The Effect of GB1 on DSS-Induced Colitis in WT and Nlrp3-/- Mice

This study investigated the protective effects of Garcinia biflavonoid 1 (GB1) against dextran sulfate sodium (DSS)-induced ulcerative colitis and its underlying mechanisms. Using wild-type (WT) and NLRP3 knockout (Nlrp3<sup>-/-</sup>) mice, we demonstrated that GB1 administration significantly ameliorated colitis symptoms, as evidenced by improved body weight, disease activity index (DAI) scores, colon length, and histological damage in WT mice. Mechanistically, GB1 downregulated pro-inflammatory mediators (IL-6, NF-κB, and CD11b) while attenuating the expression of NLRP3 inflammasome components (ASC, Caspase-1, and IL-1β). Notably, these protective effects were abolished in Nlrp3<sup>-/-</sup> mice, confirming the essential role of NLRP3 in GB1-mediated mitigation of colitis. Furthermore, GB1 reinforced intestinal barrier integrity by preserving tight junctions, reducing permeability, and attenuating mucosal inflammation. Collectively, our findings highlight GB1 as a promising therapeutic candidate for colitis treatment, primarily through NLRP3 inflammasome suppression and intestinal barrier restoration.

Authors

Institutions

Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-04-24
DOI
https://doi.org/10.3390/ijms26094016
Primary Topic
Barrier Structure and Function Studies
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The Effect of GB1 on DSS-Induced Colitis in WT and Nlrp3-/- Mice

Q. Chen, Ru-He Liao, Lixian Wang, Changsheng Deng et al.
International Journal of Molecular Sciences
Barrier Structure and Function Studies
article

The Effect of GB1 on DSS-Induced Colitis in WT and Nlrp3-/- Mice

Q. Chen, Ru-He Liao, Lixian Wang, Changsheng Deng, Xinan Huang, Changhui Liu, Jianping Song, Ziyi Zhou
article en

Abstract

This study investigated the protective effects of Garcinia biflavonoid 1 (GB1) against dextran sulfate sodium (DSS)-induced ulcerative colitis and its underlying mechanisms. Using wild-type (WT) and NLRP3 knockout (Nlrp3<sup>-/-</sup>) mice, we demonstrated that GB1 administration significantly ameliorated colitis symptoms, as evidenced by improved body weight, disease activity index (DAI) scores, colon length, and histological damage in WT mice. Mechanistically, GB1 downregulated pro-inflammatory mediators (IL-6, NF-κB, and CD11b) while attenuating the expression of NLRP3 inflammasome components (ASC, Caspase-1, and IL-1β). Notably, these protective effects were abolished in Nlrp3<sup>-/-</sup> mice, confirming the essential role of NLRP3 in GB1-mediated mitigation of colitis. Furthermore, GB1 reinforced intestinal barrier integrity by preserving tight junctions, reducing permeability, and attenuating mucosal inflammation. Collectively, our findings highlight GB1 as a promising therapeutic candidate for colitis treatment, primarily through NLRP3 inflammasome suppression and intestinal barrier restoration.

International Journal of Molecular SciencesVol. 26(9)
Guangzhou University of Chinese Medicine (CN)
Guangzhou Municipal Science and Technology Project
Openalex Percentile: Top 89%
Barrier Structure and Function Studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

The Effect of GB1 on DSS-Induced Colitis in WT and Nlrp3-/- Mice — Q. Chen, Ru-He Liao, et al. · International Journal of Molecular Sciences (2025) | TGRS Research Map | TGRS