Niflumic Acid Activates Additional Currents of the Human Glial L-Glutamate Transporter EAAT1 in a Substrate-Dependent Manner

被引:1
作者
Takahashi, Kanako [1 ]
Ishii-Nozawa, Reiko [2 ]
Takeuchi, Koichi [2 ]
Nakazawa, Ken [1 ]
Sekino, Yuko [1 ]
Sato, Kaoru [1 ]
机构
[1] Natl Inst Hlth Sci, Neuropharmacol Lab, Div Pharmacol, Tokyo, Tokyo 1588501, Japan
[2] Meiji Pharmaceut Univ, Dept Clin Pharmacol, Kiyose, Tokyo 2048588, Japan
关键词
astrocytic L-glutamate transporter; niflumic acid; additional conductance; EAAT1; voltage-dependent manner; XENOPUS OOCYTES; CHANNEL BLOCKERS; CHLORIDE CHANNEL; ION FLUXES; CL-CHANNEL; ASTROCYTES; RECEPTOR; CELLS; MODULATION; DICLOFENAC;
D O I
10.1248/bpb.b13-00702
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 CI- was involved only with the L-Asp currents. NFA activated additional currents of EAAT1 in a substrate-dependent manner.
引用
收藏
页码:1996 / 2004
页数:9
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