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The effects of coenzyme Q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise
[PURPOSE]: The aim of the study was to determine the effects of dietary CoQ10 on serum biochemical parameters, lipid peroxidation, and HSP expression in the liver and slow-twitch muscles (soleus and gastronemius deep portion) of exercise-trained rats. [METHODS]: A total of 42 Wistar albino rats were...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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한국운동영양학회
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199489/ https://www.ncbi.nlm.nih.gov/pubmed/30343554 http://dx.doi.org/10.20463/jenb.2018.0019 |
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author | Pala, Ragip Beyaz, Fahrettin Tuzcu, Mehmet Er, Besir Sahin, Nurhan Cinar, Vedat Sahin, Kazim |
author_facet | Pala, Ragip Beyaz, Fahrettin Tuzcu, Mehmet Er, Besir Sahin, Nurhan Cinar, Vedat Sahin, Kazim |
author_sort | Pala, Ragip |
collection | PubMed |
description | [PURPOSE]: The aim of the study was to determine the effects of dietary CoQ10 on serum biochemical parameters, lipid peroxidation, and HSP expression in the liver and slow-twitch muscles (soleus and gastronemius deep portion) of exercise-trained rats. [METHODS]: A total of 42 Wistar albino rats were divided into six groups: 1) Control, 2) Coenzyme Q10 (CoQ10), 3) Chronic Exercise (CE), 4) CE + CoQ10, 5) Acute Exercise (AE), and 6) AE + CoQ10. The rats were subjected to the running test 5 days a week for 6 weeks after which CoQ10 was administered via the diet. AE (running on the treadmill until the rats were exhausted) was done on the last day [RESULTS]: The results showed no significant difference in serum glucose and liver functions in any of the groups. However, CoQ10 and exercise treatment were found to lower cholesterol and triglyceride levels. Serum and muscle malondialdehyde (MDA) levels were found to be lower in the CE and CE + CoQ10 groups compared to the control group. The highest levels of HSP60, HSP70, and HSP90 in liver and muscle were found in the AE group, and the lowest levels were found in CE + CoQ10 group. CoQ10 supplementation reduced HSP expression in both CE-and AE-trained rats (P < 0.05). [CONCLUSION]: The results showed that CoQ10 supplementation could reduce MDA levels, protect against oxidative damage, and regulate HSP expression in CE-and AE-trained rats. CE and CoQ10 were shown to reduce oxidative stress synergistically. |
format | Online Article Text |
id | pubmed-6199489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | 한국운동영양학회 |
record_format | MEDLINE/PubMed |
spelling | pubmed-61994892018-11-07 The effects of coenzyme Q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise Pala, Ragip Beyaz, Fahrettin Tuzcu, Mehmet Er, Besir Sahin, Nurhan Cinar, Vedat Sahin, Kazim J Exerc Nutrition Biochem Original Articles [PURPOSE]: The aim of the study was to determine the effects of dietary CoQ10 on serum biochemical parameters, lipid peroxidation, and HSP expression in the liver and slow-twitch muscles (soleus and gastronemius deep portion) of exercise-trained rats. [METHODS]: A total of 42 Wistar albino rats were divided into six groups: 1) Control, 2) Coenzyme Q10 (CoQ10), 3) Chronic Exercise (CE), 4) CE + CoQ10, 5) Acute Exercise (AE), and 6) AE + CoQ10. The rats were subjected to the running test 5 days a week for 6 weeks after which CoQ10 was administered via the diet. AE (running on the treadmill until the rats were exhausted) was done on the last day [RESULTS]: The results showed no significant difference in serum glucose and liver functions in any of the groups. However, CoQ10 and exercise treatment were found to lower cholesterol and triglyceride levels. Serum and muscle malondialdehyde (MDA) levels were found to be lower in the CE and CE + CoQ10 groups compared to the control group. The highest levels of HSP60, HSP70, and HSP90 in liver and muscle were found in the AE group, and the lowest levels were found in CE + CoQ10 group. CoQ10 supplementation reduced HSP expression in both CE-and AE-trained rats (P < 0.05). [CONCLUSION]: The results showed that CoQ10 supplementation could reduce MDA levels, protect against oxidative damage, and regulate HSP expression in CE-and AE-trained rats. CE and CoQ10 were shown to reduce oxidative stress synergistically. 한국운동영양학회 2018-09-30 /pmc/articles/PMC6199489/ /pubmed/30343554 http://dx.doi.org/10.20463/jenb.2018.0019 Text en ©2018 The Korean Society for Exercise Nutrition ©2018 Ragip Pala et al.; License Journal of Exercise Nutrition and Biochemistry. This is an open access article distributed under the terms of the creative commons attribution license (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the orginal work is properly cited. |
spellingShingle | Original Articles Pala, Ragip Beyaz, Fahrettin Tuzcu, Mehmet Er, Besir Sahin, Nurhan Cinar, Vedat Sahin, Kazim The effects of coenzyme Q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise |
title | The effects of coenzyme Q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise |
title_full | The effects of coenzyme Q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise |
title_fullStr | The effects of coenzyme Q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise |
title_full_unstemmed | The effects of coenzyme Q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise |
title_short | The effects of coenzyme Q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise |
title_sort | effects of coenzyme q10 on oxidative stress and heat shock proteins in rats subjected to acute and chronic exercise |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199489/ https://www.ncbi.nlm.nih.gov/pubmed/30343554 http://dx.doi.org/10.20463/jenb.2018.0019 |
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