Table 3.
Baicalein, baicalin, and wogonin performance on different brain ischemia models.
| Models | Species | Baicalein | Baicalin | Wogonin | Reference(s) | |||
|---|---|---|---|---|---|---|---|---|
| Conc. | Effects | Conc. | Effects | Conc. | Effects | |||
| SCEM | Rabbit | 100 mg/kg | Improve behavioral performance | [93] | ||||
| MCAO | Rat/mouse | 20 mg/kg; 200 mg/kg | Decrease the infarct volume and neurological score; inhibiting 12/15-LOX-induced oxidative toxicity; regulate M1/M2 transformation of microglia/macrophages and block NF-κB nuclear translocation; suppress PARP-1/AIF pathway-induced neuroinflammation; antioxidant 12/15-LOX inhibitor | 5, 100, and 200 mg/kg | Reduced the neurological deficit scores, cerebral infarct volume by inhibiting TLR2/4-mediated NF-κB pathway, and expression of iNOS, COX2, and caspase3 | 20 mg/kg; 50 μM | Reduce infarct area and improve behavior performance through upregulating TGF-β1 | [92, 94, 106–109, 112–116, 118, 119] |
| GCI/R | Gerbil/rats | 100 mg/kg; 200 mg/kg | Improve learning and memory ability post-I/R injury via anti-inflammatory and antiapoptosis; perform neuroprotection by upregulating HSP70 expression and influencing MAPK cascades in the gerbil hippocampus | 0.5, 1, and 10 mg/kg | Increase neuron survival in the hippocampus area by suppressing inflammation (iNOS, TNF-α) | [100, 101, 103, 117, 118] | ||