Korean Medicine (KM)-Application Center, Korea Institute of Oriental Medicine (KIOM), 70 Cheomdan-ro, Dong-gu, Daegu, 701-300, Republic of Korea.
Mol Neurobiol. 2018 Jun;55(6):4650-4666. doi: 10.1007/s12035-017-0652-x. Epub 2017 Jul 13.
Neuronal apoptotic cell death plays an important role in many neurological disorders, including Alzheimer's disease, Parkinson's disease, and ischemic stroke. Spatholobi Caulis (SC) has been widely used in traditional herbal medicine for the treatment of cancer, inflammation, viral infection, and anemia. However, the protective effects of SC extract (SCE) against apoptotic cell death in the brain have not been reported. We investigated the protective effects of SCE against neuronal injury etoposide-induced neurotoxicity and in rats subjected to focal transient ischemic stroke middle cerebral artery occlusion (MCAO) for 45 min, followed by 7 days of reperfusion. The in vitro study demonstrated that SCE protected cells against etoposide-induced cell viability loss in SH-SY5Y cells. Apoptotic phenotypes, such as cleaved PARP and caspase-3, and oxidative stress in etoposide-treated cells were ameliorated by SCE treatment. In MCAO-reperfusion injury, SCE promoted neuronal survival and level of brain-derived neurotrophic factor (BDNF) by reducing glial activation, oxidative stress, and apoptosis in the ipsilateral cortex. These results indicated that SCE exerted protective effects under etoposide treatment and in a MCAO-reperfusion model by reducing JNK and p38 MAPK activation. This study presents the first evidence that SCE has therapeutic potential for the treatment of ischemic stroke or neurological disorder-related cell death.
神经元凋亡性细胞死亡在许多神经紊乱疾病中起着重要作用,包括阿尔茨海默病、帕金森病和缺血性中风。鸡血藤(SC)在传统草药中被广泛用于治疗癌症、炎症、病毒感染和贫血。然而,SC 提取物(SCE)对大脑中凋亡性细胞死亡的保护作用尚未报道。我们研究了 SCE 对依托泊苷诱导的神经毒性的神经保护作用,以及在大脑中动脉闭塞(MCAO)45 分钟后再灌注 7 天的大鼠中的作用。体外研究表明,SCE 可保护 SH-SY5Y 细胞免受依托泊苷诱导的细胞活力丧失。SCE 处理可改善依托泊苷处理细胞中的凋亡表型,如 PARP 和 caspase-3 的裂解,以及氧化应激。在 MCAO 再灌注损伤中,SCE 通过减少同侧皮质中的神经胶质激活、氧化应激和细胞凋亡,促进神经元存活和脑源性神经营养因子(BDNF)水平。这些结果表明,SCE 通过减少 JNK 和 p38 MAPK 的激活,在依托泊苷处理和 MCAO 再灌注模型中发挥保护作用。本研究首次证明 SCE 具有治疗缺血性中风或与神经紊乱相关的细胞死亡的潜力。