Czapski G, Goldstein S
Department of Physical Chemistry, Hebrew University of Jerusalem, Israel.
Free Radic Biol Med. 1995 Dec;19(6):785-94. doi: 10.1016/0891-5849(95)00081-8.
In this study we calculate the half-life of .NO in its reactions with superoxide and with oxygen under various conditions using the known rate constants for these reactions. The measured half-life of .NO in biological systems is 3-5 s, which agrees well with the calculated value for intracellular .NO, but not for extracellular .NO under normal physiological conditions. The autoxidation of .NO to yield NO2- as a final product cannot be responsible for such a short measured half-life under normal as well as pathologic conditions. Therefore, if there is direct evidence for the occurrence of the reaction of .NO with O2.- in the medium, one has to assume that the steady state concentrations of free .NO are much lower than those measured. The very low concentrations of free .NO in biological systems may result from its reversible strong binding to biological molecules. Simulation of the mechanism of the autoxidation of .NO indicates that the binding constants of .NO to O2 or to another .NO are too small to account for the very low concentration of free .NO in biological systems. Nevertheless, the reaction of .NO with oxygen cannot be neglected in biological systems if the intermediate ONOO. reacts rapidly with a biological target. The biological damage caused by ONOO. is expected to be due to the radical itself and to peroxynitrite, which is most probably formed via the reaction of ONOO. with the biological molecule.
在本研究中,我们利用这些反应的已知速率常数,计算了在各种条件下,一氧化氮(·NO)与超氧阴离子和氧气反应的半衰期。在生物系统中测得的·NO半衰期为3 - 5秒,这与细胞内·NO的计算值吻合良好,但与正常生理条件下细胞外·NO的计算值不符。在正常及病理条件下,·NO自氧化生成最终产物亚硝酸根离子(NO₂⁻)并不能解释如此短的实测半衰期。因此,如果有直接证据表明介质中存在·NO与超氧阴离子(O₂⁻·)的反应,那么必须假定游离·NO的稳态浓度远低于实测值。生物系统中游离·NO浓度极低可能是由于它与生物分子的可逆性强结合。·NO自氧化机制的模拟表明,·NO与氧气或另一个·NO的结合常数太小,无法解释生物系统中游离·NO的极低浓度。然而,如果中间产物过氧亚硝酸根(ONOO·)能迅速与生物靶点反应,那么在生物系统中·NO与氧气的反应就不能被忽视。预计过氧亚硝酸根造成的生物损伤是由于自由基本身以及过氧亚硝酸,过氧亚硝酸很可能是由过氧亚硝酸根与生物分子反应形成的。