Effects of harman and norharman on dopamine biosynthesis and L-DOPA-induced cytotoxicity in PC12 cells

Abstract The effects of harman and norharman on dopamine biosynthesis and L-DOPA-induced cytotoxicity in PC12 cells were investigated. Harman and norharman at a concentration of 20 μM and 100 μM showed 49.4% and 49.5% inhibition of dopamine content for 48 h, respectively. The IC 50 values of harman and norharman were 21.2 μM and 103.3 μM. Dopamine content, tyrosine hydroxylase (TH) activity and TH mRNA levels were decreased during the first 6 h, maintained for up to 48 h and then gradually recovered at 72 h after exposure to 20 μM harman and 100 μM norharman. Under the same conditions, the intracellular cyclic AMP levels and Ca 2+ concentrations were also decreased by harman and norharman. In addition, harman and norharman at concentrations higher than 80 μM and 150 μM caused cytotoxicity at 48 h in PC12 cells. Non-cytotoxic ranges of 10–30 μM harman and 50–150 μM norharman inhibited L-DOPA (20–50 μM)-induced increases in dopamine content at 48 h. Harman at 20–150 μM and norharman at 100–300 μM also enhanced L-DOPA (20–100 μM)-induced cytotoxicity at 48 h with an apoptotic process. These results suggest that harman and norharman inhibit dopamine biosynthesis by reducing TH activity and enhance L-DOPA-induced cytotoxicity in PC12 cells.