Department of Clinical Nursing, Nursing and Health College of Zhengzhou University, Zhengzhou, Henan, China (mainland).
Department of Public Nursing, Nursing and Health College of Zhengzhou University, Zhengzhou, Henan, China (mainland).
Med Sci Monit. 2020 Feb 1;26:e920325. doi: 10.12659/MSM.920325.
BACKGROUND Cerebral ischemia-reperfusion injury (CIRI) remains a serious health problem. Centella asiatica formulations are used to treat central nervous system disorders. In the present study, asiaticoside, an extract of the plant Centella asiatica, was investigated in CIRI in vivo and vitro. MATERIAL AND METHODS We made a CIRI model in vivo in SD rats treated by middle cerebral artery occlusion, and a cell model of ischemia-reperfusion injury was made in PC12 cells treated by deprivation of oxygen and glucose/restoration. CIRI in vivo was assessed by scores of neurological functions, encephaledema, and cerebral infarction area. Inflammation level and oxidative stress level were detected by the appropriate kits. TUNEL assay was performed for assessment of cell apoptosis and Western blot analysis was performed to assess protein expression levels. CCK8 assay was performed for evaluation of cell survival and flow cytometer was used to detect cell apoptosis in vitro. RESULTS Nervous function injury, brain edema, cell apoptosis, infarct size, apoptosis-related protein expressions, and protein expressions of the NOD2/MAPK/NF-kappaB signaling pathway in the CIRI model were all reversed by asiaticoside in rats. The cell apoptosis, inflammation level, and oxidative stress level in the model of cerebral ischemia-reperfusion injury were reduced by asiaticoside. The effects of asiaticoside on CIRI were reversed by NOD 2 agonists. CONCLUSIONS Asiaticoside showed a protective effect against cerebral ischemia-reperfusion injury via the NOD2/MAPK/NF-kappaB signaling pathway. These findings are vital for future research on use of asiaticoside in CIRI, providing a new avenue for alleviating CIRI.
脑缺血再灌注损伤(CIRI)仍然是一个严重的健康问题。积雪草制剂用于治疗中枢神经系统疾病。在本研究中,研究了植物积雪草的提取物积雪草苷在体内和体外的 CIRI 中的作用。
我们在 SD 大鼠中通过大脑中动脉闭塞制作 CIRI 模型,并通过缺氧和葡萄糖剥夺/恢复处理 PC12 细胞制作缺血再灌注损伤模型。通过神经功能评分、脑水肿和脑梗死面积评估体内 CIRI。通过适当的试剂盒检测炎症水平和氧化应激水平。通过 TUNEL 检测评估细胞凋亡,通过 Western blot 分析评估蛋白表达水平。通过 CCK8 测定评估细胞存活,通过流式细胞仪检测细胞凋亡。
神经功能损伤、脑水肿、细胞凋亡、梗死面积、凋亡相关蛋白表达以及 NOD2/MAPK/NF-κB 信号通路蛋白表达在 CIRI 模型中均被积雪草苷逆转。积雪草苷降低了脑缺血再灌注损伤模型中的细胞凋亡、炎症水平和氧化应激水平。NOD2 激动剂逆转了积雪草苷对 CIRI 的作用。
积雪草苷通过 NOD2/MAPK/NF-κB 信号通路对脑缺血再灌注损伤具有保护作用。这些发现对未来积雪草苷在 CIRI 中的应用研究具有重要意义,为减轻 CIRI 提供了新的途径。