Livagen
Bioregulators Research compound (not approved for human use)
Synthetic tetrapeptide bioregulator (Lys-Glu-Asp-Ala) · also known as KEDA, Lys-Glu-Asp-Ala
For reference only — not medical advice. Figures are commonly reported values compiled from published sources and may be wrong or out of date. Many compounds listed are not approved for human use. Talk to a licensed clinician before using any compound.
Livagen is mainly known from chromatin studies in lymphocytes from older people. It is a short bioregulator with a small literature from one research group, and no human trial defines a vial-based dose.
Commonly reported dosing (20 mg vial)
| Phase | Dose | Volume | U-100 units |
|---|---|---|---|
| Starting | 500 mcg | 0.075 mL | 7.5 |
| Standard | 1 mg | 0.15 mL | 15 |
| Higher | 2 mg | 0.3 mL | 30 |
Commonly reported reconstitution steps
- Vials are usually brought to room temperature (about 15-20 minutes) first.
- 3 mL of bacteriostatic water is added slowly down the inside wall of the 20 mg vial.
- The vial is swirled gently until clear, not shaken.
- This gives 6.67 mg/mL. Mixed vials are typically labeled with the date and refrigerated.
Storage
Before mixing: Lyophilized vials are commonly stored frozen (about -20 °C), dry, and protected from light.
After mixing: Reconstituted solution is commonly kept refrigerated (2-8 °C), protected from light, and freeze-thaw cycles are commonly avoided.
How it works
In cell studies it was reported to loosen condensed chromatin and activate ribosomal genes in lymphocytes from older donors; the relevance to liver tissue or whole-body effects is not established.
Researched for
- Studied in lymphocytes from older people for chromatin decondensation and ribosomal gene activity.
- Examined in a study comparing a polypeptide liver complex with the KEDA tetrapeptide.
- Examined for effects on aging-related chromosome features in cultured human cells.
Notes
- Evidence comes largely from a single research group (Khavinson and colleagues, St. Petersburg), mostly cell-culture and animal work; independent replication and controlled human trials are scarce.
- Published human work from the originating group has mostly used oral or other non-vial formats; the vial, reconstitution and dosing figures here reflect community-reported conventions rather than trial-validated regimens.
- Not FDA-approved.
Sources
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