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DSIP

Also known as: Delta Sleep-Inducing Peptide, Delta Sleep Peptide, Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu

DSIP (Delta Sleep-Inducing Peptide) is a naturally occurring nonapeptide first isolated from rabbit brain in 1977. It modulates sleep architecture, stress response, and neuroendocrine function. Research shows it promotes delta (slow-wave) sleep without sedation and normalizes disrupted sleep patterns.

Last updated: February 1, 2025Reviewed by: PeptideHub Research Team

DSIP is a 848.81 Da research peptide. DSIP (Delta Sleep-Inducing Peptide) is a naturally occurring nonapeptide first isolated from rabbit brain in 1977. It modulates sleep architecture, stress response, and neuroendocrine function. Research shows it promotes delta (slow-wave) sleep without sedation and normalizes disrupted sleep patterns.

Also called: Delta Sleep-Inducing Peptide, Delta Sleep Peptide, Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu

848.81

Molecular Weight

Daltons

0

Strong Evidence

benefits

5

Studies Cited

peer-reviewed

100-300

Typical Dose

mcg

Overview

DSIP is a naturally occurring 9-amino acid peptide (Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu) first isolated from the cerebral venous blood of rabbits during electrically induced slow-wave sleep by Schoenenberger and Monnier in 1977. Unlike conventional sedatives or hypnotics, DSIP does not force sleep onset but rather modulates sleep architecture; promoting physiological delta wave (slow-wave) sleep patterns and normalizing disrupted sleep-wake cycles. DSIP is found in both the central nervous system and peripheral tissues, with concentrations fluctuating in a circadian pattern. Beyond sleep, DSIP demonstrates unusually broad biological activity: it modulates the hypothalamic-pituitary-adrenal (HPA) axis stress response, has analgesic properties, shows anticonvulsant effects, influences thermoregulation, and modulates ACTH and cortisol secretion. It crosses the blood-brain barrier and has been found in human plasma and cerebrospinal fluid. Clinical studies, primarily conducted in European research centers in the 1980s-2000s, have examined DSIP for insomnia, chronic pain, opioid/alcohol withdrawal, and stress-related disorders. While it remains an unregulated research peptide, its unique mechanism, sleep architecture modulation without sedation — has sustained interest in the peptide therapy community.

Key Takeaways: DSIP

  • Research doses typically range from 100 to 300 mcg via subcutaneous or intramuscular injection
  • 0 benefits with strong evidence, 3 moderate, 2 preliminary
  • Half-life: ~7-8 minutes (but biological effects persist for hours, suggesting downstream cascade activation)
  • 5 cited research studies in this guide

Mechanism of Action

DSIP's mechanism remains incompletely characterized despite decades of research. It is not a classical sedative, it does not bind GABA-A receptors or produce dose-dependent sedation. Instead, DSIP appears to modulate sleep at the level of sleep-wake circuitry regulation. Proposed mechanisms include: (1) modulation of GABAergic and glutamatergic neurotransmission in sleep-regulatory nuclei (VLPO, tuberomammillary nucleus) without direct receptor binding, shifting the balance toward sleep-promoting circuits; (2) normalization of serotonin and norepinephrine metabolism; DSIP reduces the catecholamine stress response and modulates 5-HT turnover; (3) HPA axis modulation — DSIP suppresses excessive ACTH and cortisol secretion, reducing stress-mediated sleep disruption; (4) modulation of circadian clock gene expression, potentially resynchronizing disrupted circadian rhythms; (5) endogenous opioid system interaction; DSIP has analgesic properties and modulates enkephalin/endorphin signaling. The paradox of DSIP's very short half-life (~8 minutes) but long-lasting effects (hours) suggests it triggers sustained intracellular signaling cascades, possibly through gene expression changes — rather than occupying a receptor for its duration of action. DSIP may function as a 'sleep-permissive' signal that enables natural sleep architecture rather than forcing sedation.

