Table 2.
Neurobiological effects produced by some flavonoids.
| Flavonoid | Doses | Treatment duration | Effects | Reference |
|---|---|---|---|---|
| Naringenin | 5, 10, and 20 mg/kg | 21 days | Increase in BDNF concentrations in the hippocampus in male mice | [28] |
| 5, 10, and 20 mg/kg | 14 days | Increase in 5-HT, DA, and NE in the hippocampus in male ICR mice | [29] | |
| Luteolin | 10 mg/kg | 30 min before test | Increases in chloride ion flow at the GABAA receptor in male rats | [30] |
| 50 mg/kg | 23 days | Attenuation of the expression of endoplasmic reticulum stress-related proteins in the hippocampus in male ICR mice | [31] |
|
| Icariin | 60 mg/kg | 21 days | Increases in BDNF concentrations in the hippocampus in male rats | [32] |
| Hesperidin | 0.01, 0.1, 0.3, and 1 mg/kg | 21 days | Increase in BDNF concentrations in the hippocampus in male mice | [9] |
| 50 mg/kg | 13 days | Increase in BDNF and NGF concentrations in the hippocampus in male C57BL/6 mice | [33] | |
| Astilbin | 10, 20, and 40 mg/kg | 21 days | Increase in BDNF concentrations in the cerebral cortex in male mice, similar to imipramine | [34] |
| Baicalein | 10, 20, and 40 mg/kg | 14 days | Increase in dopamine and BDNF concentrations in the hippocampus in male rats | [35] |
| 1 and 4 mg/kg | Single injection or 21 days | Restoring of the reduction of extracellular signal-regulated kinase phosphorylation and BDNF expression in the hippocampus of male Kunming mice subjected to CUMS | [36] | |
| Chrysin | 5 and 20 mg/kg | 28 days | Increase in BDNF concentrations in the hippocampus and prefrontal cortex in female mice | [10] |
| 5 and 20 mg/kg | 14 days | Increase in 5-HT and BDNF concentrations in the hippocampus in male C57B/6J mice | [37] | |
| Fisetin | 5, 10, and 20 mg/kg | 60 min before test | Activation of the serotonergic system, apparently through inactivation of MAO-A enzyme in male mice | [38] |
| 5 mg/kg | 14 days | Increases in phosphorylated TrkB (pTrkB) in the hippocampus in male ICR mice | [39] | |
| Orientin | 20 and 40 mg/kg | 21 days | Increase in BDNF, serotonin, and norepinephrine concentrations in the hippocampus and prefrontal cortex in male mice | [40] |
| 7,8-Dihydroxyflavone | 1, 3, and 10 mg/kg | 60 min before test | Increase in BDNF concentrations in the hippocampus and prefrontal cortex in male mice | [41] |
| Icariin | 20 and 40 mg/kg | 35 days | Decrease in oxidative stress and neuroinflammation in the hippocampus in male rats | [42] |
| Dihydromyricetin | 10 and 20 mg/kg | 7 days | Increase in mRNA for BDNF in the hippocampus in male C57BL/6 mice | [43] |
| Silymarin | 100 and 200 mg/kg | 14 days | Increase in 5-HT, DA, NE, and BDNF concentration in the hippocampus and cerebral cortex, similar to fluoxetine in adult Wistar rats | [44] |
| Myricitrin | 10 mg/kg | 21 days | Increases in cell proliferation in the subgranular zone of the hippocampal dentate gyrus in male BALB/c mice | [45] |
| Myricetin | 50 mg/kg | 21 days | Increases in BDNF concentrations in the hippocampus in male C57BL/6 mice | [46] |
| 3,5,6,7,8,3′,4′-Heptamethoxyflavone | 50 and 100 mg/kg | 15 days | Increase in BDNF concentration, neurogenesis, and neuroplasticity in the hippocampus in male C57BL/6 mice | [47, 48] |
| Apigenin | 20 and 40 mg/kg | 21 days | Increase in BDNF concentrations in the hippocampus in male ICR mice | [49] |
| Miquelianin | 0.6 mg/kg | 14 days | Modulation of the hypothalamic-pituitary-adrenal axis by reducing plasma concentration of ACTH and corticosterone in male CD rats | [50] |
| Isoquercitrin | 0.6 mg/kg | 14–56 days | Modulation of the hypothalamic-pituitary-adrenal axis by reducing plasma concentration of ACTH and corticosterone in male CD rats | [50] |
| Liquiritin and isoliquiritin | 20 mg/kg | 30 min before sample | Increases in 5-HT and NE concentrations in the hippocampus, hypothalamus, and cortex in mice | [51] |
BDNF: brain-derived neurotrophic factor; NGF: nerve growth factor; MAO-A: monoamine oxidase type A; TrkB: tropomyosin receptor kinase B; 5-HT: serotonin; DA: dopamine; NE: norepinephrine; ACTH: adrenocorticotropic hormone.