Development of ethanol-induced working memory impairment model in Wistar rats: behavioral and neurochemical studies


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Introduction. Alcohol withdrawal is an important factor that may lead to cognitive impairment. It is known that an alcohol withdrawal leads to significant memory and learning deficits in rats in various tests. Taking into account the need to develop novel ways of pharmacological correction of alcohol dependence, the goal of this work was to develop and validate an experimental model of alcohol induced impairments associated with the function of non-spatial hippocampal-dependent working memory. Material and methods. The experiments were performed on mature male Wistar rats weighing 275-300 g. (n = 16) Wistar rats were randomly divided into control (n=8) and experimental (n=8) groups. Animals from the experimental group were injected with ethanol at intervals of 2 hours at a dose of 3 g / kg per day, intragastrically, for 7 days, animals from the control group received distilled water in the same mode at the rate of 0.1 ml/100 g of body weight. 24 hours after the last injection of the ethanol solution, the animals behavior was evaluated in the "new object recognition" test. After completing behavioral studies, the animals were decapitated, brain structures (anterior cingulate cortex, insular cortex, nucleus accumbens, and hippocampus) were extracted on ice, and frozen in liguid nitrogen. The determination of neurotransmitter monoamines and amino acids was performed by HPLC. Results. There was a decrease in dopamine turnover in the hippocampus and anterior cingulate cortex, a decrease in the activity of the serotonergic system in the insular cortex. Conclusion. Alcohol at a dose of 3 g / kg with subchronic administration per os impairs the working non-spatial memory of Wistar rats.

Full Text

Restricted Access

About the authors

V. G Konkov

Research Zakusov Institute of Pharmacology

Email: asbest321@gmail.com
Post-graduate Student, Junior Research Scientist, the Laboratory of Neurochemical Pharmacology Moscow, Russia

K. A Kasabov

Research Zakusov Institute of Pharmacology

Junior Research Scientist, the Laboratory of Neurochemical Pharmacology Moscow, Russia

P. L Naplekova

Research Zakusov Institute of Pharmacology

Ph.D. (Med.), Research Scientist, the Laboratory of Neurochemical Pharmacology Moscow, Russia

V. B Narkevich

Research Zakusov Institute of Pharmacology

Ph.D. (Med.), Senior Research Scientist, the Laboratory of Neurochemical Pharmacology Moscow, Russia

V. S Kudrin

Research Zakusov Institute of Pharmacology

Ph.D. (Med.), Head of the Laboratory of Neurochemical Pharmacology Moscow, Russia

L. G Kolik

Research Zakusov Institute of Pharmacology

Dr.Sc. (Biol.), Professor of the Russian Academy of Sciences, Head of the Laboratory of Pharmacological Regulation of Addiction States Moscow, Russia

References

  1. Baddeley A. Working memory. Curr. Biol. 2010; 20(4): 136-140.
  2. Chandler D.J., Waterhouse B.D., Gao W.J. New perspectives on catecholaminergic regulation of executive circuits: evidence for independent modulation of prefrontal functions by midbrain dopaminergic and noradrenergic neurons. Front. Neural. Circuits. 2014; 8: 53.
  3. Jacob A., Wang P. Alcohol Intoxication and Cognition: Implications on Mechanisms and Therapeutic Strategies. Front. Neuroscience. 2020; 14(102): 1-10.
  4. Farr S.A., Scherrer J.F., Banks W.A., Flood J.F., Morley J.E. Chronic ethanol consumption impairs learning and memory after cessation of ethanol. Alcohol. Clin. Exp. Res. 2005; 29(6): 971-982.
  5. Geiss J., Sagae S., Paz E., Freitas M., Souto N., Urian A., Oliveira M., Petri Guerraa G. Oral administration of lutein attenuates ethanol-induced memory deficit in rats by restoration of acetylcholinesterase activity. Physiology & Behavior. 2019; 204: 121-128.
  6. Колик Л.Г., Надорова А.В., Антипова Т.А., Круглов С.В., Кудрин В.С., Дурнев А.Д. Пептидный аналог тафтсина селанк защищает от этанолиндуцированного нарушения памяти, регулируя содержание BDNF в гиппокампе и префронтальной коре у крыс. Бюллетень экспериментальной биологии и медицины. 2019; 167(5): 581-585 (Kolik L.G., Nadorova A.V., Antipova T.A., Kruglov S.V., Kudrin V.S., Durnev A.D. Peptidnyj analog taftsina selank zashhishhaet ot jetanolinducirovannogo narushenija pamjati, reguliruja soderzhanie BDNF v gippokampe i prefrontal'noj kore u krys. Bjulleten' jeksperimental'noj biologii i mediciny. 2019; 167(5): 581-585).
  7. Литвинова С.А., Клодт П.М., Кудрин В.С., Наркевич В.Б., Воронина Т.А. Изучение поведения и содержание нейротрансмиттеров в структурах мозга крыс с моделируемой введением АР25-35 болезнью Альцгеймера. Нейрохимия. 2015; 32(1): 48-56 (Litvinova S.A., Klodt P.M., Kudrin V.S., Narkevich V.B., Voronina T.A. Izuchenie povedenija i soderzhanie nejrotransmitterov v strukturah mozga krys s modeliruemoj vvedeniem AP25-35 bolezn'ju Al'cgejmera. Nejrohimija. 2015; 32(1): 48-56).
  8. De Montis M., Grappi S., Gambarana C., Leggio B., Nanni G., Scheggi S., Tagliamonte A. Sardinian alcohol-preferring rats show low 5-HT extraneuronal levels in the mPFC and no habituation in monoaminergic response to repeated ethanol consumption in the NAcS. Brain Res. 2004; 1006(1): 18-27.
  9. Almalki A., Das S. C., Alshehri F., Althobaiti Y., Sari Y. Effects of sequential ethanol exposure and repeated high-dose methamphetamine on striatal and hippocampal dopamine, serotonin and glutamate tissue content in Wistar rats. Neurosci. Lett. 2018; 665: 61-66.
  10. Shillinglaw J.E., Morrisett R.A., Mangieri R.A. Ethanol Modulates Glutamatergic Transmission and NMDAR-Mediated Synaptic Plasticity in the Agranular Insular Cortex. Front. Pharmacol. 2018; 9: 1458.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2021 Russkiy Vrach Publishing House