q

List the different classes of adrenergic antagonists we need to know and the drugs in each class that we need to know.

A
  • α-antagonists
    • Nonselective - phenoxybenzamine & phentolamine
    • α1 selective - prazosin, terazosin, doxazosin, tamsulosin
  • β-antagonists
    • Nonselective - propranolol, nadolol, timolol
    • β1 selective - atenolol, metoprolol, esmolol,
  • α1 and β antagonists - labetalol, carvedilol
  • Partial agonists - pindolol
  • Presynaptic acting drugs
    • Inhibitors of NE synthesis - α-methyltyrosine (aka - metyrosine)
    • Inhibitors of NE storage - reserpine, tetrabenazine
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2
Q

What is the primary effect of α adrenergic blockers and why?

A

To cause vasodilation, thereby decreasing PVR.

The main receptor causing vasoconstriction and maintaining vascular tone is the α1 receptor

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3
Q

Give the MOA, effects, and uses of phenoxybenzamine.

A
  • Nonselective Irreversible antagonist of α receptors
  • Used for chronic management of inoperable pheochromocytomas and is given to patients prior to surgical removal of operable pheochromocytomas.
  • Not successful for HTN
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4
Q

Give the MOA, effects, and uses of phentolamine.

A
  • Reversibly blocks α1 and α2 receptors
  • Causes vasodilation and a drop in BP
  • Uses
    • Diagnosis of pheochromocytoma - phentolamine blocking test
    • Control of HTN during preoperative preparation and surgical excision of a pheochromocytoma
    • Sometimes NE is given to patients in shock, resulting in potent vasoconstriction which possibly leads to dermal necrosis. Phentolamine can be given to prevent this
    • HTN crisis caused by stimulant drug OD
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5
Q

Describe the concept of epinephrine reversal

A

Normally, E causes vasoconstriction via the α1 receptors. However, if an α blocker is given beforehand, E will actually cause vasodilation because it also activates the β2 receptors.

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6
Q

What is the prototye selective α1 blocker? What are these types of drugs usually used for?

A

Prazosin

  • DOC for benign prostatic hyperplasia (BPH) symptom relief (it relaxes the smooth muscle in the prostatic urethra to make urination easier)
  • Treating HTN, but they are not usually the DOC for HTN
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7
Q

Important note about α1 blocker administration

A

The first dose often produces an exaggerated hypotensive response that can result in syncope. Therefore, the first dose must be 1/3 or 1/4 the normal dose

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8
Q

List the MOA, effects, and uses for terazosin & doxazosin.

A

These are just analogs of prazosin with a longer half-life and have the same MOA, effects, and uses

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9
Q

Give the MOA, effects, and uses of tamsulosin

A
  • There are three subtypes of the α1 receptor, Tamsulosin is selective for the α1a receptor which predominate in the genitourinary smooth muscle
  • Has a very small effect on BP and is less likely to cause orthostatic hypotension than other α blockers
  • Used to treat symptoms of BPH
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10
Q

List the non-selective β blockers and their general effects on the CVS, respiratory systems, and metabolism.

A

Propranolol, Nadolol, Timolol

  • CVS - slow HR and decrease contractility
  • Respiratory - bronchoconstriction
  • Metabolism - decreases glycogenolysis and glucagon secretion
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11
Q

What’s the primary contraindication for nonselective β blockers?

A

Patients with COPD or asthma because they can precipitate a respiratory crisis.

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12
Q

Describe the MOA, effects, and uses of atenolol & metoprolol

A
  • β1 selective antagonists
  • Uses
    • Treat HTN in patients with impaired pulmonary function
    • Treat HTN in patients who are receiving insulin or oral hypoglycemic agents (a nonselective blocker would worsen the hypoglycemia)
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13
Q

Describe the MOA, effects, and uses of esmolol.

A
  • β1 selective antagonist
  • Same effects as other β1 antagonists
  • Used for rapid control of ventricular rate in patients with atrial fibrillation or atrial flutter because esmolol is ultra short acting (half life is 10 minutes)
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14
Q

Describe the MOA, effects, and uses of labetalol.