Research Benefits

DSIP at a Glance

Primary mechanism:

DSIP's mechanism remains incompletely characterized despite decades of research.

Top researched benefits:
Delta (Slow-Wave) Sleep PromotionSleep Architecture NormalizationStress Response ModulationAnalgesic PropertiesWithdrawal Symptom Management

Delta (Slow-Wave) Sleep Promotion

Moderate Evidence

Clinical studies show DSIP increases the proportion and quality of delta sleep (stages 3-4 NREM) without sedation or hangover effects, improving restorative deep sleep.

Sleep Architecture Normalization

Moderate Evidence

Rather than inducing unconsciousness, DSIP normalizes disrupted sleep-wake patterns, particularly effective for stress-related insomnia and disrupted circadian rhythms.

Stress Response Modulation

Moderate Evidence

Reduces HPA axis hyperactivation by suppressing excessive ACTH and cortisol, attenuating the physiological stress response that disrupts sleep and recovery.

Analgesic Properties

Preliminary

Clinical studies report pain reduction in chronic pain patients, likely through modulation of endogenous opioid systems and central pain processing.

Withdrawal Symptom Management

Preliminary

Studied for opioid and alcohol withdrawal with reports of reduced withdrawal symptom severity, improved sleep, and reduced craving.

Evidence Key:
Strong EvidenceMultiple human trials
Moderate EvidenceLimited human / strong preclinical
PreliminaryEarly research
AnecdotalCommunity reports

Research Dosing Protocols

Research Purposes Only: All content is for informational and research purposes only. This site does not provide medical advice, diagnosis, or treatment. Consult a qualified healthcare professional before using any peptide or supplement.

Research ProtocolDose RangeRoute
Sleep improvement protocol100300 mcgSubcutaneous or intramuscular injection
Intranasal research100500 mcgIntranasal spray
Clinical study doses (IV)2550 mcg/kgIntravenous infusion

Frequency

Once daily in the evening (30-60 minutes before desired sleep)

Timing

Evening administration; 30-60 minutes before bedtime

Cycle Length

5-14 day courses; some protocols use intermittent ongoing dosing

Research Notes

  • 1DSIP does not cause sedation — it modulates sleep architecture.
  • 2Effects may not be apparent on the first night; sleep quality typically improves over several days.
  • 3Not habit-forming based on available research; no dependency or tolerance reported.
  • 4Evening dosing aligns with the natural circadian DSIP rhythm.
  • 5Very short plasma half-life but prolonged biological effects (hours).
  • 6Not FDA-approved, unregulated research peptide.

Reconstitution Guide

Standard Reconstitution

Vial Size

5 mg

Bacteriostatic Water

2 mL

Concentration

25 mcg

per 0.1 mL (10 units)

Step-by-Step Guide

1

Gather Materials

DSIP vial, bacteriostatic water, alcohol swabs, insulin syringes.

2

Equilibrate Temperature

Remove the vial from storage and allow it to reach room temperature (5-10 minutes).

3

Sanitize

Swab the rubber stopper of both the peptide vial and bacteriostatic water vial with alcohol.

4

Draw Water

Draw 2 mL of bacteriostatic water into a syringe.

5

Add Water to Vial

Insert the needle into the peptide vial and direct the water stream against the glass wall — not directly onto the powder.

6

Mix Gently

Swirl the vial gently until the powder is fully dissolved. Never shake. The solution should be clear and colorless.

7

Store Properly

Refrigerate at Refrigerated (2-8°C) after reconstitution. Up to 21 days refrigerated.

Storage Temperature

Refrigerated (2-8°C) after reconstitution

Shelf Life

Up to 21 days refrigerated

Important Notes

  • Reconstitute with bacteriostatic water.
  • Relatively stable nonapeptide.
  • Store lyophilized powder refrigerated.
  • Protect from light.

