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DHA-rich fish oil and Tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model
BACKGROUND: Exposure to chronic stress induces oxidative damage which alters the dynamic balance between antioxidant and pro-oxidant activities in the brain. Tualang honey (TH) is a Malaysian wild multifloral honey which has been shown to contain high amount antioxidants. DHA-rich fish oil is a form...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209864/ https://www.ncbi.nlm.nih.gov/pubmed/35747355 http://dx.doi.org/10.1016/j.jtcme.2021.10.001 |
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author | Asari, Mohd Asnizam Sirajudeen, K.N.S. Mohd Yusof, Nurul Aiman Mohd Amin, Mohamad Syabil Ikhwan |
author_facet | Asari, Mohd Asnizam Sirajudeen, K.N.S. Mohd Yusof, Nurul Aiman Mohd Amin, Mohamad Syabil Ikhwan |
author_sort | Asari, Mohd Asnizam |
collection | PubMed |
description | BACKGROUND: Exposure to chronic stress induces oxidative damage which alters the dynamic balance between antioxidant and pro-oxidant activities in the brain. Tualang honey (TH) is a Malaysian wild multifloral honey which has been shown to contain high amount antioxidants. DHA-rich fish oil is a form of omega-3 fatty acids found in fish which also possesses some antioxidant activity. This study aimed to evaluate anti-stress activity of DHA-rich fish oil, TH and their combination on several parameters of oxidative stress in chronic stress rat model. METHODS: Fifty male Sprague Dawley rats were divided into (i) control, (ii) stress-exposed, (iii) stress-exposed and treated with TH (1 g/kg body weight twice daily), (iv) stress-exposed and treated with DHA-rich fish oil (450 mg/kg body weight twice daily), and (v) stress-exposed and treated with a combination of TH and DHA-rich fish oil. The chronic stress regimen consisted of a combination of restraint stress and a swim stress test for 28 days. RESULTS: DHA-rich fish oil and TH significantly (p < 0.05) supressed stress-induced elevation of serum corticosterone and lipid peroxidation, and caused a significant increase in total antioxidant capacity. For glutathione status, only TH significantly reduced stress-induced elevation of oxidised glutathione (GSSG) and normalised GSH/GSSG ratio. Conclusion: Both DHA-rich fish oil and TH have protective effects against brain oxidative stress but consuming these substances together does not seem to provide an additional benefit compared to consuming them separately. |
format | Online Article Text |
id | pubmed-9209864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92098642022-06-22 DHA-rich fish oil and Tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model Asari, Mohd Asnizam Sirajudeen, K.N.S. Mohd Yusof, Nurul Aiman Mohd Amin, Mohamad Syabil Ikhwan J Tradit Complement Med Article BACKGROUND: Exposure to chronic stress induces oxidative damage which alters the dynamic balance between antioxidant and pro-oxidant activities in the brain. Tualang honey (TH) is a Malaysian wild multifloral honey which has been shown to contain high amount antioxidants. DHA-rich fish oil is a form of omega-3 fatty acids found in fish which also possesses some antioxidant activity. This study aimed to evaluate anti-stress activity of DHA-rich fish oil, TH and their combination on several parameters of oxidative stress in chronic stress rat model. METHODS: Fifty male Sprague Dawley rats were divided into (i) control, (ii) stress-exposed, (iii) stress-exposed and treated with TH (1 g/kg body weight twice daily), (iv) stress-exposed and treated with DHA-rich fish oil (450 mg/kg body weight twice daily), and (v) stress-exposed and treated with a combination of TH and DHA-rich fish oil. The chronic stress regimen consisted of a combination of restraint stress and a swim stress test for 28 days. RESULTS: DHA-rich fish oil and TH significantly (p < 0.05) supressed stress-induced elevation of serum corticosterone and lipid peroxidation, and caused a significant increase in total antioxidant capacity. For glutathione status, only TH significantly reduced stress-induced elevation of oxidised glutathione (GSSG) and normalised GSH/GSSG ratio. Conclusion: Both DHA-rich fish oil and TH have protective effects against brain oxidative stress but consuming these substances together does not seem to provide an additional benefit compared to consuming them separately. Elsevier 2021-10-12 /pmc/articles/PMC9209864/ /pubmed/35747355 http://dx.doi.org/10.1016/j.jtcme.2021.10.001 Text en © 2021 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Asari, Mohd Asnizam Sirajudeen, K.N.S. Mohd Yusof, Nurul Aiman Mohd Amin, Mohamad Syabil Ikhwan DHA-rich fish oil and Tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model |
title | DHA-rich fish oil and Tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model |
title_full | DHA-rich fish oil and Tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model |
title_fullStr | DHA-rich fish oil and Tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model |
title_full_unstemmed | DHA-rich fish oil and Tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model |
title_short | DHA-rich fish oil and Tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model |
title_sort | dha-rich fish oil and tualang honey reduce chronic stress-induced oxidative damage in the brain of rat model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209864/ https://www.ncbi.nlm.nih.gov/pubmed/35747355 http://dx.doi.org/10.1016/j.jtcme.2021.10.001 |
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