Poulsen J P, Lun A, Scheuch C, Gruetzmann H, Saugstad O D, Gross J
Institute for Surgical Research, University of Oslo, Rikshospitalet, Norway.
Neuropediatrics. 1993 Feb;24(1):30-5. doi: 10.1055/s-2008-1071509.
The effect of the oxygen radical generating system, hypoxanthine/xanthine oxidase (Hx/XOD), on the spontaneous and potassium-stimulated outflow of the neurotransmitter dopamine (DA) from rat striatal synaptosomes was studied. The efficacy of some radical scavengers was also tested. DA outflow was measured by incubation of [3H]-DA prelabeled synaptosomes (P2) in Krebs-Ringer buffer, containing either normal or depolarizing K+ concentrations. The reactions were terminated by filtration of the synaptosomes through Sartorius filters. Hx/XOD increased the spontaneous DA outflow in a dose and time dependent manner. The reduction found in synaptosomal DA content could be explained by disturbances of DA uptake or reuptake. The K+ stimulated outflow was not altered by the lower doses of Hx/XOD, whereas, when very high doses of Hx/XOD were used, the K+ stimulated DA outflow was decreased. High doses of Hx/XOD may deplete the synaptosomal DA releasable pool, leaving little DA available for extra-stimulated outflow by high concentrations of K+. The K(+)-stimulated outflow of DA is a less sensitive process against radical attack than the spontaneous release of DA. A protective action of catalase, but no effect of superoxide dismutase was demonstrated in these experiments.
研究了氧自由基生成系统次黄嘌呤/黄嘌呤氧化酶(Hx/XOD)对大鼠纹状体突触体中神经递质多巴胺(DA)自发释放及钾离子刺激释放的影响。还测试了一些自由基清除剂的效果。通过将预先标记有[3H]-DA的突触体(P2)在含有正常或去极化钾离子浓度的 Krebs-Ringer 缓冲液中孵育来测量 DA 的释放。通过 Sartorius 滤器过滤突触体来终止反应。Hx/XOD 以剂量和时间依赖的方式增加 DA 的自发释放。突触体中 DA 含量的减少可以用 DA 摄取或再摄取的干扰来解释。较低剂量的 Hx/XOD 不会改变钾离子刺激的释放,而当使用非常高剂量的 Hx/XOD 时,钾离子刺激的 DA 释放会减少。高剂量的 Hx/XOD 可能会耗尽突触体中可释放的 DA 池,使得高浓度钾离子额外刺激释放时几乎没有 DA 可供释放。与 DA 的自发释放相比,钾离子刺激的 DA 释放对自由基攻击的敏感性较低。在这些实验中,过氧化氢酶显示出保护作用,而超氧化物歧化酶则没有效果。