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. 2012 Apr 9;209(4):837–854. doi: 10.1084/jem.20112285

Figure 2.

Figure 2.

CuII(atsm) is neuroprotective in multiple animal models of PD. (a) C57BL/6 mice were lesioned with MPTP (40 mg/kg i.p.). The SNpc count (dotted line) was determined 24 h after MPTP lesioning (when drug treatment commenced). Effect of treatment with CuII(atsm) at both 15 and 30 mg/kg on the survival of SNpc dopaminergic neurons 20 d after lesioning. (b) C57BL/6 mice were lesioned unilaterally with 6-OHDA (intranigral dose). Effect of treatment with 30 mg/kg of CuII(atsm) on the survival of SNpc dopaminergic neurons. (c) Effect of CuII(atsm) (30 mg/kg) treatment of mice overexpressing human A53T (hA53T) α-synuclein, either nonlesioned or lesioned with MPTP on the survival of SNpc dopaminergic neurons. All data are expressed as mean ± SEM; for statistical analysis, one-way ANOVA was performed with a Dunnett post-doc analysis for multisample testing using untreated MPTP-lesioned mice (a), hA53T tg untreated or MPTP-lesioned untreated hA53T tg mice (c), and Student’s t test for two-sample testing (b) as controls. *, P < 0.05; **, P < 0.01; ***, P < 0.001.