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PMID: 7545230 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Ca(2+)-permeable AMPA and NMDA receptor channels in basket cells of rat hippocampal dentate gyrus.

The Journal of physiology ·Vol. 485 ( Pt 2) ·1995-06-01 ·Pages 383-402

Koh DS, Geiger JR, Jonas P, Sakmann B

Abstract

1. Glutamate receptor (GluR) channels were studied in basket cells in the dentate gyrus of rat hippocampal slices. Basket cells were identified by their location, dendritic morphology and high frequency of action potentials generated during sustained current injection. 2. Dual-component currents were activated by fast application of glutamate to outside-out membrane patches isolated from basket cell somata (10 microM glycine, no external Mg2+). The fast component was selectively blocked by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), the slow component by D-2-amino-5-phosphonopentanoic acid (D-AP5). This suggests that the two components were mediated by alpha-amino-3- hydroxy-5-methyl-4-isoxazolepropionate receptor (AMPAR)/kainate receptor and N-methyl-D-aspartate receptor (NMDAR) channels, respectively. The mean ratio of the peak current of the NMDAR component to that of the AMPAR/kainate receptor component was 0.22 (1 ms pulses of 10 mM glutamate). 3. The AMPAR/kainate receptor component, which was studied in isolation in the presence of D-AP5, was identified as AMPAR mediated on the basis of the preferential activation by AMPA as compared with kainate, the weak desensitization of kainate-activated currents, the cross-desensitization between AMPA and kainate, and the reduction of desensitization by cyclothiazide. 4. Deactivation of basket cell AMPARs following 1 ms pulses of glutamate occurred with a time constant (tau) of 1.2 +/- 0.1 ms (mean +/- S.E.M.). During 100 ms glutamate pulses AMPARs desensitized with a tau of 3.7 +/- 0.2ms. 5. The peak current-voltage (I-V) relation of AMPAR-mediated currents in Na(+)-rich extracellular solution showed a reversal potential of -4.0 +/- 2.6 mV and was characterized by a a doubly rectifying shape. The conductance of single AMPAR channels was estimated as 22.6 +/- 1.6 pS using non-stationary fluctuation analysis. AMPARs expressed in hippocampal basket cells were highly Ca2+ permeable (PCa/PK = 1.79). 6. NMDARs in hippocampal basket cells were studied in isolation in the presence of CNQX. Deactivation of NMDARs activated by glutamate pulses occurred bi-exponentially with mean tau values of 266 +/- 23 ms (76%) and 2620 +/- 383 ms (24%). 7. The peak I-V relation of the NMDAR-mediated component in Na(+)-rich extracellular solution showed a reversal potential of 1.5 +/- 0.6 mV and a region of negative slope at negative membrane potentials in the presence of external Mg2+, due to voltage-dependent block by these ions. The conductance of single NMDAR channels in the main open state was 50.2 +/- 1.8 pS.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
Animals Benzothiadiazines/pharmacology Calcium Channels/drug effects,metabolism Dendrites/drug effects,metabolism Diuretics Glutamic Acid/pharmacology Hippocampus/cytology,drug effects,metabolism In Vitro Techniques Kainic Acid/pharmacology Kinetics Magnesium/pharmacology Patch-Clamp Techniques Rats Rats, Wistar Receptors, AMPA/antagonists & inhibitors,metabolism Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors,metabolism Sodium/metabolism Sodium Chloride Symporter Inhibitors/pharmacology alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid/pharmacology
Chemicals
Benzothiadiazines Calcium Channels Diuretics Receptors, AMPA Receptors, N-Methyl-D-Aspartate Sodium Chloride Symporter Inhibitors Glutamic Acid alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Sodium Magnesium cyclothiazide Kainic Acid
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Koh D S
Max-Planck-Institut für medizinische Forschung, Abteilung Zellphysiologie, Heidelberg, Germany.
Geiger J R
Jonas P
Sakmann B
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Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1995-06-01
Pages
383-402
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1158000
Subset
IM
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