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PMID: 8105038 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Characteristics of spontaneous and evoked EPSPs recorded from dentate spiny hilar cells in rat hippocampal slices.

Journal of neurophysiology ·Vol. 70 ·No. 2 ·1993-08-00 ·Pages 742-57

Scharfman HE

Abstract

1. Excitation of the spiny subtype of hilar neurons in the fascia dentata was characterized by intracellular recording from hilar cells in hippocampal slices. Stimulation of the outer molecular layer was used to activate the perforant path. Evoked responses were examined, as well as the large spontaneous excitatory potentials that are a distinctive characteristic of spiny hilar cells. 2. Excitatory potentials that occurred spontaneously, as well as those that occurred in response to outer molecular layer stimulation, were similar among the cells that were sampled, regardless of morphological variations such as the presence or absence of thorny excrescences. Spontaneous and evoked excitatory postsynaptic potentials (EPSPs) were complex depolarizations that often had several discrete peaks. Spontaneous EPSPs increased in amplitude slightly with hyperpolarization, and evoked EPSPs clearly increased with hyperpolarization. 3. Applications of selective antagonists of excitatory amino acid receptors were used to determine which excitatory amino acid receptor mediates EPSPs of these cells. 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) was used to block the receptor subtype selective for the agonists alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and kainic acid (the "AMPA/kainate" receptor). 2-amino-5-phosphonovaleric acid (APV) was used to block receptors specific for the agonist N-methyl-D-aspartate (NMDA; the "NMDA" receptor). Perfusion with CNQX (5-25 microM) completely blocked all spontaneous and evoked excitation, even when activity was examined at relatively depolarized membrane potentials and a low concentration of extracellular magnesium (0.5 mM) was used. Under these conditions, APV (25-50 microM) had no detectable effect on spontaneous activity but did increase the stimulus strength required to elicit responses to outer molecular layer stimulation. 4. When extracellular magnesium was lowered to 0 mM (nominally), there was strong evidence for a contribution of NMDA receptors to spontaneous and evoked EPSPs. Thus, when cells were perfused with 0 mM extracellular magnesium and 5 microM CNQX, spontaneous depolarizations were present and EPSPs could be triggered by stimulation of the outer molecular layer. Both the spontaneous and evoked EPSPs were blocked by 25 microM APV. 5. Because gamma-aminobutyric acid (GABA)A receptors can cause depolarizations in hippocampal neurons, the GABAA receptor antagonist bicuculline was used to determine whether some of the EPSPs were mediated by GABAergic neurons that are normally activated by spontaneous release of excitatory amino acids. Bicuculline (5-25 microM) had no effect on spontaneous depolarizations, and led to an enhancement of evoked depolarizations. Therefore it does not appear that GABAA receptor-mediated depolarizations contribute to hilar cell depolarizations.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
2-Amino-5-phosphonovalerate/pharmacology 6-Cyano-7-nitroquinoxaline-2,3-dione Animals Axons/drug effects,physiology Bicuculline/pharmacology Culture Techniques Dendrites/drug effects,physiology Evoked Potentials/drug effects,physiology Hippocampus/drug effects,physiology Male Neural Inhibition/drug effects,physiology Neurons/drug effects,physiology Quinoxalines/pharmacology Rats Rats, Sprague-Dawley Synapses/drug effects,physiology Synaptic Transmission/drug effects,physiology Tetrodotoxin/pharmacology
Chemicals
Quinoxalines Tetrodotoxin 6-Cyano-7-nitroquinoxaline-2,3-dione 2-Amino-5-phosphonovalerate Bicuculline
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Scharfman H E
Neurology Research Center, Helen Hayes Hospital, New York State Department of Health, West Haverstraw 10993-1195.
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Article Info
Journal
Journal of neurophysiology
Abbr.
J Neurophysiol
ISSN
0022-3077
Published
1993-08-00
Pages
742-57
Language
English
Region
United States
NLM ID
0375404
PMCID
PMC3286002
Subset
IM
Grants
NINDS NIH HHS · R01 NS038285-03 · United States
NINDS NIH HHS · NS-30831 · United States
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