Nicergoline enhances glutamate uptake via glutamate transporters in rat cortical synaptosomes

被引:12
|
作者
Nishida, A
Iwata, H
Kudo, Y
Kobayashi, T
Matsuoka, Y
Kanai, Y
Endou, H
机构
[1] Tanabe Seiyaku Co Ltd, Discovery & Pharmacol Res Labs, Toda, Saitama 3358505, Japan
[2] Tanabe Seiyaku Co Ltd, Prod Management Dept, Pharmaceut Marketing Headquarters, Chuo Ku, Osaka 5418505, Japan
[3] Natl Cardiovasc Ctr, Brain Funct Res Inst Inc, Suita, Osaka 5650873, Japan
[4] Kyorin Univ, Sch Med, Dept Pharmacol & Toxicol, Mitaka, Tokyo 1818611, Japan
关键词
glutamate transporter; nicergoline; glutamate uptake; glutamate reversed transport; synaptosome; Xenopus oocyte;
D O I
10.1248/bpb.27.817
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To elucidate the mechanisms of neuroprotective action of nicergoline, we examined its effect on glutamate transport in rat cortical synaptosomes and cloned glutamate transporters. In synaptosomes, nicergoline enhanced the glutamate uptake at 1-10 mum in standard medium and suppressed the increase of extracellular glutamate by reversed transport in low Na+ medium. Apparent increase of extracellular glutamate concentration by dihydrokinate, an inhibitor of glial glutamate transporter GLT-1, was antagonized by nicergoline. In Xenopus oocytes expressing mouse neuronal glutamate transporter (mEAAC1), the glutamate-induced inward current was enhanced by nicergoline. These results suggest that nicergoline reduces the extracellular glutamate concentration through its effect on glutamate transporters.
引用
收藏
页码:817 / 820
页数:4
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