Table 2.
Therapeutic strategy targeting microglia for CNS disorders.
| Molecular or cellular target | Pharmacological intervention | Results | Reference |
|---|---|---|---|
| (i) Inflammatory response | |||
| Immuno modulator | Minocycline | Anti-apoptotic, anti-inflammatory, and antioxidant effects on several PD models. | (131) |
| COX2 | NSAIDs | Prevention of inflammation and dyskinesia in the rotenone rat model. | (132) |
| (ii) Phenotypic transformation | |||
| Induces an M1 to M2 switch in microglia phenotype | Progesterone | Progesterone treatment reduced neurobehavioral deficits in the mouse demyelinating model. | (133) |
| Promoted transformation of microglial M1 phenotype to M2 phenotype | Fractalkine | FKN partially recovered the spatial memory of irradiated mice. | (134) |
| (iii) Microglia depletion and regeneration | |||
| Microglia depletion strategy | CSF1R inhibitors | Attenuates neurological abnormalities and brain edema. | (135) |
| Microglia repopulation strategy | Multipotent adult progenitor cells | Improved the BBB after traumatic brain injury, weakened the activated microglia macrophages in the dentate gyrus, and improved cognitive behavior. | (136) |
| (iv) Receptors and pathways | |||
| NF-κB, MAPK | Metformin | Ameliorated neurological deficit, cerebral edema, and neuronal apoptosis in rats following TBI. | (137) |
| Akt/mTOR/ STAT3 signaling pathway | 6-gingerol | Reduced the size of infarction and improved neurological functions in the ischemia brain damage rat model. | (138) |