Overview
P21 is a 21-amino-acid peptide derived from ciliary neurotrophic factor (CNTF) that retains neurogenic activity without CNTF's systemic side effects.
- Synthesized in research settings
- Subcutaneous injection (research)
Mechanism of action
Mimics CNTF-mediated neurogenic signaling, increasing hippocampal neurogenesis and BDNF expression in animal models.
- · CNTF receptor signaling
- · BDNF induction
- · Adult hippocampal neurogenesis
How it acts on the body
Native CNTF promotes neurogenesis but causes systemic effects (weight loss, antibody formation) that limited its clinical use. P21 was designed as a minimal active fragment that crosses the blood-brain barrier and reproduces the neurogenic effect without those side effects in rodents.
Reported outcomes include increased BDNF expression, enhanced spatial memory in aged mice, and reversal of cognitive deficits in Alzheimer's models. No published human trials exist.
Hormonal & endocrine impact
How this peptide is reported to shift specific hormones and signaling molecules. Directionality reflects research literature and preclinical models, not clinical prescribing data.
Curves are schematic shapes (sigmoid for increases/decreases, damped oscillation for modulation/stabilization) anchored to a 100% baseline. They communicate direction and tempo of change reported in research literature — not absolute hormone concentrations.
Effects on the body
Organ system effects
Hippocampus and cortex.
Minimal systemic involvement reported.
Reported effects
Drawn from preclinical research, anecdote, and small-scale clinical observation. No evidence grades are assigned — most peptides on this page lack rigorous human trials.
- Targets adult neurogenesis directly
- Avoids CNTF systemic side effects in animals
Potential side effects
- · No characterized human profile
- · Long-term safety unknown
Drug interactions
No notable interactions reported.
Pairing context
- Aerobic exerciseIndependently increases BDNF and adult neurogenesis.
- Active glial tumorsCNTF-pathway activation in gliomas is under-characterized.