芍药苷
神经保护
信号转导
激酶
药理学
化学
疾病
蛋白激酶C
发病机制
磷酸化
蛋白激酶A
细胞生物学
生物
中枢神经系统
丝裂原活化蛋白激酶
医学
神经退行性变
作者
Kedong Guo,Yingbo Zhang,Libo Li,Jingyan Zhang,Hua Rong,Deshui Liu,Junping Wang,Ming Jin,Nan Luo,Xiaojie Zhang
出处
期刊:Neuroreport
[Lippincott Williams & Wilkins]
日期:2021-10-21
卷期号:32 (17): 1379-1387
被引量:23
标识
DOI:10.1097/wnr.0000000000001739
摘要
OBJECTIVES: Paeoniflorin, an active component of Radix Paeoniae Alba, has a neuroprotective effect in Parkinson's animal models. However, its mechanism of action remains to be determined. METHODS: In this study, we hypothesized that the neuroprotective effect of paeoniflorin occurs through the α-synuclein/protein kinase C δ subtype (PKC-δ) signaling pathway. We tested our hypothesis in the 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced mouse model of Parkinson's disease. We evaluated the effects of paeoniflorin on the expression levels of signal components of the α-synuclein/PKC-δ pathway, cellular apoptosis and motor performance. RESULTS: Our results demonstrated that paeoniflorin restored the motor performance impairment caused by MPTP, inhibited apoptosis, and protected the ultrastructure of neurons. Paeoniflorin treatment also resulted in the dose-dependent upregulation of an antiapoptotic protein, B-cell lymphoma-2, at the mRNA and protein levels, similar to the effects of the positive control, selegiline. In contrast, paeoniflorin treatment downregulated the expression of pro-apoptotic proteins BCL2-Associated X2, α-synuclein, and PKC-δ at the mRNA and protein levels, as well as the level of the activated form of nuclear factor kappa B (p-NF-κB p65). CONCLUSIONS: Thus, our results showed that paeoniflorin exerts its neuroprotective effect by regulating the α-synuclein/PKC-δ signaling pathway to reduce neuronal apoptosis.
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