Shelkovnikov Stanislav, Merlic Craig A, Gonick Harvey C
Nephrology Section, Medical and Research Services, Veteran Affairs Greater, Los Angeles Healthcare System at West Los Angeles, Los Angeles, CA 90073, USA.
Life Sci. 2004 Apr 23;74(23):2919-28. doi: 10.1016/j.lfs.2003.11.006.
Nitric oxide (NO) and peroxynitrite (ONOO) are said to destroy norepinephrine (NE). We studied the role of NE decomposition by NO donors and ONOO as they affect the contractile activity of NE in rat denuded thoracic aorta. First, we determined the relaxing effect of NO donors (SNAP, PROLI/NO, Sodium nitrite, SIN-1) and ONOO after precontraction by NE (1 microM). SNAP and SIN-1 (EC(50) 50-110 nM) were more active than PROLI/NO, Sodium nitrite or ONOO (EC(50) 19-30 microM). The relaxing effect of NO donors and ONOO were decreased by ODQ (10 microM), a guanylate cyclase inhibitor. Second, we compared the contractile activity of NE before and after preincubation with NO donors or ONOO in presence of ODQ. NE (1 microM) was incubated with NO donors or ONOO at the concentrations of 0.1 mM in both Krebs solution or phosphate buffer (pH 7.4; 0.1 M) for 10 minutes at 37 degrees C. NE evoked the aorta contraction in the same concentrations before and after preincubation with NO donors. In contrast, ONOO decreased effect of NE, EC(50) was measured at 4.3+/-0.3 nM and 13.4+/-1.6 nM, before and after preincubation of NE with ONOO respectively. Third, we measured the NE concentration using the HPLC method. We revealed that the concentration of NE after preincubation with NO donors was unaltered. However HPLC measurement revealed that NE concentration after preincubation with ONOO was reduced 2-3-fold. Therefore, under these experimental conditions ONOO, but not NO donors, was capable of destroying NE.
一氧化氮(NO)和过氧亚硝酸盐(ONOO)据说会破坏去甲肾上腺素(NE)。我们研究了NO供体和ONOO对NE分解的作用,因为它们会影响大鼠去内皮胸主动脉中NE的收缩活性。首先,我们测定了在NE(1微摩尔)预收缩后NO供体(硝普钠、PROLI/NO、亚硝酸钠、SIN-1)和ONOO的舒张作用。硝普钠和SIN-1(半数有效浓度[EC(50)]为50 - 110纳摩尔)比PROLI/NO、亚硝酸钠或ONOO(EC(50)为19 - 30微摩尔)更具活性。鸟苷酸环化酶抑制剂ODQ(10微摩尔)可降低NO供体和ONOO的舒张作用。其次,我们比较了在ODQ存在的情况下,NE与NO供体或ONOO预孵育前后的收缩活性。在37℃下,将NE(1微摩尔)与浓度为0.1毫摩尔的NO供体或ONOO在Krebs溶液或磷酸盐缓冲液(pH 7.4;0.1摩尔)中孵育10分钟。与NO供体预孵育前后,相同浓度的NE引起的主动脉收缩情况相同。相比之下,ONOO降低了NE的作用,NE与ONOO预孵育前后的EC(50)分别测定为4.3±0.3纳摩尔和13.4±1.6纳摩尔。第三,我们使用高效液相色谱法测量NE浓度。我们发现,与NO供体预孵育后NE浓度未改变。然而,高效液相色谱测量显示,与ONOO预孵育后NE浓度降低了2 - 3倍。因此,在这些实验条件下,ONOO而非NO供体能够破坏NE。