PMID-32342318 – Functional Connectomic Approach to Semax and Selank Effects

PMID-32342318 – Functional Connectomic Approach to Semax and Selank Effects

Panikratova YR et al., "Functional connectomic approach to studying Semax and Selank effects on brain functional connectivity," Dokl Biol Sci, 2020;491(1):38-40. DOI: 10.1134/S001249662001007X

Quick Reference

Property Value
PMID 32342318
DOI 10.1134/S001249662001007X
Year 2020
Journal Doklady Biological Sciences
Study Type Observational (human interventional fMRI)
Evidence Level III
Sample 52 healthy adult volunteers
Peptide(s) Studied Semax, Selank

Key Findings

  • Resting-state fMRI demonstrated that both intranasal Semax and Selank produced significant changes in functional connectivity between the right amygdala and temporal cortex regions at 5 and 20 minutes post-administration.
  • This represents the first human neuroimaging evidence confirming that both peptides exert measurable central nervous system effects after intranasal delivery.
  • The amygdala-temporal connectivity changes suggest modulation of emotional processing and salience networks, consistent with the anxiolytic profile of Selank and the cognitive-enhancing profile of Semax.

Study Design

Randomized, controlled human study in 52 healthy adults. Participants received intranasal Semax, Selank, or placebo. Resting-state fMRI scans were acquired at baseline and at 5 and 20 minutes post-administration. Functional connectivity was analyzed using seed-based correlation with the amygdala as the primary region of interest.

Limitations

  • Short observation window (20 minutes); longer-term connectivity changes were not assessed.
  • Relatively small sample per group after randomization into three arms.

Clinical Relevance

Provides critical human-level evidence that intranasal Semax and Selank reach the brain and alter functional connectivity in emotion- and cognition-relevant circuits, bridging the gap between animal mechanistic data and clinical application.

Related

#research #observational #evidence-level-III