Evidence map›Paper›PMID 42156751›Full record

ArticleNPJ science of food2026

Structural characterization of a fructan from Polygonati Rhizoma and its anti-diabetic effects associated with insulin-signalling-related readouts and gut microbiota modulation.

Chang Xue, Zijun Li, Lulu Yao, Yicheng Zhou, Yuxin Xiao, Xinrong Fan, Dawei Song, Wei Chen, De Ji, Zhouguang Wang and 1 more

Abstract read
In one paragraph

Article in NPJ science of food, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Chang XueNational Key Laboratory of Macromolecular Drugs and Large-scale Preparation, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Zijun LiNational Key Laboratory of Macromolecular Drugs and Large-scale Preparation, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Lulu YaoResearch Institute of Pharmaceutical Sciences, College of Pharmacy, Chonnam National University, Gwangju, Republic of Korea.
Yicheng ZhouNational Key Laboratory of Macromolecular Drugs and Large-scale Preparation, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Yuxin XiaoNational Key Laboratory of Macromolecular Drugs and Large-scale Preparation, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Xinrong FanDepartment of Drug Preparation, Lishui Hospital of Traditional Chinese Medicine, Lishui, Zhejiang, China.
Dawei SongJiuhuashan Polygonati Rhizoma Research Institute, Chizhou, China.
Wei ChenJiuhuashan Polygonati Rhizoma Research Institute, Chizhou, China.
De JiSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China. de.ji@njucm.edu.cn.
Zhouguang WangNational Key Laboratory of Macromolecular Drugs and Large-scale Preparation, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China. wzhouguang@gmail.com.
Chengxi JiangNational Key Laboratory of Macromolecular Drugs and Large-scale Preparation, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China. jiangchengxi@126.com.

Funding

Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang 2023R01002the National Natural Science Foundation of China 82271629, 82301790
6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2DM) involves insulin resistance, hyperglycaemia, and metabolic stress. Polygonati Rhizoma (Huangjing), a traditional edible and medicinal plant widely used in East Asia, has gained attention as a functional food resource. In this study, a fructan-rich polysaccharide fraction (PRP-W-1) was purified and characterized by HPGPC, FT-IR, GC-MS, and NMR. PRP-W-1 showed a single HPGPC peak with a weight-average molecular weight of approximately 4.8 kDa and consisted mainly of fructose ( > 93%) with minor glucose. Linkage and NMR analyses indicated that PRP-W-1 is a low-molecular-weight fructan mainly composed of a 1,2-linked fructofuranosyl backbone, together with a minor glucosyl component and limited branching. In HFD/STZ-induced T2DM mice, PRP-W-1 mitigated body-weight loss, lowered fasting glucose, improved glucose tolerance, and enhanced insulin sensitivity. It also attenuated dyslipidaemia and liver index elevations. PRP-W-1 was associated with increased hepatic PI3K and p-AKT, reduced p-JNK, and restored adipose GLUT4 abundance. It also improved intestinal barrier-related markers, reshaped the gut microbiota, and increased cecal short-chain fatty acids (SCFAs). Collectively, these results identify PRP-W-1 as a structurally defined, low-molecular-weight fructan from Polygonati Rhizoma with hypoglycaemic and gut-modulatory effects, supporting its potential as a natural dietary ingredient for metabolic health.

Identifiers

PMID42156751
PMCPMC13451366

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