Hu Rong, Yin Chang-lin, Wu Nan, Cui Gao-yu, Meng Hui, Wu Xi-gui, Luo Hai-shui, Gang Tian, Hu Shengli, Shi Jiantao, Lin Jiang-kai, Feng Hua
Department of Neurosurgery, Southwest Hospital, Third Military Medical University, Gaotanyan 29, Chongqing 400038, People's Republic of China.
J Ethnopharmacol. 2009 Jan 30;121(3):444-50. doi: 10.1016/j.jep.2008.09.035. Epub 2008 Oct 19.
Traditional Chinese herb Dihuang Yinzi (DY) is well known to treat neurological diseases by traditional Chinese medical practitioners. This study is to elucidate its neuroprotective and anti-dementia role in ischemic brain injury.
The effects of DY on the pathohistological changes, lactate dehydrogenase (LDH) release, Morris water maze task, expression of synaptophysin (SYP) and extracellular signal-regulated protein kinase (ERK) of hippocampi of rats with ischemic brain injury were investigated.
This study showed that DY not only significantly decreased the number of TUNEL-positive cells but also reduced the LDH release of hippocampus of model rat. Morris water maze test showed that the ability of learning and memory of rats dramatically impaired after ischemic brain injury. However, DY ameliorated the impairment of learning and memory of ischemic rats. Furthermore, western blotting and immunohistochemical data showed that the expression of extracellular regulated protein and synaptophysin, which correlates with synaptic formation and function, decreased after ischemic insult. However, DY inhibited the reduction of ERK an SYP expression in a dose-dependent way.
These results suggest that DY possesses neuroprotective and anti-dementia properties, at least in part, by preventing the loss of neural cells and synapses in ischemic brain injury.
中医从业者熟知传统中药地黄饮子(DY)可治疗神经系统疾病。本研究旨在阐明其在缺血性脑损伤中的神经保护和抗痴呆作用。
研究了DY对缺血性脑损伤大鼠海马的病理组织学变化、乳酸脱氢酶(LDH)释放、莫里斯水迷宫任务、突触素(SYP)表达及细胞外信号调节蛋白激酶(ERK)的影响。
本研究表明,DY不仅显著减少了TUNEL阳性细胞数量,还降低了模型大鼠海马的LDH释放。莫里斯水迷宫试验表明,缺血性脑损伤后大鼠的学习记忆能力显著受损。然而,DY改善了缺血大鼠的学习记忆损伤。此外,蛋白质印迹法和免疫组化数据显示,与突触形成和功能相关的细胞外调节蛋白和突触素的表达在缺血损伤后降低。然而,DY以剂量依赖的方式抑制了ERK和SYP表达的降低。
这些结果表明,DY至少部分通过防止缺血性脑损伤中神经细胞和突触的丢失而具有神经保护和抗痴呆特性。