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Effect of patchouli alcohol on macrophage mediated Helicobacter pylori digestion based on intracellular urease inhibition.

Phytomedicine : international journal of phytotherapy and phytopharmacology
December 1, 2019
D W Lian et al. (7 authors)
Journal ArticleMolecular Study
Extracted Claims (8)
InterventionDirectionEndpointPopulationDosageImpactClaim #
patchouli alcohol (PA)
decrease
intracellular H. pylori urease activity
H. pylori
25 and 50 μM
inhibited
#1
patchouli alcohol (PA)
no change
isolated urease activity
H. pylori
-
did not inhibit
#2
patchouli alcohol (PA)
decrease
gene expression levels of ureB, ureE, ureI and nixA
H. pylori
-
down-regulating
#3
patchouli alcohol (PA)
decrease
protein expression level of UreB
H. pylori
-
reducing
#4
patchouli alcohol (PA)
decrease
acid resistance of H. pylori
H. pylori
-
inhibiting
#5
patchouli alcohol (PA)
increase
function of macrophage bacterial digestion
RAW264.7 macrophage cells
-
recovered
#6
patchouli alcohol (PA)
decrease
intracellular H. pylori urease function and maturation
H. pylori
-
suppressed
#7
patchouli alcohol (PA)
increase
macrophage digestion ability
RAW264.7 macrophage cells
-
increased
#8
Abstract

BACKGROUND: Helicobacter pylori infects almost half of the world population and is listed as a type I carcinoma factor since 1994. Pogostemon cablin (Blanco) Benth. (Labiatae) has been used to treat gastro-intestinal diseases for thousands of years in many east Asian countries, and the key ingredient, patchouli alcohol (PA), has been observed to exert anti-H. pylori and anti-urease activities. PURPOSE: We investigated the effect of PA on H. pylori urease and its subsequent influence on macrophage phagosome maturation and function. METHODS: In H. pylori experiment, the berthelot method and pH shock assay were adopted to evaluate the effect of PA on extracellular and intracellular H. pylori urease. And then, Q-PCR and Western blot were carried out to analyze the alterations in the expression of urease-related genes and proteins after PA treatment. In the H. pylori and macrophage cell (RAW264.7) co-culture experiment, the effects of PA on H. pylori-induced phagocytosis and intracellular killing of RAW264.7 were investigated using gentamycin protection assay, and the underlying mechanism was explored by immunofluorescence. RESULTS: PA at 25 and 50 μM inhibited intracellular H. pylori urease activity but not isolated urease by down-regulating the gene expression levels of ureB, ureE, ureI and nixA and reducing the protein expression level of UreB, thereby inhibiting the acid resistance of H. pylori. PA also recovered the function of macrophage bacterial digestion, and prior treatment with ammonium chloride inhibited the efficacy of PA. CONCLUSION: PA suppressed intracellular H. pylori urease function and maturation, which increased macrophage digestion ability.

Medical Subject Headings (MeSH)
AnimalsAnti-Bacterial AgentsBacterial ProteinsEnzyme InhibitorsGene Expression Regulation, BacterialHelicobacter InfectionsHelicobacter pyloriMacrophagesMicePhagocytosisRAW 264.7 CellsSesquiterpenesUrease
Study Links
Citation Metrics
Total Citations17
Citations/Year2.8
Relative Citation Ratio1.17
NIH Percentile56%
Research Impact Scores
APT Score0.05
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