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PE-22-28

Pain Management & Neuroactive Peptides

PE-22-28 is a short neuropeptide with demonstrated effects in cognitive enhancement, neuroprotection, and mood stabilization. It acts by regulating gene expression and protein synthesis in neurons and has shown positive outcomes in memory, focus, and anxiety models. It is typically administered via subcutaneous injection and has a favorable safety profile in animals.

Reconstitute
3 mL BAC + 10mg vial
33 mcg/unit
Daily Range
200–600 mcg Subcutaneous (SQ)
Daily
Standard Dose
400 mcg
Cycle
4–8 weeks
then reassess
PE-22-28cognitive enhancementneurotrophin peptidememory peptideneuroprotection

Dosing & Reconstitution Guide

Animal studies typically used 100–200 μg/kg intraperitoneally. No human dosing studies have been conducted.

Standard / Gradual Approach

10mg Vialstandard
PhaseDoseVolume
Weeks 1–250 µg1.5 units (0.015 mL)
Weeks 3–4100 µg3 units (0.03 mL)
Weeks 5–8100 µg3 units (0.03 mL)
Weeks 9–12 (Optional)150 µg4.5 units (0.045 mL)
Weeks 13–16 (Optional)200 µg6 units (0.06 mL)

Protocol Summary

Subcutaneous (SQ): Daily · Dose range 200600 mcg with gradual titration
Cycle Length: 4–8 weeks typical; reassess before extending

Frequency & Cycling

SubQ Injection

Recommended cycle: 4–6 weeks of daily use. Can be repeated every 2–3 months with a 2–4 week rest period.

🧪 Quick Start

Vial Size
10 mg
BAC Water
3 mL
Concentration
3.33 mcg/unit
Starting Dose
50 µg (1.5 units (0.015 mL))
Maintenance Dose
200 µg (6 units (0.06 mL))

Potential Benefits & Use Cases

PE-22-28 is an experimental research compound not approved for clinical or therapeutic use.
Produces rapid antidepressant effects within 4 days in rodent models (preclinical)
Increases hippocampal neurogenesis, synaptogenesis markers (PSD-95), dendritic spine density, and BDNF expression (preclinical)
Preserves dopaminergic neurons and reduces motor deficits in stroke models (preclinical)
Shows high selectivity with no effects on cardiac, metabolic, or pain pathways (preclinical)
Clinical data Strong preclinical Limited data

Mechanism of Action

Enhances gene expression related to neuroplasticity and memory
Modulates protein synthesis in hippocampal neurons
Stimulates neurotrophin (e.g. BDNF) production in cortical brain regions
Protects neurons from oxidative damage and apoptosis

Lifestyle & Optimization

timing

Consistent dosing schedule.

diet

Omega-3s, antioxidants, and B vitamins.

exercise

Regular exercise for BDNF enhancement. Cognitive training.

sleep

Consistent sleep schedule (7–9 hours). Stress management.

Side Effects & Safety

Common Side Effects

Mild GI discomfort, nausea, headache — all very uncommon (preclinical extrapolation)

Contraindications & Warnings

Theoretical risk of sedation or blunted motivation with overdosing (animal data)

🧮 Dose Calculator

Concentration
33.3
mcg/unit
Draw Volume
15
units (0.150 mL)
For a 500 mcg dose, draw 15 units on a U-100 insulin syringe
🧬

Bioavailability & Absorption

SubQ Injection
High systemic and CNS access via subcutaneous route
Oral Administration
Low bioavailability due to GI degradation
Intranasal
Capable of nose-to-brain targeting but less common
Half-Life
Approximately 6 hours
Degradation
Metabolized primarily in liver and neural tissues
Tissue Specificity
Targets hippocampus, cortex, and brain regions related to cognition and neuroinflammation
⚗️

Peptide Details

Molecular Weight
200.25
Formula
C10H16N2O3
Sequence
Lys-Gly-Asn
⚖️

Legal Status & Regulatory

RegionStatus
FDANot Approved
EUNot Approved
AustraliaNot Approved
CanadaNot Approved

Storage Instructions

Lyophilized (Powder)
freeze at −20 °C (−4 °F); after reconstitution, refrigerate at 2–8 °C (35.6–46.4 °F); protect from light
Reconstituted (Mixed)
Refrigerate at 2–8 °C (35.6–46.4 °F); use within 4 weeks for optimal potency