Manzoni O, Prezeau L, Desagher S, Sahuquet A, Sladeczek F, Bockaert J, Fagni L
Centre CNRS-INSERM de Pharmacologie-Endocrinologie, Montpellier, France.
Neuroreport. 1992 Jan;3(1):77-80. doi: 10.1097/00001756-199201000-00020.
The effects of a nitric oxide (NO) donor, sodium nitroprusside (SNP), on N-methyl-D-aspartate (NMDA) receptors were assessed by optical measurements of intracellular calcium concentration ([Ca2+]i) and patch-clamp techniques in cultured central neurons. SNP selectively blocked NMDA-mediated currents and increases in [Ca2+]i. SNP inhibited the binding of [3H]-CGS 19755. The blockade of NMDA responses by SNP was prevented by CPP or APV which are selective competitive NMDA receptor antagonists. These effects were not necessarily mediated by NO, since they were mimicked by ferrocyanide ions, the NO companion photolysis product of SNP.
通过光学测量培养的中枢神经元细胞内钙浓度([Ca2+]i)以及膜片钳技术,评估一氧化氮(NO)供体硝普钠(SNP)对N-甲基-D-天冬氨酸(NMDA)受体的影响。SNP选择性阻断NMDA介导的电流以及[Ca2+]i的升高。SNP抑制[3H]-CGS 19755的结合。SNP对NMDA反应的阻断作用可被选择性竞争性NMDA受体拮抗剂CPP或APV所阻止。这些效应不一定由NO介导,因为它们可被亚铁氰化物离子模拟,亚铁氰化物离子是SNP的NO伴随光解产物。