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. 2021 Feb 14;41:101896. doi: 10.1016/j.redox.2021.101896

Fig. 10.

Fig. 10

Schematic illustration of the effects of the dual-acting D2/D3 agonist and iron chelating ligand, D-607, and its multiple molecular targets in neurons affected by PD [532,533]. These include its ability to: (1) act as a D2/D3 receptor agonist; (2) bind Fe+2 and inhibit redox cycling that would prevent glutathione (GSH) depletion and lipid peroxidation; (3) bind iron and prevent the prolyl hydroxylase mediated degradation of hypoxia-inducible factor-1α (HIF1α); and (4) prevent α-synuclein aggregation as iron-depletion decreases α-synuclein expression [392,393] and may prevent fibrilization of this protein [535].