Benov L, Sztejnberg L, Fridovich I
Department of Biochemistry, Duke University Medical Center, Durham, NC 27710, USA.
Free Radic Biol Med. 1998 Nov 1;25(7):826-31. doi: 10.1016/s0891-5849(98)00163-4.
The fluorogenic oxidation of hydroethidine (HE) to ethidium (E+) has been used as a measure of O2-. Evaluation of this method confirms that O2-, but not O2 or H2O2, rapidly oxidizes HE to E+. However the ratio of E+ produced per O2- introduced decreased as the flux of O2- was increased. This suggested that HE can catalyze the dismutation of O2- and this was affirmed. HE was oxidized to a red product, distinct from E+ by ferricytochrome c and a similar oxidation may occur within Escherichia coli. HE inhibited the growth and killed a SOD-null strain to a greater extent than the SOD-replete parental strain and these effects were much diminished under anaerobic conditions. This indicated that E+ was responsible for the toxicity of HE and indeed E+ was seen to be toxic under both aerobic and anaerobic conditions. In view of the data presented HE can be recommended as a qualitative but not as a quantitative measure of O2(-1).
氢化乙锭(HE)荧光氧化为乙锭(E+)已被用作衡量超氧阴离子(O2-)的指标。对该方法的评估证实,是O2-而非O2或H2O2能迅速将HE氧化为E+。然而,随着引入的O2-通量增加,每产生一个E+所对应的O2-比例下降。这表明HE可催化O2-的歧化反应,这一点得到了证实。HE被氧化成一种红色产物,与铁细胞色素c催化生成的E+不同,并且在大肠杆菌内可能发生类似的氧化反应。与超氧化物歧化酶(SOD)充足的亲代菌株相比,HE对SOD缺失菌株的生长抑制和杀伤作用更强,且在厌氧条件下这些作用会大大减弱。这表明E+是HE毒性的原因,实际上在需氧和厌氧条件下E+均具有毒性。鉴于所呈现的数据,HE可被推荐用于定性检测O2-,但不能用于定量检测。