Pardini R S, Tilka M A, Pritsos C A, Lin A J, Sartorelli A C
Chem Biol Interact. 1981 May;35(2):241-53. doi: 10.1016/0009-2797(81)90147-2.
Mitochondrial swelling induced by 2,3-bis(chloromethyl)-1,4-naphthoquinone (CMNQ) was found to be a non-energy linked, oxygen and sulfhydryl-dependent, substrate-independent, osmotic process, that lack cation specificity. Swelling was inhibited by cysteine and DTNB, and the CMNQ induced swelling resulted in a decrease in mitochondrial reactive sulfhydryl groups; thus, mitochondrial sulfhydryl interaction was mandatory in the CMNQ swelling process. The non-enzymatic reaction of CMNQ with cysteine but not cystine resulted in the consumption of oxygen, implicating sulfhydryl redox activity in the swelling process. High level of tocopherol and histidine depressed the CMNQ induced swelling, suggesting that free radicals and singlet oxygen are important in the CMNQ induced swelling process. These findings support the proposition that CMNQ interacts with mitochondrial reductase systems and sulfhydryl groups in such a way as to generate superoxide radical which subsequently may dismute to H2O2 and produce .OH and possibly singlet oxygen. These toxic oxygen species may be responsible for the CMNQ-promoted sulfhydryl depletion and mitochondrial swelling.
2,3-双(氯甲基)-1,4-萘醌(CMNQ)诱导的线粒体肿胀是一个非能量依赖、氧和巯基依赖、底物非依赖的渗透过程,缺乏阳离子特异性。肿胀受到半胱氨酸和二硫硝基苯甲酸(DTNB)的抑制,CMNQ诱导的肿胀导致线粒体活性巯基基团减少;因此,线粒体巯基相互作用在CMNQ肿胀过程中是必需的。CMNQ与半胱氨酸而非胱氨酸的非酶反应导致氧的消耗,这表明巯基氧化还原活性参与了肿胀过程。高水平的生育酚和组氨酸抑制了CMNQ诱导的肿胀,表明自由基和单线态氧在CMNQ诱导的肿胀过程中起重要作用。这些发现支持这样的观点,即CMNQ与线粒体还原酶系统和巯基基团相互作用,以产生超氧自由基,随后超氧自由基可能歧化为过氧化氢并产生·OH以及可能产生单线态氧。这些有毒的氧物种可能是CMNQ促进的巯基消耗和线粒体肿胀的原因。