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

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. Mal...

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Bibliographic Details
Published in:Heliyon 2019-03, Vol.5 (3), p.e01357-e01357, Article e01357
Main Authors: 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
Format: Article
Language:English
Subjects:
Biochemistry
Cardiology
Life Sciences
Molecular biology
Nutrition
Physiology
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Summary: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. 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. 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. 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.
ISSN:2405-8440
2405-8440
DOI:10.1016/j.heliyon.2019.e01357