ReferenceID 1853

Evodiamine Inhibits Helicobacter pylori Growth and Helicobacter pylori-Induced Inflammation

Int J Mol Sci

Helicobacter pylori (H. pylori) classified as a class I carcinogen by the World Health Organization (WHO) plays an important role in the progression of chronic gastritis and the development of gastric cancer. A major bio

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Reference Id
1853
Evidence Id
18443
Core Evidence Id
18443
Source Reference Id
3699
Herb2 Reference Id
HBREF004496
Subject Paper Key
HBIN026264_33806161
Pubmed Id
33806161
Doi
10.3390/ijms22073385
Paper Title
Evodiamine Inhibits Helicobacter pylori Growth and Helicobacter pylori-Induced Inflammation
Paper Abstract
Helicobacter pylori (H. pylori) classified as a class I carcinogen by the World Health Organization (WHO) plays an important role in the progression of chronic gastritis and the development of gastric cancer. A major bioactive component of Evodia rutaecarpa, evodiamine, has been known for its anti-bacterial effect and anti-cancer effects. However, the inhibitory effect of evodiamine against H. pylori is not yet known and the inhibitory mechanisms of evodiamine against gastric cancer cells are yet to be elucidated concretely. In this study, therefore, anti-bacterial effect of evodiamine on H. pylori growth and its inhibitory mechanisms as well as anti-inflammatory effects and its mechanisms of evodiamine on H. pylori-induced inflammation were investigated in vitr. Results of this study showed the growth of the H. pylori reference strains and clinical isolates were inhibited by evodiamine. It was considered one of the inhibitory mechanisms that evodiamine downregulated both gene expressions of replication and transcription machineries of H. pylori. Treatment of evodiamine also induced downregulation of urease and diminished translocation of cytotoxin-associated antigen A (CagA) and vacuolating cytotoxin A (VacA) proteins into gastric adenocarcinoma (AGS) cells. This may be resulted from the reduction of CagA and VacA expressions as well as the type IV secretion system (T4SS) components and secretion system subunit protein A (SecA) protein which are involved in translocation of CagA and VacA into host cells, respectively. In particular, evodiamine inhibited the activation of signaling proteins such as the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappaB) and the mitogen-activated protein kinase (MAPK) pathway induced by H. pylori infection. It consequently might contribute to reduction of interleukin (IL)-8 production in AGS cells. Collectively, these results suggest anti-bacterial and anti-inflammatory effects of evodiamine against H. pylori.
Journal
Int J Mol Sci
Publish Year
2021
Experiment Subject
ags cells
Experiment Type
Cell Experiment
Phenotype Related
Helicobacter Pylori; Chronic Gastritis; Gastric Cancer; Gastric Adenocarcinoma
Paper Title Cn
Paper Title En
Evodiamine Inhibits Helicobacter pylori Growth and Helicobacter pylori-Induced Inflammation
Bilingual Status
semi_complete