<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hwang S</submitter><funding>NRF-2017-Fostering Core Leaders of the Future Basic Science Program/Global Ph.D. Fellowship Program</funding><funding>National Research Foundation of Korea</funding><pagination>E4560</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6770904</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(18)</volume><pubmed_abstract>Enterotoxigenic Bacteroides fragilis (ETBF) is human intestinal commensal bacterium and a potent initiator of colitis through secretion of the metalloprotease Bacteroides fragilis toxin (BFT). BFT induces cleavage of E-cadherin in colon cells, which subsequently leads to NF-κB activation. Zerumbone is a key component of the Zingiber zerumbet (L.) Smith plant and can exhibit anti-bacterial and anti-inflammatory effects. However, whether zerumbone has anti-inflammatory effects in ETBF-induced colitis remains unknown. The aim of this study was to determine the anti-inflammatory effect of orally administered zerumbone in a murine model of ETBF infection. Wild-type C57BL/6 mice were infected with ETBF and orally administered zerumbone (30 or 60 mg/kg) once a day for 7 days. Treatment of ETBF-infected mice with zerumbone prevented weight loss and splenomegaly and reduced colonic inflammation with decreased macrophage infiltration. Zerumbone treatment significantly decreased expression of IL-17A, TNF-α, KC, and inducible nitric oxide synthase (iNOS) in colonic tissues of ETBF-infected mice. In addition, serum levels of KC and nitrite was also diminished. Zerumbone-treated ETBF-infected mice also showed decreased NF-κB signaling in the colon. HT29/C1 colonic epithelial cells treated with zerumbone suppressed BFT-induced NF-κB signaling and IL-8 secretion. However, BFT-mediated E-cadherin cleavage was unaffected. Furthermore, zerumbone did not affect ETBF colonization in mice. In conclusion, zerumbone decreased ETBF-induced colitis through inhibition of NF-κB signaling.</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Zerumbone Suppresses Enterotoxigenic Bacteroides fragilis Infection-Induced Colonic Inflammation through Inhibition of NF-κΒ.</pubmed_title><pmcid>PMC6770904</pmcid><funding_grant_id>2017-52-0078</funding_grant_id><funding_grant_id>2017R1D1A1A02018088</funding_grant_id><funding_grant_id>2017H1A2A1045727</funding_grant_id><pubmed_authors>Jo M</pubmed_authors><pubmed_authors>Park CO</pubmed_authors><pubmed_authors>Hong JE</pubmed_authors><pubmed_authors>Yun M</pubmed_authors><pubmed_authors>Hwang S</pubmed_authors><pubmed_authors>Lee CG</pubmed_authors><pubmed_authors>Rhee KJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Zerumbone Suppresses Enterotoxigenic Bacteroides fragilis Infection-Induced Colonic Inflammation through Inhibition of NF-κΒ.</name><description>Enterotoxigenic Bacteroides fragilis (ETBF) is human intestinal commensal bacterium and a potent initiator of colitis through secretion of the metalloprotease Bacteroides fragilis toxin (BFT). BFT induces cleavage of E-cadherin in colon cells, which subsequently leads to NF-κB activation. Zerumbone is a key component of the Zingiber zerumbet (L.) Smith plant and can exhibit anti-bacterial and anti-inflammatory effects. However, whether zerumbone has anti-inflammatory effects in ETBF-induced colitis remains unknown. The aim of this study was to determine the anti-inflammatory effect of orally administered zerumbone in a murine model of ETBF infection. Wild-type C57BL/6 mice were infected with ETBF and orally administered zerumbone (30 or 60 mg/kg) once a day for 7 days. Treatment of ETBF-infected mice with zerumbone prevented weight loss and splenomegaly and reduced colonic inflammation with decreased macrophage infiltration. Zerumbone treatment significantly decreased expression of IL-17A, TNF-α, KC, and inducible nitric oxide synthase (iNOS) in colonic tissues of ETBF-infected mice. In addition, serum levels of KC and nitrite was also diminished. Zerumbone-treated ETBF-infected mice also showed decreased NF-κB signaling in the colon. HT29/C1 colonic epithelial cells treated with zerumbone suppressed BFT-induced NF-κB signaling and IL-8 secretion. However, BFT-mediated E-cadherin cleavage was unaffected. Furthermore, zerumbone did not affect ETBF colonization in mice. In conclusion, zerumbone decreased ETBF-induced colitis through inhibition of NF-κB signaling.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Sep</publication><modification>2025-04-04T10:33:20.338Z</modification><creation>2019-11-07T08:06:42Z</creation></dates><accession>S-EPMC6770904</accession><cross_references><pubmed>31540059</pubmed><doi>10.3390/ijms20184560</doi></cross_references></HashMap>