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Mechanistic investigations in human somatic cell cultures have suggested that Epithalon may: Activate telomerase in vitro Support telomere maintenance and reduce the accumulation of DNA replicationassociated errors Potentially modulate the balance between cellular senescence and replicative capacity in experimental systems In parallel, Epithalon has been examined for its ability to interact with oxidative stress pathways and free radical markers, which may contribute to observed longevity-related effects in certain preclinical models

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Results: The whole blood (WB) group showed greater improvements in pain and function over the PRP group before 12 weeks, whereas the PRP group showed improved outcomes over whole blood (WB) at 6 months