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The impact of sugar-sweetened beverage intake on rat cardiac function

AIMS: Although there is evidence linking sugar-sweetened beverage (SSB) intake with the development of cardio-metabolic diseases, the underlying mechanisms remain unclear. The current study therefore evaluated the effects of SSB consumption by establishing a unique in-house in vivo experimental mode...

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Autores principales: Driescher, Natasha, Joseph, Danzil E., Human, Veronique R., Ojuka, Edward, Cour, Martin, Hadebe, Nkanyiso, Bester, Dirk, Marnewick, Jeanine L., Lecour, Sandrine, Lochner, Amanda, Essop, M. Faadiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429811/
https://www.ncbi.nlm.nih.gov/pubmed/30949605
http://dx.doi.org/10.1016/j.heliyon.2019.e01357
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author Driescher, Natasha
Joseph, Danzil E.
Human, Veronique R.
Ojuka, Edward
Cour, Martin
Hadebe, Nkanyiso
Bester, Dirk
Marnewick, Jeanine L.
Lecour, Sandrine
Lochner, Amanda
Essop, M. Faadiel
author_facet Driescher, Natasha
Joseph, Danzil E.
Human, Veronique R.
Ojuka, Edward
Cour, Martin
Hadebe, Nkanyiso
Bester, Dirk
Marnewick, Jeanine L.
Lecour, Sandrine
Lochner, Amanda
Essop, M. Faadiel
author_sort Driescher, Natasha
collection PubMed
description AIMS: Although there is evidence linking sugar-sweetened beverage (SSB) intake with the development of cardio-metabolic diseases, the underlying mechanisms remain unclear. The current study therefore evaluated the effects of SSB consumption by establishing a unique in-house in vivo experimental model. MAIN METHODS: Male Wistar rats were divided into two groups: a) one consuming a popular local SSB (SSB- Jive), and b) a control group (Control-water) for a period of three and six months (n = 6 per group), respectively. Rats were gavaged on a daily basis with an experimental dosage amounting to half a glass per day (in human terms) (SSB vs. water). Cardiac function was assessed at baseline (echocardiography) and following ex vivo ischemia-reperfusion of the isolated perfused working rat heart. Oral glucose tolerance tests and mitochondrial respiratory analyses were also performed. In addition, the role of non-oxidative glucose pathways (NOGPs), i.e. the polyol pathway, hexosamine biosynthetic pathway (HBP) and PKC were assessed. KEY FINDINGS: These data show that SSB intake: a) resulted in increased weight gain, but did not elicit major effects in terms of insulin resistance and cardiac function after three and six months, respectively; b) triggered myocardial NOGP activation after three months with a reversion after six months; and c) resulted in some impairment in mitochondrial respiratory capacity in response to fatty acid substrate supply after six months. SIGNIFICANCE: SSB intake did not result in cardiac dysfunction or insulin resistance. However, early changes at the molecular level may increase risk in the longer term.
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spelling pubmed-64298112019-04-04 The impact of sugar-sweetened beverage intake on rat cardiac function Driescher, Natasha Joseph, Danzil E. Human, Veronique R. Ojuka, Edward Cour, Martin Hadebe, Nkanyiso Bester, Dirk Marnewick, Jeanine L. Lecour, Sandrine Lochner, Amanda Essop, M. Faadiel Heliyon Article AIMS: Although there is evidence linking sugar-sweetened beverage (SSB) intake with the development of cardio-metabolic diseases, the underlying mechanisms remain unclear. The current study therefore evaluated the effects of SSB consumption by establishing a unique in-house in vivo experimental model. MAIN METHODS: Male Wistar rats were divided into two groups: a) one consuming a popular local SSB (SSB- Jive), and b) a control group (Control-water) for a period of three and six months (n = 6 per group), respectively. Rats were gavaged on a daily basis with an experimental dosage amounting to half a glass per day (in human terms) (SSB vs. water). Cardiac function was assessed at baseline (echocardiography) and following ex vivo ischemia-reperfusion of the isolated perfused working rat heart. Oral glucose tolerance tests and mitochondrial respiratory analyses were also performed. In addition, the role of non-oxidative glucose pathways (NOGPs), i.e. the polyol pathway, hexosamine biosynthetic pathway (HBP) and PKC were assessed. KEY FINDINGS: These data show that SSB intake: a) resulted in increased weight gain, but did not elicit major effects in terms of insulin resistance and cardiac function after three and six months, respectively; b) triggered myocardial NOGP activation after three months with a reversion after six months; and c) resulted in some impairment in mitochondrial respiratory capacity in response to fatty acid substrate supply after six months. SIGNIFICANCE: SSB intake did not result in cardiac dysfunction or insulin resistance. However, early changes at the molecular level may increase risk in the longer term. Elsevier 2019-03-19 /pmc/articles/PMC6429811/ /pubmed/30949605 http://dx.doi.org/10.1016/j.heliyon.2019.e01357 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Driescher, Natasha
Joseph, Danzil E.
Human, Veronique R.
Ojuka, Edward
Cour, Martin
Hadebe, Nkanyiso
Bester, Dirk
Marnewick, Jeanine L.
Lecour, Sandrine
Lochner, Amanda
Essop, M. Faadiel
The impact of sugar-sweetened beverage intake on rat cardiac function
title The impact of sugar-sweetened beverage intake on rat cardiac function
title_full The impact of sugar-sweetened beverage intake on rat cardiac function
title_fullStr The impact of sugar-sweetened beverage intake on rat cardiac function
title_full_unstemmed The impact of sugar-sweetened beverage intake on rat cardiac function
title_short The impact of sugar-sweetened beverage intake on rat cardiac function
title_sort impact of sugar-sweetened beverage intake on rat cardiac function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429811/
https://www.ncbi.nlm.nih.gov/pubmed/30949605
http://dx.doi.org/10.1016/j.heliyon.2019.e01357
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