DSIP for Health & Longevity - Quick Reference Sheet

DSIP for Health & Longevity

Created on 09/30/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5.5 – Audit

DSIP, a chain of nine amino acids sold as an injectable research product for sleep, stress resilience and healthy aging, has promised benefits unconfirmed in people. Its discoverers reported better sleep, but independent controlled studies found only small changes. Longevity evidence rests entirely on animal studies. Reported side effects were mild in the few hundred people studied over weeks; unregulated manufacturing and combining with other sleep-promoting drugs pose larger risks. (Full Review)

Protocol

Basel clinical protocol
25–30 nmol/kg intravenous
About 1.5 mg for 70 kg by slow injection, usually evening, 4–7 consecutive days; used in all controlled insomnia trials
Peptide-clinic protocol
100–300 µg subcutaneous
1–3 hours before bed in short cycles; never tested in trials
Time of day
Evening, single daily dose
Split twice-daily dosing reduced effectiveness in the Basel studies
Time to effect
Insomnia normalized
~4 doses
About four consecutive doses; effects built up over doses
Older adults
Up to 2 weeks
Including follow-up, to reach normal sleep
Sleep pressure
~1 hour
After intravenous injection

Benefits

Contraindications
  • Pregnant or breastfeeding women (any trimester)
  • People under 18 years of age
  • Untreated moderate-to-severe obstructive sleep apnea (≥15 breathing pauses per hour)
  • Heart attack, unstable angina (chest pain at rest or rapidly worsening) or stroke within the past 90 days
  • Active alcohol or opioid withdrawal outside medical supervision
  • Competitive athletes under World Anti-Doping Agency testing (prohibited class S0)
  • Known allergy to DSIP or any other product ingredient
Key Interactions
  • Prescription sleep medications (zolpidem, eszopiclone, temazepam, lorazepam)
  • Opioids (oxycodone, morphine, methadone, buprenorphine)
  • Opioid antagonists (naltrexone, naloxone)
  • Other sedating prescription drugs (gabapentin, pregabalin, trazodone, mirtazapine, quetiapine)
  • Over-the-counter sleep aids and sedating antihistamines (diphenhydramine, doxylamine)
  • Alcohol
  • Supplements with additive sleep effects (melatonin, magnesium glycinate, glycine, valerian, kava)
  • L-tryptophan supplements

Risk & Side Effects

  • High:
  • Medium: Unintended daytime sleepiness
  • Low: Headache; faster heart rate and reduced heart rate variability
  • Speculative: Impurities, contamination and immune reactions; harm during acutely blocked blood flow to the heart or brain; unknown long-term effects

Monitoring

Marker Target Why
Insomnia Severity Index (ISI) 0–7 Primary insomnia outcome
Sleep efficiency ≥90% Main outcome in DSIP trials
Sleep onset latency 10–20 min Tracks faster sleep onset
Deep (slow-wave) sleep No established target; track change from own baseline DSIP's proposed target
Apnea–hypopnea index (AHI) <5 events/hour Excludes sleep apnea before use
Fasting glucose 75–90 mg/dL Claimed glucose effects
HbA1c 4.8–5.4% Three-month glucose average
Morning cortisol 10–18 µg/dL Claimed stress-hormone effects
ALT <25 U/L Liver safety of unregulated injectable
eGFR >90 mL/min/1.73 m² Kidney function baseline

Cadence: Baseline (including at least one week of sleep-diary or wearable data); at 1 week and 2 weeks into each course (sleep questionnaire, diary or wearable, morning alertness); every 3–6 months for repeated courses (blood tests)

Qualitative Assessment

  • Subjective sleep quality and feeling rested on waking
  • Morning grogginess or unintended daytime sleepiness
  • Daytime alertness, concentration and mood
  • Headache frequency after doses
  • Injection-site redness, swelling or pain