Table 2.
Disease | Animal Model | Treatment | Tissue Sample | Result | References |
---|---|---|---|---|---|
PD | PD mouse model. | TQ (10 mg/kg was given for 1 week before administration of MPTP (25 mg/kg). | Striatal region | Inhibition effect against α-synuclein aggregation and cellular death. | [3] |
PD | Primary dopaminergic cell culture neurons. | dopaminergic neurons tissue was received TQ (0.01, 0.1, 1, and 10 μM) on day 6 i.v. for 6 days. | NA | Protective effects against MPP+ and rotenone. | [56] |
PD | Embryonic mouse mesencephala at gestation day 14. | Four groups: group 1 control group, group 2 received TQ on the 8th day for 4 days, group 3: received 1-methyl-4-phenylpyridinium (MPP+) on the 10th for 48 h, group 4:co-treated with TQ and MPP+. | NA | Protective effects on the dopaminergic neurons and inhibition of their apoptosis. | [61] |
PD | 6-hydroxydopamine (6-OHDA)-lesioned rats. | Oral TQ at different doses of 5 and/or 10 mg/kg administered 3 times daily for 1 week. | Substantia nigra pars compacta and midbrain |
Protective effect against 6-OHDA neurotoxicity. | [62] |
PD | Male Wistar rats (8–10 months) received rotenone. | TQ (7.5 and 15 mg/kg/day, po) given as pretreatment for one hour before administration of rotenone injection. | Substantia nigra (SN) and striatum (ST) | Protection and antioxidant effects against rotenone. | [63] |
PD | Adult Wistar rats of either sex, CPZ dosing for 21 days to induce Parkinson’s. | Extracts of Nigella sativa at 200 and 400 mg/kg doses were given orally. | Whole-brain | Increased anti-Parkinson’s activity | [64] |