Patel M, Day B J, Crapo J D, Fridovich I, McNamara J O
Department of Medicine, Duke University, Durham, North Carolina 27710, USA.
Neuron. 1996 Feb;16(2):345-55. doi: 10.1016/s0896-6273(00)80052-5.
We tested the pathogenic role of O2-) radicals in excitotoxic injury. Inactivation of the TCA cycle enzyme, aconitase, was used as a marker of intracellular O2- levels, and a porphyrin SOD mimetic was used to scavenge O2-. The selective, reversible, and SOD-sensitive inactivation of aconitase by known O2- generators was used to validate aconitase activity as a marker of O2- generation. Treatment of rat cortical cultures with NMDA, KA, or the intracellular O2- generator PQ2+ produced a selective and reversible inactivation of aconitase, which closely correlated with subsequent cell death produced by these agents. The SOD mimetic, but not its less active congener, attenuated both aconitase inactivation and cell death produced by NMDA, KA, and PQ2+. These results provide direct evidence implicating O2(-) generation in the pathway to excitotoxic injury.
我们测试了超氧阴离子(O2-)自由基在兴奋性毒性损伤中的致病作用。三羧酸循环酶乌头酸酶的失活被用作细胞内O2-水平的标志物,并且一种卟啉超氧化物歧化酶模拟物被用于清除O2-。已知的O2-生成剂对乌头酸酶的选择性、可逆性以及对超氧化物歧化酶敏感的失活作用被用于验证乌头酸酶活性作为O2-生成的标志物。用N-甲基-D-天冬氨酸(NMDA)、 kainic acid(KA)或细胞内O2-生成剂百草枯二价阳离子(PQ2+)处理大鼠皮层培养物会导致乌头酸酶的选择性和可逆性失活,这与这些试剂随后产生的细胞死亡密切相关。超氧化物歧化酶模拟物,而非其活性较低的同类物,减轻了由NMDA、KA和PQ2+导致的乌头酸酶失活和细胞死亡。这些结果提供了直接证据,表明O2(-)生成参与了兴奋性毒性损伤途径。