Kitamura S, Tatsumi K
Institute of Pharmaceutical Science, Hiroshima University School of Medicine, Japan.
Biochem Mol Biol Int. 1997 Jun;42(2):271-6. doi: 10.1080/15216549700202661.
This study demonstrates the menadione-dependent reduction of imipramine N-oxide, a tertiary amine N-oxide, to imipramine by rat liver cytosol in the presence of NADH or NADPH. A mechanism for the cytosolic reduction of the tertiary amine N-oxide is proposed. Menadione is converted to its reduced form by a menadione-reducing enzyme such as DT-diaphorase and the reduced pyridine nucleotide, followed by reduction of the tertiary amine N-oxide to the amine by the heme group of catalytic hemoproteins in the presence of reduced menadione as an electron donor.
本研究表明,在NADH或NADPH存在的情况下,大鼠肝细胞溶胶可将叔胺N-氧化物亚胺丙嗪N-氧化物以甲萘醌依赖的方式还原为亚胺丙嗪。提出了一种叔胺N-氧化物胞质还原的机制。甲萘醌通过甲萘醌还原酶(如DT-黄递酶)和还原型吡啶核苷酸转化为其还原形式,随后在还原型甲萘醌作为电子供体的存在下,催化血红素蛋白的血红素基团将叔胺N-氧化物还原为胺。