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

被引:25
作者
Lian, D. W. [1 ,4 ,5 ]
Xu, Y. F. [2 ,5 ]
Deng, Q. H. [3 ]
Lin, X. M. [3 ]
Huang, B. [2 ]
Xian, S. X. [1 ,4 ]
Huang, P. [3 ]
机构
[1] Guangzhou Univ Chinese Med, Affiliated Hosp 1, 12 Airport Rd, Guangzhou 510407, Guangdong, Peoples R China
[2] Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Fourth Clin Med Coll, Shenzhen 518033, Guangdong, Peoples R China
[3] Guangzhou Univ Chinese Med, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
[4] Guangzhou Univ Chinese Med, Lingnan Med Res Ctr, Key Lab Chron Heart Failure, Guangzhou 510407, Guangdong, Peoples R China
[5] Guangzhou Univ Chinese Med, Postdoctoral Res Stn, Guangzhou 510006, Guangdong, Peoples R China
基金
美国国家科学基金会; 中国博士后科学基金;
关键词
Helicobacter pylori; Patchouli alcohol; Urease; Macrophage; Phagocytosis; PHAGOCYTOSIS; CELLS;
D O I
10.1016/j.phymed.2019.153097
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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 mu M 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.
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页数:8
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