AITC for Health & Longevity - Quick Reference Sheet

AITC for Health & Longevity

Created on 07/16/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 4.8 Audit

The pungent compound in mustard, horseradish, and wasabi. At food-level amounts it gently activates the body's own cleanup and antioxidant defenses and fights bacteria and fungi. Cancer-protective and anti-inflammatory hints rest mostly on lab and animal work. Concentrated amounts irritate and burn; the safety margin is wide at food levels, but human evidence is thin. (Full Review)

Protocol

Primary Approach
Whole foods
AITC is delivered through mustard, horseradish, wasabi, and ~1 cup/day of cruciferous vegetables rather than the isolated compound
Preparation
Raw or lightly prepared
Foods are eaten raw, or a raw myrosinase source (mustard powder) is added to cooked cruciferous foods, since prolonged heat destroys the enzyme that forms AITC
Dosing
Divided, with meals
Intake is spread across the day and paired with meals to sustain pathway activation and buffer gastrointestinal irritation
Time to effect
Enzyme Induction
Hours–days
Phase II detoxification-enzyme activity is measurable within hours to a few days of exposure
Cancer / Longevity Benefit
Years
Any cancer-preventive or longevity benefit is a long-term, cumulative proposition from sustained dietary pattern

Benefits

Contraindications
  • Pregnancy and breastfeeding
  • Active peptic ulcer disease or acute gastrointestinal inflammation
  • Poorly controlled reactive airway disease
  • Iodine-deficient thyroid disease
Key Interactions
  • Cytochrome P450–metabolized drugs (e.g., acetaminophen, CYP1A2 substrates)
  • Topical counterirritants and rubefacients
  • Anticoagulant and antiplatelet agents (e.g., warfarin, aspirin, clopidogrel)
  • Other Nrf2-activating isothiocyanate supplements (e.g., sulforaphane)
  • Iodine and thyroid-support supplements
  • Glutathione-depleting stress (heavy alcohol, acetaminophen overdose risk)

Risk & Side Effects

  • High: Gastrointestinal and oral mucosal irritation; skin irritation and allergic contact dermatitis
  • Medium: High-dose genotoxicity and rodent bladder carcinogenicity; respiratory and airway irritation
  • Low: Drug-metabolizing enzyme interactions; pro-oxidant effects at high concentrations
  • Speculative: Goitrogenic / thyroid effects; reproductive and developmental concerns

Monitoring

Marker Target Why
TSH 0.5–2.5 mIU/L Screens for thyroid suppression from high isothiocyanate intake
Free T4 1.0–1.5 ng/dL Confirms adequate thyroid output alongside TSH
Free T3 3.0–4.0 pg/mL Detects reduced conversion or thyroid output
Urinary iodine 100–200 µg/L Confirms iodine adequacy that offsets goitrogenic risk
Urinary isothiocyanate Higher reflects greater intake (research marker) Objective marker of actual isothiocyanate exposure

Cadence: Baseline, follow-up at ~3 months, then every 6–12 months

Qualitative Assessment

  • Digestive tolerance: no mouth, throat, or stomach burning after intake
  • Energy and general well-being: stable energy without new fatigue
  • Skin and airway comfort: no new dermatitis or airway irritation