A patch clamp study of the effects of ciprofloxacin and biphenyl acetic acid on rat hippocampal neurone GABA(A) and ionotropic glutamate receptors

被引:17
作者
Halliwell, RF [1 ]
Davey, PG [1 ]
Lambert, JJ [1 ]
机构
[1] UNIV DUNDEE,NINEWELLS HOSP & MED SCH,DEPT PHARMACOL & CLIN PHARMACOL,DUNDEE DD1 9SY,SCOTLAND
关键词
quinolones; ciprofloxacin; GABA(A) receptor; hippocampal neurones; biphenyl acetic acid; ionotropic glutamate receptors;
D O I
10.1016/0028-3908(95)00106-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neurotoxic effects of 4-quinolones alone and in combination with certain non-steroidal anti-inflammatory drugs (NSAIDs) may be related to an interaction at GABA(A) and/or ionotropic glutamate receptors. In the present study, the effects of the fluoroquinolone, ciprofloxacin, alone and in combination with the NSAID, biphenyl acetic acid (BPAA), were examined on GABA(A)-, NMDA-, AMPA-, and kainate-evoked current responses recorded from cultured rat hippocampal neurones, using the whole cell patch clamp technique. GABA-evoked currents were reversibly inhibited by bicuculline (3 mu M) and ciprofloxacin (100 mu M) to 11 +/- 5 and 38 +/- 7% of control, respectively. BPAA (100 mu M) had little affect on the GABA current (the response was 82 +/- 4% of control) but enhanced the inhibitory potency of ciprofloxacin by approx. 3000-fold. The antagonist effects of ciprofloxacin (30 mu M) and ciprofloxacin (0.03 mu M) together with BPAA (100 mu M) on the GABA-evoked current were not voltage-dependent. Whole cell currents evoked by NMDA, AMPA or kainate were little influenced by ciprofloxacin (100 mu M), BPAA (100 mu M), or ciprofloxacin plus BPAA (both at 100 mu M); the responses being greater than or equal to 90% of control in all cases. These data suggest that the proconvulsant effects of quinolones when combined with BPAA may be related to antagonism of central GABA(A) receptors but not to an interaction at ionotropic glutamate receptors.
引用
收藏
页码:1615 / 1624
页数:10
相关论文
共 35 条
[1]   POSSIBLE INTERMOLECULAR INTERACTION BETWEEN QUINOLONES AND BIPHENYLACETIC ACID INHIBITS GAMMA-AMINOBUTYRIC-ACID RECEPTOR-SITES [J].
AKAHANE, K ;
KIMURA, Y ;
TSUTOMI, Y ;
HAYAKAWA, I .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (10) :2323-2329
[2]   STRUCTURE-EPILEPTOGENICITY RELATIONSHIP OF QUINOLONES WITH SPECIAL REFERENCE TO THEIR INTERACTION WITH GAMMA-AMINOBUTYRIC ACID RECEPTOR-SITES [J].
AKAHANE, K ;
SEKIGUCHI, M ;
UNE, T ;
OSADA, Y .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (10) :1704-1708
[3]   INVOLVEMENT OF INHIBITORY AND EXCITATORY NEUROTRANSMITTERS IN LEVOFLOXACIN-INDUCED AND CIPROFLOXACIN-INDUCED CONVULSIONS IN MICE [J].
AKAHANE, K ;
KATO, M ;
TAKAYAMA, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (09) :1764-1770
[4]   QUINOLONES AND FENBUFEN INTERACT WITH GABA-A RECEPTOR IN DISSOCIATED HIPPOCAMPAL CELLS OF RAT [J].
AKAIKE, N ;
SHIRASAKI, T ;
YAKUSHIJI, T .
JOURNAL OF NEUROPHYSIOLOGY, 1991, 66 (02) :497-504
[5]   NEUROTRANSMITTER RECEPTORS .2. AMPA AND KAINATE RECEPTORS [J].
BETTLER, B ;
MULLE, C .
NEUROPHARMACOLOGY, 1995, 34 (02) :123-139
[6]   CENTRAL-NERVOUS-SYSTEM TOXICITY OF QUINOLONES - HUMAN AND ANIMAL FINDINGS [J].
CHRIST, W .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 26 :219-225
[7]  
DALHOFF A, 1989, QUINOLONES
[8]   ONLY SOME ANTICONVULSANTS PROTECT AGAINST SEIZURES INDUCED BY AMINOPHYLLINE IN QUINOLONE-TREATED GENETICALLY EPILEPSY-PRONE RATS [J].
DESARRO, A ;
AMMENDOLA, D ;
JULIANO, M ;
GARERI, P ;
DESARRO, G .
GENERAL PHARMACOLOGY, 1993, 24 (06) :1393-1401
[9]   HIPPOCAMPAL ACTIVITY IN THE PRESENCE OF QUINOLONES AND FENBUFEN INVITRO [J].
DIMPFEL, W ;
SPULER, M ;
DALHOFF, A ;
HOFMANN, W ;
SCHLUTER, G .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (06) :1142-1146
[10]  
DODD PR, 1989, PHARM TOXIC, V64, P401