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Protective effect of vitamin C, vitamin B12 and omega-3 on lead-induced memory impairment in rat

Lead belongs to the heavy metal group and is considered as an environmental contaminant. Acute or chronic contact to lead can change the physiological function of human organs. One of the most important disorders following the lead exposure is neurotoxicity. Lead neurotoxicity consists of the neurob...

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Autores principales: Moosavirad, Saeedeh Alsadat, Rabbani, Mohammad, Sharifzadeh, Mohammad, Hosseini-Sharifabad, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122828/
https://www.ncbi.nlm.nih.gov/pubmed/27920821
http://dx.doi.org/10.4103/1735-5362.192490
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author Moosavirad, Saeedeh Alsadat
Rabbani, Mohammad
Sharifzadeh, Mohammad
Hosseini-Sharifabad, Ali
author_facet Moosavirad, Saeedeh Alsadat
Rabbani, Mohammad
Sharifzadeh, Mohammad
Hosseini-Sharifabad, Ali
author_sort Moosavirad, Saeedeh Alsadat
collection PubMed
description Lead belongs to the heavy metal group and is considered as an environmental contaminant. Acute or chronic contact to lead can change the physiological function of human organs. One of the most important disorders following the lead exposure is neurotoxicity. Lead neurotoxicity consists of the neurobehavioral disturbances like cognitive impairment. The aim of the current study is to evaluate the possible protective effect of vitamin C (Vit C), vitamin B12 (Vit B12), omega 3 (ω-3), or their combination on the lead-induced memory disorder. Adult wistar rats were orally administered Vit C (120 mg/kg/day) or Vit B12 (1 mg/kg/day) or ω-3 (1000 mg/kg/day) or their combination for 3 weeks in groups of 7 animals each. Then lead acetate (15 mg/kg/day) was injected intraperitoneally for one week to all pretreated animals. The control group received normal saline as a vehicle while the positive control for cognitive impairment received just lead acetate. At the end of treatments animal memories were evaluated in Object Recognition Task. The results showed, although 15 mg/kg lead acetate significantly declines the memory-evaluating parameters, pretreatment with Vit C, Vit B12, ω-3, or their combination considerably inverted the lead induced reduction in discrimination (d2) index (P < 0.001) and recognition (R) index (P < 0.001, P < 0.05, P < 0.05, and P < 0.001, respectively). Our findings indicate while lead acetate impairs spatial memory in rat, administration of Vit C, Vit B12, ω-3, or their combination prior to the lead exposure inhibits the lead induced cognitive loss. There was no remarkable difference in this effect between the used supplements.
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spelling pubmed-51228282016-12-05 Protective effect of vitamin C, vitamin B12 and omega-3 on lead-induced memory impairment in rat Moosavirad, Saeedeh Alsadat Rabbani, Mohammad Sharifzadeh, Mohammad Hosseini-Sharifabad, Ali Res Pharm Sci Original Article Lead belongs to the heavy metal group and is considered as an environmental contaminant. Acute or chronic contact to lead can change the physiological function of human organs. One of the most important disorders following the lead exposure is neurotoxicity. Lead neurotoxicity consists of the neurobehavioral disturbances like cognitive impairment. The aim of the current study is to evaluate the possible protective effect of vitamin C (Vit C), vitamin B12 (Vit B12), omega 3 (ω-3), or their combination on the lead-induced memory disorder. Adult wistar rats were orally administered Vit C (120 mg/kg/day) or Vit B12 (1 mg/kg/day) or ω-3 (1000 mg/kg/day) or their combination for 3 weeks in groups of 7 animals each. Then lead acetate (15 mg/kg/day) was injected intraperitoneally for one week to all pretreated animals. The control group received normal saline as a vehicle while the positive control for cognitive impairment received just lead acetate. At the end of treatments animal memories were evaluated in Object Recognition Task. The results showed, although 15 mg/kg lead acetate significantly declines the memory-evaluating parameters, pretreatment with Vit C, Vit B12, ω-3, or their combination considerably inverted the lead induced reduction in discrimination (d2) index (P < 0.001) and recognition (R) index (P < 0.001, P < 0.05, P < 0.05, and P < 0.001, respectively). Our findings indicate while lead acetate impairs spatial memory in rat, administration of Vit C, Vit B12, ω-3, or their combination prior to the lead exposure inhibits the lead induced cognitive loss. There was no remarkable difference in this effect between the used supplements. Medknow Publications & Media Pvt Ltd 2016-10 /pmc/articles/PMC5122828/ /pubmed/27920821 http://dx.doi.org/10.4103/1735-5362.192490 Text en Copyright: © Research in Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Moosavirad, Saeedeh Alsadat
Rabbani, Mohammad
Sharifzadeh, Mohammad
Hosseini-Sharifabad, Ali
Protective effect of vitamin C, vitamin B12 and omega-3 on lead-induced memory impairment in rat
title Protective effect of vitamin C, vitamin B12 and omega-3 on lead-induced memory impairment in rat
title_full Protective effect of vitamin C, vitamin B12 and omega-3 on lead-induced memory impairment in rat
title_fullStr Protective effect of vitamin C, vitamin B12 and omega-3 on lead-induced memory impairment in rat
title_full_unstemmed Protective effect of vitamin C, vitamin B12 and omega-3 on lead-induced memory impairment in rat
title_short Protective effect of vitamin C, vitamin B12 and omega-3 on lead-induced memory impairment in rat
title_sort protective effect of vitamin c, vitamin b12 and omega-3 on lead-induced memory impairment in rat
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122828/
https://www.ncbi.nlm.nih.gov/pubmed/27920821
http://dx.doi.org/10.4103/1735-5362.192490
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