首页> 外文期刊>Journal of pharmacological sciences. >Two Non-steroidal Anti-inflammatory Drugs, Niflumic Acid and Diclofenac, Inhibit the Human Glutamate Transporter EAAT1 Through Different Mechanisms
【24h】

Two Non-steroidal Anti-inflammatory Drugs, Niflumic Acid and Diclofenac, Inhibit the Human Glutamate Transporter EAAT1 Through Different Mechanisms

机译:两种非甾体类抗炎药尼氟酸和双氯芬酸通过不同机制抑制人谷氨酸转运蛋白EAAT1。

获取原文
           

摘要

References(12) Supplementary materials(2) 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 (Erev) of L-Glu-induced current and increased current amplitude at the potentials more negative than −100 mV. Diclofenac had no effects on Erev 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. [Supplementary methods and Figure: available only at http://dx.doi.org/10.1254/jphs.09260SC]
机译:参考文献(12)补充材料(2)我们研究了非甾体类抗炎药对非洲爪蟾卵母细胞中底物诱导的L-谷氨酸(L-Glu)转运蛋白EAAT1电流的影响。尼氟酸(NFA)和双氯芬酸以非竞争性方式抑制L-Glu诱导的通过EAAT1的电流。 NFA使L-Glu感应的电流的反向电位(Erev)向左移动,并且在比-100 mV负的电位上增加了电流幅度。双氯芬酸对Erev没有影响,并且在所有负电位下都将电流幅度抑制到相同程度。这些结果表明NFA和双氯芬酸通过不同的机制抑制L-Glu诱导的EAAT1电流。 [补充方法和图:仅在http://dx.doi.org/10.1254/jphs.09260SC上提供]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号