Two non-steroidal anti-inflammatory drugs, niflumic acid and diclofenac, inhibit the human glutamate transporter EAAT1 through different mechanisms

J Pharmacol Sci. 2010;112(1):113-7. doi: 10.1254/jphs.09260sc. Epub 2010 Jan 6.

Abstract

We investigated the effects of non-steroidal anti-inflammatory drugs on substrate-induced currents of L-glutamate (L-Glu) transporter EAAT1 expressed in Xenopus laevis oocytes. Niflumic acid (NFA) and diclofenac inhibited L-Glu-induced current through EAAT1 in a non-competitive manner. NFA produced a leftward shift in reversal potential (E(rev)) of L-Glu-induced current and increased current amplitude at the potentials more negative than -100 mV. Diclofenac had no effects on E(rev) and inhibited the current amplitude to the same extent at all negative potentials. These results indicate that NFA and diclofenac inhibit the L-Glu-induced EAAT1 current via different mechanisms.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal / blood
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Diclofenac / adverse effects
  • Diclofenac / pharmacology*
  • Excitatory Amino Acid Transporter 1 / antagonists & inhibitors*
  • Excitatory Amino Acid Transporter 1 / metabolism
  • Female
  • Humans
  • Niflumic Acid / adverse effects
  • Niflumic Acid / pharmacology*
  • Oocytes / drug effects
  • Oocytes / metabolism
  • Xenopus laevis

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Excitatory Amino Acid Transporter 1
  • SLC1A3 protein, human
  • Diclofenac
  • Niflumic Acid