Restarting the brain's repair factory (IGF-1 & HGF) through systemic intake.
Exogenous Supplementation
Supplementing neurotransmitters (Donepezil). Symptom control only.
Endogenous Induction (Oral)
Binding Siglec receptors to upregulate factors by >50%. Structural repair & regeneration.
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SAO mimics endogenous Polysialic Acid (PSA), acting as a "molecular decoy" to bind Siglec-11 receptors on Microglia.
Result: Anti-inflammatory "Ceasefire" signal sent to brain immune cells.
Clinical observation confirms patients recover "Facial Recognition" (Social Memory) after 60 days (8 weeks). This is not a miracle, but a precise alignment with the Adult Hippocampal Neurogenesis (AHN) cycle triggered by SAO intake.
IGF-1 activates mTOR pathway, increasing AMPA receptors.
Unblocks CD33 receptors, restoring Microglia phagocytosis.
IGF-1 triggers Neural Stem Cell division. Sleep quality improves.
New neurons extend axons towards CA2/CA3. HGF fuels energy.
Clinical Breakthrough: Synapses connect to memory net. Facial recognition restored.
How paralyzed patients regain walking ability through "Vicariation" (Neural Compensation).
Unlike VEGF, HGF induces angiogenesis in the Ischemic Penumbra without causing brain edema. It delivers Oxygen & Glucose to dormant neurons.
Senolytic Action: Specifically induces apoptosis in senescent Glial Scar cells that block nerve regeneration.
*HGF activates Rho/ROCK pathway guiding axons through the cleared path to reconnect with the spinal cord.
Topical application of SAO lotion demonstrates powerful endogenous regeneration, acting on fibroblasts to accelerate wound healing and moisture retention.
Compared to non-additive control, SAO induction increased Type 1 Collagen production by approximately 20 times.
Significant increase in skin hydration after 4 weeks of topical SAO lotion application.
Consistent hydration improvement observed across different facial zones.
In Dan-syl chloride fluorescence tests, skin treated with SAO lotion showed faster disappearance of fluorescence compared to control, indicating significantly accelerated skin cell turnover and metabolic activity, particularly in subjects aged 50s-60s.
Clinical data on Sarcopenia (Muscle Loss) and Hair Growth using SAO combinations.