The sensitivity of Purkinje cells to short pulse applications of L-aspartate, L-glutamate and related derivatives in their dendritic fields was tested in normal and staggerer mutant mice using cerebellar slices maintained in vitro. In normal mice, the response of Purkinje cells to L-aspartate and L-glutamate consisted of a transient and dose-dependent increase of their firing of simple spikes. The potency of L-aspartate in exciting Purkinje cells was lower than that of L-glutamate when the two drugs were released from adjacent barrels of the same iontophoretic electrode. Quisqualate was an even more potent excitant of these cells than L-aspartate and L-glutamate, whereas N-methyl-DL-aspartate had little or no effect. In staggerer mutant mice, the sensitivity of Purkinje cells to L-aspartate, L-glutamate and quisqualate was not significantly altered. On the contrary, N-methyl-DL-aspartate had a much stronger potency than normal in exciting Purkinje cells although this was still smaller than that of the other agonists tested. These results suggest that the sensitivity of Purkinje cells to L-aspartate and L-glutamate, i.e. the putative neurotransmitters of the climbing and parallel fibers respectively, remains largely normal in staggerer mice. In contrast, in the mutant, N-methyl-D-aspartate receptors are likely to be much more developed than normal.