We have shown previously that a selective metabotropic glutamate receptor (mGluR) agonist, 1S,3R-1-aminocyclopentane-1,3-dicarboxylate (1S,3R-ACPD), evokes an inward current in CA1 pyramidal neurons of rat hippocampal slices in the presence of K ϩ channel blockers (Cré pel et al., 1994). This current has been characterized as a Ca 2ϩ -activated nonselective cationic (CAN) current. Using whole-cell patch-clamp recordings and intracellular dialysis, we now have identified the mGluR subtype and the mechanisms underlying the CAN current (I CAN ) and report for the first time the presence of a synaptic I CAN in the mammalian CNS. First, we have shown pharmacologically that activation of I CAN by 1S,3R-ACPD involves the group I mGluRs (and not the groups II and III) and a G-protein-dependent process. We also report that I CAN is modulated by the divalent cations (Mg 2ϩ , Cd 2ϩ , and Zn 2ϩ ). Second, we have isolated a slow synaptic inward current evoked by a high-frequency stimulation in the presence of K ϩ channel blockers, ionotropic glutamate, and GABA A receptor antagonists. This current shows similar properties to the exogenously evoked I CAN : its reversal potential is close to the reversal potential of the 1S,3R-ACPD-evoked I CAN , and it is G-protein-and Ca 2ϩ -dependent. Because the amplitude and duration of I CAN increased in the presence of a glutamate uptake blocker, we suggest that this synaptic current is generated via the activation of mGluRs. We propose that the synaptic I CAN , activated by a brief tetanic stimulation and leading to a long-lasting inward current, may be involved in neuronal plasticity and synchronized network-driven oscillations.