Oxygen-glucose deprivation activates 5-lipoxygenase mediated by oxidative stress through the p38 mitogen-activated protein kinase pathway in PC12 cells

✍ Scribed by Cheng-Tan Li; Wei-Ping Zhang; Yun-Bi Lu; San-Hua Fang; Yu-Mei Yuan; Ling-Ling Qi; Li-Hui Zhang; Xiao-Jia Huang; Lei Zhang; Zhong Chen; Er-Qing Wei

• Publisher: John Wiley and Sons
• Year: 2009
• Tongue: English
• Weight: 842 KB
• Volume: 87
• Category: Article
• ISSN: 0360-4012
• DOI: 10.1002/jnr.21913

✦ Synopsis

Abstract

5‐Lipoxygenase (5‐LOX) is a key enzyme catalyzing arachidonic acid to form leukotrienes. We have reported that ischemic‐like injury activates 5‐LOX in PC12 cells; however, the mechanisms are unknown. To determine whether ischemic‐like injury activates 5‐LOX mediated by oxidative stress through the p38 MAPK pathway, we transfected GFP‐5‐LOX into PC12 cells and induced ischemic‐like injury by oxygen‐glucose deprivation (OGD). We found that the transfected GFP‐5‐LOX was localized primarily in the nuclei and translocated to the nuclear envelope after OGD/recovery reaching a maximum 2 hr after a 2‐hr exposure to OGD. The nonselective 5‐LOX inhibitor caffeic acid, 5‐LOX‐activating protein inhibitor MK886, and selective 5‐LOX inhibitor zileuton attenuated the cell injury and reduced the production of 5‐LOX products, cysteinyl leukotrienes, after OGD/recovery. However, only caffeic acid inhibited OGD/recovery‐induced 5‐LOX translocation. OGD/recovery also increased reactive oxygen species (ROS), which was inhibited by caffeic acid only. Hydrogen peroxide, an exogenous ROS, evoked similar cell injury and 5‐LOX translocation, and the inhibitors had effects on the changes after H~2~O~2~ similar to those after OGD/recovery. Both OGD/recovery and H~2~O~2~ increased the phosphorylated p38 MAPK level, which was inhibited by caffeic acid and the ROS scavenger edaravone, but not by MK886 or zileuton. Moreover, SB203580 (a p38 MAPK inhibitor) and edaravone inhibited the cell injury and 5‐LOX translocation induced by OGD/recovery and H~2~O~2~. Thus, we conclude that OGD/recovery‐induced ischemic‐like injury induces 5‐LOX activation, which is mediated by oxidative stress through activating the p38 MAPK pathway. © 2008 Wiley‐Liss, Inc.