Fucoidan from sea cucumber protects against high-fat high-sucrose diet-induced hyperglycaemia and insulin resistance in mice

•Improvement in insulin resistance by Am-FUC is reported for the first time.•Am-FUC reduced blood glucose, improved insulin resistance, and regulated cytokines.•Am-FUC improved hepatic glucose metabolism via regulation of key enzymes’ activities.•Activation of PKB/GLUT4 pathway caused glucose uptake...

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Veröffentlicht in:Journal of functional foods 2014-09, Vol.10, p.128-138
Hauptverfasser: Hu, Shiwei, Xia, Guanghua, Wang, Jingfeng, Wang, Yuming, Li, Zhaojie, Xue, Changhu
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Sprache:eng
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Zusammenfassung:•Improvement in insulin resistance by Am-FUC is reported for the first time.•Am-FUC reduced blood glucose, improved insulin resistance, and regulated cytokines.•Am-FUC improved hepatic glucose metabolism via regulation of key enzymes’ activities.•Activation of PKB/GLUT4 pathway caused glucose uptake in skeletal muscle by Am-FUC.•Am-FUC is a novel and significant functional factor for insulin resistant therapy. The amelioration in hyperglycaemia and insulin resistance of fucoidan from sea cucumber can be speculated due to these effects of fucoidan from marine phaeophyta. We examined the effect of fucoidan from Acaudina molpadioides (Am-FUC) on anti-hyperglycaemia and improvement in insulin resistance in high-fat high-sucrose diet-induced insulin resistant mice. Results showed that Am-FUC significantly reduced blood glucose, insulin, leptin, resistin, and TNF-α levels, and increased adiponectin and hepatic glycogen contents. Am-FUC improved glucose metabolism via an increase in hexokinase and pyruvate kinase activities, and a reduction in glycogen phosphorylase and glucose-6-phosphates activities. Am-FUC enhanced glucose transport through successively activated insulin signalling cascadeinduced GLUT4 translocation. Am-FUC also enhanced the effects of rosiglitazone. No signs of toxicity were observed in acute oral toxicity study. It indicates that Am-FUC acutely reduces blood glucose level and improves insulin resistance via normalization of cytokines and glucose metabolism-related enzyme activities and up-regulation of the PKB/GLUT4 pathway.
ISSN:1756-4646
2214-9414
DOI:10.1016/j.jff.2014.05.012