Guzik Tomasz J, Channon Keith M
Department of Pharmacology, Jagiellonian University, Cracow, Poland.
Methods Mol Med. 2005;108:73-89. doi: 10.1385/1-59259-850-1:073.
Reactive oxygen species (ROS) play important roles in the pathogenesis of vascular disease states. In particular, superoxide anion participates in endothelial dysfunction mainly owing to its rapid interaction with NO, but also as it causes direct biological effects and serves as a progenitor for many other ROS. Detection of ROS in intact tissues and cells is much more difficult than in chemical systems. We describe advantages and potential pitfalls of chemiluminescent methods of vascular ROS detection. Lucigenin and luminol-enhanced chemiluminescent methods are described in the detection of vascular superoxide and peroxynitrite production and NAD(P)H oxidase activity. We also describe the use of new chemiluminescent probes, including cypridina luciferin analogs (coelenterazine; CLA and MCLA) and pholasin. The validity of some of these chemiluminescent methods (in particular lucigenin-enhanced chemiluminescence) recently has been questioned. It has been suggested that lucigenin itself, especially at high concentrations (>50 micromol/L), may produce superoxide via redox cycling. Using intact human vascular rings and vascular homogenates, we show that lucigenin, particularly at lower concentrations (5 micromol/L), provides an accurate assessment of the rate of superoxide production as assessed by close correlations with the SOD inhibitable ferricytochrome c reduction assay. Chemiluminescent techniques provide a useful approach for vascular ROS measurements, but should be always interpreted in the context of measurements obtained using other complementary techniques.
活性氧(ROS)在血管疾病状态的发病机制中起重要作用。特别是,超氧阴离子主要通过与一氧化氮(NO)的快速相互作用参与内皮功能障碍,但也因其引起直接的生物学效应并作为许多其他ROS的前体。在完整组织和细胞中检测ROS比在化学系统中困难得多。我们描述了用于检测血管ROS的化学发光方法的优点和潜在陷阱。介绍了光泽精和鲁米诺增强化学发光法在检测血管超氧化物、过氧亚硝酸盐生成及烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H)氧化酶活性方面的应用。我们还描述了新化学发光探针的使用,包括海萤荧光素类似物(腔肠素;CLA和MCLA)和船蛆素。最近,其中一些化学发光方法(特别是光泽精增强化学发光法) 的有效性受到了质疑。有人提出,光泽精本身,尤其是在高浓度(>50 μmol/L)时,可能通过氧化还原循环产生超氧化物。使用完整的人体血管环和血管匀浆,我们发现,光泽精,特别是在较低浓度(5 μmol/L)时,与超氧化物歧化酶(SOD)可抑制的高铁细胞色素c还原测定法密切相关,能准确评估超氧化物的产生速率。化学发光技术为测量血管ROS提供了一种有用的方法,但应始终结合使用其他互补技术获得的测量结果来进行解释。