Effect of Quercetin on PC12 Alzheimer’s Disease Cell Model Induced by Aβ25-35 and Its Mechanism Based on Sirtuin1/Nrf2/HO-1 Pathway
Autor: | Yicai Li, Xinjun Yu, Xiaohua Mu |
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Rok vydání: | 2020 |
Předmět: |
Article Subject
Cell Survival NF-E2-Related Factor 2 Aché Models Neurological PC12 Cells Neuroprotection General Biochemistry Genetics and Molecular Biology chemistry.chemical_compound Sirtuin 1 Western blot Alzheimer Disease medicine Animals Amyloid beta-Peptides General Immunology and Microbiology medicine.diagnostic_test Chemistry Cell growth General Medicine medicine.disease Molecular biology Peptide Fragments language.human_language Rats Mechanism of action Heme Oxygenase (Decyclizing) Toxicity language Medicine Quercetin medicine.symptom Alzheimer's disease Research Article Signal Transduction |
Zdroj: | BioMed Research International BioMed Research International, Vol 2020 (2020) |
ISSN: | 2314-6141 2314-6133 |
DOI: | 10.1155/2020/8210578 |
Popis: | Objective. This study is aimed at studying the effect of quercetin on the Alzheimer disease cell model induced by Aβ25-35 in PC12 cells and its mechanism of action. Methods. The AD cell model was established by Aβ25-35. Quercetin was used at different concentrations (0, 10, 20, 40, and 80 μmol/L). The morphology of cells was observed, and the effect on cell survival rate was detected by the MTT method. Cell proliferation was detected by the SRB method. The contents of LDH, SOD, MDA, GSH-Px, AChE, CAT, and T-AOC were detected by kits. The expression of sirtuin1/Nrf2/HO-1 was detected by RT-qPCR and Western blot. Results. PC12 cells in the control group grew quickly and adhered well to the wall, most of which had extended long axons and easily grew into clusters. In the model group, cells were significantly damaged and the number of cells was significantly reduced. It was found that PC12 cells were swollen, rounded, protruding, and retracting, with reduced adherent function and floating phenomenon. Quercetin could increase the survival rate and proliferation rate of PC12 cells; reduce the levels of LDH, AChE, MDA, and HO-1 protein; and increase the levels of SOD, GSH-Px, CAT, T-AOC, sirtuin1, and Nrf2 protein. Conclusion. Quercetin can increase the survival rate of PC12 injured by Aβ25-35, promote cell proliferation, and antagonize the toxicity of Aβ; it also has certain neuroprotective effects. Therefore, quercetin is expected to become a drug for the treatment of AD. |
Databáze: | OpenAIRE |
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