Review Article
Chelators in the Treatment of Iron Accumulation in Parkinson's Disease
Table 1
Iron chelators in brief. Summary of key information regarding iron chelators currently undergoing research as possible PD therapies.
| Chelator name | BBB-permeable | Stage of research | Relevant findings | References |
| Synthetic | | | | | Desferal | No | Clinically used for systemic iron accumulation. Cellular and animal models of PD | Neuroprotective in rat 6-OHDA model | [64] | Deferiprone | Yes | Phase II trials | Efficacious. Can reduce iron levels but not always with symptomatic improvement | [65, 66] | Apomorphine | Yes | Animal models | Effective against iron-induced toxicity and MPTP-induced cell death | [67] | VK-28 | Yes | Animal models | Protective in 6-OHDA rat model | [68] | M30 | Yes | Animals models | MAO-A and -B inhibitor. Selective. Effective in MPTP mouse model | [69] | M10 | Yes | Cell culture | Hydroxide scavenger. Inhibits lipid peroxidation | [70, 71] | CQ | Yes | Animal models | Neuroprotective in MPTP mouse model | [72, 73] |
| Natural | | | | | EGCG | Yes | Animal models | Multiple protective actions. Can be used in combination with rasagiline. Effective in MPTP mouse model but not in 6-OHDA rat model | [74, 75] | Phytic acid | Unknown | Cell culture | Protects against MPP+ and 6-OHDA toxicity in normal and excess iron | [76, 77] |
|
|