Protective mechanism of kaempferol against Aβ 25-35 -mediated apoptosis of pheochromocytoma (PC-12) cells through the ER/ERK/MAPK signalling pathway

• Published in: Archives of medical science Vol. 17; no. 2; p. 406
• Main Authors: Zhang, Ning, Xu, Hongdan, Wang, Yueying, Yao, Yuan, Liu, Guoliang, Lei, Xia, Sun, Huifeng, Wu, Xiuhong, Li, Jianmin
• Format: Journal Article
• Language: English
• Published: Poland 2021
• Subjects: Alzheimer’s disease; kaempferol; MAPK signalling pathway; pheochromocytoma; oestrogen receptors
• ISSN: 1734-1922

Progressive accumulation of amyloid-β (Aβ) is a pathological trait of Alzheimer's disease (AD). Amyloid-β increases free radical production in neuronal cells, leading to neuronal cell death. Hormone replacement therapy can reduce the incidence of AD, and oestrogen significantly improves the clinical signs in patients with AD. However, the long-term use of oestrogen causes a variety of diseases. Phytoestrogens have been reported to bind and activate oestrogen receptors in mammals and humans to produce oestrogen-like or anti-oestrogen-like effects. Kaempferol is a flavonoid phytoestrogen that can produce a certain protective effect in neurons. However, the molecular mechanism of kaempferol in AD is unclear. This study used pheochromocytoma (PC-12) cells that were damaged by Aβ as an model of AD, and oestradiol was a positive control. The cells were incubated with kaempferol alone or in combination with fulvestrant (an antagonist of ER) and U0126 (an inhibitor of ERK) in Aβ culture. Cell activity was measured by the MTT method. Cell apoptosis was evaluated by flow cytometry. Gene and protein expression levels were tested by qRT-PCR and Western blotting. This study demonstrated that kaempferol protected PC-12 cells from Aβ -induced cell death and apoptosis in a dose-dependent manner. Treatment with fulvestrant (an antagonist of ER) and U0126 (an inhibitor of ERK) significantly increased the apoptosis of PC-12 cells. Moreover, kaempferol promoted the expression of anti-apoptotic molecules and inhibited the expression of pro-apoptotic molecules, which were blocked by fulvestrant and U0126. Kaempferol protected PC-12 cells against Aβ -induced cell apoptosis through the ER/ERK/MAPK signalling pathway.