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Effects of dietary creatine supplementation on kidney and striated skeletal muscles of rats submitted to ischemia and reperfusion of hind limbs
PURPOSE: To evaluate the effect of creatine supplementation in the diet of rats subjected to ischemia and reperfusion of hind limbs. METHODS: Eighteen male Wistar rats were randomized to receive dietary creatine supplementation (G1) or no supplementation (G2), before being subjected to 4 h of ischem...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128404/ https://www.ncbi.nlm.nih.gov/pubmed/33909821 http://dx.doi.org/10.1590/ACB360305 |
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author | Moreira, Antonio Augusto Francisco, Acácio Moreira, Fernanda Macedo dos Reis Rigopoulos, Lawani Tsunemi, Douglas Soufen, Marco Antônio |
author_facet | Moreira, Antonio Augusto Francisco, Acácio Moreira, Fernanda Macedo dos Reis Rigopoulos, Lawani Tsunemi, Douglas Soufen, Marco Antônio |
author_sort | Moreira, Antonio Augusto |
collection | PubMed |
description | PURPOSE: To evaluate the effect of creatine supplementation in the diet of rats subjected to ischemia and reperfusion of hind limbs. METHODS: Eighteen male Wistar rats were randomized to receive dietary creatine supplementation (G1) or no supplementation (G2), before being subjected to 4 h of ischemia followed by 4 h of reperfusion. In addition, 10 rats (G3) underwent the same surgical procedure, without ischemia, but with supplementation. After reperfusion, kidney and musculature were evaluated for histological damage and serum levels of alanine aminotransferase, urea and creatinine were obtained. RESULTS: The urea dosage showed significant differences between the groups (averages G1 = 155.1; G2 = 211.27; G3 = 160.42). Histological analysis found significant differences between G1 and G2 (but not between G1 and G3) in renal myoglobin cylinders and vacuolar degeneration variables and in hypereosinophilia and karyopyknosis variables in muscle fibers. There were no significant differences in the other variables studied. CONCLUSIONS: Creatine supplementation was related to fewer histological lesions, as well as lower levels of plasma urea, which may suggest a protective effect against lesions caused by ischemia and reperfusion of posterior paws muscles in Wistar rats. |
format | Online Article Text |
id | pubmed-8128404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia |
record_format | MEDLINE/PubMed |
spelling | pubmed-81284042021-05-24 Effects of dietary creatine supplementation on kidney and striated skeletal muscles of rats submitted to ischemia and reperfusion of hind limbs Moreira, Antonio Augusto Francisco, Acácio Moreira, Fernanda Macedo dos Reis Rigopoulos, Lawani Tsunemi, Douglas Soufen, Marco Antônio Acta Cir Bras Original Article PURPOSE: To evaluate the effect of creatine supplementation in the diet of rats subjected to ischemia and reperfusion of hind limbs. METHODS: Eighteen male Wistar rats were randomized to receive dietary creatine supplementation (G1) or no supplementation (G2), before being subjected to 4 h of ischemia followed by 4 h of reperfusion. In addition, 10 rats (G3) underwent the same surgical procedure, without ischemia, but with supplementation. After reperfusion, kidney and musculature were evaluated for histological damage and serum levels of alanine aminotransferase, urea and creatinine were obtained. RESULTS: The urea dosage showed significant differences between the groups (averages G1 = 155.1; G2 = 211.27; G3 = 160.42). Histological analysis found significant differences between G1 and G2 (but not between G1 and G3) in renal myoglobin cylinders and vacuolar degeneration variables and in hypereosinophilia and karyopyknosis variables in muscle fibers. There were no significant differences in the other variables studied. CONCLUSIONS: Creatine supplementation was related to fewer histological lesions, as well as lower levels of plasma urea, which may suggest a protective effect against lesions caused by ischemia and reperfusion of posterior paws muscles in Wistar rats. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2021-04-21 /pmc/articles/PMC8128404/ /pubmed/33909821 http://dx.doi.org/10.1590/ACB360305 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Moreira, Antonio Augusto Francisco, Acácio Moreira, Fernanda Macedo dos Reis Rigopoulos, Lawani Tsunemi, Douglas Soufen, Marco Antônio Effects of dietary creatine supplementation on kidney and striated skeletal muscles of rats submitted to ischemia and reperfusion of hind limbs |
title | Effects of dietary creatine supplementation on kidney and striated
skeletal muscles of rats submitted to ischemia and reperfusion of hind
limbs |
title_full | Effects of dietary creatine supplementation on kidney and striated
skeletal muscles of rats submitted to ischemia and reperfusion of hind
limbs |
title_fullStr | Effects of dietary creatine supplementation on kidney and striated
skeletal muscles of rats submitted to ischemia and reperfusion of hind
limbs |
title_full_unstemmed | Effects of dietary creatine supplementation on kidney and striated
skeletal muscles of rats submitted to ischemia and reperfusion of hind
limbs |
title_short | Effects of dietary creatine supplementation on kidney and striated
skeletal muscles of rats submitted to ischemia and reperfusion of hind
limbs |
title_sort | effects of dietary creatine supplementation on kidney and striated
skeletal muscles of rats submitted to ischemia and reperfusion of hind
limbs |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128404/ https://www.ncbi.nlm.nih.gov/pubmed/33909821 http://dx.doi.org/10.1590/ACB360305 |
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