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Inhibition of GABAA receptor-mediated current responses by enoxacin (new quinolone) and felbinac (non-steroidal anti-inflammatory drug) in Xenopus oocytes injected with mouse-brain messenger RNA.

作者信息

Kawakami J, Shimokawa M, Yamamoto K, Sawada Y, Asanuma A, Yanagisawa K, Iga T

机构信息

Department of Pharmacy, University of Tokyo Hospital, Faculty of Medicine, Japan.

出版信息

Biol Pharm Bull. 1993 Jul;16(7):726-8. doi: 10.1248/bpb.16.726.

DOI:10.1248/bpb.16.726
PMID:7691340
Abstract

The convulsant interaction between enoxacin (ENX), a new quinolone antibacterial agent (NQ), and felbinac (FLB), a non-steroidal anti-inflammatory drug (NSAID), in vivo was reproduced as the change of GABA-induced current response in Xenopus oocytes injected with mouse brain mRNA. GABA (10 microM) response was inhibited by ENX in a dose-dependent manner, and IC50 of ENX was 96 microM. Moreover, the inhibitory effect of ENX was 80-fold potentiated in the presence of 10 microM FLB. The GABAA-antagonistic interaction between these two drugs in vitro was considered a possible mechanism of convulsant reaction after concomitant administration of NQs and NSAIDs in vivo.

摘要

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引用本文的文献

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In vivo and in vitro toxicodynamic analyses of new quinolone-and nonsteroidal anti-inflammatory drug-induced effects on the central nervous system.新型喹诺酮类和非甾体抗炎药对中枢神经系统影响的体内和体外毒代动力学分析
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2
Pharmacokinetic-pharmacodynamic drug interactions with nonsteroidal anti-inflammatory drugs.非甾体抗炎药的药代动力学-药效学药物相互作用
Clin Pharmacokinet. 1994 Dec;27(6):462-85. doi: 10.2165/00003088-199427060-00005.