Diaminodiphenyl sulfone-induced parkin ameliorates age-dependent dopaminergic neuronal loss

Abstract During normal aging, the number of dopaminergic (DA) neurons in the substantia nigra (SN) progressively diminishes, while massive DA neuronal loss is a hallmark sign of Parkinson’s disease (PD). Unfortunately, there is little known about the molecular events involved in age-related DA neuronal loss. In this study, we found that (1) the level of parkin was decreased in the cerebellum, brain stem, SN, and striatum of aged mice, (2) diaminodiphenyl sulfone (DDS) restored the level of parkin, (3) DDS prevented age-dependent DA neuronal loss, and (4) DDS protected SH-SY5Y cells from MPP+ and H2 O2 . Furthermore, pre/post-treatment of DDS in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced PD model attenuated DA neuronal loss and restored motor behavior. DDS transcriptionally activated parkin via PERK-ATF4 signaling and DDS not only failed to induce parkin expression, but also failed to rescue SH-SY5Y cells from MPP+ in the absence of ATF4. Herein, we demonstrated for the first time that DDS increased parkin level and served as a neuroprotective agent for age-dependent DA neuronal loss. Thus, DDS may be a potential therapeutic agent for age-related neurodegeneration.