A
  • Competitive antagonist of α1 and β receptors but more potently antagonizes β receptors
  • Used to treat HTN
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15
Q

Describe the MOA, effects, and uses of carvedilol

A

Very similar to labetalol but also has antioxidant properties

Used to treat HTN and CHF

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16
Q

Describe the MOA and uses of pindolol.

A
  • Partial β agonist.
  • May be used in individuals with diminished cardiac reserve or a propensity to bradycardia
17
Q

List the most common uses of β blockers and briefly explain how they work for these purposes.

A
  • Lower BP by decreasing CO.
  • Decreasing IOP by reducing aqueous humore secretions
  • Prevention of migraines (not treatment of migraines)
  • Blunt sympathetic stimulation of the heart in hyperthyroidic patients
  • Chronic management (not acute) of angina pectoris by reducing O2 requirements of the heart
  • Control atrial fibrillations
  • Given to patients who’ve had an MI to reduce further stress on heart
  • Control performance anxiety
  • Treatment of essential tremor
18
Q

Describe the adverse effects and contrainidcations of non-selective and selective β blockers on the respiratory system.

A
  • Nonselective β blockers cause a relatively strong bronchoconstriction
  • β1-selective blockers are less likely to evoke bronchoconstriction

The use of these drugs should be avoided in COPD and asthma patients whenever possible. β1 selective drugs are preferred if they have to be used

19
Q

Describe the adverse effects and contrainidcations of non-selective and selective β blockers on sugar metabolism.

A
  • Nonselective β blockers will antagonize the β2 receptors in the liver, decreasing glycogenolysis and gluconeogenesis. This can make recovery from hypoglycemia (particularly with insulin dependent diabetics) difficult.
  • A major warning sign for patients prone to hypoglycemia is tachycardia. A nonselective β blocker will suppress this increasing the chances of a person becoming dangerous hypoglycemic
  • For patients prone to hypocglycemia, a β1 selective blocker is preferred
20
Q

Describe the adverse effects and contrainidcations of non-selective and selective β blockers on lipid metabolism. Which β blockers don’t seem to have this effect?

A
  • Even though a β receptor blockade inhibits the release of FFAs from adipose tissue, both nonselective and selective β blockers increase plasma TG and decrease HDL
  • The α1 and β blocker, labetalol, along with the partial β agonist, pindolol, do not seem to have these effects
21
Q

Describe the adverse effects and contrainidcations of non-selective and selective β blockers on the CNS.

A
  • Sedation
  • Dizziness
  • Lethargy
  • Fatigue
22
Q

Impotant notes about how to administer β blockers

A

When β recetors are blocked, the body will upregulate the amount of receptors. This effect typically isn’t seen, because they are also being blocked. Because of this, it is very important to gradually taper a patient off of β blockers to avoid acute tachycardia, HTN, and/or ischemia.

23
Q

Describe the MOA and uses for α-methyltyrosine

A
  • Inhibits synthesis of NE in the presynaptic terminal by competitively inhibiting tyrosine hydroxylase
  • Use for management of malignant pheochromocytoma and for preoperative preparation of patients for resection of an operable pheochromocytoma
24
Q

Describe the MOA, effects, and uses of reserpine.

A
  • Inhibits NE storage in the presynaptic terminal by irreversibly blocking VMAT
  • This causes depletion of NE, since MAO degrades it in the cytoplasm. This is seen as a gradual decrease in BP and HR
  • Used in the past to treat HTN (but still tested on the STEP)
25
Q

Describe the MOA, effects, and uses of tetrabenazine.

A
  • Inhibits storage of NE in the presynaptic terminal by reversibly inhibiting VMAT
  • Causes presynaptic depletion of NE
  • Indicated for the treatment of chorea (jerky involuntary movements) associated with Huntington’s Disease
26
Q

List the tissues in the eye controlled by the ANS that we need to know. Include their receptors and response to receptor stimulation

A
  • Dilator pupillae - α1 - mydriasis
  • Constrictor pupilae - M3 - miosis
  • Ciliary muscle - M3 - lens accommodation for near vision and facilitation fo aqueous humor outflow
  • Ciliary epithelium - ß2 - secretion of aqueous humor