Sympathetic Depressants Flashcards

(56 cards)

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:

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 ```