Table 2.
Clemastine in vitro study.
Cells | Cell origin | Intervention | Clemastine doses and incubation time | Major findings | Mechanisms | Ref. |
---|---|---|---|---|---|---|
OPCs | Cerebral cortices from 2-day-old postnatal rat | Co-culture with human neural progenitor cells, | 1 μM for 48 hr | Enhanced OPCs differentiation | – | Nicaise et al. (2017) |
Cerebral hemispheres from 1-day-old postnatal SD rats | IL-1β | 20 ng/ml for 7 days | Promoted the maturation of primary OPCs | Activated ERK phosphorylation | Xie et al. (2020) | |
Primary microglial cells | Brain cortex from 1-day old postnatal SOD1G93A mice | P2X7 receptor agonist BzATP | 30 μM for 18 hr | Inhibited M1 phenotype, promoted M2 phenotype | – | Apolloni et al. (2016b) |
Cerebral hemispheres from 1-day-old postnatal SD rats | Oxygen glucose deprivation | 20 ng/ml for 1 hr | Inhibited activation of microglial cells | Inhibited p38 phosphorylation | Xie et al. (2020) | |
Spinal cord from 120-day-old postnatal SOD1G93A mice | – | 30 μM for 6 hr | Decreased inflammation and SOD1, enhanced autophagic activity | Inhibited mTOR signaling pathway | Apolloni et al. (2016a) | |
BV2 microglial cells | Lysed murine RBC | 20 or40 μM for 72 hr | Suppressed microglia activation | – | Zhi et al. (2021) | |
Primary cortical neurons | Brain cortex from 14-days-old postnatal mouse | Co-culture with activated microglia | 20 or 40 μM for 72 hr | Protected against neuronal apoptosis induced by activated microglia | – | Zhi et al. (2021) |