Pharmacology - Gastrointestinal Flashcards
Name some classes of antiemetics and their mechanism of action
- serotonin 5-HT3 antagonists: ondansetron (serotonin antagonist)
- corticosteroids: dexamethasone (unknown)
- phenothiazines: stemetil (D2 blocker), largactil (D2+ blocker), phenergen (H1+ blocker)
- substituted benzamides: metoclopramide (D2 blocker)
- butyrophenones: droperidol (D2 blocker)
What is the mechanism of action and adverse effects of Metoclopramide
Mechanism: dopamine (D2) antagonist at the chemoreceptor trigger zone
centrally acts as antiemetic, peripherally acts as a prokinetic
Side effects: restlessness, drowsiness, insomnia, anxiety, agitation, EPSE, NMS
What is the mechanism of action, routes of administration and side effects of Ondansetron
- mechanism: 5-HT3 receptor antagonist (mostly peripheral)
- administration: 4-8mg PO/IV/SC/IM
- uses: chemotherapy, post-operation nausea
- side effects: headache, dizziness, constipation, diarrhoea, prolonged QT
- modify dosing in hepatic failure (not renal failure)
What are the adverse effects of Prochlorperazine (stemetil)
EPSE
sedation
anticholinergic effects
allergy
What are the classes and mechanism of action of laxatives
-bulk forming laxatives: psyllium
colloids that absorb water and forms bulky gel that promotes peristalsis
-stool softener: docusate
softens stool to permit water and lipids to penetrate
-osmotic laxatives: lactulose
soluble but non-absorbable compounds that increase stool liquidity
-stimulant laxatives: senna
direct stimulation of enteric nervous system
-opioid receptor antagonist: methylnaltrexone
blocks intestinal mu opioid receptor
What is polyethylene glycol
- laxative used as preparation for endoscopic procedures
- balanced isotonic solution so that no significant intravascular fluid shift occurs
- osmotically active sugar, not absorbed
What is the mechanism of action of PPI
- mechanism: forms covalent disulfide bond with H+/K+ATPase causing irreversible inhibition of the proton pump
- IV infusion is preferred because PPI only inactivates actively secreting pumps
How do you increase bioavailability of oral PPI
- lipophilic weak bases so best absorbed in basic environment (small bowel)
- taken as inactive prodrugs
- acid resistant enteric coat prevents gastric elimination
- take on empty stomach because food decreases bioavailability (take 1 hour prior to meal)