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Memory Impairment Induced by Chronic Psychosocial Stress Is Prevented by L-Carnitine
INTRODUCTION: Psychosocial stress (STS) negatively influences memory. This might be associated to oxidative stress-induced progressive destruction of numerous brain structures and functions. L-carnitine (L-CAR) is a widely used antioxidant compound that is endogenously made in mammalian species. The...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927795/ https://www.ncbi.nlm.nih.gov/pubmed/31908419 http://dx.doi.org/10.2147/DDDT.S225264 |
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author | Rababa’h, Suzie Y Alzoubi, Karem H Hammad, Hana M Alquraan, Laiali El-Salem, Khalid |
author_facet | Rababa’h, Suzie Y Alzoubi, Karem H Hammad, Hana M Alquraan, Laiali El-Salem, Khalid |
author_sort | Rababa’h, Suzie Y |
collection | PubMed |
description | INTRODUCTION: Psychosocial stress (STS) negatively influences memory. This might be associated to oxidative stress-induced progressive destruction of numerous brain structures and functions. L-carnitine (L-CAR) is a widely used antioxidant compound that is endogenously made in mammalian species. The current study investigated the effect of L-CAR on STS-induced memory impairment in the rat hippocampus. METHODS: The STS was induced using intruder model, where two rats were randomly switched from each one cage to another, once/day for 6 weeks. Concurrently, L-CAR (300mg/kg/day) was intraperitoneally administered for 6 weeks. After that, radial arm water maze (RAWM) was used to assess spatial learning memory in rats. Hippocampal biomarkers of oxidative stress, including thiobarbituric acid reactive substance (TBARs), oxidized glutathione (GSSG), reduced glutathione (GSH), glutathione peroxidase (GPx), catalase, and superoxide dismutase (SOD), and Brain-derived neurotrophic factor (BDNF) were examined. RESULTS: The results showed impairment of short-term memory (P < 0.05) during STS, whereas L-CAR treatment protected against this effect. Furthermore, while no change was observed in GSH, GSSG, GPx, catalase, and SOD, L-carnitine normalized STS-induced reduction in the hippocampal BDNF levels and increase in TBARS levels. DISCUSSION: Chronic psychosocial stress-induced memory impairment was prevented via L-CAR administration, which could have been achieved via normalizing changes in lipid peroxidation (TBARs) and BDNF levels in the hippocampus. |
format | Online Article Text |
id | pubmed-6927795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-69277952020-01-06 Memory Impairment Induced by Chronic Psychosocial Stress Is Prevented by L-Carnitine Rababa’h, Suzie Y Alzoubi, Karem H Hammad, Hana M Alquraan, Laiali El-Salem, Khalid Drug Des Devel Ther Original Research INTRODUCTION: Psychosocial stress (STS) negatively influences memory. This might be associated to oxidative stress-induced progressive destruction of numerous brain structures and functions. L-carnitine (L-CAR) is a widely used antioxidant compound that is endogenously made in mammalian species. The current study investigated the effect of L-CAR on STS-induced memory impairment in the rat hippocampus. METHODS: The STS was induced using intruder model, where two rats were randomly switched from each one cage to another, once/day for 6 weeks. Concurrently, L-CAR (300mg/kg/day) was intraperitoneally administered for 6 weeks. After that, radial arm water maze (RAWM) was used to assess spatial learning memory in rats. Hippocampal biomarkers of oxidative stress, including thiobarbituric acid reactive substance (TBARs), oxidized glutathione (GSSG), reduced glutathione (GSH), glutathione peroxidase (GPx), catalase, and superoxide dismutase (SOD), and Brain-derived neurotrophic factor (BDNF) were examined. RESULTS: The results showed impairment of short-term memory (P < 0.05) during STS, whereas L-CAR treatment protected against this effect. Furthermore, while no change was observed in GSH, GSSG, GPx, catalase, and SOD, L-carnitine normalized STS-induced reduction in the hippocampal BDNF levels and increase in TBARS levels. DISCUSSION: Chronic psychosocial stress-induced memory impairment was prevented via L-CAR administration, which could have been achieved via normalizing changes in lipid peroxidation (TBARs) and BDNF levels in the hippocampus. Dove 2019-12-19 /pmc/articles/PMC6927795/ /pubmed/31908419 http://dx.doi.org/10.2147/DDDT.S225264 Text en © 2019 Rababa’h et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Rababa’h, Suzie Y Alzoubi, Karem H Hammad, Hana M Alquraan, Laiali El-Salem, Khalid Memory Impairment Induced by Chronic Psychosocial Stress Is Prevented by L-Carnitine |
title | Memory Impairment Induced by Chronic Psychosocial Stress Is Prevented by L-Carnitine |
title_full | Memory Impairment Induced by Chronic Psychosocial Stress Is Prevented by L-Carnitine |
title_fullStr | Memory Impairment Induced by Chronic Psychosocial Stress Is Prevented by L-Carnitine |
title_full_unstemmed | Memory Impairment Induced by Chronic Psychosocial Stress Is Prevented by L-Carnitine |
title_short | Memory Impairment Induced by Chronic Psychosocial Stress Is Prevented by L-Carnitine |
title_sort | memory impairment induced by chronic psychosocial stress is prevented by l-carnitine |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927795/ https://www.ncbi.nlm.nih.gov/pubmed/31908419 http://dx.doi.org/10.2147/DDDT.S225264 |
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