Last updated: March 2026
Opioid antagonist at 1/10th to 1/50th the addiction dose. Brief receptor blockade causes rebound endorphin increase. Modulates TLR4 for anti-inflammatory effects.
Low-Dose Naltrexone uses naltrexone at micro-doses (1-4.5mg vs 50mg for addiction treatment). The low dose creates a brief receptor blockade followed by upregulation of the body's own opioid system.
Brief opioid receptor blockade (4-6 hours) triggers compensatory increase in endogenous endorphins. Patients report improved mood, energy, and pain relief.
Naltrexone at low doses modulates toll-like receptor 4 (TLR4) on microglia and immune cells. This reduces pro-inflammatory cytokine release.
LDN appears to modulate immune function in autoimmune conditions — reducing disease activity in MS, Crohn's, fibromyalgia. Mechanism still being elucidated.
Standard naltrexone is 50mg tablets. LDN doses (1-4.5mg) require compounding pharmacy. Not available at regular pharmacies.
Context: ~90% of LDN research is off-label. Naltrexone FDA-approved for addiction (50mg). LDN research is mostly case series, small trials, and patient-reported outcomes. Growing interest from functional medicine.
Support supplements for LDN therapy.
Dosing schedules, interaction warnings, and cycle protocols for 50+ compounds — all in one place.
LDN is OFF-LABEL — naltrexone is FDA-approved for addiction treatment (50mg), but LDN (1-4.5mg) is not approved for any medical condition. Requires compounding pharmacy. This is not medical advice. Always consult a healthcare provider. Off-Label Use Compounding Required