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Morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats

In the developed and developing world, opioid consumption in combination with alcohol has become one of the substances abused. In this experiment, we examined the effects of alcohol, morphine, and morphine+alcohol combination on cognitive functions and neuroinflammatory responses in the medial prefr...

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Autores principales: Adedayo, Adekomi Damilare, Aderinola, Adegoke Adebiyi, Adekilekun, Tijani Ahmad, Olaolu, Olaniyan Olayinka, Olanike, Alabi Mutiyat, Olayemi, Ijomone Kafilat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Anatomists 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890016/
https://www.ncbi.nlm.nih.gov/pubmed/29644109
http://dx.doi.org/10.5115/acb.2018.51.1.41
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author Adedayo, Adekomi Damilare
Aderinola, Adegoke Adebiyi
Adekilekun, Tijani Ahmad
Olaolu, Olaniyan Olayinka
Olanike, Alabi Mutiyat
Olayemi, Ijomone Kafilat
author_facet Adedayo, Adekomi Damilare
Aderinola, Adegoke Adebiyi
Adekilekun, Tijani Ahmad
Olaolu, Olaniyan Olayinka
Olanike, Alabi Mutiyat
Olayemi, Ijomone Kafilat
author_sort Adedayo, Adekomi Damilare
collection PubMed
description In the developed and developing world, opioid consumption in combination with alcohol has become one of the substances abused. In this experiment, we examined the effects of alcohol, morphine, and morphine+alcohol combination on cognitive functions and neuroinflammatory responses in the medial prefrontal cortex (mPFC) of juvenile male rats. Alcohol (1.0 ml of 15% v/v ethanol twice daily, subcutaneously, 7 hours apart), morphine (0.5 ml/kg of 0.4 mg/kg morphine chlorate twice daily, subcutaneously, 7 hours apart), morphine+alcohol co-treatment (0.5 ml/kg of 0.4 mg/kg morphine chlorate+1.0 ml of 15% v/v ethanol twice daily, subcutaneously, 7 hours apart) were administered for 21 days. Treatment with morphine+alcohol significantly impairs cognition functions in the Morris water maze, passive avoidance, and novel object recognition tests, furthermore, the treatment significantly increased the quantitative count of astrocytic cells and also conferred marked neuronal cell death in the mPFC, which were studied by glial fibrillary acidic protein immunochemistry for astrocytes and Cresyl violet for Nissl's substance distribution in neurons respectively. These results suggest that alcohol, morphine, and morphine+alcohol co-treatment may trigger cognitive deficits and neuroinflammatory responses in the brain.
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spelling pubmed-58900162018-04-11 Morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats Adedayo, Adekomi Damilare Aderinola, Adegoke Adebiyi Adekilekun, Tijani Ahmad Olaolu, Olaniyan Olayinka Olanike, Alabi Mutiyat Olayemi, Ijomone Kafilat Anat Cell Biol Original Article In the developed and developing world, opioid consumption in combination with alcohol has become one of the substances abused. In this experiment, we examined the effects of alcohol, morphine, and morphine+alcohol combination on cognitive functions and neuroinflammatory responses in the medial prefrontal cortex (mPFC) of juvenile male rats. Alcohol (1.0 ml of 15% v/v ethanol twice daily, subcutaneously, 7 hours apart), morphine (0.5 ml/kg of 0.4 mg/kg morphine chlorate twice daily, subcutaneously, 7 hours apart), morphine+alcohol co-treatment (0.5 ml/kg of 0.4 mg/kg morphine chlorate+1.0 ml of 15% v/v ethanol twice daily, subcutaneously, 7 hours apart) were administered for 21 days. Treatment with morphine+alcohol significantly impairs cognition functions in the Morris water maze, passive avoidance, and novel object recognition tests, furthermore, the treatment significantly increased the quantitative count of astrocytic cells and also conferred marked neuronal cell death in the mPFC, which were studied by glial fibrillary acidic protein immunochemistry for astrocytes and Cresyl violet for Nissl's substance distribution in neurons respectively. These results suggest that alcohol, morphine, and morphine+alcohol co-treatment may trigger cognitive deficits and neuroinflammatory responses in the brain. Korean Association of Anatomists 2018-03 2018-03-28 /pmc/articles/PMC5890016/ /pubmed/29644109 http://dx.doi.org/10.5115/acb.2018.51.1.41 Text en Copyright © 2018. Anatomy & Cell Biology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Adedayo, Adekomi Damilare
Aderinola, Adegoke Adebiyi
Adekilekun, Tijani Ahmad
Olaolu, Olaniyan Olayinka
Olanike, Alabi Mutiyat
Olayemi, Ijomone Kafilat
Morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats
title Morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats
title_full Morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats
title_fullStr Morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats
title_full_unstemmed Morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats
title_short Morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats
title_sort morphine-alcohol treatment impairs cognitive functions and increases neuro-inflammatory responses in the medial prefrontal cortex of juvenile male rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890016/
https://www.ncbi.nlm.nih.gov/pubmed/29644109
http://dx.doi.org/10.5115/acb.2018.51.1.41
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