4.7 Article

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

Journal

INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 35, Issue -, Pages 43-52

Publisher

ELSEVIER
DOI: 10.1016/j.intimp.2016.02.022

Keywords

Patchouli alcohol; Helicobacter pylori urease; Human gastric epithelial cells; Apoptosis; Oxidative; Inflammatory

Funding

  1. Guangdong International Cooperation Project [2012B050300002]
  2. National Science Foundation of China [81374043, 81173534, 81503202]
  3. Guangdong Natural Science Foundation [2015 A030310217]
  4. Science and Technology Planning Project of Guangdong Province [2014A020221042]
  5. Science and Technological Program for Dongguan's Higher Education, Science and Research, and Health Care Institutions [2012105102009]
  6. Ph.D. Programs Foundation of Ministry of Education of China [20134425110009]
  7. Science and Technology Innovation Project of Guangdong Provincial Department of Education [2013KJCX0045]
  8. Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme
  9. Special Funds from Central Finance of China in Support of the Development of Local Colleges and University - Educational finance Grant [276(2014)]

Ask authors/readers for more resources

(-)-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, 20.0 mu M) was able to remarkably ameliorate the cytotoxicity induced by 17.0 U/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-alpha (TNF-alpha), 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 antiapoptotic, antioxidative, anti-inflammatory and HPU inhibitory actions. (C) 2016 Published by Elsevier B.V.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available