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Reversal of age-associated oxidative stress in mice by PFT, a novel kefir product
INTRODUCTION: Oxidative stress is a key contributor to aging and age-related diseases. In the present study, we examine the protective effects of PFT, a novel kefir product, against age-associated oxidative stress using aged (10-month-old) mice. METHODS: Mice were treated with PFT orally at a daily...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466882/ https://www.ncbi.nlm.nih.gov/pubmed/32862733 http://dx.doi.org/10.1177/2058738420950149 |
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author | Ghoneum, Mamdooh Abdulmalek, Shaymaa Pan, Deyu |
author_facet | Ghoneum, Mamdooh Abdulmalek, Shaymaa Pan, Deyu |
author_sort | Ghoneum, Mamdooh |
collection | PubMed |
description | INTRODUCTION: Oxidative stress is a key contributor to aging and age-related diseases. In the present study, we examine the protective effects of PFT, a novel kefir product, against age-associated oxidative stress using aged (10-month-old) mice. METHODS: Mice were treated with PFT orally at a daily dose of 2 mg/kg body weight over 6 weeks, and antioxidant status, protein oxidation, and lipid peroxidation were studied in the brain, liver, and blood. RESULTS: PFT supplementation significantly reduced the oxidative stress biomarkers malondialdehyde (MDA) and nitric oxide; reversed the reductions in glutathione (GSH) levels, total antioxidant capacity (TAC), and anti-hydroxyl radical (AHR) content; enhanced the antioxidant enzyme activities of glutathione peroxidase (GPx), catalase (CAT), and superoxide dismutase (SOD); inhibited the liver enzyme levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT); significantly reduced triglyceride (TG), total cholesterol (TC), and low density lipoprotein (LDL) levels; and significantly elevated high density lipoprotein (HDL) levels. Interestingly, PFT supplementation reversed the oxidative changes associated with aging, thus bringing levels to within the limits of the young control mice in the brain, liver, and blood. We also note that PFT affects the redox homeostasis of young mice and that it is corrected post-treatment with PFT. CONCLUSION: Our findings show the effectiveness of dietary PFT supplementation in modulating age-associated oxidative stress in mice and motivate further studies of PFT’s effects in reducing age-associated disorders where free radicals and oxidative stress are the major cause. |
format | Online Article Text |
id | pubmed-7466882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-74668822020-09-16 Reversal of age-associated oxidative stress in mice by PFT, a novel kefir product Ghoneum, Mamdooh Abdulmalek, Shaymaa Pan, Deyu Int J Immunopathol Pharmacol Original Research Article INTRODUCTION: Oxidative stress is a key contributor to aging and age-related diseases. In the present study, we examine the protective effects of PFT, a novel kefir product, against age-associated oxidative stress using aged (10-month-old) mice. METHODS: Mice were treated with PFT orally at a daily dose of 2 mg/kg body weight over 6 weeks, and antioxidant status, protein oxidation, and lipid peroxidation were studied in the brain, liver, and blood. RESULTS: PFT supplementation significantly reduced the oxidative stress biomarkers malondialdehyde (MDA) and nitric oxide; reversed the reductions in glutathione (GSH) levels, total antioxidant capacity (TAC), and anti-hydroxyl radical (AHR) content; enhanced the antioxidant enzyme activities of glutathione peroxidase (GPx), catalase (CAT), and superoxide dismutase (SOD); inhibited the liver enzyme levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT); significantly reduced triglyceride (TG), total cholesterol (TC), and low density lipoprotein (LDL) levels; and significantly elevated high density lipoprotein (HDL) levels. Interestingly, PFT supplementation reversed the oxidative changes associated with aging, thus bringing levels to within the limits of the young control mice in the brain, liver, and blood. We also note that PFT affects the redox homeostasis of young mice and that it is corrected post-treatment with PFT. CONCLUSION: Our findings show the effectiveness of dietary PFT supplementation in modulating age-associated oxidative stress in mice and motivate further studies of PFT’s effects in reducing age-associated disorders where free radicals and oxidative stress are the major cause. SAGE Publications 2020-08-31 /pmc/articles/PMC7466882/ /pubmed/32862733 http://dx.doi.org/10.1177/2058738420950149 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Article Ghoneum, Mamdooh Abdulmalek, Shaymaa Pan, Deyu Reversal of age-associated oxidative stress in mice by PFT, a novel kefir product |
title | Reversal of age-associated oxidative stress in mice by PFT, a novel kefir product |
title_full | Reversal of age-associated oxidative stress in mice by PFT, a novel kefir product |
title_fullStr | Reversal of age-associated oxidative stress in mice by PFT, a novel kefir product |
title_full_unstemmed | Reversal of age-associated oxidative stress in mice by PFT, a novel kefir product |
title_short | Reversal of age-associated oxidative stress in mice by PFT, a novel kefir product |
title_sort | reversal of age-associated oxidative stress in mice by pft, a novel kefir product |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466882/ https://www.ncbi.nlm.nih.gov/pubmed/32862733 http://dx.doi.org/10.1177/2058738420950149 |
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