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Ceftriaxone improves senile neurocognition damages induced by D-galactose in mice
OBJECTIVE(S): Ceftriaxone (Cef), a beta-lactam antibiotic, is accompanied by antioxidant and anti-inflammatory properties. It has been shown that Cef has beneficial effects on Alzheimer’s disease. In the current investigation, the effect of Cef in a mice model of aging was investigated. MATERIALS AN...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229512/ https://www.ncbi.nlm.nih.gov/pubmed/32440324 http://dx.doi.org/10.22038/IJBMS.2019.40344.9556 |
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author | Hakimizadeh, Elham Kaeidi, Ayat Taghipour, Zahra Mehrzadi, Saeed Allahtavakoli, Mohammad Shamsizadeh, Ali Bazmandegan, Gholamreza Hassanshahi, Jalal Aflatoonian, Mohammad Reza Fatemi, Iman |
author_facet | Hakimizadeh, Elham Kaeidi, Ayat Taghipour, Zahra Mehrzadi, Saeed Allahtavakoli, Mohammad Shamsizadeh, Ali Bazmandegan, Gholamreza Hassanshahi, Jalal Aflatoonian, Mohammad Reza Fatemi, Iman |
author_sort | Hakimizadeh, Elham |
collection | PubMed |
description | OBJECTIVE(S): Ceftriaxone (Cef), a beta-lactam antibiotic, is accompanied by antioxidant and anti-inflammatory properties. It has been shown that Cef has beneficial effects on Alzheimer’s disease. In the current investigation, the effect of Cef in a mice model of aging was investigated. MATERIALS AND METHODS: Forty male mice were equally aliquoted into four groups as follows: Control (as healthy normal animals), D-galactose (DG) group (treated with 500 mg/kg/day DG for 6 weeks), DG + Cef group (treated with DG plus Cef 200 mg/kg/day for 6 weeks), and Cef group (treated with Cef 200 mg/kg/day for 6 weeks). A battery of behavioral tests was done to evaluate age-related neurocognitive changes. The activities of catalase (CAT), glutathione peroxidase (GPx), and superoxide dismutase (SOD), as well as the level of malondialdehyde (MDA) in the brain, were measured by biochemical methods. Also, to determine the brain damage, histopathological alterations in the hippocampus were measured using hematoxylin and eosin (H&E) staining. RESULTS: Our results indicate that neurobehavioral dysfunctions of DG can be prevented by co-administration of Cef. We also found that Cef increases the activity of SOD, GPx, and CAT as well as decreasing the level of MDA in the brain of aged mice. CONCLUSION: Based on our findings, Cef declines neurocognitive dysfunctions in the DG-induced model of aging, possibly through its antioxidative properties. |
format | Online Article Text |
id | pubmed-7229512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-72295122020-05-21 Ceftriaxone improves senile neurocognition damages induced by D-galactose in mice Hakimizadeh, Elham Kaeidi, Ayat Taghipour, Zahra Mehrzadi, Saeed Allahtavakoli, Mohammad Shamsizadeh, Ali Bazmandegan, Gholamreza Hassanshahi, Jalal Aflatoonian, Mohammad Reza Fatemi, Iman Iran J Basic Med Sci Original Article OBJECTIVE(S): Ceftriaxone (Cef), a beta-lactam antibiotic, is accompanied by antioxidant and anti-inflammatory properties. It has been shown that Cef has beneficial effects on Alzheimer’s disease. In the current investigation, the effect of Cef in a mice model of aging was investigated. MATERIALS AND METHODS: Forty male mice were equally aliquoted into four groups as follows: Control (as healthy normal animals), D-galactose (DG) group (treated with 500 mg/kg/day DG for 6 weeks), DG + Cef group (treated with DG plus Cef 200 mg/kg/day for 6 weeks), and Cef group (treated with Cef 200 mg/kg/day for 6 weeks). A battery of behavioral tests was done to evaluate age-related neurocognitive changes. The activities of catalase (CAT), glutathione peroxidase (GPx), and superoxide dismutase (SOD), as well as the level of malondialdehyde (MDA) in the brain, were measured by biochemical methods. Also, to determine the brain damage, histopathological alterations in the hippocampus were measured using hematoxylin and eosin (H&E) staining. RESULTS: Our results indicate that neurobehavioral dysfunctions of DG can be prevented by co-administration of Cef. We also found that Cef increases the activity of SOD, GPx, and CAT as well as decreasing the level of MDA in the brain of aged mice. CONCLUSION: Based on our findings, Cef declines neurocognitive dysfunctions in the DG-induced model of aging, possibly through its antioxidative properties. Mashhad University of Medical Sciences 2020-03 /pmc/articles/PMC7229512/ /pubmed/32440324 http://dx.doi.org/10.22038/IJBMS.2019.40344.9556 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hakimizadeh, Elham Kaeidi, Ayat Taghipour, Zahra Mehrzadi, Saeed Allahtavakoli, Mohammad Shamsizadeh, Ali Bazmandegan, Gholamreza Hassanshahi, Jalal Aflatoonian, Mohammad Reza Fatemi, Iman Ceftriaxone improves senile neurocognition damages induced by D-galactose in mice |
title | Ceftriaxone improves senile neurocognition damages induced by D-galactose in mice |
title_full | Ceftriaxone improves senile neurocognition damages induced by D-galactose in mice |
title_fullStr | Ceftriaxone improves senile neurocognition damages induced by D-galactose in mice |
title_full_unstemmed | Ceftriaxone improves senile neurocognition damages induced by D-galactose in mice |
title_short | Ceftriaxone improves senile neurocognition damages induced by D-galactose in mice |
title_sort | ceftriaxone improves senile neurocognition damages induced by d-galactose in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229512/ https://www.ncbi.nlm.nih.gov/pubmed/32440324 http://dx.doi.org/10.22038/IJBMS.2019.40344.9556 |
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