...
首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Inhibition of excitotoxic neuronal death by methanol extract of Acori graminei rhizoma in cultured rat cortical neurons.
【24h】

Inhibition of excitotoxic neuronal death by methanol extract of Acori graminei rhizoma in cultured rat cortical neurons.

机译:在培养的大鼠皮质神经元中,Acori graminei rhizoma甲醇提取物抑制兴奋性神经元死亡。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Acori graminei rhizoma (AGR) are reported to exhibit a number of pharmacological actions in the central nervous system. The effects of the methanol extract of AGR on excitotoxic neuronal death were evaluated in the present study using cultured rat cortical neurons. Based on the phase-contrast microscopic examinations of cultures and lactate dehydrogenase activities measured in the culture media, the glutamate-induced excitotoxicity was significantly inhibited by the extract. The inhibitory action of the extract was more potent and selective for the N-methyl-D-aspartate (NMDA) receptor-mediated toxicity. The AGR extract competed with [3H]MDL 105,519 for the specific binding to the glycine site of the NMDA receptor with the IC(50) value of 164.7 microg/ml. Modulation of the NMDA receptor activity by the extract was determined using [3H]MK-801 binding studies. The reduction of the binding in the presence of the extract indicated the receptor inactivation by AGR. These results demonstrated that the methanol extract of AGR exhibited protective action against excitotoxic neuronal death, and that the neuroprotective action was primarily due to the blockade of NMDA receptor function by the interaction with the glycine binding site of the receptor.
机译:据报道,Acori graminei rhizoma(AGR)在中枢神经系统中表现出许多药理作用。在本研究中,使用培养的大鼠皮层神经元评估了AGR甲醇提取物对兴奋性神经元死亡的影响。基于培养物的相差显微镜检查和在培养基中测量的乳酸脱氢酶活性,谷氨酸诱导的兴奋性毒性被提取物显着抑制。提取物的抑制作用对N-甲基-D-天冬氨酸(NMDA)受体介导的毒性更有效和更具选择性。 AGR提取物与[3H] MDL 105,519竞争与NMDA受体的甘氨酸位点的特异性结合,IC(50)值为164.7 microg / ml。使用[3H] MK-801结合研究确定提取物对NMDA受体活性的调节。在提取物存在下结合的减少表明AGR使受体失活。这些结果表明,AGR的甲醇提取物表现出针对兴奋性神经元死亡的保护作用,并且神经保护作用主要是由于与受体的甘氨酸结合位点的相互作用而阻断了NMDA受体功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号