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PeptideWADA Status UnclearCompare

DSIP

Also known as: Delta Sleep Inducing Peptide, Delta Sleep Peptide, Factor Delta

1
1 · Natty510 · Enhanced

Lower numbers = closer to natural. Higher numbers = more enhanced.

Why this rating?

DSIP is a sleep-focused neuropeptide with no direct anabolic mechanism. It does not stimulate protein synthesis or act as a GH secretagogue the way CJC-1295/Ipamorelin do. Animal studies (Iyer et al. 1987/1988) suggested it could trigger nocturnal GH pulses and blunt stress-hormone responses, but the controlled human trials that actually tested this found no effect: Giusti et al. (1993) reported no change in GH or prolactin in healthy women, and Späth-Schwalbe et al. (1995) reported no change in CRH- or meal-induced ACTH/cortisol. Any real-world benefit is indirect, via better sleep quality and recovery. Rated 1 (basically natty): it is a sleep aid, not a muscle-, fat-, or hormone-altering compound, and the human data show no measurable GH or cortisol effect, so it does not move the muscular/physique ceiling beyond natural by any established path.

Overview

A 9-amino acid neuropeptide (Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu, ~849 Da) first isolated from rabbit cerebral venous blood in 1974 and chemically characterized by Schoenenberger & Monnier in 1977. Promotes delta wave (slow-wave) sleep stages 3-4 NREM. Modulates GABA and serotonin systems. Animal studies report increased nocturnal GH pulses and altered stress-hormone responses, but the controlled human trials that tested this directly found no effect on GH/prolactin (Giusti et al. 1993) or on CRH-/meal-induced ACTH/cortisol (Späth-Schwalbe et al. 1995): so the often-repeated GH and cortisol claims are largely unproven in humans. Research peaked in the 1980s-90s but development stalled due to very short half-life and inconsistent clinical results. Evidence quality is low-moderate with mostly small, outdated studies.

Important Warnings

  • •NOT approved for human therapeutic use anywhere
  • •Evidence quality is LOW-MODERATE (small, outdated studies from 1980s-90s)
  • •Inconsistent results in clinical trials - effects vary by individual
  • •Very short plasma half-life creates formulation challenges
  • •Quality control varies significantly between peptide suppliers
  • •No pharmaceutical-grade product exists
  • •Avoid with sedatives, benzodiazepines, alcohol (additive sedation)
  • •Avoid driving or operating machinery after administration
  • •Long-term safety data is absent
  • •Mechanism of action incompletely understood

Purpose & Use Cases

Sleep Quality Improvement

Promotes slow-wave (delta) sleep. Reduced sleep latency and improved sleep efficiency in some insomnia studies. Effects may be more pronounced in sleep-disordered individuals than healthy subjects.

GH Enhancement (unproven in humans)

Animal studies (Iyer et al. 1987/1988) report increased nocturnal GH pulse amplitude, often cited as "30-50%" though that figure traces to older/animal work rather than a controlled human trial. The one controlled human trial that tested this, Giusti et al. (1993), found no significant change in GH or prolactin. Not comparable to exogenous GH.

Stress/Cortisol Normalization (unproven in humans)

Improved stress tolerance and stress-hormone markers in animal models (e.g., preserved hypothalamic substance P, blunted adrenal/thymus stress response, Salieva et al. 1992). However, a controlled human trial (Späth-Schwalbe et al. 1995) found DSIP did not alter CRH- or meal-induced ACTH/cortisol secretion, so cortisol-normalizing claims are not established in humans.

Recovery Support

Theoretical improvement through better sleep quality alone (the cortisol-lowering pathway is not confirmed in humans). Any enhanced recovery capacity during intense training periods is indirect.

Benefits

  • May improve slow-wave sleep quality
  • GH pulse increases seen in animal studies, but not confirmed in the one controlled human trial
  • Stress-protective effects seen in animal models; a controlled human trial found no cortisol/ACTH effect
  • Acts as an endogenous stress-limiting factor in animal research
  • Generally well-tolerated with mild side effects (largest human trial, n=107, reported good tolerance aside from occasional headache)
  • No evidence of dependence or tolerance in short-term studies
  • Not currently WADA prohibited
  • Crosses blood-brain barrier effectively

Good to Know

A sleep peptide, not an anabolic

DSIP's job is to promote delta (slow-wave) sleep. Any physique benefit is indirect. Better sleep can support recovery. It does not build muscle or burn fat directly, which is why it sits at a 2, in line with other pure health/recovery peptides (Epithalon, GHK-Cu, ARA-290, Cerebrolysin) that don't move muscular potential beyond natural.

The growth-hormone and cortisol claims are weak in humans

The often-repeated '30-50% increase in nocturnal GH' comes largely from rat studies (Iyer et al. 1987/1988) and older work. The one controlled human trial that tested it, Giusti et al. (1993), found infusing DSIP in healthy women did not change GH or prolactin secretion. Likewise, a separate human trial (Späth-Schwalbe et al. 1995) found DSIP did not affect CRH- or meal-induced ACTH/cortisol. Any GH or recovery benefit is probably secondary to improved sleep, and is nothing like exogenous GH or a secretagogue. Treat the GH/cortisol angle as unproven in humans.

