Yang Min, Cai Wanhao, Li Xinxin, Deng Yixuan, Li Jinjun, Wang Xin, Zhu Liying, Wang Chong, Li Xiaoqiong
Key Laboratory of Applied Technology on Green-Eco-Healthy Animal Husbandry of Zhejiang Province, College of Animal Science and Technology and College of Veterinary Medicine, Zhejiang Agriculture and Forestry University, Hangzhou 311300, China.
State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-Products & Institute of Food Sciences, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China.
Foods. 2024 May 23;13(11):1625. doi: 10.3390/foods13111625.
Owing to the interplay of genetic and environmental factors, obesity has emerged as a significant global public health concern. To gain enhanced control over obesity, we examined the effects of type 2 resistant starch (RS2) and its promoted microbial-derived metabolite, indole-3-propionic acid (IPA), on hepatic steatosis, antioxidant activity, and gut microbiota in obese mice. Neither RS2 nor low-dose IPA (20 mg kg) exhibited a reduction in body weight or improved glucose and lipid metabolism in post-obesity state mice continuously fed the high-fat diet (HFD). However, both interventions improved hepatic steatosis, with RS2 being more effective in all measured parameters, potentially due to changes in gut microbiota and metabolites not solely attributed to IPA. LC-MS/MS analysis revealed increased serum IPA levels in both RS2 and IPA groups, which positively correlated with and Clostridium. Moreover, RS2 exhibited a more significant restoration of gut dysbiosis by promoting the abundance of health-promoting bacteria including and . These findings suggest that the regulatory role of RS2 on tryptophan metabolism only partially explains its prebiotic activity. Future studies should consider increasing the dose of IPA and combining RS2 and IPA to explore their potential interventions in obesity.
由于遗传和环境因素的相互作用,肥胖已成为一个重大的全球公共卫生问题。为了更好地控制肥胖,我们研究了2型抗性淀粉(RS2)及其促进产生的微生物衍生代谢产物吲哚-3-丙酸(IPA)对肥胖小鼠肝脂肪变性、抗氧化活性和肠道微生物群的影响。在持续喂食高脂饮食(HFD)的肥胖后状态小鼠中,RS2和低剂量IPA(20毫克/千克)均未使体重减轻,也未改善葡萄糖和脂质代谢。然而,两种干预措施均改善了肝脂肪变性,RS2在所有测量参数上更有效,这可能是由于肠道微生物群和代谢产物的变化不仅仅归因于IPA。液相色谱-串联质谱(LC-MS/MS)分析显示,RS2组和IPA组的血清IPA水平均升高,且与梭菌属呈正相关。此外,RS2通过促进包括[未提及的细菌属1]和[未提及的细菌属2]在内的有益健康细菌的丰度,对肠道生态失调表现出更显著的恢复作用。这些发现表明,RS2对色氨酸代谢的调节作用仅部分解释了其益生元活性。未来的研究应考虑增加IPA的剂量,并将RS2和IPA联合使用,以探索它们对肥胖的潜在干预作用。