Evidence map›Paper›PMID 42603129›Full record

ArticleJournal of food science2026

Hericium erinaceus β-Glucan Improves Post-Prandial Glycemic Homeostasis in Association With Changes in Akkermansia muciniphila, Serum Metabolites, and Gut Hormones.

Zhineng Wang, Yuzhu Shu, Pin Gong, Wenbo Yao

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

4 authors.

Zhineng WangCollege of Agriculture and Animal Husbandry, Qinghai University, Xining, China.ORCID https://orcid.org/0000-0001-9414-7043
Yuzhu ShuSchool of Food Science and Engineering, Shaanxi University of Science & Technology, Xi'an, China.
Pin GongSchool of Food Science and Engineering, Shaanxi University of Science & Technology, Xi'an, China.ORCID https://orcid.org/0000-0002-4795-7569
Wenbo YaoKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, Institute of Immunology, The First Hospital, Jilin University, Changchun, China.

Funding

Fundamental Research Funds for the Central UniversitiesGuangxi Key Lab of Agricultural Resources Chemistry and Biotechnology 2024KF06Key Projects of Shaanxi Provincial-Core Technology Breakthroughs-Agriculture and Rural Field 2024NC2-GJHX-25Key Projects of Shaanxi Provincial-Core Technology Breakthroughs-Social Development Field 2024SF-GJHX-08
6 · The paper itself

Abstract

Post-prandial glycemia is an important indicator of metabolic health and early glucose dysregulation. Mushroom-derived β-glucans have potential as functional ingredients for glycemic control, but their comparative efficacy and regulatory mechanisms remain unclear. In this study, β-glucans from oyster mushroom (OMBG), Ganoderma lucidum (GBG), and Hericium erinaceus (HEBG) were evaluated using structural characterization, functional assays, simulated digestion, colonic fermentation, and in vivo experiments, with oat β-glucan (OBG) included as a reference. OBG showed strong glucose diffusion-retarding and enzyme-inhibitory activities in vitro, whereas HEBG exhibited the best overall performance among mushroom-derived β-glucans, particularly in glucose adsorption, glucose diffusion retardation, and α-glucosidase inhibition. During simulated gastrointestinal digestion, HEBG reduced starch hydrolysis and glucose release, and during colonic fermentation it supported microbial growth and carbohydrate utilization. In mice, HEBG improved oral glucose tolerance without affecting body weight, food intake, or organ indices. HEBG treatment was associated with reduced intestinal Sglt-1 expression, enhanced barrier-related markers, including tight junction proteins and Muc2, and increased GLP-1 and PYY secretion. Multi-omics analyses further indicated that HEBG altered gut microbiota composition, particularly enriching Akkermansia muciniphila, and was associated with changes in serum metabolites related to carbohydrate and lipid metabolism. These findings suggest that HEBG may improve post-prandial glucose homeostasis in association with a gut microbiota-metabolite-gut hormone network. PRACTICAL APPLICATIONS: HEBG may serve as a mushroom-derived functional ingredient for post-prandial glycemic management and could be incorporated into supplements, beverages, or starch-based foods to help delay starch digestion and glucose release. Further studies should assess its processing stability and functional retention during food manufacturing.

Indexed as

Akkermansiabeta-GlucansBlood GlucoseGastrointestinal HormonesHericiumAnimalsDigestionFermentationGastrointestinal MicrobiomeHomeostasisMaleMicePostprandial Periodbeta-GlucansBlood GlucoseGastrointestinal Hormones

Identifiers

PMID42603129
PMCPMC13476955

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.