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. 2022 Jan 10;23(2):726. doi: 10.3390/ijms23020726

Table 1.

Potential mutation-independent treatments for IRDs which showed preserved cone and/or rod survival in animal models.

Cellular Process Method Model
Apoptosis ↓ Calpain Cnga3−/− mouse [29]
Rd1 mouse [33]
Necroptosis ↓ RIP3 Pde6c−/− zebrafish [71]
Rd10 mouse [72]
Rho S334ter rat [73]
Autophagy ↑ RdCVF Rho P23H rat [86]
Rd1 and Rho P23H mice [87]
↑ mTOR Pde6b−/−, Pde6g−/−, Rho−/−,
Rho P23H mice [54]
Oxidative Stress ↓ ROS Rd1 mouse [99,100]
Endoplasmic
Reticulum Stress
↓ PKG Cnga3−/−Nrl−/− mouse [29]
Rd1 and Rd2 mice [112]
TUDCA
injection
Lrat−/− mouse [115]
Rd10 mouse [116]
Epigenetic Changes ↓ HDACs Cpfl1 mouse [121,123]
Rd1 mouse [120,122]
Rd10 mouse [122,123]
Immunological
Changes
Müller glia
differentiation
Rho P23H rat [150]
Stimulation in healthy mice [153]
NMDA retinal damaged mouse [154]
Microglia
inhibition
Rd1 mouse [159]
Rd10 mouse [159,160]
Mutant Mer tyrosine kinase associated retinitis pigmentosa (mutMerTK-RP) rat [161]

↓ Decrease in expression; ↑ Increase in expression