Livagen
A tetrapeptide hepatic bioregulator (Lys-Glu-Asp-Ala) from the Khavinson series targeting liver cell chromatin and gene expression to support hepatic function and longevity.
⚠ Research & Educational Use Only. Livagen is a research chemical documented here for scientific education. All information references peer-reviewed literature and preclinical/clinical study data. Not for human consumption. Not medical advice. Consult a licensed researcher or healthcare professional before any laboratory use.
- Targets liver cell chromatin - demonstrated ability to activate transcriptionally silent chromatin regions in hepatocytes
- Supports hepatocyte gene expression and liver-specific protein synthesis
- Promotes liver cell differentiation and maintains hepatic identity markers
- Livagen is not FDA-approved for human use. It is a research chemical for scientific study only.
Research At a Glance
- Targets liver cell chromatin - demonstrated ability to activate transcriptionally silent chromatin regions in hepatocytes
- Supports hepatocyte gene expression and liver-specific protein synthesis
- Promotes liver cell differentiation and maintains hepatic identity markers
- Anti-aging effects on liver tissue - part of comprehensive longevity bioregulator protocols
What is Livagen?
Livagen (Lys-Glu-Asp-Ala, KEDA) is a synthetic tetrapeptide bioregulator developed by Professor Vladimir Khavinson's research group at the St. Petersburg Institute of Biogerontology, specifically targeting hepatic tissue. It represents the liver-specific component of the comprehensive organ-targeted bioregulator system that includes peptides for nearly every major organ system.
The liver is the body's primary metabolic organ - responsible for glucose homeostasis, lipid metabolism, protein synthesis, detoxification, bile production, and immune function. Age-related hepatic decline manifests as reduced regenerative capacity, impaired metabolic efficiency, increased susceptibility to hepatic injury, and progressive fibrosis. The development of Livagen aimed to address these age-related changes through targeted bioregulation of hepatic gene expression.
The fundamental mechanism by which Livagen is proposed to act involves interaction with chromatin - the complex of DNA and histone proteins that governs gene accessibility and expression. Research has demonstrated that Livagen can interact with DNA regulatory sequences in liver cells, particularly with regions that become transcriptionally silenced during aging. This epigenetic reactivation of silenced chromatin regions could restore expression of genes that are progressively downregulated in the aging liver - a direct molecular mechanism for reversing some aspects of hepatic aging at the gene expression level.
The practical applications studied for Livagen span several domains of hepatic medicine. In age-related liver decline, the goal is to maintain hepatocyte identity, proliferative capacity, and metabolic efficiency. In the context of regenerative medicine, the restoration of hepatocyte differentiation gene expression could support liver recovery after injury. In metabolic disease research, the normalisation of hepatic gene expression patterns may help restore proper metabolic regulation.
Livagen is most commonly combined with Pancragen in research protocols targeting the metabolic organ system broadly - as both the liver and pancreas are central to glucose and lipid homeostasis, their bioregulators are complementary. Both peptides are often included in comprehensive Khavinson longevity protocols alongside immune bioregulators (Thymalin, Vilon) and neuroendocrine bioregulators (Epitalon).
Key Research Benefits
Documented effects observed in preclinical and clinical studies on Livagen. See all Healing & Recovery peptides for comparison.
Side Effects & Risks
Adverse effects reported in the research literature. All data sourced from preclinical and clinical study reports.
Dosing Data from the Literature
Doses referenced below are sourced from published preclinical and clinical studies. Use the peptide dose calculator to convert these values to injection volume.
Standard bioregulator protocol: 10 mg IM daily for 10 days, 2-3 courses per year.
Research dose: 10 mg intramuscularly, daily for 10 consecutive days Often combined with Pancragen in metabolic/liver health protocols
Administration in Research Settings
Standard reconstitution and administration methodology for laboratory research use.
Reconstitute with physiological saline. Administer intramuscularly once daily for 10 consecutive days.
Explore Further
Quick Reference
Research Use Only
This information is for educational research purposes only. This is not medical advice. Consult a qualified healthcare professional.