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

• Published in: Neuropharmacology 1995-12, Vol.34 (12), p.1615-1624
• Main Authors: HALLIWELL, R. F, DAVEY, P. G, LAMBERT, J. J
• Format: Article
• Language: English
• Subjects: alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology; Animals; Anti-Infective Agents - pharmacology; Anti-Inflammatory Agents, Non-Steroidal - pharmacology; Bicuculline - pharmacology; Biological and medical sciences; Cells, Cultured; Ciprofloxacin - pharmacology; Drug Interactions; Drug toxicity and drugs side effects treatment; Hippocampus - drug effects; Hippocampus - metabolism; Kainic Acid - pharmacology; Medical sciences; N-Methylaspartate - pharmacology; Patch-Clamp Techniques; Pharmacology. Drug treatments; Phenylacetates - pharmacology; Rats; Rats, Sprague-Dawley; Receptors, GABA-A - drug effects; Receptors, Glutamate - drug effects; Toxicity: nervous system and muscle
• ISSN: 0028-3908; 1873-7064

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 GABAA 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 GABAA-, 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 microM) and ciprofloxacin (100 microM) to 11 +/- 5 and 38 +/- 7% of control, respectively. BPAA (100 microM) 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 microM) and ciprofloxacin (0.03 microM) together with BPAA (100 microM) on the GABA-evoked current were not voltage-dependent. Whole cell currents evoked by NMDA, AMPA or kainate were little influenced by ciprofloxacin (100 microM), BPAA (100 microM), or ciprofloxacin plus BPAA (both at 100 microM); the responses being > or = 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 GABAA receptors but not to an interaction at ionotropic glutamate receptors.