Safety & Side Effects

Reported Side Effects

  • !Mild warmth or flushing after injection (transient)
  • !Headache (uncommon)
  • !No sedation or hangover effects reported
  • !No respiratory depression (unlike sedative-hypnotics)
  • !No dependency or withdrawal effects reported
  • !Generally well tolerated in published clinical studies

Potential Interactions

  • May potentiate effects of other sleep-promoting agents (melatonin, GABA agonists).
  • Interaction with HPA axis — caution with corticosteroid therapy.
  • Endogenous opioid modulation, theoretical interaction with opioid medications.
  • No significant adverse interactions identified in published literature.
  • Compatible with standard sleep hygiene practices.

Important: Side effects and interactions listed here are compiled from published research and community reports. This is not a complete list. No formal drug interaction studies have been conducted for most research peptides. Always consult a qualified healthcare provider.

Research Studies

The following studies are referenced in this profile. PubMed IDs are provided where available for independent verification.

Delta sleep-inducing peptide: isolation and characterization

Schoenenberger GA, Monnier M.1977Proceedings of the National Academy of Sciences
PMID: 265521

Original discovery paper isolating DSIP from rabbit cerebral venous blood during electrically induced slow-wave sleep, characterizing its sleep-inducing properties.

DSIP for chronic insomnia: clinical trial

Schneider-Helmert D, Schoenenberger GA.1983European Neurology
PMID: 6196209

Clinical trial in chronic insomnia patients showing DSIP improved sleep quality, increased delta sleep proportion, and normalized sleep architecture without sedation or hangover.

DSIP modulates HPA axis and stress response

Graf MV, Kastin AJ.1984Annals of the New York Academy of Sciences
PMID: 6099244

Demonstrated DSIP modulates ACTH and cortisol secretion, suppressing HPA axis hyperactivation and reducing physiological stress response.

DSIP in opioid withdrawal management

Dick P, et al.1984European Neurology
PMID: 6548739

Clinical study showing DSIP reduced withdrawal symptom severity and improved sleep in patients undergoing opioid withdrawal.

DSIP analgesic effects in chronic pain

Nakamura A, et al.2003Peptides
PMID: 12732341

Demonstrated DSIP's analgesic properties in chronic pain models, with modulation of endogenous opioid pathways and central pain processing.

Note: This is not an exhaustive list of all published research. Studies are selected for relevance and quality. Click PubMed IDs to verify sources independently. Inclusion does not imply endorsement of the peptide for any clinical use.

Frequently Asked Questions

DSIP (Delta Sleep-Inducing Peptide) is a naturally occurring 9-amino acid peptide that modulates sleep architecture, promoting restorative slow-wave (delta) sleep without sedation. It also modulates stress response, pain processing, and circadian rhythms.

No. Unlike sleeping pills (benzodiazepines, Z-drugs), DSIP does not force sedation. It normalizes sleep architecture; promoting natural delta sleep patterns, improving sleep quality rather than inducing unconsciousness. There is no hangover, no respiratory depression, and no reported dependency.

DSIP's effects on sleep quality often develop over several days rather than immediately. The first night may show subtle changes, but optimal sleep architecture normalization typically occurs over a 5-14 day course.

No dependency or tolerance has been reported in published research. DSIP does not bind GABA-A receptors (the mechanism behind benzodiazepine dependency) and appears to work through sleep architecture modulation rather than sedation.

This is a key paradox. DSIP likely triggers sustained intracellular signaling cascades and gene expression changes that persist long after the peptide itself is cleared. It functions as a 'signal' that initiates hours-long downstream biological programs.

⚠️

Research & Educational Use Only

All content is for informational and research purposes only. This site does not provide medical advice, diagnosis, or treatment. Consult a qualified healthcare professional before using any peptide or supplement.

The information presented here is compiled from published research studies and is intended for informational purposes only. Individual results may vary. Always consult with a licensed healthcare provider.