Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
35 Cards in this Set
- Front
- Back
disease caused by excess ergot alkaloids
|
St. Anthony's fire
|
|
endogenous substances commonly interpreted as histamine, serotonin, prostaglandins, and vasoactive peptides
|
autocoids
|
|
syndrome of hypersecretion of gastric acid and usually caused by gastrinoma; associated with peptic ulceration and diarrhea
|
Zollinger-Ellison syndrome
|
|
drug that causes contraction of the uterus
|
oxytocin
|
|
distribution of histamine receptors H1, H2, and H3
|
H1: smooth muscle
H2: stomach, heart, mast cells H3: nerve endings, CNS |
|
prototype antagonist of H1 and H2 receptors
|
diphenydramine and ranitidine, respectively
|
|
1st generation antihistamine that is highly sedating
|
diphenhydramine
|
|
1st generation antihistamine that is least sedating
|
chlorpheniramine or cyclizine
|
|
2nd generation antihistamines
|
fexofenadine, loratadine, cetirizine
|
|
generation of antihistamine that has most CNS
|
1st generation because more lipid soluble
|
|
Major indication for H1 receptor antagonist
|
use in IgE mediated allergic reaction
|
|
antihistamine that can be used for anxiety and is not addictive
|
hydroxyzine (atarax)
|
|
H1 antagonist used in motion sickness
|
dimenhydrinate, meclizine, and other 1st generation
|
|
most common side effect of 1st generation antihistamines
|
sedation
|
|
lethal arrhythmias resulting from concurrent therapy with azole antifungals (metabolized by CYP3A4) and these antihistamines which inhibit 3A4 isoenzyme
|
terfenadine and astemizole (both removed from market)
|
|
H2 blocker that causes the most interactions with other drugs
|
cimetidine
|
|
clinical use for H2 blockers
|
acid reflux disease, duodenal ulcer and peptic ulcer disease
|
|
receptors for serotonin (5HT-1) are located
|
mostly in the brain, and they mediate synaptic inhibition via increased K+ conductance
|
|
5-HT1d agonist used for migraine headaches
|
sumatriptan, naratriptan, and rizatriptan
|
|
triptan available in parenteral and nasal formulation
|
sumatriptan
|
|
H1 blocker that is also a serotonin antagonist
|
cyproheptadine
|
|
agents for reduction of postpartum bleeding
|
oxytocin, ergonovine, ergotamine
|
|
5HT-3 antagonist used in chemotherapeutic induced emesis
|
ondansetron, granisetron, dolasetron, alosetron
|
|
agents used in treatment of carcinoid tumor
|
ketanserin, cyproheptadine, phenoxybenzamine
|
|
5HT-3 antagonist that has been associated with QRS and QTc prolongation and should not be used in patients with heart disease
|
dolasetron
|
|
DOC for chemo induced nausea and vomiting
|
ondansetron
|
|
drug used in ergot alkaloids overdose, ischemia and pregnancy
|
nitroprusside
|
|
reason ergot alkaloids are contraindicated in pregnancy
|
uterine contraction- abortion
|
|
ergot alkaloid used as an illicit drug
|
LSD
|
|
SE of ergot alkaloids
|
hallucinations resembling psychosis
|
|
dopamine agonist used in hyperprolactinemia
|
bromocriptine
|
|
peptide causing increased capillary permeability and edema
|
bradykinin and histamine
|
|
mediator of tissue pain, edema, inactivated by ACE and may be a contributing factor to the development of angioedema
|
bradykinin
|
|
drug causing depletion of substance P (vasodilator)
|
capsaicin
|
|
prostaglandins that cause abortions
|
prostaglandin E1 (misoprostol), PGE2, and PGF2alpha
|