Apomorphine is a potent dopamine agonist that displays efficient antiparkin
sonian properties. However, it is a catechol that easily autoxidates, formi
ng both potentially toxic quinone-related compounds and reactive oxygen spe
cies. The consequences of its oxidant and toxic properties have been poorly
investigated on in vitro models. In a recent work, we studied apomorphine
autoxidation by recording the formation of a neuromelanin product. We also
investigated apomorphine toxicity on cultures of rat glioma C6 cells and pr
imary cultures of neurons using different concentrations of the drug. Apomo
rphine-promoted cell death was proportional to its concentration and was ti
me-dependent. Both toxicity of apomorphine and neuromelanin formation were
partially prevented by thiol reagents, suggesting the involvement of an oxi
dative stress in the toxicity promoted by apomorphine.