PE-22-28
Shortened spadin / TREK-1 blocker class — preclinical antidepressant models; CID TBD.
Editorial review:Evidence snapshot
This drawer marks papers. It is not a plan, a dose, or a source. A paper is a bounded report. It is not a protocol. Grades name the object. They are not a safety rating.
Identity lock. PE-22-28 is a shortened spadin analogue (sortilin / NTSR3 propeptide lineage) developed as a TREK-1 (K2P2.1) blocker with antidepressant-like activity in models. It is not a generic “PE” growth factor fragment, not PEG-MGF, and not PT-141. No clean PubChem CID was locked in this pass for the exact PE-22-28 sequence object — treat sequence / analogue naming as To be confirmed against the Djillani / Pietri primary papers before UI badges. This drawer marks papers. It is not use advice.
Bottom line
PubMed object-matched literature is small and preclinical / translational. Core paper Djillani 2017 characterizes shortened spadin analogues (including PE-22-28 framing) with TREK-1 inhibition, in vivo stability, and antidepressant-like activity. Related spadin / sortilin reviews and stroke-recovery / post-stroke depression protective reports expand the class but are not human PE-22-28 RCTs. No approved human antidepressant indication for PE-22-28 is assumed here.
Papers
PE-22-28 / shortened spadin core
PMID 28955242 — Djillani 2017
Tested: shortened spadin analogues (PE-22-28 lineage) with improved TREK-1 inhibition, in vivo stability, and antidepressant activity in animal models.
Does not show: a completed human Phase 3 antidepressant RCT for PE-22-28.
PMID 31325429 — Pietri 2019
Tested: protective effects of sortilin-derived peptides on stroke recovery and post-stroke depression models.
Does not show: that PE-22-28 is an approved post-stroke drug.
PMID 25080852 — Veyssiere 2015
Tested: retroinverso spadin analogues with increased antidepressant effects (related spadin chemistry).
Does not show: identity equivalence of every retroinverso analogue to PE-22-28.
PMID 30291907 — Djillani 2019
Tested: review of TREK-1 blockers for depression with focus on spadin.
Does not show: new primary human PE-22-28 efficacy data.
PMID 30670975 — Mazella 2018
Tested: sortilin/NTSR3 involvement in depression as progenitor of spadin and role in TREK-1 membrane expression.
Does not show: a human PE-22-28 trial.
PMID 27816451 — Hivelin 2017
Tested: sortilin-derived propeptide regulation during adipocyte differentiation and inflammation (class biology).
Does not show: PE-22-28 metabolic indication in humans.
What is not established
Human clinical efficacy for PE-22-28 as an antidepressant or post-stroke therapy. A locked PubChem CID / CAS for UI badges without sequence confirmation. Equivalence to PEG-MGF, PT peptides, or unrelated “PE-” shop SKUs. This drawer does not provide use advice, schedules, or sourcing.
Selected sources
Reported experiences
Reported topics are not established benefits.Risks and unknowns
Compare experiences with care.
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