Effects of coconut oil long-term supplementation in Wistar rats during metabolic syndrome - regulation of metabolic conditions involving glucose homeostasis, inflammatory signals, and oxidative stress

• Published in: The Journal of nutritional biochemistry 2023-04, Vol.114, p.109272-109272, Article 109272
• Main Authors: Mautone Gomes, Henrique, Silveira, Alexandre K., Gasparotto, Juciano, Bortolin, Rafael Calixto, Terra, Silvia R., Brum, Pedro O., Gelain, Daniel P., Fonseca Moreira, José C.
• Format: Article
• Language: English
• Subjects: Animals; Blood Glucose - metabolism; Coconut Oil; Coconut Oil - pharmacology; Coconut Oil - therapeutic use; Conjugated Dienes; Diabetes Mellitus, Type 2 - etiology; Diabetes Mellitus, Type 2 - metabolism; Dietary Supplements; Fructosamine - metabolism; Fructosamine - pharmacology; Fructose - metabolism; Glucose - metabolism; Hepatic Oxidative Stress; Homeostasis; Inflammation - diet therapy; Inflammation - metabolism; Liver - metabolism; Metabolic Syndrome; Metabolic Syndrome - diet therapy; Metabolic Syndrome - metabolism; Oxidative Stress; Rats; Rats, Wistar
• ISSN: 0955-2863; 1873-4847
• DOI: 10.1016/j.jnutbio.2023.109272

This study was designed to evaluate the long-term effects of Fructose (20%) feeding in rats, simulating metabolic syndrome (MetS), and the effects of coconut oil (C.O.) supplementation when administered in a MetS context. MetS is a cluster of systemic conditions that represent an increased chance of developing cardiovascular diseases and type 2 diabetes in the future. C.O. has been the target of media speculation, and recent studies report inconsistent results. C.O. improved glucose homeostasis and reduced fat accumulation in Fructose-fed rats while decreasing the levels of triglycerides (TGs) in the liver. C.O. supplementation also increased TGs levels and fructosamine in serum during MetS, possibly due to white adipose tissue breakdown and high fructose feeding. Pro-inflammatory cytokines IL-1β and TNF-α were also increased in rats treated with Fructose and C.O. Oxidative stress marker nitrotyrosine is increased in fructose-fed animals, and C.O. treatment did not prevent this damage. No significant changes were observed in lipoperoxidation marker 4-Hydroxynonenal; however, fructose feeding increased total conjugated dienes and caused conjugated dienes to switch their conformation from cis-trans to trans-trans, which was not prevented by C.O. treatment. Potential benefits of C.O. have been reported with inconsistent results, and indeed we observed some benefits of C.O. supplementation in aiding weight loss, fat accumulation, and improving glucose homeostasis. Nonetheless, we also demonstrated that long-term C.O. supplementation could present some problematic effects with higher risk for individuals suffering MetS, including increased TGs and fructosamine levels and conformational changes in dienes. [Display omitted]