WE reported here the first evidence that endothelin (ET)-1 and ET-3 pr
oduced an increase in intracellular Ca2+ concentrations ([Ca2+](1)), c
onsisting of a transient and a sustained component, in cultured neuron
es and in slices of the rat hippocampus. In the neurones, the removal
of Ca2+ or the addition of Cd2+ remarkably inhibited the ET-3-evoked s
ustained but not the transient response. The [Ca2+](i) increased by ET
s was observed in the dentate gyrus and in the vicinity of CA1 and CA3
pyramidal cell layer in the hippocampus, findings in good accord with
regions where the glutamate receptor agonists have an elevated [Ca2+]
(i). The possible causal link between ETs and the increased [Ca2+](i)
in the development of hippocampal neuronal death is discussed.