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(-)-Patchouli alcohol protects against Helicobacter pylori urease-induced apoptosis, oxidative stress and inflammatory response in human gastric epithelial cells.

International immunopharmacology
June 1, 2016
Jianhui Xie et al. (12 authors)
Journal ArticleMolecular Study
Extracted Claims (13)
InterventionDirectionEndpointPopulationDosageImpactClaim #
(-)-Patchouli alcohol (PA)
decrease
cytotoxicity induced by 17.0U/mg HPU
GES-1 cells
-
remarkably ameliorate
#1
(-)-Patchouli alcohol (PA)
decrease
HPU-induced apoptosis
GES-1 cells
-
effectively attenuated
#2
(-)-Patchouli alcohol (PA)
decrease
HPU-induced disruption of MMP
GES-1 cells
-
associated with amelioration
#3
(-)-Patchouli alcohol (PA)
decrease
intracellular ROS
GES-1 cells
-
decreasing contents
#4
(-)-Patchouli alcohol (PA)
decrease
MDA
GES-1 cells
-
decreasing contents
#5
(-)-Patchouli alcohol (PA)
increase
superoxide dismutase (SOD) enzymatic activities
GES-1 cells
-
increasing
#6
(-)-Patchouli alcohol (PA)
increase
catalase (CAT) enzymatic activities
GES-1 cells
-
increasing
#7
(-)-Patchouli alcohol (PA)
decrease
nitric oxide (NO)
HPU-stimulated GES-1 cells
-
markedly attenuated the secretion
#8
(-)-Patchouli alcohol (PA)
decrease
pro-inflammatory cytokines such as interleukin-2 (IL-2)
HPU-stimulated GES-1 cells
-
markedly attenuated the secretion
#9
(-)-Patchouli alcohol (PA)
decrease
pro-inflammatory cytokines such as interleukin-4 (IL-4)
HPU-stimulated GES-1 cells
-
markedly attenuated the secretion
#10
(-)-Patchouli alcohol (PA)
decrease
pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α)
HPU-stimulated GES-1 cells
-
markedly attenuated the secretion
#11
(-)-Patchouli alcohol (PA)
increase
anti-inflammatory cytokine interleukin-13 (IL-13)
HPU-stimulated GES-1 cells
-
elevated
#12
(-)-Patchouli alcohol (PA)
decrease
active urease catalysis conformation
-
-
engaged in the active site of urease bearing nickel ions and interacted with important residues via covalent binding
#13
Abstract

(-)-Patchouli alcohol (PA), the major active principle of Pogostemonis Herba, has been reported to have anti-Helicobacter pylori and gastroprotective effects. In the present work, we aimed to investigate the possible protective effect of PA on H. pylori urease (HPU)-injured human gastric epithelial cells (GES-1) and to elucidate the underlying mechanisms of action. Results showed that pre-treatment with PA (5.0, 10.0, 20.0μM) was able to remarkably ameliorate the cytotoxicity induced by 17.0U/mg HPU in GES-1 cells. Flow cytometric analysis on cellular apoptosis showed that pre-treatment with PA effectively attenuated GES-1 cells from the HPU-induced apoptosis. Moreover, the cytoprotective effect of PA was found to be associated with amelioration of the HPU-induced disruption of MMP, attenuating oxidative stress by decreasing contents of intracellular ROS and MDA, and increasing superoxide dismutase (SOD) and catalase (CAT) enzymatic activities. In addition, pre-treatment with PA markedly attenuated the secretion of nitric oxide (NO) and pro-inflammatory cytokines such as interleukin-2 (IL-2), interleukin-4 (IL-4) and tumor necrosis factor-α (TNF-α), whereas elevated the anti-inflammatory cytokine interleukin-13 (IL-13) in the HPU-stimulated GES-1 cells. Molecular docking assay suggested that PA engaged in the active site of urease bearing nickel ions and interacted with important residues via covalent binding, thereby restricting the active urease catalysis conformation. Our experimental findings suggest that PA could inhibit the cellular processes critically involved in the pathogenesis of H. pylori infection, and its protective effects against the HPU-induced cytotoxicity in GES-1 cells are believed to be associated with its anti-apoptotic, antioxidative, anti-inflammatory and HPU inhibitory actions.

Medical Subject Headings (MeSH)
ApoptosisBacterial ProteinsCatalysisCell LineCytokinesCytoprotectionHelicobacter InfectionsHelicobacter pyloriHumansInflammationIntestinal MucosaOxidative StressPogostemonSesquiterpenesUrease
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Citation Metrics
Total Citations32
Citations/Year3.6
Relative Citation Ratio1.46
NIH Percentile64.2%
Research Impact Scores
APT Score0.05
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