Overview
PE-22-28 is a synthetic peptide derived from spadin, the natural sortilin-propeptide fragment, and is studied as a modulator of the TREK-1 background potassium channel. Its short, targeted structure gives it a research-friendly profile for probing a single, well-defined ion-channel mechanism.
In preclinical models, PE-22-28 has been investigated for its blockade of TREK-1 channels, a mechanism associated in the research literature with neuroplasticity, mood-related signaling, and neurogenesis in the hippocampus. Investigators examining background-potassium-channel pharmacology have used it as a research material to model how TREK-1 activity shapes neuronal excitability and downstream plasticity pathways.
What makes PE-22-28 notable for a cognitive and neurological catalog is the relative specificity of its studied target, which allows the TREK-1 pathway to be examined with limited confounding. Whether these mechanisms translate to female physiology remains an open research question; our evidence review tracks how many of the underlying studies included women.
Summary
PE-22-28 is a synthetic analog of spadin that blocks the TREK-1 potassium channel, studied preclinically for rapid antidepressant-like effects. All evidence is preclinical; there are no human trials and no female-specific data.
Evidence in women
Mechanism
Blocks the TREK-1 background potassium channel, an action linked to fast-acting antidepressant effects in preclinical models.
Free research guide
How to tell real female data from male-extrapolated claims, with the questions to ask about any compound.
Citations (PMID)
Related peptides
Educational information for laboratory and research use only. Not medical advice, a recommendation, or a claim of safety or efficacy; no personal dosing. “Unstudied” means no qualifying study was found, not that a compound is safe or unsafe.