Cargando…

Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia

Oxidative stress is involved in the pathogenesis of vascular dementia. Studies have shown that lycopene can significantly inhibit oxidative stress; therefore, we hypothesized that lycopene can reduce the level of oxidative stress in vascular dementia. A vascular dementia model was established by per...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Ning-Wei, Yin, Xiao-Lan, Lin, Ren, Fan, Xiao-Lan, Chen, Shi-Jie, Zhu, Yuan-Ming, Zhao, Xiao-Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905346/
https://www.ncbi.nlm.nih.gov/pubmed/31552907
http://dx.doi.org/10.4103/1673-5374.265565
_version_ 1783478152919515136
author Zhu, Ning-Wei
Yin, Xiao-Lan
Lin, Ren
Fan, Xiao-Lan
Chen, Shi-Jie
Zhu, Yuan-Ming
Zhao, Xiao-Zhen
author_facet Zhu, Ning-Wei
Yin, Xiao-Lan
Lin, Ren
Fan, Xiao-Lan
Chen, Shi-Jie
Zhu, Yuan-Ming
Zhao, Xiao-Zhen
author_sort Zhu, Ning-Wei
collection PubMed
description Oxidative stress is involved in the pathogenesis of vascular dementia. Studies have shown that lycopene can significantly inhibit oxidative stress; therefore, we hypothesized that lycopene can reduce the level of oxidative stress in vascular dementia. A vascular dementia model was established by permanent bilateral ligation of common carotid arteries. The dosage groups were treated with lycopene (50, 100 and 200 mg/kg) every other day for 2 months. Rats without bilateral carotid artery ligation were prepared as a sham group. To test the ability of learning and memory, the Morris water maze was used to detect the average escape latency and the change of search strategy. Hematoxylin-eosin staining was used to observe changes of hippocampal neurons. The levels of oxidative stress factors, superoxide dismutase and malondialdehyde, were measured in the hippocampus by biochemical detection. The levels of reactive oxygen species in the hippocampus were observed by dihydroethidium staining. The distribution and expression of oxidative stress related protein, neuron-restrictive silencer factor, in hippocampal neurons were detected by immunofluorescence histochemistry and western blot assays. After 2 months of drug administration, (1) in the model group, the average escape latency was longer than that of the sham group, and the proportion of straight and tend tactics was lower than that of the sham group, and the hippocampal neurons were irregularly arranged and the cytoplasm was hyperchromatic. (2) The levels of reactive oxygen species and malondialdehyde in the hippocampus of the model group rats were increased, and the activity of superoxide dismutase was decreased. (3) Lycopene (50, 100 and 200 mg/kg) intervention improved the above changes, and the lycopene 100 mg/kg group showed the most significant improvement effect. (4) Neuron-restrictive silencer factor expression in the hippocampus was lower in the sham group and the lycopene 100 mg/kg group than in the model group. (5) The above data indicate that lycopene 100 mg/kg could protect against the learning-memory ability impairment of vascular dementia rats. The protective mechanism was achieved by inhibiting oxidative stress in the hippocampus. The experiment was approved by the Animal Ethics Committee of Fujian Medical University, China (approval No. 2014-025) in June 2014.
format Online
Article
Text
id pubmed-6905346
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-69053462020-02-27 Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia Zhu, Ning-Wei Yin, Xiao-Lan Lin, Ren Fan, Xiao-Lan Chen, Shi-Jie Zhu, Yuan-Ming Zhao, Xiao-Zhen Neural Regen Res Research Article Oxidative stress is involved in the pathogenesis of vascular dementia. Studies have shown that lycopene can significantly inhibit oxidative stress; therefore, we hypothesized that lycopene can reduce the level of oxidative stress in vascular dementia. A vascular dementia model was established by permanent bilateral ligation of common carotid arteries. The dosage groups were treated with lycopene (50, 100 and 200 mg/kg) every other day for 2 months. Rats without bilateral carotid artery ligation were prepared as a sham group. To test the ability of learning and memory, the Morris water maze was used to detect the average escape latency and the change of search strategy. Hematoxylin-eosin staining was used to observe changes of hippocampal neurons. The levels of oxidative stress factors, superoxide dismutase and malondialdehyde, were measured in the hippocampus by biochemical detection. The levels of reactive oxygen species in the hippocampus were observed by dihydroethidium staining. The distribution and expression of oxidative stress related protein, neuron-restrictive silencer factor, in hippocampal neurons were detected by immunofluorescence histochemistry and western blot assays. After 2 months of drug administration, (1) in the model group, the average escape latency was longer than that of the sham group, and the proportion of straight and tend tactics was lower than that of the sham group, and the hippocampal neurons were irregularly arranged and the cytoplasm was hyperchromatic. (2) The levels of reactive oxygen species and malondialdehyde in the hippocampus of the model group rats were increased, and the activity of superoxide dismutase was decreased. (3) Lycopene (50, 100 and 200 mg/kg) intervention improved the above changes, and the lycopene 100 mg/kg group showed the most significant improvement effect. (4) Neuron-restrictive silencer factor expression in the hippocampus was lower in the sham group and the lycopene 100 mg/kg group than in the model group. (5) The above data indicate that lycopene 100 mg/kg could protect against the learning-memory ability impairment of vascular dementia rats. The protective mechanism was achieved by inhibiting oxidative stress in the hippocampus. The experiment was approved by the Animal Ethics Committee of Fujian Medical University, China (approval No. 2014-025) in June 2014. Wolters Kluwer - Medknow 2019-09-24 /pmc/articles/PMC6905346/ /pubmed/31552907 http://dx.doi.org/10.4103/1673-5374.265565 Text en Copyright: © Neural Regeneration Research http://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 Research Article
Zhu, Ning-Wei
Yin, Xiao-Lan
Lin, Ren
Fan, Xiao-Lan
Chen, Shi-Jie
Zhu, Yuan-Ming
Zhao, Xiao-Zhen
Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia
title Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia
title_full Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia
title_fullStr Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia
title_full_unstemmed Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia
title_short Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia
title_sort possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6905346/
https://www.ncbi.nlm.nih.gov/pubmed/31552907
http://dx.doi.org/10.4103/1673-5374.265565
work_keys_str_mv AT zhuningwei possiblemechanismsoflycopeneameliorationoflearningandmemoryimpairmentinratswithvasculardementia
AT yinxiaolan possiblemechanismsoflycopeneameliorationoflearningandmemoryimpairmentinratswithvasculardementia
AT linren possiblemechanismsoflycopeneameliorationoflearningandmemoryimpairmentinratswithvasculardementia
AT fanxiaolan possiblemechanismsoflycopeneameliorationoflearningandmemoryimpairmentinratswithvasculardementia
AT chenshijie possiblemechanismsoflycopeneameliorationoflearningandmemoryimpairmentinratswithvasculardementia
AT zhuyuanming possiblemechanismsoflycopeneameliorationoflearningandmemoryimpairmentinratswithvasculardementia
AT zhaoxiaozhen possiblemechanismsoflycopeneameliorationoflearningandmemoryimpairmentinratswithvasculardementia