TPPU Downregulates Oxidative Stress Damage and Induces BDNF Expression in PC-12 Cells
Autor: | Qiong Wu, Minlin Lin, Peng Wu, Chongyan Zhao, Shuang Yang, Haiying Yu, Wenjiao Xian, Jingfang Song |
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Rok vydání: | 2022 |
Předmět: |
Epoxide Hydrolases
General Immunology and Microbiology Article Subject Caspase 3 Applied Mathematics Brain-Derived Neurotrophic Factor Phenylurea Compounds General Medicine Hydrogen Peroxide General Biochemistry Genetics and Molecular Biology Rats Oxidative Stress Piperidines Modeling and Simulation Animals Enzyme Inhibitors |
Zdroj: | Computational and mathematical methods in medicine. 2022 |
ISSN: | 1748-6718 |
Popis: | Objective. Ischemia-reperfusion is an ongoing clinical challenge that can lead to a series of pathological changes including oxidative stress. The inhibition of soluble epoxide hydrolase inhibitor (sEH) by 1-(1-propanoylpiperidin-4-yl)-3-[4-(trifluoromethoxy)phenyl]urea (TPPU) results in an anti-inflammatory, cardioprotective, and blood vessel growth-promoting effects. Therefore, this study focused on the protective effect of TPPU on a rat pheochromocytoma (PC-12) cell oxidative stress model induced by H2O2. Methods. CCK-8 and Hoechst 33342 were used to evaluate cell apoptosis and western blot to detect the apoptotic proteins and brain-derived neurotrophic factor (BDNF) expression. Result. The incubation with 100 μM, 50 μM, and 25 μM TPPU significantly increased PC-12 cell viability. Epoxyeicosatrienoic acid (EET) pretreatment also protected PC-12 cells from oxidative stress. In addition, TPPU reduced caspase-3 and Bax expression and induced Bcl-2 expression, and EETs exerted the same effect on caspase-3 expression as TPPU. A positive relationship was found between TPPU or EET incubation and BDNF expression. Conclusion. These results revealed that TPPU reduced PC-12 cell oxidative stress injury induced by H2O2 and promoted BDNF expression. |
Databáze: | OpenAIRE |
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