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A Neurochemical and Electrophysiological Study on the Combined Effects of Caffeine and Nicotine in the Cortex of Rats

INTRODUCTION: Caffeine and nicotine are the most widely consumed psychostimulants worldwide. Although the effects of each drug alone on the central nervous system have been studied extensively, the literature on the neurochemical and electrophysiological effects of their combined treatments is scarc...

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Autores principales: Mourad, Iman M., Noor, Neveen A., Mohammed, Haitham S., Aboul Ezz, Heba S., Khadrawy, Yasser A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Neuroscience Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818121/
https://www.ncbi.nlm.nih.gov/pubmed/35173922
http://dx.doi.org/10.32598/bcn.2021.2100.1
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author Mourad, Iman M.
Noor, Neveen A.
Mohammed, Haitham S.
Aboul Ezz, Heba S.
Khadrawy, Yasser A.
author_facet Mourad, Iman M.
Noor, Neveen A.
Mohammed, Haitham S.
Aboul Ezz, Heba S.
Khadrawy, Yasser A.
author_sort Mourad, Iman M.
collection PubMed
description INTRODUCTION: Caffeine and nicotine are the most widely consumed psychostimulants worldwide. Although the effects of each drug alone on the central nervous system have been studied extensively, the literature on the neurochemical and electrophysiological effects of their combined treatments is scarce. The present study investigated the cortical electrophysiological and neurochemical alterations induced by acute administration of caffeine and nicotine in rats. METHODS: The rats received caffeine and nicotine at a 1-hour interval between the two treatments. RESULTS: Caffeine and nicotine administration resulted in a significant decrease in the concentrations of cortical amino acid neurotransmitters, namely glutamate, aspartate, glycine, and taurine, while γ-aminobutyric acid (GABA) significantly increased. Increased cortical lipid peroxidation and reduced glutathione and nitric oxide levels and acetylcholinesterase and Na(+)/K(+)-ATPase activities were also observed. The Electroencephalogram (EEG) showed an increase in delta frequency power band, whereas theta, beta-1, and beta-2 decreased after caffeine and nicotine treatment. CONCLUSION: These findings suggest that caffeine and nicotine adversely exacerbate their stimulant effects manifested by the EEG changes mediated by increasing cholinergic transmission and disturbing the balance between the excitatory and inhibitory amino acids leading to oxidative stress.
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spelling pubmed-88181212022-02-15 A Neurochemical and Electrophysiological Study on the Combined Effects of Caffeine and Nicotine in the Cortex of Rats Mourad, Iman M. Noor, Neveen A. Mohammed, Haitham S. Aboul Ezz, Heba S. Khadrawy, Yasser A. Basic Clin Neurosci Research Paper INTRODUCTION: Caffeine and nicotine are the most widely consumed psychostimulants worldwide. Although the effects of each drug alone on the central nervous system have been studied extensively, the literature on the neurochemical and electrophysiological effects of their combined treatments is scarce. The present study investigated the cortical electrophysiological and neurochemical alterations induced by acute administration of caffeine and nicotine in rats. METHODS: The rats received caffeine and nicotine at a 1-hour interval between the two treatments. RESULTS: Caffeine and nicotine administration resulted in a significant decrease in the concentrations of cortical amino acid neurotransmitters, namely glutamate, aspartate, glycine, and taurine, while γ-aminobutyric acid (GABA) significantly increased. Increased cortical lipid peroxidation and reduced glutathione and nitric oxide levels and acetylcholinesterase and Na(+)/K(+)-ATPase activities were also observed. The Electroencephalogram (EEG) showed an increase in delta frequency power band, whereas theta, beta-1, and beta-2 decreased after caffeine and nicotine treatment. CONCLUSION: These findings suggest that caffeine and nicotine adversely exacerbate their stimulant effects manifested by the EEG changes mediated by increasing cholinergic transmission and disturbing the balance between the excitatory and inhibitory amino acids leading to oxidative stress. Iranian Neuroscience Society 2021 2021-09-01 /pmc/articles/PMC8818121/ /pubmed/35173922 http://dx.doi.org/10.32598/bcn.2021.2100.1 Text en Copyright© 2021 Iranian Neuroscience Society https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Research Paper
Mourad, Iman M.
Noor, Neveen A.
Mohammed, Haitham S.
Aboul Ezz, Heba S.
Khadrawy, Yasser A.
A Neurochemical and Electrophysiological Study on the Combined Effects of Caffeine and Nicotine in the Cortex of Rats
title A Neurochemical and Electrophysiological Study on the Combined Effects of Caffeine and Nicotine in the Cortex of Rats
title_full A Neurochemical and Electrophysiological Study on the Combined Effects of Caffeine and Nicotine in the Cortex of Rats
title_fullStr A Neurochemical and Electrophysiological Study on the Combined Effects of Caffeine and Nicotine in the Cortex of Rats
title_full_unstemmed A Neurochemical and Electrophysiological Study on the Combined Effects of Caffeine and Nicotine in the Cortex of Rats
title_short A Neurochemical and Electrophysiological Study on the Combined Effects of Caffeine and Nicotine in the Cortex of Rats
title_sort neurochemical and electrophysiological study on the combined effects of caffeine and nicotine in the cortex of rats
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818121/
https://www.ncbi.nlm.nih.gov/pubmed/35173922
http://dx.doi.org/10.32598/bcn.2021.2100.1
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