Abstract
Glial glutamate transporters, GLAST and GLT-1, are co-localized in processes of Bergmann glia (BG) wrapping excitatory synapses on Purkinje cells (PCs). Although GLAST is expressed 6-fold more abundantly than GLT-1, no change is detected in the kinetics of climbing fiber (CF)-mediated excitatory postsynaptic currents (CF-EPSCs) in PCs in GLAST(-/-) mice compared to the wild-type mice (WT). The prolongation of the decay kinetics of CF-EPSCs in GLAST(-/-) mice is found only in the presence of cyclothiazide (CTZ), which attenuates the desensitization of AMPA receptors. We attempted to clarify the mechanism(s) underlying this unexpected finding using a selective GLT-1 blocker, dihydrokainate (DHK), and a novel antagonist of glial glutamate transporters, (2S,3S)-3-[3-(4-methoxybenzoylamino)benzyloxy]aspartate (PMB-TBOA). In the presence of CTZ, DHK prolonged the decay time constant (τw) of CF-EPSCs in WT, indicating that GLT-1 plays a partial role in the removal of glutamate. The application of 100 nM PMB-TBOA, which inhibited CF-mediated transporter currents in BG by ∼80%, caused no change in τw in WT in the absence of CTZ, whereas it prolonged τw in the presence of CTZ. This prolonged value of τw was similar to that in GLAST(-/-) mice in the presence of CTZ. These results indicate that glial glutamate transporters can apparently retain the fast decay kinetics of CF-EPSCs if a small proportion (∼20%) of functional transporters is preserved, and that GLT-1 alone in GLAST(-/-) mice is sufficient to keep the fast kinetics of EPSCs in the absence of CTZ. [J Physiol Sci. 2006;56 Suppl:S45]
