...
首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Arachidonic acid and lysophosphatidylcholine modulate excitatory transmitter amino acid release from the rat cerebral cortex.
【24h】

Arachidonic acid and lysophosphatidylcholine modulate excitatory transmitter amino acid release from the rat cerebral cortex.

机译:花生四烯酸和溶血磷脂酰胆碱调节从大鼠大脑皮层释放的兴奋性递质氨基酸。

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

The involvement of phospholipase A2 (PLA2) products in ischemia-evoked release of excitatory neurotransmitter amino acids (EAAs) from the cerebral cortex was studied in a four vessel occlusion rat model of cerebral ischemia/reperfusion. In comparison with untreated animals, arachidonic acid (AA; 5 x 10(-7) M to 5 x 10(-5) M) significantly reduced the ischemia-evoked efflux of glutamate and aspartate into cortical superfusates. Direct application of lysophosphatidylcholine (LysoPC; 55.4 micrograms/ml) to the cerebral cortex of non-ischemic animals resulted in a significant increase in glutamate levels. These results indicate that the immediate products of PLA2 action on plasma membrane phospholipids can either enhance or inhibit excitotoxic amino acid release following cerebral ischemia. The effect of AA is likely to be a result of its ability to inhibit PLA2; that of LysoPC, a consequence of its detergent action.
机译:在脑缺血/再灌注的四血管阻塞大鼠模型中研究了磷脂酶A2(PLA2)产物参与缺血诱发的大脑皮层兴奋性神经递质氨基酸(EAA)的释放。与未经处理的动物相比,花生四烯酸(AA; 5 x 10(-7)M到5 x 10(-5)M)显着降低了缺血诱发的谷氨酸和天冬氨酸向皮质超融合产物的外排。将溶血磷脂酰胆碱(LysoPC; 55.4微克/毫升)直接应用到非缺血性动物的大脑皮层会导致谷氨酸水平显着增加。这些结果表明,PLA2对质膜磷脂作用的直接产物可以增强或抑制脑缺血后兴奋性毒性氨基酸的释放。 AA的作用可能是其抑制PLA2的能力的结果。这是LysoPC的清洁剂作用的结果。

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