Abstract
Sodium L-glutamate inhibited the growth (due to inhibition of cell division and cell death) of mouse neuroblastoma (NB) cells in culture in a dose dependent fashion. The sensitivity of adrenergic (NBA 2(1)) and cholinergic (NBE −) clones to L-glutamate was similar. Sodium D-glutamate, L-aspartate, α-ketoglutarate, glutamine, γ-aminobutyric acid and carbachol did not inhibit the growth of NB cells. Methylmercuric chloride (CH 3HgCl), inorganic mercury (HgCl 2), manganese chloride (MnCl 2) and lead tri-butyl acetate, by themselves inhibited the growth of NB cells in culture to a varying degree ranging from 41% to 49%. However, the combination of glutamate with CH 3HgCl, HgCl 2 and MnCl 2, produced a synergestic effect on growth inhibition of NB cells in culture. The combination of glutamate with lead tri-butyl acetate produced only an additive effect. Sodium kainate neither inhibited the growth nor potentiated the growth inhibitory effect of L-glutamate on NB cells. Neuroblastoma cells contained high levels of receptors for glutamate but not for kainate. These results show that neuroblastoma culture may be a useful model to study the mechanisms of glutamate effects and their modification by various agents.
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