Yamamoto N, Oliveira M B, Campello A de P, Lopes L C, Klüppel M L
Departamento de Bioquímica, Universidade Federal do Paraná, Brasil.
Cell Biochem Funct. 1988 Jan;6(1):61-6. doi: 10.1002/cbf.290060110.
Effect of methotrexate (MTX) on mitochondrial oxygen uptake, oxidative phosphorylation and on the activity of several enzymes linked to respiratory chain was studied. MTX was able to inhibit state III respiration activated by ADP and to decrease the respiratory coefficient with the substrates alpha-ketoglutarate and glutamate; these effects became pronounced when mitochondria were pre-incubated with MTX for 10 min. No effect was observed on ATPase activity of undamaged or broken mitochondria; the same was true for NADH-oxidase, NADH-dehydrogenase, NADH-cytochrome c reductase, succinate oxidase, and cytochrome c oxidase activity. The effect on the steady-state of cytochrome b, as well as, the inhibitory effect on state III of respiration with NAD+-linked substrates, offers a reasonable possibility to suggesting that the inhibition site of MTX could be in a place anterior to cytochrome b region, and not linked to respiratory chain.
研究了甲氨蝶呤(MTX)对线粒体氧摄取、氧化磷酸化以及与呼吸链相关的几种酶活性的影响。MTX能够抑制由ADP激活的状态III呼吸,并降低α-酮戊二酸和谷氨酸作为底物时的呼吸系数;当线粒体与MTX预孵育10分钟时,这些作用变得明显。未受损或破损线粒体的ATP酶活性未观察到影响;NADH氧化酶、NADH脱氢酶、NADH-细胞色素c还原酶、琥珀酸氧化酶和细胞色素c氧化酶活性也是如此。对细胞色素b稳态的影响以及对NAD+连接底物呼吸状态III的抑制作用,为表明MTX的抑制位点可能在细胞色素b区域之前且与呼吸链无关提供了合理的可能性。