Yang Chengcheng, Du Yao, Wei Lusha, Tan Zhengwei, Zhou Ting, Wang Lulu, Yang Xingbin, Zhao Yan
Shaanxi Engineering Laboratory for Food Green Processing and Safety Control, and Shaanxi Key Laboratory for Hazard Factors Assessment in Processing and Storage of Agricultural Products, College of Food Engineering and Nutritional Science, Shaanxi Normal University, Xi'an 710119, China.
Key Laboratory of Ministry of Education for Medicinal Resource and Natural Pharmaceutical Chemistry, College of Life Sciences, Shaanxi Normal University, Xi'an 710119, China.
Food Funct. 2025 May 6;16(9):3613-3626. doi: 10.1039/d5fo01001b.
This study is the first to investigate the antidiabetic effect of turmeric powder (TP) and its underlying molecular mechanism in type 2 diabetes mellitus (T2DM) mice. The T2DM mice were supplemented with or without TP (8%) for 8 weeks. The results indicated that the glucolipid metabolism disorder and insulin resistance in T2DM mice were significantly ameliorated through supplementation with TP. The consumption of TP also ameliorated the T2DM-induced gut microbiota dysbiosis, as reflected by a dramatic increase in the relative abundance of beneficial bacteria such as , and at the genus level. Besides, TP significantly increased the colonic levels of short-chain fatty acids (SCFAs) and subsequently activated the IRS1/PI3K/Akt and AMPK-mediated gluconeogenesis signaling pathways to improve insulin resistance in T2DM mice. Interestingly, TP-activated IRS1/PI3K/Akt and AMPK-mediated gluconeogenesis signaling pathways were highly correlated with the reconstruction of the gut microbiome and the formation of SCFAs. Collectively, these findings, for the first time, highlight a novel antidiabetic mechanism of TP by alleviating intestinal microbiota dysbiosis and promoting SCFA production to trigger the IRS1/PI3K/Akt and AMPK-mediated gluconeogenesis signaling axis.
本研究首次探究了姜黄粉(TP)对2型糖尿病(T2DM)小鼠的抗糖尿病作用及其潜在分子机制。给T2DM小鼠补充或不补充8%的TP,持续8周。结果表明,补充TP可显著改善T2DM小鼠的糖脂代谢紊乱和胰岛素抵抗。TP的摄入还改善了T2DM诱导的肠道微生物群失调,这在属水平上表现为有益细菌如[具体细菌名称1]、[具体细菌名称2]和[具体细菌名称3]的相对丰度显著增加。此外,TP显著提高了结肠短链脂肪酸(SCFAs)水平,随后激活了IRS1/PI3K/Akt和AMPK介导的糖异生信号通路,以改善T2DM小鼠的胰岛素抵抗。有趣的是,TP激活的IRS1/PI3K/Akt和AMPK介导的糖异生信号通路与肠道微生物群的重建以及SCFAs的形成高度相关。总的来说,这些发现首次突出了TP通过减轻肠道微生物群失调和促进SCFA产生来触发IRS1/PI3K/Akt和AMPK介导的糖异生信号轴的新型抗糖尿病机制。