Sympathetic Depressants Flashcards

1
Q

Non-selective α & β agonists:

A

Adrenalin
Dopamine
Ephedrine
Amphetamine

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2
Q

α1 selective agonists:

A
Phenylephrine
Methoxamine
Mephenteramine
Metaraminol
Oxymetazoline
Xylometazoline
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3
Q

α2 selective agonists:

A

Clonidine
Methyldopa
Guanfacine

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4
Q

β1 agonists:

A

Dobutamine

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5
Q

β2 agonists:

A

Salbutamol
Terbutaline
Salmeterol
Formoterol

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6
Q

Non-selective α blockers:

A

Phenoxybenzamine
Phentolamine
Ergotamine

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7
Q

α1 selective blockers:

A
Prazosin
Terazosin
Tamsulosin
Alfuzosin
Doxazosin
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8
Q

α2 selective blockers:

A

Yohimbine

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9
Q

Non-selective β blockers:

A

Propranolol
Pindolol
Timolol

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10
Q

α & β blockers:

A

Labetalol

Carvedilol

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11
Q

β1 blockers:

A

Atenolol
Metoprolol
Esmolol

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12
Q

Adrenergic neuron blockers:

A

Reserpine
Guanethidine
Methyldopa
Bethanidine

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13
Q

Ganglionic blockers:

A

Trimetaphan

Mecamylamine

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14
Q

Side effects associated with interference in sympathetic neuron function:

A
Postural hypotension (GGb)
Sedation or depression
Increase GI motility and diarrhea
Sexual dysfunction
Increase blood volume and Na retention
Nasal stuffiness
Extrapyramidal syndrome
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15
Q

α2 agonists have an ___ effect on sympathetic discharge from the ___ in the brainstem:

A

inhibitory; VMC

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16
Q

Adverse effects of α2 agonists:

A
Drowsiness or sedation
Dry mouth (xerostomia)
Decrease in BP
Bradycardia
Rebound hypertension (acute withdrawal)
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17
Q

When given ___, postsynaptic α2 receptors result in a transient ___:

A

parenterally; rise in BP

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18
Q

These drugs block the antihypertensive effect of clonidine:

A

Tri-cyclic antidepressants

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19
Q

Guanfacine has ___ effects similar to Clonidine but is slower to enter the __:

A

hemodynamic; CNS

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20
Q

α2 agonists undergoing extensive 1st pass metabolism:

A

Methyldopa

Guanabenz

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21
Q

α2 agonist which gives a (+) Coombs test:

A

Methyldopa

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22
Q

α2 agonist that may activate imidazoline receptors:

A

Clonidine

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23
Q

Therapeutic uses of clonidine:

A
HTN
Reduce diarrhea in diabetics
Treatment for withdrawal
Menopausal hot flashes
Diagnosis of pheochromocytoma
24
Q

Usual half-life of α2 agonists:

A

6-24 hours

25
Advantages of Guanfacine over Clonidine
More selective for α2 receptors Adverse effects milder Withdrawal symptom milder
26
These drugs should never be given alone when treating α2 agonist withdrawal:
β-blockers
27
Used in the treatment of ADHD in children 16-17:
Guanfacine
28
Drugs causing extrapyramidal symptoms:
Methyldopa | Reserpine
29
α2 agonist used for ocular hypertension and open-angle glaucoma:
Apraclonidine | Brimonidine
30
Glaucoma therapy drug the crosses the BBB and is more selective for α2:
Brimonidine
31
Blockade of presynaptic α2 receptors leads to enhanced release of ___ and stimulation of ___ receptors and ____:
norepinephrine; postsynaptic β1; JG cells
32
Blockade of α1 receptors inhibits vasoconstriction, leading to:
``` Decreased blood pressure (orthostatic hypertension) Fluid retention (RAA activation) ```
33
Therapeutic uses of phenoxybenzamine:
``` Pheochromocytoma Reverse local anesthesia Prevent dermal necrosis Treat rebound hypertension Sexual dysfunction Peripheral vascular disease ```
34
Phenoxybenzamine generally has a ___ onset and ___ duration:
slow (1 hr); long (12-14 hrs)
35
Phenoxybenzamine exhibits a 100:1 selectivity for __ receptors vs. __ receptors:
α1; α2 SNS excitation and increased motor activity)
36
CNS effects of phenoxybenzamine depend on:
``` Slow IV administration (sedation, fatigue, nausea) Rapid IV (SNS excitation and increased motor activity) ```
37
α1a (uroselective) blockers:
Tamsulosin Silodosin Afluzosin
38
Nonselective α1 blockers are more prone to:
1st dose effect
39
Phentolamine has a ___ onset and ___ duration:
rapid (1 hr); short
40
Contraindications of phentolamine:
Coronary Artery Disease | History of peptic ulcer
41
Other receptors stimulated by phentolamine:
Muscarinic, H1, H2 (increased gastric acid secretion)
42
Phenoxybenzamine and Phentolamine are both used to treat:
Pheochromocytoma
43
Blockade of __ receptors are responsible for reflex tachycardia:
α2
44
Therapeutic uses of Prazosin:
Mild to moderate HTN Congestive heart failure Impaired bladder emptying
45
α1 blockers from longest to shortest half-life:
Terazosin (12) > Tamsulosin > Alfuzosin > Prazosin (2-3)
46
α1a selection blockers exhibit no ___ and are metabolized by ___:
1st dose effect; CYP450
47
α1 blockers with apoptotic effects on prostrate smooth muscle:
Terazosin | Doxazosin
48
Ergot preparation with greatest α blocking property:
Ergotoxine
49
Ergot preparation with highest selectivity for dopamine receptors
Cabergoline Pergolide Bromocriptine (suppress prolactin)
50
Ergot preparations with agonist effects at α receptors:
Ergotamine Ergonovine Methysergide
51
Ergot derivatives with increased α blocking action:
Dihydro
52
Ergot DOC in preventing postpartum bleeding:
Ergonovine
53
Ergot alkaloids are combined with __ to facilitate absorption when used to treat ___:
Caffeine; migraines
54
Ergot used for senile cerebral insufficiency:
Dihydroergotoxine
55
Erogt used to treat parkinsonism:
Bromocriptine
56
Depressants that will cause hypotension:
``` Ganglionic blockers Guanethidine Methyldopa Reserpine Clonidine Conventional α blockers ```