Pütter J
Eur J Drug Metab Pharmacokinet. 1979;4(1):1-7. doi: 10.1007/BF03189392.
Drug metabolizing enzymes which are not located in the microsomes such as oxidoreductases are reviewed. It has been reported that a cytoplasmic NAD+-dependent dehydrogenase could be involved in the dehydrogenation of secondary or primary alcohols, and that peroxidases, located in all extranuclear cell-fractions, are able to oxidize certain drugs. Among the conjugating enzymes, mainly the glucuronidases and 0-Methyltransferases have been reported to be localised in the microsomes. Sulfatation, mercapturic acid formation and acetylation seem to occur in the supernatant of animal liver cells. Binding to glycine has been found in the mitochondria. Examples of combined action of microsomes and other cell fractions are presented. Esterases are found in the microsomes and cytoplasmic fraction of animal cells and also in the extracellular fluid (blood-plasma). They are more stable than monooxygenases whose activity depends on the intact microsomal structure and are therefore readily accessible in human biological material. Metabolic problems involving human esterases can often easily be solved by in vitro experiments. Results concerning the biochemical degradation of propanidid, mefrusid, acetyl salicylic acid and an acetyl salicylic acid ester are reported.
本文综述了位于微粒体之外的药物代谢酶,如氧化还原酶。据报道,一种胞质NAD+依赖的脱氢酶可能参与仲醇或伯醇的脱氢反应,并且位于所有核外细胞组分中的过氧化物酶能够氧化某些药物。在结合酶中,主要是葡萄糖醛酸酶和O-甲基转移酶已被报道定位于微粒体中。硫酸化、硫醚氨酸形成和乙酰化似乎发生在动物肝细胞的上清液中。与甘氨酸的结合已在线粒体中被发现。本文还列举了微粒体与其他细胞组分联合作用的例子。酯酶存在于动物细胞的微粒体和胞质组分中,也存在于细胞外液(血浆)中。它们比单加氧酶更稳定,单加氧酶的活性依赖于完整的微粒体结构,因此在人类生物材料中很容易获得。涉及人类酯酶的代谢问题通常可以通过体外实验轻松解决。本文报道了有关丙泮尼地、甲呋酰胺、乙酰水杨酸和一种乙酰水杨酸酯的生化降解结果。