Effects of organophosphates on rabbit pyramidal cells firing pattern and hippocampal theta rhythm

The effects of the irreversible acetylcholinesterase (AChE) antagonist paraoxon (Px) on hippocampal neurophysiology were investigated and compared to those of physostigmine in urethane-anaesthetized rabbits. Hippocampal CA1 EEG signals were analyzed by power spectra. Following intracarotid administr...

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Published inBrain research bulletin Vol. 33; no. 3; pp. 241 - 248
Main Authors Nio, Jacques, Breton, Patrick
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 1994
Elsevier Science
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Abstract The effects of the irreversible acetylcholinesterase (AChE) antagonist paraoxon (Px) on hippocampal neurophysiology were investigated and compared to those of physostigmine in urethane-anaesthetized rabbits. Hippocampal CA1 EEG signals were analyzed by power spectra. Following intracarotid administration, the two drugs induced a similar fundamental low-frequency theta power peak while the appearance of a second theta harmonic was commonly found under Px. Again, inhibition of CA1 pyramidal cells firing was significantly more pronounced after Px injection than after physostigmine. A potent inhibitory action was also described following local Px iontophoretic application. However, a discrepancy appeared between the effects of Px and the classical cholinergic drugs (acetylcholine, physostigmine). The results indicate that Px and physostigmine have a rather similar influence on the septo-hippocampal pathway and support suggestions that Px could act within local hippocampal circuitry through other systems than the cholinergic system exclusively.
AbstractList The effects of the irreversible acetylcholinesterase (AChE) antagonist paraoxon (Px) on hippocampal neurophysiology were investigated and compared to those of physostigmine in urethane-anaesthetized rabbits. Hippocampal CA1 EEG signals were analyzed by power spectra. Following intracarotid administration, the two drugs induced a similar fundamental low-frequency theta power peak while the appearance of a second theta harmonic was commonly found under Px. Again, inhibition of CA1 pyramidal cells firing was significantly more pronounced after Px injection than after physostigmine. A potent inhibitory action was also described following local Px iontophoretic application. However, a discrepancy appeared between the effects of Px and the classical cholinergic drugs (acetylcholine, physostigmine). The results indicate that Px and physostigmine have a rather similar influence on the septo-hippocampal pathway and support suggestions that Px could act within local hippocampal circuitry through other systems than the cholinergic system exclusively.
Author Breton, Patrick
Nio, Jacques
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Issue 3
Keywords Physostigmine
Extracellular recording
Pyramidal cells
Hippocampus
Organophosphates
Toxicity
Central nervous system
Discharge pattern
Rabbit
Lagomorpha
Cholinergic pathway
Vertebrata
Mammalia
Animal
Acetylcholine
Organophosphorus compounds
Anticholinesterase agent
Pyramidal neuron
θ-Rhythm
Brain (vertebrata)
Language English
License CC BY 4.0
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Snippet The effects of the irreversible acetylcholinesterase (AChE) antagonist paraoxon (Px) on hippocampal neurophysiology were investigated and compared to those of...
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SubjectTerms Animals
Biological and medical sciences
Carotid Arteries
Chemical and industrial products toxicology. Toxic occupational diseases
Electroencephalography
Extracellular recording
Female
Hippocampus
Hippocampus - drug effects
Hippocampus - physiology
Injections, Intra-Arterial
Iontophoresis
Male
Medical sciences
Organophosphates
Organophosphorus Compounds - pharmacology
Paraoxon - pharmacology
Physostigmine
Physostigmine - pharmacology
Pyramidal cells
Pyramidal Cells - drug effects
Pyramidal Cells - physiology
Rabbits
Theta Rhythm - drug effects
Toxicology
Various organic compounds
Title Effects of organophosphates on rabbit pyramidal cells firing pattern and hippocampal theta rhythm
URI https://dx.doi.org/10.1016/0361-9230(94)90190-2
https://www.ncbi.nlm.nih.gov/pubmed/8293309
https://search.proquest.com/docview/16768412
https://search.proquest.com/docview/76338287
Volume 33
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