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No effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats
BACKGROUND: Exacerbated oxidative stress is thought to be a mediator of arterial hypertension. It has been postulated that creatine (Cr) could act as an antioxidant agent preventing increased oxidative stress. The aim of this study was to investigate the effects of nine weeks of Cr or placebo supple...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342894/ https://www.ncbi.nlm.nih.gov/pubmed/22480293 http://dx.doi.org/10.1186/1550-2783-9-13 |
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author | Alves, Christiano RR Murai, Igor H Ramona, Pamella Nicastro, Humberto Bechara, Luiz RG Lancha, Antonio H Brum, Patrícia C Irigoyen, Maria C Gualano, Bruno |
author_facet | Alves, Christiano RR Murai, Igor H Ramona, Pamella Nicastro, Humberto Bechara, Luiz RG Lancha, Antonio H Brum, Patrícia C Irigoyen, Maria C Gualano, Bruno |
author_sort | Alves, Christiano RR |
collection | PubMed |
description | BACKGROUND: Exacerbated oxidative stress is thought to be a mediator of arterial hypertension. It has been postulated that creatine (Cr) could act as an antioxidant agent preventing increased oxidative stress. The aim of this study was to investigate the effects of nine weeks of Cr or placebo supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats (SHR). FINDINGS: Lipid hydroperoxidation, one important oxidative stress marker, remained unchanged in the coronary artery (Cr: 12.6 ± 1.5 vs. Pl: 12.2 ± 1.7 nmol·mg(-1); p = 0.87), heart (Cr: 11.5 ± 1.8 vs. Pl: 14.6 ± 1.1 nmol·mg(-1); p = 0.15), plasma (Cr: 67.7 ± 9.1 vs. Pl: 56.0 ± 3.2 nmol·mg(-1); p = 0.19), plantaris (Cr: 10.0 ± 0.8 vs. Pl: 9.0 ± 0.8 nmol·mg(-1); p = 0.40), and EDL muscle (Cr: 14.9 ± 1.4 vs. Pl: 17.2 ± 1.5 nmol·mg(-1); p = 0.30). Additionally, Cr supplementation affected neither arterial blood pressure nor heart structure in SHR (p > 0.05). CONCLUSIONS: Using a well-known experimental model of systemic arterial hypertension, this study did not confirm the possible therapeutic effects of Cr supplementation on oxidative stress and cardiovascular dysfunction associated with arterial hypertension. |
format | Online Article Text |
id | pubmed-3342894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33428942012-05-04 No effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats Alves, Christiano RR Murai, Igor H Ramona, Pamella Nicastro, Humberto Bechara, Luiz RG Lancha, Antonio H Brum, Patrícia C Irigoyen, Maria C Gualano, Bruno J Int Soc Sports Nutr Short Report BACKGROUND: Exacerbated oxidative stress is thought to be a mediator of arterial hypertension. It has been postulated that creatine (Cr) could act as an antioxidant agent preventing increased oxidative stress. The aim of this study was to investigate the effects of nine weeks of Cr or placebo supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats (SHR). FINDINGS: Lipid hydroperoxidation, one important oxidative stress marker, remained unchanged in the coronary artery (Cr: 12.6 ± 1.5 vs. Pl: 12.2 ± 1.7 nmol·mg(-1); p = 0.87), heart (Cr: 11.5 ± 1.8 vs. Pl: 14.6 ± 1.1 nmol·mg(-1); p = 0.15), plasma (Cr: 67.7 ± 9.1 vs. Pl: 56.0 ± 3.2 nmol·mg(-1); p = 0.19), plantaris (Cr: 10.0 ± 0.8 vs. Pl: 9.0 ± 0.8 nmol·mg(-1); p = 0.40), and EDL muscle (Cr: 14.9 ± 1.4 vs. Pl: 17.2 ± 1.5 nmol·mg(-1); p = 0.30). Additionally, Cr supplementation affected neither arterial blood pressure nor heart structure in SHR (p > 0.05). CONCLUSIONS: Using a well-known experimental model of systemic arterial hypertension, this study did not confirm the possible therapeutic effects of Cr supplementation on oxidative stress and cardiovascular dysfunction associated with arterial hypertension. BioMed Central 2012-04-05 /pmc/articles/PMC3342894/ /pubmed/22480293 http://dx.doi.org/10.1186/1550-2783-9-13 Text en Copyright ©2012 Alves et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 original work is properly cited. |
spellingShingle | Short Report Alves, Christiano RR Murai, Igor H Ramona, Pamella Nicastro, Humberto Bechara, Luiz RG Lancha, Antonio H Brum, Patrícia C Irigoyen, Maria C Gualano, Bruno No effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats |
title | No effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats |
title_full | No effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats |
title_fullStr | No effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats |
title_full_unstemmed | No effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats |
title_short | No effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats |
title_sort | no effect of creatine supplementation on oxidative stress and cardiovascular parameters in spontaneously hypertensive rats |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342894/ https://www.ncbi.nlm.nih.gov/pubmed/22480293 http://dx.doi.org/10.1186/1550-2783-9-13 |
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