Disease | Model | Administration | Molecular mechanism | Effect | References |
---|---|---|---|---|---|
MS | EAE Rat | Intravenous | Regulated polarization of microglia M1-M2 | Attenuated demyelination and decreased inflammation | [141] |
 | EAE Mice | Intravenous | Reduced T-cell proliferation and increased regulatory T-cell activity through anti-inflammatory cytokines | Improved functional outcomes and clinical score, reduced demyelination | [138] |
 | EAE Mice | Intravenous | Induced anti-inflammatory TH-2 cytokines and TGF-β | Modulated immune response and induced peripheral tolerance | [132] |
 | TMEV-IDD Mice | Intravenous | Decreased Th-1/Th-17 cytokines | Improved motor deficits | [131] |
Alzheimer | APP/PS1 Mice | Intravenous | Inhibited astrocyte activation, decreased pro-inflammatory and increased anti-inflammatory cytokines | Alleviated plaque deposition and Aβ accumulation, improving cognitive function | [148] |
 | 3xTg Mice | Intranasal | Regulated polarization of microglia M1-M2 | Neuroprotective effects, increased dendritic spine density | [143] |
Status Epilepticus | Pilocarpine Mice | Intranasal | Decreased glutamatergic and GABAergic neurons, regulation of pro/anti-inflammatory cytokines | Neuroprotective effects, preserved cognitive and memory function | [128] |
Stroke | MCAO Rats | Intravenous | miR-133b regulated CTGF in astrocytes, increasing axonal plasticity | Induced functional recovery | [149] |
Glaucoma | ONC Mice | Intravitreal | Improved retinal ganglion cell survival, downregulated cis-p tau | Improved cognitive visual behavior | [150] |
 | ONC Rats | Intravitreal | Modulated inflammatory response through miR-based mechanisms | Neuroprotection of retinal ganglion cells | [130] |