Research Applications for Striatech Products
Biomedicines (Jan 15, 2026)
Targeting AKT via SC79 for Photoreceptor Preservation in Retinitis Pigmentosa Mouse Models
Brunet AA, Gilbert K, Miller AL, James RE, Lim XR, Harvey AR, Carvalho LS
DOI: 10.3390/biomedicines14010195 >>
Brunet et al tested SC79, and activator of the pro-survival kinase AKT, as a neuroprotective strategy in retinitis pigmentosa mouse models. Intravitreal SC79 (10–100 µM) was well tolerated in wildtype mice. In rd1.GFP mice, it partially preserved peripheral photoreceptor cell layer thickness, rod-driven contrast sensitivity, and cone morphology. In RhoP23H.GFP mice, the effects of SC79 were minimal. AKT pathway markers confirmed target engagement, but overall functional rescue remained modest, indicating that dosing and delivery require further optimization.
Background/Objectives: Retinitis pigmentosa is a degenerative retinal disease and a major cause of inherited blindness globally. The pro-survival kinase AKT is downregulated in degenerating photoreceptors in retinitis pigmentosa, and its activation has shown neuroprotective effects in retinitis pigmentosa and other neurodegenerative disorders. In this study, we evaluated the therapeutic potential of SC79, a pharmaceutical AKT activator, in two mouse models of retinitis pigmentosa, rd1.GFP and RhoP23H.GFP.
Methods: SC79 was administered intravitreally at postnatal day 12 (P12) and analysis was conducted at P16.
Results: SC79 at 10 µM was well tolerated in wildtype mice, with no reduction in retinal function or thickness. In rd1.GFP mice, SC79 partially preserved peripheral outer nuclear layer (ONL) thickness, improved rod photoreceptor-driven optomotor contrast sensitivity responses, and improved cone photoreceptor morphology. Immunohistochemistry of retinal sections indicated AKT-related protein expression changes in both sham and SC79-treated rd1.GFP retinas, with sham injections leading to decreases in this pathway and SC79 injections restoring this back to uninjected protein levels or higher, indicating the damage from intravitreal injections can induce AKT-related protein expression changes. In RhoP23H.GFP mice, changes to the visual response from the therapeutic effects of SC79 were not detectable. An increased dosage of SC79 at 100 µM was evaluated in wildtype mice and showed no major toxic effects, although it did not confer neuroprotective benefits in either disease model.
Conclusions: These results demonstrate the potential therapeutic effect of AKT pathway modulation for preserving photoreceptors in recessive retinitis pigmentosa, with further optimisation of treatment delivery required.
