Chang Guoli, Tian Siyi, Luo Xinyu, Xiang Yannan, Cai Chenggang, Zhu Ruiyu, Cai Haiying, Yang Hailong, Gao Haiyan
School of Biological and Chemical Engineering, Zhejiang Provincial Key Lab for Chem & Bio Processing Technology for Farm Product, Zhejiang University of Science and Technology, Hangzhou, China.
College of Life and Environmental Science, Wenzhou University, Wenzhou, China.
Mol Nutr Food Res. 2025 May;69(10):e202400523. doi: 10.1002/mnfr.202400523. Epub 2025 Apr 2.
The Myrica rubra pomace polyphenols (MRPP) were used to study their hypoglycemic effects and mechanisms using Type 2 diabetes (T2D) (db/db) mice as the model. The results showed that the oral administration of MRPP (low-dose myricitrin, 50 mg/kg BW by gavage; high-dose myricitrin, 250 mg/kg BW by gavage; and Myrica rubra pomace, 500 mg/kg BW by gavage) for 4 weeks significantly reduced fasting blood glucose, glycated serum protein, serum insulin, and insulin resistance index in mice, as well as the dyslipidemia in mice was improved. MRPP was able to improve the structural morphology of hepatocytes and pancreatic β-cells in diabetic mice. Its hypoglycemic mechanism may involve the upregulation of GLUT-4 and IRS-1 genes expression in the PI3K and AMPK signaling pathways, downregulation of GSK-3β, AMPK, PI3K, and AKT genes expression, and enhancement of the activity of enzymes related to glycogen synthesis and glucose metabolism. Research findings on 16S rRNA suggest that MRPP has the ability to alter the composition of the gut microbiota, impede the growth of harmful bacteria, and foster the growth of beneficial bacteria. Therefore, MRPP was capable of reshaping the specific gut microbial community and supporting its application as a novel supplement in functional foods for the treatment of T2D.
以2型糖尿病(T2D)(db/db)小鼠为模型,研究杨梅渣多酚(MRPP)的降血糖作用及其机制。结果表明,连续4周口服MRPP(低剂量杨梅素,灌胃50 mg/kg体重;高剂量杨梅素,灌胃250 mg/kg体重;以及杨梅渣,灌胃500 mg/kg体重)可显著降低小鼠的空腹血糖、糖化血清蛋白、血清胰岛素和胰岛素抵抗指数,同时改善小鼠的血脂异常。MRPP能够改善糖尿病小鼠肝细胞和胰腺β细胞的结构形态。其降血糖机制可能涉及上调PI3K和AMPK信号通路中GLUT-4和IRS-1基因的表达,下调GSK-3β、AMPK、PI3K和AKT基因的表达,并增强与糖原合成和葡萄糖代谢相关的酶的活性。关于16S rRNA的研究结果表明,MRPP有能力改变肠道微生物群的组成,抑制有害细菌的生长,并促进有益细菌的生长。因此,MRPP能够重塑特定的肠道微生物群落,并支持其作为一种新型补充剂应用于治疗T2D的功能性食品中。