Academic Thesis

Basic information

Name Iseki Masanori
Belonging department
Occupation name
researchmap researcher code 7000027512
researchmap agency Okayama University of Science

Title

Partially hydrolyzed guar gum intake alleviates lipopolysaccharide-induced systemic inflammation via gut microbial alteration in mice

Bibliography Type

Author

Chihiro Watanabe, Hinako Hirai, Takafumi Aoki, Hiromi Kataoka, Masanori Iseki, Hiroki Hamada, Masato Kawashima, Michael J. Kremenik, Hiromi Yano, Eri Oyanagi

Summary

Background

Interactions between dietary fiber and the gut microbiota appear to be associated with potential mechanisms to alleviate systemic inflammation. We hypothesized that partially hydrolyzed guar gum (PHGG), a soluble dietary fiber, acts on the immune system via the fermentation of gut microbiota.

Objective

In this study, we investigated the effect of PHGG intake on LPS-induced systemic inflammation and changes in gut microbiota.

Methods

Nine-wk-old male C3H/HeN mice were randomly divided into three groups: non-fiber (NF), 5% cellulose (Cellu), and 5% PHGG (PHGG) diet groups. After a 6-wk dietary intervention, all mice were injected with LPS (1 mg/kg, i.v.), after which plasma tumor necrosis factor (TNF)-α and interleukin-10 (IL-10) concentrations were measured. In addition, the relative abundance of gut microbiota in feces, short-chain fatty acids (SCFAs) in the cecum contents, and regulatory T (Treg) cell differentiation was measured.

Results

LPS-induced TNF-α, but not IL-10, production in PHGG mice was significantly lower than that in both the NF and Cellu groups (P < 0.01). The α- and β-diversities of gut microbiota were different among the three groups. SCFAs in the cecum contents of PHGG mice were significantly higher than that in the Cellu group (P < 0.05). Furthermore, Treg cells in the colonic lamina propria were increased by PHGG intake (P < 0.05).

Conclusions

Taken together, the habitual intake of PHGG suppresses systemic inflammation, suggesting that this phenomenon may be related to adaptations in immune function with the induction of differentiation into Treg cells via changes in SCFA production by the gut microbiota.

Magazine(name)

Nutrition

Publisher

Elsevier BV

Volume

142

Number Of Pages

StartingPage

113009

EndingPage

113009

Date of Issue

2026/02

Referee

Exist

Invited

Not exist

Language

English

Thesis Type

Research papers (academic journals)

ISSN

DOI

10.1016/j.nut.2025.113009

NAID

PMID

J-GLOBAL ID

arXiv ID

ORCID Put Code

DBLP ID