Trigger Attack Console

Stack triggers to push the patient toward an AIP attack. Watch the severity bar rise, symptoms light up. Apply the right treatments to bring it down.

Patient · Quiet at baseline

Each trigger induces hepatic ALA synthase. Stack enough and the partial PBG deaminase block becomes a clinical attack. Treatments bypass the trigger or shut down ALA synthase directly.

Attack severity Quiet
Add a trigger
Symptoms (light up as severity climbs)
Vague abdominal pain
Severe colicky pain + nausea
Dark / port-wine urine
Tachycardia + HTN (autonomic)
Motor weakness, neuropathy
Anxiety, hallucinations, seizures
Respiratory paralysis (crisis)
Treatments (subtract from severity)
No events yet.
From the Attending

AIP is a setup, not a constant. Patient is fine until the liver gets pushed to make more heme · sulfa / barbiturate / OCP / fasting / alcohol / infection / smoking induce ALA synthase. PBG deaminase can\'t keep up · ALA + porphobilinogen pile up · the nervous system gets toxic. Treat in this order: stop the trigger, IV glucose (turns off ALA synthase upstream), then IV hemin (negative feedback at ALA synthase). Don\'t treat porphyria with phenobarb · you\'ll make it worse.

BIOCHEM · Heme Synthesis

Acute Intermittent Porphyria

Trigger opens the faucet. PBG deaminase blocks the pipe. ALA/PBG spill out, and the patient gets NEUROVISCERAL.

Here is your patient: A 24-year-old woman has severe cramping abdominal pain, constipation, anxiety, and reddish urine after starting an antiseizure drug. Her abdomen is tender but has no rebound or guarding. Which enzyme is most likely deficient?
Ferrochelatase
Porphobilinogen deaminase
Uroporphyrinogen decarboxylase
Glucose-6-phosphate dehydrogenase
The clue is not just dark urine. It is dark urine plus neurovisceral chaos: abdominal pain, constipation, anxiety, neuropathy, tachycardia, or hypertension after a trigger. A trigger raises hepatic heme demand, ALA synthase opens the faucet, and the blocked PBG deaminase step makes ALA/PBG pile up. Those precursors irritate nerves. AIP = PBG deaminase deficiency = abdominal pain + psych/autonomic symptoms + dark urine.
1 / 7

The Heme Factory

Run the trigger. Watch the blocked assembly line spill neurotoxic precursors.

Chapter I · Hector Idles
HECTOR
"Hector the hepatocyte is quiet. ALA synthase idles. PBG deaminase is narrow, but nothing is overflowing yet."
ALA input PBG checkpoint HEME product NORMAL FLOW No trigger. No attack. Factory pressure normal.
Baseline: Hector makes heme calmly. ALA becomes PBG, PBG moves downstream, and finished heme keeps the faucet quiet.
Chapter II · Hector Gets Pushed
ALA SYNTHASE UP
"Barbiturate, alcohol, fasting, hormones. Liver demands more heme."
FAUCET OPEN ALA PBG HEME Triggers induce hepatic enzymes and increase heme demand.
A trigger tells Hector to make more heme. He opens the ALA synthase faucet, so more raw material rushes into the line.
Chapter III · Hector Overflows
PBG DEAMINASE BLOCK
"PBG cannot clear. ALA/PBG back up and spill into nerves and urine."
TOXIC BACKUP ALA / PBG NERVES + URINE HEME
Now the chain becomes clinical: more inflow meets the PBG deaminase block, ALA/PBG back up, and the spill irritates nerves.
Pattern Locked · AIP
The AIP Chain
RouteTrigger → ALA synthase up → PBG deaminase block → ALA/PBG accumulate → nerves irritated
PatternUrine δ-ALA + porphobilinogen, abdominal pain, neuropathy, red-dark urine.
PearlSevere abdominal pain with a quiet exam is wiring pain, not peritoneal fire.
🎯Board clue chain: high porphyrin precursors, urine δ-ALA and porphobilinogen, then abdominal pain, neuropathy, and red-dark urine.
Move: stop the trigger, then give glucose and hemin to turn down ALA synthase upstream.
Board trap: dark urine after a drug can look like G6PD, but G6PD gives hemolysis signs. AIP gives nerve signs.
From the Attending

Heme synthesis is the playground for the porphyrias. ALA synthase (mitochondria) is the rate-limiter, induced by anything that depletes hepatic heme: alcohol, sulfa, antifungals, OCPs, smoking, fasting, infection. PBG deaminase (cytosol) is broken in AIP · ALA + porphobilinogen pile up · both are neurotoxic, neither photosensitizes the skin (no porphyrins past this block). That's why AIP gives abdominal pain + neuropathy + psychiatric symptoms but NEVER photosensitivity. Porphyria cutanea tarda blocks LATER in the pathway (uroporphyrinogen decarboxylase) → porphyrins build up → sun-exposed skin blisters. Position in the pathway predicts the symptom set.

Medically reviewed by Kaitlyn Cocuzzo, MD and Fatima Ali, DO · Last reviewed June 2026
Bone Wizardry is an independent educational resource for visual learning in the medical sciences. It is not affiliated with, endorsed by, or sponsored by any licensing or examination board, contains no real or recalled examination questions, and does not guarantee any educational or examination outcome.