Liu D M, Wu J N, Chiou A L, Liu J Y, Wang Y
Department of Pharmacology, National Defense Medical Center, Taipei, Taiwan, ROC.
Neurosci Lett. 1997 Feb 28;223(3):145-8. doi: 10.1016/s0304-3940(97)13431-0.
We and others have previously reported that N-methyl-D-aspartate (NMDA) induces nitric oxide (NO) release from the rat cerebral cortex in vivo. It is crucial to determine if this phenomenon also exists in human brain tissue. In this study, we investigated the interactions of NMDA and NO in human primary neocortical cell cultures obtained from elective abortions. Extracellular NO concentration was monitored through Nafion- and porphyrine-coated carbon fiber electrodes, which have previously been demonstrated sensitive and selective responses to NO. We found that local application of NMDA induced NO release from neocortical neuron-enriched cultures but not from glial cultures. Pretreatment with NG-nitro-L-arginine methyl ester hydrochloride (L-NAME), a nitric oxide synthase inhibitor, or MK801 significantly attenuated NMDA-induced NO overflow. This is the first time, to our knowledge, that extracellular NO concentration evoked by exogenous NMDA has been directly measured from the fetal human cortical neurons.
我们及其他研究人员之前曾报道,N-甲基-D-天冬氨酸(NMDA)可在体内诱导大鼠大脑皮层释放一氧化氮(NO)。确定这种现象是否也存在于人类脑组织中至关重要。在本研究中,我们调查了从选择性堕胎获取的人类原代新皮层细胞培养物中NMDA与NO的相互作用。通过涂有萘酚和卟啉的碳纤维电极监测细胞外NO浓度,该电极先前已被证明对NO具有灵敏且选择性的反应。我们发现,局部应用NMDA可诱导富含新皮层神经元的培养物释放NO,但不能诱导神经胶质细胞培养物释放NO。用一氧化氮合酶抑制剂盐酸NG-硝基-L-精氨酸甲酯(L-NAME)或MK801预处理可显著减弱NMDA诱导的NO溢出。据我们所知,这是首次直接测量外源性NMDA诱发的胎儿人类皮层神经元细胞外NO浓度。