The aim of our research was the evaluation in vitro of the neurotoxic
effects of fenthion and its metabolites on human neuroblastoma cells,
as a model for their toxicity in humans. The results indicate that 24
hours exposure was sufficient to produce dose related effects on SK-N-
BE and IMR 32 cell viability causing detachment and loss of cells at t
he effective doses. In the two cell lines fenthion metabolites display
an increased cytotoxicity respect to the parent compound with a disti
nct pattern of toxicity on neurons. Our data suggest that cultured neu
ronal cells of human origin are discriminating experimental systems, s
ensitive to minor differences,of correlating in vivo and in vitro neur
otoxicants.