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Separate acute from chronic, and put a boundary on duration If someone is intent on using it, the least risky scenario is short-term use around a clearly defined acute injury window, not ongoing use for months for chronic pain

This biology underlies the prominence of GHRH + GHRP combinations in pituitary research

In rodent models, Dihexa at 5mg/kg orally for 7 days increased hippocampal synapse formation by 42% compared to vehicle controls, while Cerebrolysin required intravenous administration at 2.5ml/kg daily to achieve comparable synaptogenesis

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