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Aluminium Induced Neurodegeneration in Rat Cerebellum in the Presence of Ethanol Coexposure

INTRODUCTION: Both aluminium and ethanol are pro-oxidants and neurotoxic. Moderately intake of alcohol may favor the body in coronary heart disease and diabetes mellitus etc. Being cheaper aluminium and increasing consumption of alcohol in India mixed with each other and may induce neurotoxicity. Th...

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Autores principales: Ghosh, Buddhadeb, Sharma, Ravi Kant, Yadav, Suman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687035/
https://www.ncbi.nlm.nih.gov/pubmed/35017961
http://dx.doi.org/10.4103/jpbs.jpbs_377_21
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author Ghosh, Buddhadeb
Sharma, Ravi Kant
Yadav, Suman
author_facet Ghosh, Buddhadeb
Sharma, Ravi Kant
Yadav, Suman
author_sort Ghosh, Buddhadeb
collection PubMed
description INTRODUCTION: Both aluminium and ethanol are pro-oxidants and neurotoxic. Moderately intake of alcohol may favor the body in coronary heart disease and diabetes mellitus etc. Being cheaper aluminium and increasing consumption of alcohol in India mixed with each other and may induce neurotoxicity. The present study was planned to identify the level of aluminium induced neurodegeneration in presence of ethanol coexposure in the cerebellum. MATERIALS AND METHODS: An experimental study was carried out at Dr. RP Government Medical College, Kangra, and Government Medical College, Amritsar, India after due approval from the Institute Animal Ethics Committee. Thirty-two Wistar rats were divided into one vehicle control and three experimental groups. Group I received the normal saline water as the vehicle control group. Group II received aluminium chloride 4.2 mg/kg body weight as the experimental group. Group III received ethanol 1 g/kg body weight as the experimental group. Group IV received both aluminium chloride 4.2 mg/kg body weight and ethanol 1 g/kg body weight as the experimental group. After 3 months of treatment, cerebellum was processed for histopathological observation under the microscope. RESULTS: Experimental group treated with aluminium and ethanol separately showed reduction in the number of Purkinje cells, without a prominent nucleolus and well-defined nuclear membrane. Eosinophilic swelling adjacent to Purkinje cell bodies observed. The effects of combined administration of aluminium ethanol treated groups showed with acute neurodegeneration of Purkinje cell layer and granular layer. Pyknosis and neurofibrillary tangle seen in Purkinje cells. CONCLUSIONS: It has been suggested that the ethanol-induced the effects of aluminium on the cerebellum and plays a significant role in neurotoxicity.
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spelling pubmed-86870352022-01-10 Aluminium Induced Neurodegeneration in Rat Cerebellum in the Presence of Ethanol Coexposure Ghosh, Buddhadeb Sharma, Ravi Kant Yadav, Suman J Pharm Bioallied Sci Original Article INTRODUCTION: Both aluminium and ethanol are pro-oxidants and neurotoxic. Moderately intake of alcohol may favor the body in coronary heart disease and diabetes mellitus etc. Being cheaper aluminium and increasing consumption of alcohol in India mixed with each other and may induce neurotoxicity. The present study was planned to identify the level of aluminium induced neurodegeneration in presence of ethanol coexposure in the cerebellum. MATERIALS AND METHODS: An experimental study was carried out at Dr. RP Government Medical College, Kangra, and Government Medical College, Amritsar, India after due approval from the Institute Animal Ethics Committee. Thirty-two Wistar rats were divided into one vehicle control and three experimental groups. Group I received the normal saline water as the vehicle control group. Group II received aluminium chloride 4.2 mg/kg body weight as the experimental group. Group III received ethanol 1 g/kg body weight as the experimental group. Group IV received both aluminium chloride 4.2 mg/kg body weight and ethanol 1 g/kg body weight as the experimental group. After 3 months of treatment, cerebellum was processed for histopathological observation under the microscope. RESULTS: Experimental group treated with aluminium and ethanol separately showed reduction in the number of Purkinje cells, without a prominent nucleolus and well-defined nuclear membrane. Eosinophilic swelling adjacent to Purkinje cell bodies observed. The effects of combined administration of aluminium ethanol treated groups showed with acute neurodegeneration of Purkinje cell layer and granular layer. Pyknosis and neurofibrillary tangle seen in Purkinje cells. CONCLUSIONS: It has been suggested that the ethanol-induced the effects of aluminium on the cerebellum and plays a significant role in neurotoxicity. Wolters Kluwer - Medknow 2021-11 2021-11-10 /pmc/articles/PMC8687035/ /pubmed/35017961 http://dx.doi.org/10.4103/jpbs.jpbs_377_21 Text en Copyright: © 2021 Journal of Pharmacy and Bioallied Sciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Ghosh, Buddhadeb
Sharma, Ravi Kant
Yadav, Suman
Aluminium Induced Neurodegeneration in Rat Cerebellum in the Presence of Ethanol Coexposure
title Aluminium Induced Neurodegeneration in Rat Cerebellum in the Presence of Ethanol Coexposure
title_full Aluminium Induced Neurodegeneration in Rat Cerebellum in the Presence of Ethanol Coexposure
title_fullStr Aluminium Induced Neurodegeneration in Rat Cerebellum in the Presence of Ethanol Coexposure
title_full_unstemmed Aluminium Induced Neurodegeneration in Rat Cerebellum in the Presence of Ethanol Coexposure
title_short Aluminium Induced Neurodegeneration in Rat Cerebellum in the Presence of Ethanol Coexposure
title_sort aluminium induced neurodegeneration in rat cerebellum in the presence of ethanol coexposure
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687035/
https://www.ncbi.nlm.nih.gov/pubmed/35017961
http://dx.doi.org/10.4103/jpbs.jpbs_377_21
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