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Peptide encyclopedia/ PE-22-28
Illustration for PE-22-28

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PE-22-28

TREK-1 blockade in depression models

Research topics · Sources checked 2026-10-04

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PE-22-28 AT A GLANCE

The question behind the molecule.

Read findings and limitations ↓
1 selected publicationContext mattersMouse behavior tests are screening models, not a diagnosis of depression. The work comes from the group that discovered spadin, has not been confirmed in human trials, and does not establish a safe or effective use in people.

What is PE-22-28?

PE-22-28 is a seven-amino-acid peptide designed from spadin, a naturally occurring fragment of the sortilin propeptide. Its published evidence comes from cell-channel experiments and mouse behavior tests, not studies in people.

Biological role or research focus

TREK-1 blockade in depression models.

Mouse behavior tests are screening models, not a diagnosis of depression. The work comes from the group that discovered spadin, has not been confirmed in human trials, and does not establish a safe or effective use in people.

Role reference: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

Names you may encounter

PE 22-28 · Spadin analog

Search terms can include brands, combinations, or historical names. They are not automatic product equivalents.

Class / identity
Seven-residue peptide designed from spadin, a sortilin-propeptide fragment; TREK-1 channel blocker in laboratory studies
Research focus
TREK-1 blockade in depression models
Featured evidence
Cell and animal study
Source check
October 4, 2026

Source: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

Biology & proposed mechanism

Spadin and PE-22-28 block TREK-1, a potassium channel linked to mood regulation in animal research. In engineered human cells, PE-22-28 blocked TREK-1 at a far lower concentration than spadin, and its effect lasted longer in mice. Blocking a channel and changing mouse behavior do not show an antidepressant effect in humans.

Source: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

Research context & identity

This profile covers preclinical neuroscience research. PE-22-28 has no approved medical use, and no published human trials were found when this page was checked.

Source: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

What does the evidence show?

Selected published evidence, with the population, findings, and limits kept together. These original summaries draw on publication abstracts; they are not a systematic review.

Cell and animal study · 2017

Shortened spadin analogs in TREK-1 cells and mouse depression models

What did this publication test, and what did it find?

Population / model
Cell lines expressing human TREK-1, mouse cortical neurons, and mice in behavioral depression models.
Study design
Patch-clamp channel experiments, then mouse forced-swim and novelty-suppressed feeding tests, neurogenesis and synapse-marker measurements, and duration-of-action comparisons with spadin.
Main finding
The authors reported stronger and more selective TREK-1 inhibition than spadin, less immobility in the forced-swim test, a shorter latency to feed after four days, more neurogenesis and synapse-marker expression, and action lasting up to about 23 hours in mice versus about 7 hours for spadin.
Limits & context
Mouse behavior tests are screening models, not a diagnosis of depression. The work comes from the group that discovered spadin, has not been confirmed in human trials, and does not establish a safe or effective use in people.

Source: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

Read the original paper for methods, adverse events, funding, and conflicts of interest. Publisher access may require a subscription.

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Safety & precautions

Safety & what remains unknown

The publication does not include a human safety assessment. TREK-1 channels occur in many tissues, so effects outside the brain, long-term exposure and interactions remain unknown.

Source: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

Evidence boundaries

Mouse behavior tests are screening models, not a diagnosis of depression. The work comes from the group that discovered spadin, has not been confirmed in human trials, and does not establish a safe or effective use in people.

Source: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

This is not a complete list of contraindications, interactions, or adverse effects. Medicine labels apply to specific products and indications; research-use listings are not interchangeable with approved medicines.

What are people discussing?

No editorial transcript note has been reviewed for this profile yet. Below are the matching video records available for exploration; title and caption matches are not verified claims.

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Sources & supplier listings

Listings are grouped by the vendor’s stated identity. Blends and modified derivatives are labeled separately. Inclusion is not a quality assessment or an endorsement.

Named compound

PE-22-28 (10 mg)

American Peptides · Vendor-labeled research use only

$70.00

Listed in stock · Snapshot 2026-10-05
Options may vary. Shipping and tax excluded.

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Affiliate link · PepsRadar may earn a commission from purchases through this link. Affiliate disclosure.

Catalog checked 2026-10-04. Seller listings retain their stated intended use. Shops covered: BioLongevity Labs, BioLongevity Supplements, American Peptides, PSPeptides. This is not a market-wide comparison. Affiliate participation does not determine evidence or editorial coverage.

Questions worth asking

  • Has PE-22-28 been tested in people?
  • What material, population, and route were actually studied?
  • Mouse behavior tests are screening models, not a diagnosis of depression. The work comes from the group that discovered spadin, has not been confirmed in human trials, and does not establish a safe or effective use in people.
  • What adverse effects, uncertainty, and conflicts of interest does the original source report?

Frequently asked questions

Has PE-22-28 been tested in people?

Not in the publications checked for this page. Its evidence comes from cell and mouse experiments, and mouse behavior tests cannot show that it treats depression in humans.

Source: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

Does the publication verify a supplier’s product?

No. The tested material and a commercial listing need separate identity and batch checks. A research-use disclaimer does not establish clinical suitability.

Source: Shortened Spadin Analogs Display Better TREK-1 Inhibition, In Vivo Stability and Antidepressant Activity · 2017 ↗

References & editorial record

Source notes checked 2026-10-04. Original PepsRadar summaries. Not reviewed by a medical professional. Topic grouping is editorial navigation, not a treatment recommendation. Video notes specify which excerpts were reviewed; no full transcripts are published.

For research and education only. This page does not provide medical advice, diagnosis, or treatment. Research-only listings are not instructions for human use.

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