Savel'ev S A
Ross Fiziol Zh Im I M Sechenova. 2005 Aug;91(8):942-8.
By means of in vivo microdialysis combined with HPLC analysis, we have shown that local infusions of 1 mM N-nitro-L-arginine (NO-synthase inhibitors) in the rat striatum reduced, and infusions of 100 microM apomorphine (agonists of the dopamine receptors) increased the level of citrulline (a NO co-product) in extracellular space of this structure. The apomorphine-induced increase in citrulline extracellular levels in the striatum was completely prevented by infusions of N-nitro-L-arginine in this structure, and 10 microM raclopride (dopamine D2 receptor blocker), but not by infusions of 50 microM SCH-23390 (dopamine D1 receptor blocker). The data obtained suggest that the increase in citrulline extracellular levels in striatum resulted from local activation of NO-synthase, and this effect is mediated by D2 rather than D1 dopamine receptors.
通过体内微透析结合高效液相色谱分析,我们发现,向大鼠纹状体局部注入1 mM N-硝基-L-精氨酸(一氧化氮合酶抑制剂)会降低该结构细胞外空间中瓜氨酸(一种一氧化氮副产物)的水平,而注入100 microM阿扑吗啡(多巴胺受体激动剂)则会使其升高。在该结构中注入N-硝基-L-精氨酸以及10 microM雷氯必利(多巴胺D2受体阻滞剂)可完全阻止阿扑吗啡诱导的纹状体瓜氨酸细胞外水平升高,但注入50 microM SCH-23390(多巴胺D1受体阻滞剂)则不能。所获得的数据表明,纹状体瓜氨酸细胞外水平升高是由一氧化氮合酶的局部激活所致,且这种效应是由D2而非D1多巴胺受体介导的。