Abstract
The astrocytic L-glutamate (L-Glu) transporter EAAT1 participates in the removal of L-Glu from the synaptic cleft and maintenance of non-toxic concentrations in the extracellular fluid. We have shown that niflumic acid (NFA), a non-steroidal anti-inflammatory drug (NSAIDs), alters L-Glu-induced EAAT1 currents in a voltage-dependent manner using the two-electrode voltage clamp technique in Xenopus oocytes expressing EAAT1. In this study, we characterised the effects of NFA on each type of ion-flux through EAAT1. NFA modulated currents induced by both L-Glu and L-aspartate (L-Asp) in a voltage-dependent manner. Ion-substitution experiments revealed that the activation of additional H conductance was involved in the modulation of currents induced by L-Asp and L-Glu, but Cl-was involved only with the L-Asp currents. NFA activated additional currents of EAAT1 in a substrate-dependent manner. © 2013 The Pharmaceutical Society of Japan.
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Takahashi, K., Ishii-Nozawa, R., Takeuchi, K., Nakazawa, K., Sekino, Y., & Sato, K. (2013). Niflumic acid activates additional currents of the human glial l-glutamate transporter eaat1 in a substrate-dependent manner. Biological and Pharmaceutical Bulletin, 36(12), 1996–2004. https://doi.org/10.1248/bpb.b13-00702
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