Jia Rui-Bo, Wu Juan, Luo Donghui, Lin Lianzhu, Chen Chong, Xiao Chuqiao, Zhao Mouming
Chaozhou Branch of Chemistry and Chemical Engineering Guangdong Laboratory, Chaozhou 521000, China.
School of Food Science and Engineering, South China University of Technology, Guangzhou 510640, China.
Foods. 2022 May 13;11(10):1416. doi: 10.3390/foods11101416.
The current study aimed to assess the anti-diabetic effects and potential mechanisms of two polysaccharide fractions (SFPs, named SFP-1 and SFP-2). The carbohydrate-loading experiment revealed that SFP-2 could control postprandial hyperglycemia by inhibiting the activity of digestive enzymes in rats. The analysis of diabetic symptoms and serum profiles indicated that SFPs could mitigate diabetes accompanied by dyslipidemia, and SFP-2 showed better regulatory effects on body weight, food intake and the levels of total cholesterol (TC), triglycerides (TG), low density lipoprotein-cholesterol (LDL-C) and free fatty acid (FFA) in diabetic rats. Intestinal bacterial analysis showed that SFP treatment could reshape the gut flora of diabetic rats, and SFP-2 possessed a greater regulatory effect on the growth of and than SFP-1. RT-qPCR analysis revealed that SFPs could regulate the genes involved in the absorption and utilization of blood glucose, hepatic glucose production and lipid metabolism, and the effects of SFP-2 on the relative expressions of Protein kinase B (Akt), Glucose-6-phosphatase (G-6-Pase), Glucose transporter 2 (GLUT2), AMP-activated protein kinase- (AMPK), Peroxisome proliferator-activated receptor (PPAR) and Cholesterol 7-alpha hydroxylase (CYP7A1) were greater than SFP-1. All above results indicated that SFPs could be exploited as functional foods or pharmaceutical supplements for the treatment of diabetes and its complications.
本研究旨在评估两种多糖组分(SFP,命名为SFP-1和SFP-2)的抗糖尿病作用及其潜在机制。碳水化合物负荷实验表明,SFP-2可通过抑制大鼠消化酶活性来控制餐后高血糖。对糖尿病症状和血清指标的分析表明,SFP可减轻伴有血脂异常的糖尿病,且SFP-2对糖尿病大鼠的体重、食物摄入量以及总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)和游离脂肪酸(FFA)水平具有更好的调节作用。肠道细菌分析表明,SFP处理可重塑糖尿病大鼠的肠道菌群,且SFP-2对[具体细菌名称1]和[具体细菌名称2]生长的调节作用大于SFP-1。RT-qPCR分析显示,SFP可调节参与血糖吸收与利用、肝脏葡萄糖生成及脂质代谢的基因,且SFP-2对蛋白激酶B(Akt)、葡萄糖-6-磷酸酶(G-6-Pase)、葡萄糖转运蛋白2(GLUT2)、AMP激活的蛋白激酶α(AMPKα)、过氧化物酶体增殖物激活受体α(PPARα)和胆固醇7α-羟化酶(CYP7A1)相对表达的影响大于SFP-1。上述所有结果表明,SFP可开发为功能性食品或药物补充剂用于治疗糖尿病及其并发症。