Home LiteratureArticle Details
PMID: 1697209 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Miniature excitatory synaptic currents in cultured hippocampal neurons.

Brain research ·Vol. 518 ·No. 1-2 ·1990-06-04 ·Pages 257-68

Finch DM, Fisher RS, Jackson MB

Abstract

We performed patch clamp recordings in the whole cell mode from cultured embryonic mouse hippocampal neurons. In bathing solutions containing tetrodotoxin (TTX), the cells showed spontaneous inward currents (SICs) ranging in size from 1 to 100 pA. Several observations indicated that the SICs were miniature excitatory synaptic currents mediated primarily by non-NMDA (N-methyl-D-aspartate) excitatory amino acid receptors: the rising phase of SICs was fast (1 ms to half amplitude at room temperature) and smooth, suggesting unitary events. The SICs were blocked by the broad-spectrum glutamate receptor antagonist gamma-D-glutamylglycine (DGG), but not by the selective NMDA-receptor antagonist D-2-amino-5-phosphonovaleric acid (5-APV). SICs were also blocked by desensitizing concentrations of quisqualate. Incubating cells in tetanus toxin, which blocks exocytotic transmitter release, eliminated SICs. The presence of SICs was consistent with the morphological arrangement of glutamatergic innervation in the cell cultures demonstrated immunohistochemically. Spontaneous outward currents (SOCs) were blocked by bicuculline and presumed to be mediated by GABAA receptors. This is consistent with immunohistochemical demonstration of GABAergic synapses. SIC frequency was increased in a calcium dependent manner by bathing the cells in a solution high in K+, and application of the dihydropyridine L-type calcium channel agonist BAY K 8644 increased the frequency of SICs. Increases in SIC frequency produced by high K+ solutions were reversed by Cd2+ and omega-conotoxin GVIA, but not by the selective L-type channel antagonist nimodipine. This suggested that presynaptic L-type channels were in a gating mode that was not blocked by nimodipine, and/or that another class of calcium channel makes a dominant contribution to excitatory transmitter release.

MeSH Terms
2-Amino-5-phosphonovalerate/pharmacology 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester/pharmacology Action Potentials/drug effects Animals Aspartic Acid/analogs & derivatives,pharmacology Calcium Channel Blockers/pharmacology Cells, Cultured Dipeptides/pharmacology Electrophysiology/methods Fetus Hippocampus/physiology Kinetics Membrane Potentials/drug effects Mice N-Methylaspartate Neurons/cytology,drug effects,physiology Oxadiazoles/pharmacology Potassium/pharmacology Quisqualic Acid Synapses/drug effects,physiology Tetrodotoxin/pharmacology
Chemicals
Calcium Channel Blockers Dipeptides Oxadiazoles gamma-glutamylglycine Aspartic Acid Tetrodotoxin N-Methylaspartate 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester 2-Amino-5-phosphonovalerate Quisqualic Acid Potassium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Finch D M
Department of Neurology, Reed Neurological Research Center, University of California, Los Angeles 90024.
Fisher R S
Jackson M B
Article Info
Journal
Brain research
Abbr.
Brain Res
ISSN
0006-8993
Published
1990-06-04
Pages
257-68
Language
English
Region
Netherlands
NLM ID
0045503
Subset
IM
Grants
NICHD NIH HHS · HD 05958 · United States
NINDS NIH HHS · NS 21908 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]