[Effect of semax on the temporary dynamics of brain-derived neurotrophic factor and nerve growth factor gene expression in the rat hippocampus and frontal cortex].
Agapova. T Iu TIu; Agniullin. Ia V IaV; Silachev. D N DN; Shadrina. M I MI; Slominskiĭ. P A PA; Shram. S I SI; Limborskaia. S A SA; Miasoedov. N F NF
Key Findings
- Semax (50 mg/kg, intranasal) altered BDNF and NGF gene expression within 20 minutes in rat brain regions
- Hippocampus showed an early decrease then a later increase, while frontal cortex showed an early increase then a return to baseline before rising again
- The gene‑expression changes persisted up to 8 hours after a single dose
Practical Outcomes
- Semax can rapidly and temporarily boost neurotrophic factor activity in the brain, suggesting potential for short‑term cognitive or neuroprotective effects. However, the study is in rats and uses a high dose, so human dosing, safety, and real‑world benefits remain unclear. Biohackers should view this as mechanistic evidence rather than a ready‑to‑use protocol.
Summary
In rats, a single intranasal dose of the peptide semax quickly changed the levels of brain‑growth genes (BDNF and NGF) in two brain areas, with early drops in the hippocampus and rises in the frontal cortex, then both areas showed a later increase that lasted several hours.
Abstract
Semax is a synthetic peptide, which consists of the N-terminal adrenocorticotropic hormone fragment (4-7) (ACTH4-7) and C-terminal Pro-Gly-Pro peptide. Semax promotes neuron survival in hypoxia, increases selective attention and memory storage. It was shown that this synthetic peptide exerted a number of gene expressions, especially brain derived neurotrophic factor gene (Bdnf) and nerve growth factor gene (Ngf). Temporary dynamics of Bdnf and Ngf ex- pression in rat hippocampus and frontal cortex under Semax action (50 mg/kg, single intranasal administration) was studied in this work. It was shown that the studied gene expression levels changed significantly both in the hippocampus and the frontal cortex tissues 20 minutes after the peptide preparation application. The expression levels decreased in the hippocampus and increased in the frontal cortex. Forty minutes after Semax administration both gene expression levels returned to the level typical of control tissues. After that they increased significantly by 90 minutes after experiment start. Bdnf and Ngf expression levels decreased up to the control levels by 8 hours after medicine applying maximum gene expression levels were attained. Thus, Semax administration results in rapid, long-term, and specific activation of Bdnf and Ngf expression changes in different rat brain departments.
Study Information
pubmed
2008