首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Neuroprotective effects of a standardized extract of Diospyros kaki leaves on MCAO transient focal cerebral ischemic rats and cultured neurons injured by glutamate or hypoxia.
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Neuroprotective effects of a standardized extract of Diospyros kaki leaves on MCAO transient focal cerebral ischemic rats and cultured neurons injured by glutamate or hypoxia.

机译:柿叶标准化提取物对MCAO短暂性局灶性脑缺血大鼠和受谷氨酸或低氧损伤的培养神经元的神经保护作用。

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Naoxinqing (NXQ, a standardized extract of Diospyros kaki leaves) is a patented and approved drug of Traditional Chinese Medicine (TCM) used for the treatment of apoplexy syndrome for years in China, but its underlying mechanism remains to be further elucidated. The present study investigates the effects of NXQ against focal ischemia/reperfusion injury induced by middle cerebral artery occlusion (MCAO) in rats and against glutamate-induced cell injury of hippocampal neurons as well as against hypoxia injury of cortical neurons. Oral administrations of NXQ at 20, 40, 80 mg/kg/day for 7 days (3 days before MCAO and 4 days after MCAO) significantly reduced the lesion of the insulted brain hemisphere and improved the neurological behavior of the rats. In primary rat hippocampal neuron cultures, treatment with NXQ at 5 - 20 microg mL concentration protects the neurons against glutamate-induced excitotoxic death in a dose-dependent manner. In primary rat cerebral cortical neuron cultures, pretreatment with 5- 100 microg/mL NXQ also attenuates hypoxia-reoxygen induced neuron death and apoptosis in a dose-dependent manner. These results suggest that NXQ significantly protects the rats from MCAO ischemic injury in vivo and the hippocampal neurons from glutamate-induced excitotoxic injury as well as cortical neurons from hypoxia injury in vitro by synergistic mechanisms involving its antioxidative effects. NXQ:Naoxinqing CNS:central nervous system MCAO:middle cerebral artery occlusion I/R:ischemia and reperfusion.
机译:脑辛清(NXQ,柿叶的标准提取物)是在中国多年用于中风综合征治疗的已获专利和批准的中药(TCM),但其潜在机制仍有待进一步阐明。本研究研究了NXQ对大鼠大脑中动脉闭塞(MCAO)引起的局灶性缺血/再灌注损伤,谷氨酸诱导的海马神经元细胞损伤以及皮质神经元缺氧损伤的作用。 NXQ口服给药20、40、80 mg / kg / day的时间为7天(MCAO之前3天,MCAO之后4天),可显着减轻所损伤的大脑半球的病变并改善大鼠的神经行为。在原代大鼠海马神经元培养物中,以5-20微克/毫升的浓度进行NXQ处理可保护神经元免受谷氨酸诱导的兴奋性毒性死亡,并呈剂量依赖性。在原代大鼠大脑皮层神经元培养物中,用5-100微克/毫升NXQ进行预处理也以剂量依赖的方式减弱了缺氧-复氧诱导的神经元死亡和细胞凋亡。这些结果表明,NXQ通过涉及其抗氧化作用的协同机制,可显着保护大鼠免受MCAO体内缺血性损伤,并保护海马神经元免受谷氨酸诱导的兴奋性毒性损伤,并使皮质神经元免受缺氧损伤。 NXQ:脑心清中枢神经系统:中枢神经系统MCAO:大脑中动脉闭塞I / R:缺血和再灌注。

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