Department of Neurosurgery, Tong Liao City Hospital of Inner Mongolia Autonomous Region, TongLiao 028000, China.
Department of Neurosurgery, the Second Affiliated Hospital of Henan University of Science and Technology, Luoyang 471000, China.
Int J Biol Macromol. 2020 Aug 15;157:759-768. doi: 10.1016/j.ijbiomac.2020.01.180. Epub 2020 Jan 24.
In the present study, we investigated the neuroprotective effects of a purified Corydalis yanhusuo polysaccharide (CYP) on Aβ -induced neurotoxicity and explored its underlying molecular mechanisms in PC12 cells. The results showed pretreatment with CYP (25, 50, and 100 μg/ml) prior to Aβ exposure significantly protected PC12 cells from Aβ -induced cell death, lactate dehydrogenase (LDH) release, DNA fragmentation, mitochondrial dysfunction and mitochondrial cytochrome c release. Moreover, Aβ -induced increase of ratio between Bax and Bcl-2 protein expression was dramatically reversed by CYP pretreatment. Furthermore, the addition of CYP led to a significant repressing effect on the elevated protein expression of cleaved caspase-8, caspase-9, and caspase-3 in Aβ -treated PC12 cells. Taken together, these findings indicated that protective effect of CYP against Aβ -induced toxicity in PC12 cells was probably mediated by inhibition of apoptosis via both mitochondrial apoptotic pathway and death receptor pathway.
在本研究中,我们研究了一种纯化的延胡索乙素多糖(CYP)对 Aβ 诱导的神经毒性的神经保护作用,并探讨了其在 PC12 细胞中的潜在分子机制。结果表明,在 Aβ 暴露前用 CYP(25、50 和 100μg/ml)预处理可显著保护 PC12 细胞免受 Aβ 诱导的细胞死亡、乳酸脱氢酶(LDH)释放、DNA 片段化、线粒体功能障碍和线粒体细胞色素 c 释放。此外,CYP 预处理可显著逆转 Aβ 诱导的 Bax 和 Bcl-2 蛋白表达比值的增加。此外,CYP 的加入对 Aβ 处理的 PC12 细胞中 cleaved caspase-8、caspase-9 和 caspase-3 蛋白表达的升高有显著的抑制作用。综上所述,这些发现表明 CYP 对 PC12 细胞中 Aβ 诱导的毒性的保护作用可能是通过抑制线粒体凋亡途径和死亡受体途径的细胞凋亡来介导的。