胰岛素抵抗
糖原
内分泌学
糖尿病
2型糖尿病
内科学
糖异生
氧化应激
血糖
多糖
生物
化学
医学
生物化学
新陈代谢
作者
Rui‐Bo Jia,Zhao‐Rong Li,Juan Wu,Zhirong Ou,Bingwu Liao,Baoguo Sun,Lianzhu Lin,Mouming Zhao
标识
DOI:10.1016/j.ijbiomac.2020.08.154
摘要
The objective of current work was to explore the potential anti-diabetic mechanisms of Hizikia fusifarme polysaccharide (HFP) in type 2 diabetic rats. The carbohydrate loading experiment illustrated that HFP supplement could reduce blood sugar fluctuations caused by eating through inhibiting the hydrolysis of starch in mice. The analysis of typically diabetic symptoms and serum profiles showed that oral administration of HFP could mitigate hyperglycemia, insulin resistance, dyslipidemia, chronic inflammation and oxidative stress in rats. The 16s rRNA gene sequencing analysis indicated that HFP treatment could restore beneficial composition of gut flora in diabetic rats, and the correlation analysis revealed that the improvement of diabetes is closely related to the modification of gut flora by HFP intervention. Furthermore, the RT-qPCR and western blotting analysis clarified that HFP administration could increase glycogen storage in liver and skeletal muscle of diabetic rats through activating IRS/PI3K/AKT/GLUT signaling pathway and restrain gluconeogenesis via affecting the relative expression of Egr-1 and PEPCK genes.
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