Literature DB >> 2400909

Patterns of changes in field potentials in the isolated hippocampal slice on withdrawal from chronic ethanol treatment of mice in vivo.

M A Whittington1, H J Little.   

Abstract

Extracellular recordings were made from isolated hippocampal slices, CA1 area, following withdrawal from chronic ethanol administration to mice of the C57 strain. The field potentials were followed for 7 h from preparation of the slices, in the absence of ethanol. Paired pulse potentiation was increased, and paired pulse inhibition decreased, in slices from ethanol-treated mice during the first four hours of the recording period. Orthodromic thresholds for elicitation of single and multiple population spikes were decreased by the ethanol treatment, in the later part of the recording period. The input/output curves for population spike area and population excitatory postsynaptic potential slope showed a shift to the left for the slices from ethanol-treated animals, but no change in the maximal response. Antidromic stimulation also demonstrated decreases in thresholds for single and multiple population spikes in tissues from ethanol-treated animals, during the later half of the recording period. The results indicate that there are several mechanisms by which neuronal excitability increases on withdrawal from chronic ethanol treatment. The changes follow different time courses and suggest multiple mechanisms underlying the behavioural signs seen during the ethanol withdrawal syndrome.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2400909     DOI: 10.1016/0006-8993(90)91492-y

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  8 in total

1.  The effects of chronic treatment with the dihydropyridine, Bay K 8644, on hyperexcitability due to ethanol withdrawal, in vivo and in vitro.

Authors:  M A Whittington; A R Butterworth; S J Dolin; T L Patch; H J Little
Journal:  Br J Pharmacol       Date:  1992-02       Impact factor: 8.739

Review 2.  Glutamate plasticity in the drunken amygdala: the making of an anxious synapse.

Authors:  Brian A McCool; Daniel T Christian; Marvin R Diaz; Anna K Läck
Journal:  Int Rev Neurobiol       Date:  2010       Impact factor: 3.230

3.  Do GABAB receptors have a role in causing behavioural hyperexcitability, both during ethanol withdrawal and in naive mice?

Authors:  A J Mead; H J Little
Journal:  Psychopharmacology (Berl)       Date:  1995-01       Impact factor: 4.530

4.  Chronic Intermittent Ethanol Exposure Selectively Increases Synaptic Excitability in the Ventral Domain of the Rat Hippocampus.

Authors:  Sarah E Ewin; James W Morgan; Farr Niere; Nate P McMullen; Samuel H Barth; Antoine G Almonte; Kimberly F Raab-Graham; Jeffrey L Weiner
Journal:  Neuroscience       Date:  2018-11-24       Impact factor: 3.590

5.  Nitrendipine prevents the decrease caused by chronic ethanol intake in the maintenance of tetanic long-term potentiation.

Authors:  T L Ripley; H J Little
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

6.  Nitrendipine, given during drinking, decreases the electrophysiological changes in the isolated hippocampal slice, seen during ethanol withdrawal.

Authors:  M A Whittington; H J Little
Journal:  Br J Pharmacol       Date:  1991-07       Impact factor: 8.739

7.  Changes in intrinsic inhibition in isolated hippocampal slices during ethanol withdrawal; lack of correlation with withdrawal hyperexcitability.

Authors:  M A Whittington; H J Little; J D Lambert
Journal:  Br J Pharmacol       Date:  1992-10       Impact factor: 8.739

8.  A calcium channel antagonist stereoselectively decreases ethanol withdrawal hyperexcitability but not that due to bicuculline, in hippocampal slices.

Authors:  M A Whittington; H J Little
Journal:  Br J Pharmacol       Date:  1991-06       Impact factor: 8.739

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.