Atropine
Key Board Facts Grid
Target Receptors
Non-selective M1–M5 muscarinic antagonist
BBB Penetration
Tertiary amine; crosses the BBB at high doses
Primary Indication
Symptomatic bradycardia, high-grade AV block, organophosphate poisoning muscarinic effects
First-Line Antidote
Physostigmine for isolated anticholinergic toxidrome
Mechanism of Action
- Competitive antagonism at all muscarinic ACh receptors.
- M2 blockade in SA/AV nodes increases heart rate and AV conduction.
- M3 blockade produces mydriasis, cycloplegia, dry mouth, urinary retention, decreased GI motility.
- M3 sweat-gland blockade causes anhidrosis and hyperthermia.
- No nicotinic receptor blockade at usual clinical doses.
Adverse Effects & Toxicities
- Classic anticholinergic toxidrome: delirium, mydriasis, cycloplegia, dry mouth, urinary retention, constipation, tachycardia, hyperthermia.
- Can precipitate acute angle-closure glaucoma in shallow anterior chambers.
- Infants are especially prone to hyperthermia; elderly to delirium.
- Contraindications: narrow-angle glaucoma, severe BPH/urinary retention, GI obstruction, paralytic ileus, tachycardia.
DO / OMM Board Pearl
Blunts vagal tone (CN X) at the SA and AV nodes. Mimics a relative sympathetic state. In OMT, this correlates with reduced parasympathetic influence over cardiopulmonary structures T1–T5.