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Epithalon (also known as Epitalon or AEDG) is a synthetic tetrapeptide composed of alanine, glutamic acid, aspartic acid, and glycine. It has been widely researched for its potential role in regulating aging, telomere activity, and oxidative stress. Epithalon is strictly intended for research use only and not for human consumption [1].
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Epithalon is a synthetic peptide modeled after a naturally occurring compound produced in the pineal gland. It has been studied for its potential to influence gene expression and delay cellular aging by modulating biological mechanisms like telomere elongation and oxidative balance. It is of particular interest in gerontology and neurobiology research [2].
Epithalon is a tetrapeptide with the sequence Ala-Glu-Asp-Gly. Its short structure and stability under experimental conditions make it an attractive candidate for research applications in molecular aging and regenerative biology [3].
Research shows that Epithalon can promote neuronal differentiation by increasing expression of neurogenic markers such as GAP43 and β-Tubulin III in human embryonic stem cells. This suggests potential roles in neurogenesis and regenerative medicine [1].
Epithalon has been shown to activate telomerase in human somatic cells, resulting in measurable telomere elongation. This mechanism is associated with delayed cellular senescence and extended cell lifespan, making Epithalon a focal point in anti-aging research [4].
Studies indicate that Epithalon enhances antioxidant defense by upregulating superoxide dismutase, glutathione peroxidase, and catalase activity. These effects contribute to reduced oxidative stress and may protect against age-related cellular damage [5].
In rodent models, Epithalon administration resulted in delayed age-associated changes and extended lifespan. One study reported a 12.3% increase in maximum lifespan and a 13.3% increase in the lifespan of the final 10% of subjects [6].
Epithalon has been explored for its possible anti-cancer properties. In mice, it significantly reduced the incidence of spontaneous tumors and slowed the progression of experimentally induced neoplasms. While results are promising, further study is needed to clarify its mechanisms [6].
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