Very short half-life, but effects outlast the peptide

DSIP is cleared from plasma on the order of minutes (estimates across sources range roughly 7-25 minutes) via peptidase degradation, yet its sleep effects have been reported to persist for hours, up to ~20 hours after IV dosing in one human study (Schneider-Helmert & Schoenenberger 1983). It appears to trigger downstream GABA/serotonin cascades that outlast the molecule. The flip side: the short half-life and formulation challenges mean no pharmaceutical-grade product exists and evidence quality is low-to-moderate.

Additive sedation: mind the stack

Because it works partly through GABA, DSIP can add to the sedation of benzodiazepines, alcohol, opioids, and other CNS depressants. Dose it 30-60 min before bed, and do not drive or operate machinery afterward.

Dosage Guidelines

Experience LevelDosage Range
Beginner100 – 100 mcg/day
Intermediate100 – 200 mcg/day
Advanced200 – 300 mcg/day
Frequency
Once daily, 30-60 minutes before bed. Some use 5 days on/2 days off.
Typical Cycle Length
4 – 8 weeks
Notes

Research doses: 25-100 mcg/kg intranasal/IV. Bodybuilding: 100-300mcg SC before bed. Very short plasma half-life (~7-25 min, estimates vary) but biological effects persist. Phosphorylated DSIP (DSIP-P) may have extended half-life.

Half-Life

Plasma clearance is very fast (rapidly degraded by peptidases; estimates vary by source), but behavioral/sleep effects have been reported to persist for hours, up to ~20 hours after IV dosing in one human study (Schneider-Helmert & Schoenenberger 1983).

Side Effects

Transient Warmth/Flushing

common
Severity
1/5

Brief sensation of warmth after injection.

Mitigation

Self-limiting. No intervention needed.

Drowsiness

common
Severity
1/5

Expected effect - indicates activity. Take before bed.

Mitigation

Ensure administration before bedtime.

Mild Headache

uncommon
Severity
1/5

Occasional headache reported.

Mitigation

Usually transient. Stay hydrated.

Injection Site Reaction

uncommon
Severity
1/5

Mild irritation at injection site.

Mitigation

Rotate injection sites.

Transient Hypotension

rare
Severity
1.5/5

Brief blood pressure reduction reported rarely.

Mitigation

Lie down if dizzy. Usually resolves quickly.

General Mitigation Strategies

DSIP is generally well-tolerated. The largest human trial to date (Dick et al. 1984, n=107, IV dosing for withdrawal syndromes) reported good tolerance aside from headaches in a few patients, with no serious adverse events. Side effects at typical research doses are typically mild and transient. No significant cardiovascular concerns reported at research doses. Long-term safety data is limited. No evidence of dependence or tolerance in short-term use.

Support Supplements

Ancillary supplements commonly run alongside DSIP to manage side effects, support the target tissue, or fill nutrient demands it creates.

Magnesium (glycinate/threonate)

Well-tolerated sleep-quality aid that complements a sleep-focused peptide, supports GABAergic tone and muscle relaxation. Deficiency is common in hard-training lifters.

Dose
~200-400mg elemental
Timing
Evening, with the pre-bed DSIP dose
When
General sleep support rather than a DSIP-specific requirement.

Glycine

Amino acid shown to improve subjective sleep quality and lower core body temperature at sleep onset; pairs logically with a slow-wave-sleep peptide.

Dose
~3g
Timing
30-60 min before bed
When
Optional add-on; modest, evidence-backed effect on sleep onset.

Post Cycle Therapy (PCT)

✓PCT Not Required

Does not suppress the HPT axis. No PCT required. May indirectly support recovery through improved sleep quality (direct cortisol-normalizing effects have not been confirmed in controlled human trials).

How It Works

Incompletely understood. Modulates GABA-A receptor activity (possibly allosteric). Influences serotonin release and 5-HT receptor sensitivity. Promotes delta wave sleep without significantly altering REM. Stimulated GH release during sleep phases and blunted stress-hormone responses in animal models, but controlled human trials found no effect on GH/prolactin or on CRH-/meal-induced ACTH/cortisol secretion. Crosses blood-brain barrier despite peptide nature.

Fundamentals

Common Stacks

  • DSIP 100-200mcg before bed + Ipamorelin/Mod GRF - sleep and GH optimization
  • DSIP + Melatonin - enhanced sleep quality (start melatonin low)
  • DSIP during contest prep - sleep support during stressful deficit
  • Avoid CNS depressants (benzos, alcohol, opioids) - additive sedation risk
  • Take 30-60 minutes before intended sleep time

WADA Status

❓WADA Status Unclear

DSIP (Delta Sleep-Inducing Peptide) is not explicitly listed on the WADA Prohibited List. It has no direct performance-enhancing effect, but as a non-approved research peptide it could still be argued under S0 (non-approved substances) for tested athletes, so its status is genuinely unclear. Verify before competition.

References

Last updated: July 19, 2026