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Improved islet function is associated with anti-inflammatory, antioxidant and hypoglycemic potential of cinnamaldehyde on metabolic syndrome induced by high tail fat in rats

•High fat diet (HFD) induced obesity, insulin resistance and high blood pressure.•HFD enhanced oxidative stress and inflammation by increase in MDA and TNF-α.•Cinnamaldehyde (CNMA) prevented metabolic syndrome induced by high fat.•CNMA enhanced anti-oxidative, anti-inflammatory and insulin like acti...

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Published in:Journal of functional foods 2014-09, Vol.10, p.397-406
Main Authors: Farrokhfall, Khadije, Khoshbaten, Ali, Zahediasl, Saleh, Mehrani, Hossein, Karbalaei, Narges
Format: Article
Language:English
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Summary:•High fat diet (HFD) induced obesity, insulin resistance and high blood pressure.•HFD enhanced oxidative stress and inflammation by increase in MDA and TNF-α.•Cinnamaldehyde (CNMA) prevented metabolic syndrome induced by high fat.•CNMA enhanced anti-oxidative, anti-inflammatory and insulin like action.•CNMA preserved islet insulin reserve and hypertrophy associated with HFD. Cinnamon is used in traditional medicine and foods. In this study the protective effects of cinnamaldehyde, one of the most abundant compound of cinnamon against metabolic syndrome induced by high fat diet, were investigated. To induce metabolic syndrome, male Wistar rats were given high fat diet for 16 weeks. Cinnamaldehyde was administrated orally (143.8 µmol/kg body weight) concomitant with high fat feed. Changes in islet morphology, lipid profile, TNF-α, TBARS, insulin resistance were analyzed. Metabolic syndrome was induced by high fat diet. Cinnamaldehyde reversed this process and significantly reduced insulin secretion and content in isolated islets of high fat diet. Beta cell enlargement, TNF-α and TBARS significantly increased with high fat diet, cinnamaldehyde restored both to the control level. Cinnamaldehyde prevented all symptoms of metabolic syndrome by improving oxidative and inflammatory conditions in pancreatic islets with no effect on insulin secretion but by enhancing insulin reserve and preventing beta cell damage.
ISSN:1756-4646
2214-9414
DOI:10.1016/j.jff.2014.07.014