Suppr超能文献

牛膝中的格兰尼苷型果聚糖通过调节肠道微生物群预防糖尿病小鼠的肾脏损伤。

A graminan type fructan from Achyranthes bidentata prevents the kidney injury in diabetic mice by regulating gut microbiota.

机构信息

State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, China.

Department of Food Nutrition and Safety, School of Engineering, China Pharmaceutical University, Nanjing, China.

出版信息

Carbohydr Polym. 2024 Sep 1;339:122275. doi: 10.1016/j.carbpol.2024.122275. Epub 2024 May 15.

Abstract

Diabetic kidney disease (DKD) is the main cause of end-stage renal disease, and few therapeutic options are available. The root of Achyranthis bidentatae (AB) is commonly used for DKD treatment in Traditional Chinese medicine. However, its mechanisms are still unclear. Here, a graminan type fructan ABPW1 with molecular weight of 3998 Da was purified from AB. It was composed of β-1,2-linked Fruf, β-2,6-linked-Fruf and β-1,2,6-linked-Fruf backbone, and terminated with T-Glcp and 2-Fruf residues. ABPW1 protected against kidney injuries and intestinal barrier disruption in Streptozotocin (STZ)/High fat diet (HFD) mice. It could modulate gut microbiota composition, evidenced by a rise in the abundance of Bacteroide and decreases of Rikenella, Alistipes, Laedolimicola and Faecalibaculum. ABPW1 intervention promoted short chain fatty acids (SCFAs) production in STZ/HFD mice, especially propionate and isobutyric acid. Antibiotic treatment further demonstrated the key role of gut microbiota in the renal protective action of ABPW1. In addition, in vitro simulated digestion and fermentation together with in vivo fluorescent labeling studies demonstrated ABPW1 was indigestible in upper digestive tract but could reach the colon and be degraded into SCFAs by gut microbiota there. Overall, these data suggested ABPW1 has the potential application on DKD prevention.

摘要

糖尿病肾病(DKD)是终末期肾病的主要原因,目前可用的治疗选择很少。牛膝是一种常用于治疗 DKD 的中药,但它的作用机制尚不清楚。本研究从牛膝中纯化得到一种分子量为 3998 Da 的格兰马宁型果聚糖 ABPW1。它由β-1,2 连接的 Fruf、β-2,6 连接的 Fruf 和β-1,2,6 连接的 Fruf 组成,末端连接有 T-Glcp 和 2-Fruf 残基。ABPW1 可减轻链脲佐菌素(STZ)/高脂饮食(HFD)诱导的小鼠肾损伤和肠屏障破坏。它可以调节肠道微生物群落组成,表现在厚壁菌门和拟杆菌门丰度增加,而变形菌门、理研菌科、阿克曼菌属和粪杆菌属丰度降低。ABPW1 干预促进了 STZ/HFD 小鼠短链脂肪酸(SCFAs)的产生,特别是丙酸和异丁酸。抗生素处理进一步证明了肠道微生物群在 ABPW1 肾保护作用中的关键作用。此外,体外模拟消化和发酵以及体内荧光标记研究表明,ABPW1 在上消化道不可消化,但可到达结肠并被肠道微生物群降解为 SCFAs。总的来说,这些数据表明 ABPW1 具有预防 DKD 的应用潜力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验