Niflumic acid activates additional currents of the human glial l-glutamate transporter eaat1 in a substrate-dependent manner

1Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free