Abstract
The effects of low-level lead exposure on survival and neurite length of rat E15 primary ventral mesencephalic dopaminergic neurons were studied. Lead acetate (0.001–10 μM) added to primary cultures for 48 h (in serum-free defined media [DM]) caused a loss of tyrosine hydroxylase (TH)-positive neurons only at the highest concentrations (1 and 10 μM). In contrast, significant effects on neurite length were observed at concentrations as low as 0.001 μM. Lead-induced decrease in neurite length became more apparent at concentrations of 0.01 μM (mean 37.9% decrease) and 0.10 μM lead acetate (mean 43.9% decrease). These data show that very low concentrations of lead, well below the level necessary to adversely affect neuronal survival, can have dramatic effects on neurite growth. These results support recent clinical findings of detrimental effects of low-level lead exposure on brain development.
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