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Structural Modification The modification involves deletion of the first three N-terminal amino acids (glycine-proline-glutamate) from the 70-amino acid native IGF-1 sequence, creating a 67-amino acid variant with profound implications for receptor binding, bioavailability, and biological activity

Mechanistically, this was associated with increased BrdU-positive neurons, preservation of dopaminergic neurons (via elevated tyrosine hydroxylase and dopamine transporter levels), enhanced antioxidant defenses (e.g., catalase, GPX1/2, HO-1), and upregulation of autophagy markers such as LC3-II and Beclin-1

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Surface functionalization of nanoparticles for nanomedicine