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Neuroprotective Effects of Natural Antioxidants Against Branched-Chain Fatty Acid-Induced Oxidative Stress in Cerebral Cortex and Cerebellum Regions of the Rat Brain
[Image: see text] Valproic acid (VPA) is short branched-chain fatty acid (BCFA) derived from valeric acids which are naturally produced by Valeriana officinalis (flowering plant). Neurotoxicity caused by BCFA-like VPA may be mediated by oxidative stress, according to research involving the cerebral...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631910/ https://www.ncbi.nlm.nih.gov/pubmed/36340064 http://dx.doi.org/10.1021/acsomega.2c00163 |
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author | Chaudhary, Shaista Pinky, Parvez, Suhel |
author_facet | Chaudhary, Shaista Pinky, Parvez, Suhel |
author_sort | Chaudhary, Shaista |
collection | PubMed |
description | [Image: see text] Valproic acid (VPA) is short branched-chain fatty acid (BCFA) derived from valeric acids which are naturally produced by Valeriana officinalis (flowering plant). Neurotoxicity caused by BCFA-like VPA may be mediated by oxidative stress, according to research involving the cerebral cortex and cerebellum. In the present study, we explored the possible protective effect of different antioxidants such as melatonin, quercetin, and piperine on VPA exposure by using a supernatant preparation of the cerebral cortex and cerebellum regions of the rat brain. The present study revealed that melatonin, quercetin, and piperine significantly prevented VPA-induced oxidative stress in the cerebral cortex and cerebellum regions. VPA was also observed to lower the level of reduced glutathione, and this effect was significantly mitigated by these antioxidants. Melatonin, quercetin, and piperine also ameliorated and altered the activities of AChE, Na(+), K(+)ATPase, and MAO in the cerebral cortex and cerebellum. Results of this study also suggest that prior treatment of antioxidants like melatonin, quercetin, and piperine helps in combating the oxidative stress induced by VPA in the cerebral cortex and cerebellum region of the rat brain. Thus, sufficient dietary intake of these antioxidants by individuals at high risk of VPA exposure could prove beneficial in combating the adverse effect of VPA. |
format | Online Article Text |
id | pubmed-9631910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96319102022-11-04 Neuroprotective Effects of Natural Antioxidants Against Branched-Chain Fatty Acid-Induced Oxidative Stress in Cerebral Cortex and Cerebellum Regions of the Rat Brain Chaudhary, Shaista Pinky, Parvez, Suhel ACS Omega [Image: see text] Valproic acid (VPA) is short branched-chain fatty acid (BCFA) derived from valeric acids which are naturally produced by Valeriana officinalis (flowering plant). Neurotoxicity caused by BCFA-like VPA may be mediated by oxidative stress, according to research involving the cerebral cortex and cerebellum. In the present study, we explored the possible protective effect of different antioxidants such as melatonin, quercetin, and piperine on VPA exposure by using a supernatant preparation of the cerebral cortex and cerebellum regions of the rat brain. The present study revealed that melatonin, quercetin, and piperine significantly prevented VPA-induced oxidative stress in the cerebral cortex and cerebellum regions. VPA was also observed to lower the level of reduced glutathione, and this effect was significantly mitigated by these antioxidants. Melatonin, quercetin, and piperine also ameliorated and altered the activities of AChE, Na(+), K(+)ATPase, and MAO in the cerebral cortex and cerebellum. Results of this study also suggest that prior treatment of antioxidants like melatonin, quercetin, and piperine helps in combating the oxidative stress induced by VPA in the cerebral cortex and cerebellum region of the rat brain. Thus, sufficient dietary intake of these antioxidants by individuals at high risk of VPA exposure could prove beneficial in combating the adverse effect of VPA. American Chemical Society 2022-10-20 /pmc/articles/PMC9631910/ /pubmed/36340064 http://dx.doi.org/10.1021/acsomega.2c00163 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Chaudhary, Shaista Pinky, Parvez, Suhel Neuroprotective Effects of Natural Antioxidants Against Branched-Chain Fatty Acid-Induced Oxidative Stress in Cerebral Cortex and Cerebellum Regions of the Rat Brain |
title | Neuroprotective
Effects of Natural Antioxidants Against
Branched-Chain Fatty Acid-Induced Oxidative Stress in Cerebral Cortex
and Cerebellum Regions of the Rat Brain |
title_full | Neuroprotective
Effects of Natural Antioxidants Against
Branched-Chain Fatty Acid-Induced Oxidative Stress in Cerebral Cortex
and Cerebellum Regions of the Rat Brain |
title_fullStr | Neuroprotective
Effects of Natural Antioxidants Against
Branched-Chain Fatty Acid-Induced Oxidative Stress in Cerebral Cortex
and Cerebellum Regions of the Rat Brain |
title_full_unstemmed | Neuroprotective
Effects of Natural Antioxidants Against
Branched-Chain Fatty Acid-Induced Oxidative Stress in Cerebral Cortex
and Cerebellum Regions of the Rat Brain |
title_short | Neuroprotective
Effects of Natural Antioxidants Against
Branched-Chain Fatty Acid-Induced Oxidative Stress in Cerebral Cortex
and Cerebellum Regions of the Rat Brain |
title_sort | neuroprotective
effects of natural antioxidants against
branched-chain fatty acid-induced oxidative stress in cerebral cortex
and cerebellum regions of the rat brain |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631910/ https://www.ncbi.nlm.nih.gov/pubmed/36340064 http://dx.doi.org/10.1021/acsomega.2c00163 |
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