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Role of L-carnitine in protection against the cardiac oxidative stress induced by aspartame in Wistar albino rats

Aspartame (ASP) has been used as an alternative to sucrose for diabetics and obese people worldwide. Co-administration of L-carnitine (LC) with ASP has a protective effect against the liver and kidney toxicity induced of ASP. The goal of the investigation was to assess the enhancement of LC effect o...

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Autores principales: Al-Eisa, Rasha A., Al-Salmi, Fawziah A., Hamza, Reham Z., El-Shenawy, Nahla S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221268/
https://www.ncbi.nlm.nih.gov/pubmed/30403670
http://dx.doi.org/10.1371/journal.pone.0204913
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author Al-Eisa, Rasha A.
Al-Salmi, Fawziah A.
Hamza, Reham Z.
El-Shenawy, Nahla S.
author_facet Al-Eisa, Rasha A.
Al-Salmi, Fawziah A.
Hamza, Reham Z.
El-Shenawy, Nahla S.
author_sort Al-Eisa, Rasha A.
collection PubMed
description Aspartame (ASP) has been used as an alternative to sucrose for diabetics and obese people worldwide. Co-administration of L-carnitine (LC) with ASP has a protective effect against the liver and kidney toxicity induced of ASP. The goal of the investigation was to assess the enhancement of LC effect on the cardiac toxicity caused of ASP. The rats were divided into 6 groups: control with saline, LC (10 mg/kg), ASP (75 mg/kg), ASP (150 mg/kg), LC with 75 mg/kg of ASP, and LC with 150 mg/kg ASP. The antioxidants were determined by measuring the activities of myeloperoxidase, xanthine oxidase, superoxide dismutase, catalase, and glutathione peroxidase, and by assessing the levels of lipid peroxidation, total thiols, and glutathione. There was a significant elevation in LPO, in conjunction with a significant decline in the enzymatic antioxidants superoxide dismutase, catalase, and glutathione peroxidase and the non-enzymatic antioxidants glutathione and thiols. The cardiac myofibrils were found in a disarrayed pattern in ASP treated-animals as compared to the control rats. The animals treated with ASP-HD showed more than one apoptotic cell with a large tail and a small head, and the relaxed loops of the damaged DNA were extended to form a comet-shaped structure. These effects may be due to the excessive generation of reactive oxygen species by ASP, which reduces cardiac function. Co-administration of LC with ASP improved all of the above-mentioned parameters that were disrupted of ASP alone. This study evidences a sufficient originality in showing how LC plays a positive role against cardiac toxicity of ASP.
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spelling pubmed-62212682018-11-19 Role of L-carnitine in protection against the cardiac oxidative stress induced by aspartame in Wistar albino rats Al-Eisa, Rasha A. Al-Salmi, Fawziah A. Hamza, Reham Z. El-Shenawy, Nahla S. PLoS One Research Article Aspartame (ASP) has been used as an alternative to sucrose for diabetics and obese people worldwide. Co-administration of L-carnitine (LC) with ASP has a protective effect against the liver and kidney toxicity induced of ASP. The goal of the investigation was to assess the enhancement of LC effect on the cardiac toxicity caused of ASP. The rats were divided into 6 groups: control with saline, LC (10 mg/kg), ASP (75 mg/kg), ASP (150 mg/kg), LC with 75 mg/kg of ASP, and LC with 150 mg/kg ASP. The antioxidants were determined by measuring the activities of myeloperoxidase, xanthine oxidase, superoxide dismutase, catalase, and glutathione peroxidase, and by assessing the levels of lipid peroxidation, total thiols, and glutathione. There was a significant elevation in LPO, in conjunction with a significant decline in the enzymatic antioxidants superoxide dismutase, catalase, and glutathione peroxidase and the non-enzymatic antioxidants glutathione and thiols. The cardiac myofibrils were found in a disarrayed pattern in ASP treated-animals as compared to the control rats. The animals treated with ASP-HD showed more than one apoptotic cell with a large tail and a small head, and the relaxed loops of the damaged DNA were extended to form a comet-shaped structure. These effects may be due to the excessive generation of reactive oxygen species by ASP, which reduces cardiac function. Co-administration of LC with ASP improved all of the above-mentioned parameters that were disrupted of ASP alone. This study evidences a sufficient originality in showing how LC plays a positive role against cardiac toxicity of ASP. Public Library of Science 2018-11-07 /pmc/articles/PMC6221268/ /pubmed/30403670 http://dx.doi.org/10.1371/journal.pone.0204913 Text en © 2018 Al-Eisa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Al-Eisa, Rasha A.
Al-Salmi, Fawziah A.
Hamza, Reham Z.
El-Shenawy, Nahla S.
Role of L-carnitine in protection against the cardiac oxidative stress induced by aspartame in Wistar albino rats
title Role of L-carnitine in protection against the cardiac oxidative stress induced by aspartame in Wistar albino rats
title_full Role of L-carnitine in protection against the cardiac oxidative stress induced by aspartame in Wistar albino rats
title_fullStr Role of L-carnitine in protection against the cardiac oxidative stress induced by aspartame in Wistar albino rats
title_full_unstemmed Role of L-carnitine in protection against the cardiac oxidative stress induced by aspartame in Wistar albino rats
title_short Role of L-carnitine in protection against the cardiac oxidative stress induced by aspartame in Wistar albino rats
title_sort role of l-carnitine in protection against the cardiac oxidative stress induced by aspartame in wistar albino rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221268/
https://www.ncbi.nlm.nih.gov/pubmed/30403670
http://dx.doi.org/10.1371/journal.pone.0204913
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