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Publication : Protective effects of metallothionein against dopamine quinone-induced dopaminergic neurotoxicity.

First Author  Miyazaki I Year  2007
Journal  FEBS Lett Volume  581
Issue  25 Pages  5003-8
PubMed ID  17910954 Mgi Jnum  J:126937
Mgi Id  MGI:3762324 Doi  10.1016/j.febslet.2007.09.046
Citation  Miyazaki I, et al. (2007) Protective effects of metallothionein against dopamine quinone-induced dopaminergic neurotoxicity. FEBS Lett 581(25):5003-8
abstractText  Dopamine (DA) quinone as DA neuron-specific oxidative stress conjugates with cysteine residues in functional proteins to form quinoproteins. Here, we examined the effects of cysteine-rich metal-binding proteins, metallothionein (MT)-1 and -2, on DA quinone-induced neurotoxicity. MT quenched DA semiquinones in vitro. In dopaminergic cells, DA exposure increased quinoproteins and decreased cell viability; these were ameliorated by pretreatment with MT-inducer zinc. Repeated L-DOPA administration markedly elevated striatal quinoprotein levels and reduced the DA nerve terminals specifically on the lesioned side in MT-knockout parkinsonian mice, but not in wild-type mice. Our results suggested that intrinsic MT protects against L-DOPA-induced DA quinone neurotoxicity in parkinsonian mice by its quinone-quenching property.
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