Shirasaki T, Harata N, Nakaye T, Akaike N
Department of Neurophysiology, Tohoku University School of Medicine, Sendai, Japan.
Brain Res. 1991 Oct 25;562(2):329-31. doi: 10.1016/0006-8993(91)90641-8.
Interaction of various non-steroidal anti-inflammatory drugs (NSAIDs) and quinolone antimicrobials with gamma-aminobutyric acid (GABA)A receptor-Cl- channel complex was investigated in rat dissociated hippocampal CA1 neurons by using whole-cell mode patch-clamp technique. Neither NSAIDs nor quinolones alone affected the GABA-induced chloride current (ICl). In the presence of norfloxacin (NFLX), one of quinolones, some NSAIDs suppressed the GABA response in a concentration-dependent manner. The inhibitory potency of NSAIDs was 4-biphenylacetic acid (BPA), a metabolite of fenbufen much greater than indomethacin = naproxen greater than mefenamic acid greater than diclofenac greater than piroxicam. The results suggest that fenbufen, indomethacin and naproxen in the presence of quinolones may induce the epileptogenic neurotoxicities via pharmacological interaction with GABAA receptor.
采用全细胞膜片钳技术,在大鼠离体海马CA1神经元中研究了多种非甾体抗炎药(NSAIDs)和喹诺酮类抗菌药物与γ-氨基丁酸(GABA)A受体-Cl-通道复合物的相互作用。单独使用NSAIDs或喹诺酮类药物均不影响GABA诱导的氯离子电流(ICl)。在喹诺酮类药物之一诺氟沙星(NFLX)存在的情况下,一些NSAIDs以浓度依赖的方式抑制GABA反应。NSAIDs的抑制效力为:联苯乙酸(BPA,芬布芬的一种代谢产物)远大于吲哚美辛 = 萘普生大于甲芬那酸大于双氯芬酸大于吡罗昔康。结果表明,在喹诺酮类药物存在的情况下,芬布芬、吲哚美辛和萘普生可能通过与GABAA受体的药理相互作用诱导致癫痫性神经毒性。