Department of Biochemistry, Faculty of Medicine, Kuwait University, Kuwait.
Department of Biochemistry, Faculty of Medicine, Kuwait University, Kuwait.
Chem Biol Interact. 2020 Sep 25;329:109222. doi: 10.1016/j.cbi.2020.109222. Epub 2020 Aug 7.
Extensive application of methylene blue (MB) for therapeutic and diagnostic purposes, and reports for unwanted side effects, demand better understanding of the mechanisms of biological action of this thiazine dye. Because MB is redox-active, its biological activities have been attributed to transfer of electrons, generation of reactive oxygen species, and antioxidant action. Results of this study show that MB is more toxic to a superoxide dismutase-deficient Escherichia coli mutant than to its SOD-proficient parent, which indicates that superoxide anion radical is involved. Incubation of E. coli with MB induced the enzymes fumarase C, SOD, nitroreductase A, and glucose-6-phosphate dehydrogenase, all controlled by the soxRS regulon. Induction of these enzymes was prevented by blocking protein synthesis with chloramphenicol and was not observed when soxRS-negative mutants were incubated with MB. These results show that MB is capable of inducing the soxRS regulon of E. coli, which plays a key role in protecting bacteria against oxidative stress and redox-cycling compounds. Irrespective of the abundance of heme-containing proteins in living cells, which are preferred acceptors of electrons from the reduced form of MB, reduction of oxygen to superoxide radical still takes place. Induction of the soxRS regulon suggests that in humans, beneficial effects of MB could be attributed to activation of redox-sensitive transcription factors like Nrf2 and FoxO. If defense systems are compromised or genes coding for protective proteins are not induced, MB would have deleterious effects.
由于亚甲蓝(MB)在治疗和诊断方面的广泛应用,以及其不良反应的报告不断增加,人们对这种噻嗪染料的生物学作用机制有了更好的了解。由于 MB 具有氧化还原活性,其生物学活性归因于电子转移、活性氧物种的生成和抗氧化作用。本研究结果表明,超氧化物歧化酶缺陷型大肠杆菌突变体比其 SOD 丰富的亲本对 MB 更为敏感,这表明超氧阴离子自由基参与其中。用 MB 孵育大肠杆菌诱导了顺乌头酸酶 C、SOD、硝基还原酶 A 和葡萄糖-6-磷酸脱氢酶,所有这些酶都受 soxRS 调控子控制。用氯霉素阻断蛋白质合成可阻止这些酶的诱导,而当 soxRS 阴性突变体用 MB 孵育时则观察不到这种情况。这些结果表明,MB 能够诱导大肠杆菌的 soxRS 调控子,该调控子在保护细菌免受氧化应激和氧化还原循环化合物的侵害中起着关键作用。无论细胞内血红素蛋白的丰度如何,这些蛋白都是 MB 还原形式的电子的首选受体,但氧仍被还原为超氧自由基。soxRS 调控子的诱导表明,在人类中,MB 的有益作用可能归因于激活了 Nrf2 和 FoxO 等氧化还原敏感转录因子。如果防御系统受损或编码保护性蛋白的基因未被诱导,则 MB 会产生有害影响。