Overview
Endogenous sleep hormone; low doses (0.3–0.5 mg) typically outperform mega-doses.
- Synthesized; pineal gland
- Immediate-release
- Sustained-release
- Sublingual
Mechanism of action
Activates MT1/MT2 receptors in SCN to entrain circadian rhythm.
- · MT1/MT2 receptor activation
- · Melatonin
Effects on the body
Organ system effects
Effective for circadian misalignment (jet lag, shift work).
Evidence-based benefits
Reduces jet lag and sleep latency in circadian disorders
Strong evidencePotential side effects
- · Vivid dreams
- · Morning grogginess (high dose)
- · Headache
Drug interactions
Safety & non-supplemental interactions
Educational summary — always confirm with your clinician or pharmacist before starting, stopping, or combining with prescription therapy.
- ·Alcohol, benzodiazepines, opioids, sedating antihistamines (additive CNS depression)
Supplement interactions
None listed.
No specific avoidances listed.
Dosing & bioavailability
Where to buy
Affiliate-style search links to reputable retailers. We don't endorse specific brands — verify third-party testing (USP, NSF, Informed Sport) before purchase.
Scientific evidence (8)
Low-dose melatonin for insomnia in older adults
Zhdanova IV, et al.
RCT of 0.3 mg melatonin in older insomniacs.
Physiologic doses restored sleep architecture; higher doses less effective.
PubMed: Melatonin (low-dose physiologic) — Reduces jet lag and sleep latency in circadian disorders
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PubMed: Melatonin (low-dose physiologic) — randomized controlled trial
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PubMed: Melatonin (low-dose physiologic) — meta-analysis
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PubMed: Melatonin (low-dose physiologic) — pharmacokinetics
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PubMed: Melatonin (low-dose physiologic) — safety adverse events
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PubMed: Melatonin (low-dose physiologic) — dose response
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Google Scholar: Melatonin (low-dose physiologic) — clinical evidence
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