Chen Ahong, Wang Hongyun, Zhang Yuqin, Wang Xiaoying, Yu Lishuang, Xu Wen, Xu Wei, Lin Yu
College of Pharmacy of Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian 350122, P.R. China.
Int J Mol Med. 2017 Sep;40(3):825-833. doi: 10.3892/ijmm.2017.3076. Epub 2017 Jul 20.
Paeoniflorin (PF) is an active ingredient of Radix Paeoniae, which is known to exert neuroprotective effects. However, the mechanims behind the neuroprotective effects of PF are not yet fully understood. The apoptosis of neurons plays an important role in the cerebral ischemia-induced cascade response. This study aimed to investigate neuroprotective effects of PF against glutamate‑induced PC12 cellular cytotoxicity and to determine whether these effects are mediated via the inhibition of apoptosis in vitro and the activity of mitochondrial apoptosis-associated proteins in PC12 cells. Exposure of the PC12 cells to glutamate induced cell morphological changes, significantly decreased cell viability and induced apoptosis, with similar results being observed from the Hoechst 33342 staining and Annexin V/PI staining experiments. Glutamate also increased the lactate dehydrogenase release by the PC12 cells. However, treatment with PF prevented these effects. Furthermore, PF inhibited Bax and Bad expression and increased Bcl-2 and Bcl-xL expression; it also decreased the levels of downstream protein (caspase-3 and caspase-9). Collectively, our results indicate that PF protects PC12 cells against glutamate-induced neurotoxicity possibly through the inhibition of the expression of mitochondrial apoptosis-associated proteins.
芍药苷(PF)是芍药根的一种活性成分,已知其具有神经保护作用。然而,PF神经保护作用背后的机制尚未完全明确。神经元凋亡在脑缺血诱导的级联反应中起重要作用。本研究旨在探讨PF对谷氨酸诱导的PC12细胞毒性的神经保护作用,并确定这些作用是否通过体外抑制PC12细胞凋亡及线粒体凋亡相关蛋白的活性介导。PC12细胞暴露于谷氨酸会诱导细胞形态变化,显著降低细胞活力并诱导凋亡,Hoechst 33342染色和Annexin V/PI染色实验也观察到类似结果。谷氨酸还增加了PC12细胞乳酸脱氢酶的释放。然而,PF处理可防止这些效应。此外,PF抑制Bax和Bad表达并增加Bcl-2和Bcl-xL表达;它还降低了下游蛋白(caspase-3和caspase-9)的水平。总体而言,我们的结果表明,PF可能通过抑制线粒体凋亡相关蛋白的表达来保护PC12细胞免受谷氨酸诱导的神经毒性。