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Aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism
Chronic alcoholism seriously damages the central nervous system and leads to impaired learning and memory. Cell damage in chronic alcoholism is strongly associated with elevated levels of hydrogen sulfide (H(2)S) and calcium ion overload. Aminooxyacetic acid is a cystathionine-β-synthase activity in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126113/ https://www.ncbi.nlm.nih.gov/pubmed/30127117 http://dx.doi.org/10.4103/1673-5374.237120 |
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author | Du, Ai-Lin Qin, Hao-Zhi Jiang, Hong-Bo Fu, Peng-Yan Lou, Ke Xu, Yu-Ming |
author_facet | Du, Ai-Lin Qin, Hao-Zhi Jiang, Hong-Bo Fu, Peng-Yan Lou, Ke Xu, Yu-Ming |
author_sort | Du, Ai-Lin |
collection | PubMed |
description | Chronic alcoholism seriously damages the central nervous system and leads to impaired learning and memory. Cell damage in chronic alcoholism is strongly associated with elevated levels of hydrogen sulfide (H(2)S) and calcium ion overload. Aminooxyacetic acid is a cystathionine-β-synthase activity inhibitor that can reduce H(2)S formation in the brain. This study sought to observe the effect of aminooxyacetic acid on learning and memory in a chronic alcoholism rat model. Rats were randomly divided into three groups. Rats in the control group were given pure water for 28 days. Rats in the model group were given 6% alcohol for 28 days to establish an alcoholism rat model. Rats in the aminooxyacetic acid remedy group were also given 6% alcohol for 28 days and were also intraperitoneally injected daily with aminooxyacetic acid (5 mg/kg) from day 15 to day 28. Learning and memory was tested using the Morris water maze test. The ultrastructure of mitochondria in the hippocampus was observed by electron microscopy. H(2)S levels in the hippocampus were measured indirectly by spectrophotometry, and ATPase activity was measured using a commercial kit. The expression of myelin basic protein was determined by immunohistochemistry and western blotting. Compared with the control group, latency and swimming distance were prolonged in the navigation test on days 2, 3, and 4 in the model group. In the spatial probe test on day 5, the number of platform crosses was reduced in the model group. Cristae cracks, swelling or deformation of mitochondria appeared in the hippocampus, the hippocampal H(2)S level was increased, the mitochondrial ATPase activity was decreased, and the expression of myelin basic protein in the hippocampus was down-regulated in the model group compared with the control group. All the above indexes were ameliorated in the aminooxyacetic acid remedy group compared with the model group. These findings indicate that aminooxyacetic acid can improve learning and memory in a chronic alcoholism rat model, which may be associated with reduction of hippocampal H(2)S level and mitochondrial ATPase activity, and up-regulation of myelin basic protein levels in the hippocampus. |
format | Online Article Text |
id | pubmed-6126113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61261132018-09-12 Aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism Du, Ai-Lin Qin, Hao-Zhi Jiang, Hong-Bo Fu, Peng-Yan Lou, Ke Xu, Yu-Ming Neural Regen Res Research Article Chronic alcoholism seriously damages the central nervous system and leads to impaired learning and memory. Cell damage in chronic alcoholism is strongly associated with elevated levels of hydrogen sulfide (H(2)S) and calcium ion overload. Aminooxyacetic acid is a cystathionine-β-synthase activity inhibitor that can reduce H(2)S formation in the brain. This study sought to observe the effect of aminooxyacetic acid on learning and memory in a chronic alcoholism rat model. Rats were randomly divided into three groups. Rats in the control group were given pure water for 28 days. Rats in the model group were given 6% alcohol for 28 days to establish an alcoholism rat model. Rats in the aminooxyacetic acid remedy group were also given 6% alcohol for 28 days and were also intraperitoneally injected daily with aminooxyacetic acid (5 mg/kg) from day 15 to day 28. Learning and memory was tested using the Morris water maze test. The ultrastructure of mitochondria in the hippocampus was observed by electron microscopy. H(2)S levels in the hippocampus were measured indirectly by spectrophotometry, and ATPase activity was measured using a commercial kit. The expression of myelin basic protein was determined by immunohistochemistry and western blotting. Compared with the control group, latency and swimming distance were prolonged in the navigation test on days 2, 3, and 4 in the model group. In the spatial probe test on day 5, the number of platform crosses was reduced in the model group. Cristae cracks, swelling or deformation of mitochondria appeared in the hippocampus, the hippocampal H(2)S level was increased, the mitochondrial ATPase activity was decreased, and the expression of myelin basic protein in the hippocampus was down-regulated in the model group compared with the control group. All the above indexes were ameliorated in the aminooxyacetic acid remedy group compared with the model group. These findings indicate that aminooxyacetic acid can improve learning and memory in a chronic alcoholism rat model, which may be associated with reduction of hippocampal H(2)S level and mitochondrial ATPase activity, and up-regulation of myelin basic protein levels in the hippocampus. Medknow Publications & Media Pvt Ltd 2018-09 /pmc/articles/PMC6126113/ /pubmed/30127117 http://dx.doi.org/10.4103/1673-5374.237120 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 Du, Ai-Lin Qin, Hao-Zhi Jiang, Hong-Bo Fu, Peng-Yan Lou, Ke Xu, Yu-Ming Aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism |
title | Aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism |
title_full | Aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism |
title_fullStr | Aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism |
title_full_unstemmed | Aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism |
title_short | Aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism |
title_sort | aminooxyacetic acid improves learning and memory in a rat model of chronic alcoholism |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126113/ https://www.ncbi.nlm.nih.gov/pubmed/30127117 http://dx.doi.org/10.4103/1673-5374.237120 |
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