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Effects of agents that inactivate free radical NO (NO • ) on nitroxyl anion‐mediated relaxations, and on the detection of NO • released from the nitroxyl anion donor Angeli's salt

2001; Wiley; Volume: 134; Issue: 3 Linguagem: Inglês

10.1038/sj.bjp.0704287

1476-5381

Anthie Ellis, Hong Lu, Chun Guang Li, M. J. Rand,

Neuroscience of respiration and sleep

The effects of agents that inactivate free radical nitric oxide (carboxy‐PTIO, hydroxocobalamin and pyrogallol) were tested on relaxations produced by the nitroxyl anion (NO − ) donor Angeli's salt in rat aortic rings and anococcygeus muscles. The amount of NO • generated from Angeli's salt in the presence of these agents was measured using a NO • ‐selective electrode sensor. Carboxy‐PTIO (100, 300 μ M ), hydroxocobalamin (30, 100 μ M ) and pyrogallol (10, 30 μ M ) significantly reduced relaxations produced by Angeli's salt (0.3 μ M ) in aortic rings but not in anococcygeus muscles. NO • generated from Angeli's salt (0.1 – 10 μ M ), as detected by the sensor electrode, was less than 0.5% of the amount of Angeli's salt added. Carboxy‐PTIO (100 μ M ) and hydroxocobalamin (30 μ M ), but not pyrogallol significantly increased the amount of NO • detected. In the presence of an oxidizing agent copper [II] (as CuSO 4 100 μ M ), the amount of NO • detected from 0.3 μ M of Angeli's salt increased from an undetectable level of 142.7±15.7 n M (equivalent to 47.6% of Angeli's salt added). Under these conditions, carboxy‐PTIO, hydroxocobalamin and pyrogallol significantly reduced the amount of NO • detected from Angeli's salt as well as the signal generated by an equivalent amount of authentic NO (0.33 μ M ). The difference in effects of these agents on relaxations to Angeli's salt in the aorta and the anococcygeus muscle may be explained by the ready conversion of NO − to NO • in the aorta through an unidentified mechanism, which makes NO − susceptible to inactivation by these agents. Furthermore, in addition to inactivating NO • , carboxy‐PTIO and hydroxocobalamin may themselves oxidize NO − to NO • , albeit slightly. British Journal of Pharmacology (2001) 134 , 521–528; doi: 10.1038/sj.bjp.0704287