This invention proposes the application of MTA targeting SMS in the preparation of anti-intraocular
inflammation products, relating to the biomedical field. Specifically, MTA, as an active molecule, inhibits inflammatory signaling pathways and improves RPE / external blood-
retinal barrier damage by targeting and binding to SMS and remodeling
polyamine metabolism. Remodeling
polyamine metabolism involves MTA targeting and binding to SMS, inhibiting its enzymatic activity and / or expression, thereby blocking the conversion of SPD to SPM. This invention clarifies the
direct binding relationship and key binding sites between MTA and SMS, elucidating the technical basis for MTA inhibiting inflammatory signaling pathways and improving RPE / external blood-
retinal barrier damage by inhibiting SMS and remodeling
polyamine metabolism. It addresses the problems of existing intraocular
inflammation treatments primarily relying on broad-spectrum
immunosuppression, lacking metabolic target intervention, and struggling to simultaneously control
inflammation and protect tissue barriers; providing a new direction for
drug development for the precise intervention of intraocular inflammatory diseases, especially acute anterior
uveitis and related acute intraocular inflammations.