Vesugen

Also known as: KED, KED peptide, Lys-Glu-Asp

Evidence: Preclinical

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Overview

Khavinson-series synthetic tripeptide KED (Lys-Glu-Asp), sold as a vascular bioregulator; studied in endothelial cell cultures and a mouse Alzheimer model, with uncontrolled Russian human reports.

Vesugen is the tripeptide KED (Lys-Glu-Asp) from the St. Petersburg Institute of Bioregulation and Gerontology. Cell work covers vascular endothelial cell proliferation during aging (Khavinson 2014) and molecular markers relevant to atherosclerosis and restenosis (Kozlov 2016). In a mouse model of Alzheimer's disease it was among tripeptides with reported neuroprotective effects (Khavinson 2021). Human data are uncontrolled Russian reports: 41 older patients with chronic lower-limb arterial insufficiency (Kitachev 2014), a polymorbid cohort with organic brain syndrome (Meshchaninov 2015) and truck drivers with neurotic disorders, given with Pinealon (Bashkireva 2012). No randomized trial has been published.

Benefits

Vascular endothelial cell proliferation in aging cultures (in vitro), markers in atherosclerosis and restenosis models (preclinical), neuroprotection in a mouse Alzheimer model (rodent), chronic lower-limb arterial insufficiency in older adults (human, uncontrolled, n=41)

Dosing reference

Research dose
200 to 1000 mcg daily: vendor/community range; not compared with the doses in the uncontrolled human reports
Range
200 to 1000 mcg, 1x daily

Sold as oral capsules and as lyophilized powder for injection. Community protocols run 10 to 20 day courses two or three times a year; no study compared schedules. Doses in the uncontrolled Russian human reports have not been compared with this range.

Mechanism

Proposed, from the developing group. The peptide is reported to act epigenetically on vascular endothelial cell proliferation in aging cultures (Khavinson 2014) and to change molecular markers in models of atherosclerosis and restenosis (Kozlov 2016). Other work describes effects on neurogenesis genes relevant to Alzheimer's disease (Khavinson 2021) and on cells of the neuroimmunoendocrine system (Chalisova 2012). Gene regulation by direct DNA binding is the group's hypothesis and has not been tested independently. The old claims about nitric oxide and vessel tone had no source.

Evidence

Preclinical: animal or in vitro data only

  • In 41 older patients with chronic lower-limb arterial insufficiency, an uncontrolled study reported benefit from vascular peptide bioregulators (Kitachev et al., 2014)
  • Given with Pinealon to patients with chronic polymorbidity and organic brain syndrome, the peptides showed prooxidant activity and lowered CD34+ cell counts (Meshchaninov et al., 2015)
  • Given with Pinealon to professional truck drivers with neurotic disorders (Bashkireva et al., 2012)
  • Reported neuroprotective effects in a mouse model of Alzheimer's disease (Khavinson et al., 2021)
  • Studied for epigenetic effects on vascular endothelial cell proliferation in aging cultures (Khavinson et al., 2014)
  • Human-trial status: no randomized trial; the human reports are uncontrolled Russian-language studies, and nearly all work comes from the developing group

References

Side effects

No controlled safety study has been published. Given with Pinealon in an uncontrolled study, the peptides showed prooxidant activity and a fall in CD34+ cells (Meshchaninov 2015). Commonly reported (anecdotal): injection-site irritation with injectable forms.

Storage

Storage
Room temperature
Lyophilized
24+ months

Pharmacology

Half-life
No published pharmacokinetic data in any species
Bioavailability
Not measured in any species
Molecular weight
390.39 Da
Sequence
Lys-Glu-Asp

Stacks with

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