Santamaría A, Santamaría D, Díaz-Muñoz M, Espinoza-González V, Ríos C
Department of Neurochemistry, National Institute of Neurology and Neurosurgery Manuel Velasco Suárez, México D.F., Mexico.
Toxicol Lett. 1997 Dec;93(2-3):117-24. doi: 10.1016/s0378-4274(97)00082-9.
The effects of a nitric oxide synthase inhibitor, N omega-nitro-L-arginine (L-NARG), and a nitric oxide precursor, L-arginine (L-ARG), on the lipid peroxidation induced by quinolinic acid (QUIN, an NMDA receptor agonist), were both tested in synaptosomal fractions from whole rat brain. Baseline of lipid peroxidation was found at 2.43 +/- 0.24 fluorescence units/mg protein or 14.27 +/- 1.24 nmoles of TBARS/mg protein (100%). QUIN (100 microM)-induced lipid peroxidation in synaptosomes (256% and 166% vs. control, as measured by lipid fluorescent products and thiobarbituric acid-reactive substances, respectively) was inhibited by concentrations of 10, 40, 100, 200 and 400 microM of L-NARG (74%, 58%, 56%, 48% and 48% vs. quinolinate value, respectively). Coincubation of synaptosomes with QUIN plus L-ARG (100 microM), which alone resulted a potent pro-oxidant (277% vs. control), increased the lipoperoxidative effect induced by QUIN alone in 120% (290% vs. control). Synaptosomes simultaneously exposed to QUIN (100 microM) plus L-ARG (100 microM) plus L-NARG (200 microM) showed levels of lipid peroxidation similar to those of quinolinate alone. These findings suggest that nitric oxide may contribute to the oxidative damage induced in vitro by QUIN.
在来自大鼠全脑的突触体组分中,测试了一氧化氮合酶抑制剂Nω-硝基-L-精氨酸(L-NARG)和一氧化氮前体L-精氨酸(L-ARG)对喹啉酸(QUIN,一种NMDA受体激动剂)诱导的脂质过氧化的影响。脂质过氧化的基线为2.43±0.24荧光单位/毫克蛋白质或14.27±1.24纳摩尔丙二醛/毫克蛋白质(100%)。喹啉酸(100μM)诱导的突触体脂质过氧化(分别通过脂质荧光产物和硫代巴比妥酸反应性物质测量,相对于对照组分别为256%和166%)被10、40、100、200和400μM浓度的L-NARG抑制(相对于喹啉酸盐值分别为74%、58%、56%、48%和48%)。突触体与喹啉酸加L-精氨酸(100μM)共同孵育,单独使用L-精氨酸时是一种强效促氧化剂(相对于对照组为277%),使喹啉酸单独诱导的脂质过氧化作用增加了120%(相对于对照组为290%)。同时暴露于喹啉酸(100μM)加L-精氨酸(100μM)加L-NARG(200μM)的突触体显示出的脂质过氧化水平与单独使用喹啉酸盐时相似。这些发现表明一氧化氮可能促成了喹啉酸在体外诱导的氧化损伤。