3AA Limited Human

Vesugen

Synthetic vascular tripeptide (Lys-Glu-Asp) from the Khavinson school that epigenetically restores endothelial proliferation and connexin signalling in aged blood vessel tissue.

In Plain English: Vesugen is a three-amino-acid chain — lysine, glutamic acid, and aspartic acid — modelled on a peptide sequence found in vascular wall proteins. Small Russian clinical studies report improvements in arterial blood flow, reductions in erectile dysfunction linked to atherosclerosis, and benefits in lower-limb arterial insufficiency in elderly patients. In cell and mouse experiments, it restores the Ki-67 proliferation marker in aged endothelial cells, normalises gap-junction proteins (connexins), upregulates SIRT1, and — at a separate neurological level — recovers mushroom-spine density in an Alzheimer's mouse model. Western replication is absent; all human clinical data originates from a single Russian research group.

Research Maturity Limited Human (~15-20 peer-reviewed papers (2012-2021); 2 small human trials (n=41 each); no independent replication+ Studies)
Quick Facts
Focus
Cardiovascular Support Healthy Aging Microcirculation
Route
SubQ
Origin
Identified and synthesised by Vladimir Kh. Khavinson at the St. Petersburg Institute of Bioregulation and Gerontology, Russia. Derived from the amino-acid sequence of bovine vascular-wall proteins; later produced synthetically from plant-derived amino acids. Introduced into Russian clinical practice as a food-supplement cytogen (peptide complex AC-2) alongside the full Khavinson bioregulator series.
Mechanism
Binds the promoter region of the MKI67 gene (molecular docking confirmed) and stimulates Ki-67 protein synthesis, counteracting the age-related decline in endothelial cell proliferation. Normalises endothelin-1 (EDN1) expression in atherosclerotic aortic endothelium. Restores connexin gap-junction proteins (Cx37, Cx40, Cx43), maintaining endothelial cell-to-cell communication. Upregulates SIRT1, linking it to calorie-restriction-like vasoprotective phenotypes. In neural tissue, binds promoter regions of CASP3, GAP43, APOE, SOD2, PPARA, and PPARG; increases mushroom-spine density in 5xFAD Alzheimer's mice (sex-specific, pronounced in males). Stimulates proliferation and inhibits apoptosis in organotypic neuroimmunoendocrine cultures (Ki-67 up, p53 down). May promote nitric-oxide-dependent relaxation and prostaglandin-mediated vasorelaxation.
Outcome
Ki-67 expression in aged vascular endothelial cultures (in vitro), endothelin-1 levels (atherosclerotic cell culture), connexin expression (Cx37/Cx40/Cx43), SIRT1 expression, penile arterial blood flow (duplex Doppler, n=41 RCT), International Index of Erectile Function score, lower-limb blood flow (clinical + Doppler, n=41), mushroom-spine density in 5xFAD mice (in vivo), memory/attention scores in elderly with CNS disorders (clinical observation), mesenchymal stem-cell proliferation markers.

Safety Flags & Warnings

No Independent Western Replication No Published Pharmacokinetic Data Cell Proliferation Stimulation Prooxidant Activity Reported (in vitro) Small Human Trial Sizes Contraindicated in Pregnancy / Breastfeeding Generally Well Tolerated in Short Courses

Always consult a licensed physician. Research purposes only.

3.5 / mg