Vesugen
Vesugen is a synthetic tripeptide (Lys-Glu-Asp or KED) developed as a blood vessel bioregulator. Research indicates it supports vascular health by improving microcirculation, enhancing endothelial cell function, and potentially mitigating age-related vascular changes like atherosclerosis.
01Dosing reference
02Mechanism of action
Endothelial Targeting
The KED tripeptide binds to specific DNA sequences in vascular endothelial cells.
Gene Expression Regulation
It stimulates the synthesis of proteins necessary for the repair and regeneration of the vascular wall.
Vascular Normalization
This leads to improved elasticity of blood vessels, reduced arterial stiffness, and enhanced microcirculation.
03Human evidence
Improved microcirculation and reduced symptoms in patients with atherosclerosis and hypertension.
Clinical studies in older adults showed improved lipid profiles, decreased vascular stiffness, and better overall cardiovascular function when used as an adjunct therapy.
Enhanced recovery and functional capacity in patients with ischemic heart disease.
Observational trials in Russia demonstrated improved exercise tolerance and reduced angina episodes in elderly patients.
04Preclinical evidence
Normalization of vascular endothelial cell function under stress.
In vitro studies on human vascular cells showed that the KED peptide increases cell proliferation and reduces apoptosis in aging cell cultures.
Reduction in the progression of atherosclerotic plaques.
Animal models of atherosclerosis demonstrated that administration of the peptide slowed the development of vascular lesions and improved arterial compliance.
05What is known vs. unknown
- Vesugen is a synthetic tripeptide (Lys-Glu-Asp) belonging to the Khavinson bioregulator family.
- It is designed to mimic the effects of the natural vascular peptide complex, Ventfort.
- Research primarily focuses on its ability to restore endothelial function and improve microcirculation.
- It is frequently studied in the context of gerontology for combating age-related cardiovascular decline.
- There is a lack of large-scale, double-blind, placebo-controlled clinical trials in Western populations.
- Long-term safety and efficacy data outside of Russian clinical studies remain limited.
- The exact molecular binding sites and comprehensive pharmacokinetics are not fully characterized in international literature.
06Safety & regulatory context
07Compared with Ventfort
08Glossary
09Knowledge check
10Sources
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