PMID- 12367599 OWN - NLM STAT- MEDLINE DCOM- 20021224 LR - 20190726 IS - 0028-3908 (Print) IS - 0028-3908 (Linking) VI - 43 IP - 4 DP - 2002 Sep TI - Complex effects of CNQX on CA1 interneurons of the developing rat hippocampus. PG - 523-9 AB - We have investigated the effect of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist, 6-cyano-7-nitro-quinoxaline-2,3-dione (CNQX), on spontaneous GABA(A) receptor-mediated transmission in the hippocampal CA1 subfield. On average, simultaneous recordings from CA1 str. radiatum interneurons and pyramidal cells showed that CNQX application doubled the frequency of bicuculline sensitive spontaneous inhibitory postsynaptic currents (sIPSCs) without apparently changing their amplitude. However, despite the increase in sIPSC frequency, current-clamp recording showed that CNQX application was sufficient in most cases to depolarize interneurons to firing threshold. In contrast, CNQX application could not induce firing in pyramidal cells. In the presence of tetrado-toxin (TTX), CNQX increased interneuron membrane conductance, and depolarized interneurons from resting potentials. The axons of the studied interneurons ramify widely in the CA1 region and suggest that the cells of our sample are mostly involved with control of dendritic excitability. Our results indicate that CNQX-induced increase of sIPSC frequency is not limited to excitatory cells, but also impacts GABAergic interneurons. However, despite the increase of sIPSC frequency, CNQX-induced depolarization is sufficient to selectively generate firing in interneurons and thus modify the network properties mediated by GABA(A) receptors in the hippocampus. FAU - Maccaferri, G AU - Maccaferri G AD - Department of Physiology, Tarry Bldg, Rm 5-707 M211, 303 E. Chicago Ave., IL 60611, USA. g-maccaferri@northwestern.edu FAU - Dingledine, R AU - Dingledine R LA - eng GR - R01 MH067561/MH/NIMH NIH HHS/United States GR - R01 MH067561-01/MH/NIMH NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - England TA - Neuropharmacology JT - Neuropharmacology JID - 0236217 RN - 0 (Excitatory Amino Acid Antagonists) RN - 0 (GABA Antagonists) RN - 6OTE87SCCW (6-Cyano-7-nitroquinoxaline-2,3-dione) RN - H030S2S85J (Kynurenic Acid) RN - Y37615DVKC (Bicuculline) SB - IM MH - 6-Cyano-7-nitroquinoxaline-2,3-dione/*pharmacology MH - Animals MH - Axons/drug effects/physiology MH - Bicuculline/pharmacology MH - Electrophysiology MH - Excitatory Amino Acid Antagonists/*pharmacology MH - Excitatory Postsynaptic Potentials/drug effects MH - GABA Antagonists/pharmacology MH - Hippocampus/*cytology/drug effects/*growth & development MH - Image Processing, Computer-Assisted MH - In Vitro Techniques MH - Interneurons/*drug effects/ultrastructure MH - Kynurenic Acid/pharmacology MH - Membrane Potentials/physiology MH - Nerve Net/drug effects MH - Patch-Clamp Techniques MH - Pyramidal Cells/drug effects MH - Rats MH - Rats, Sprague-Dawley EDAT- 2002/10/09 04:00 MHDA- 2002/12/27 04:00 CRDT- 2002/10/09 04:00 PHST- 2002/10/09 04:00 [pubmed] PHST- 2002/12/27 04:00 [medline] PHST- 2002/10/09 04:00 [entrez] AID - S0028390802001612 [pii] AID - 10.1016/s0028-3908(02)00161-2 [doi] PST - ppublish SO - Neuropharmacology. 2002 Sep;43(4):523-9. doi: 10.1016/s0028-3908(02)00161-2.