Literature DB >> 381004

Extramicrosomal drug metabolism.

J Pütter.   

Abstract

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.

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Year:  1979        PMID: 381004     DOI: 10.1007/BF03189392

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  10 in total

1.  [Inactivation of L-asparaginase by cathepsin].

Authors:  J Pütter; K Otto
Journal:  Arzneimittelforschung       Date:  1972-10

2.  Proceedings: Studies on the esterase hydrolyzing pivampicillin.

Authors:  T Yokota; T Oshima; S Totsuka; M Tanaka
Journal:  Jpn J Pharmacol       Date:  1974

3.  Human liver microsomal drug metabolism.

Authors:  F J Darby; W Newnes; D A Price Evans
Journal:  Biochem Pharmacol       Date:  1970-04       Impact factor: 5.858

4.  Studies on an unusual N-dealkylation reaction. II. Characteristics of the enzyme system and a proposed pathway for the reaction.

Authors:  J J Kamm; A Szuna
Journal:  J Pharmacol Exp Ther       Date:  1973-03       Impact factor: 4.030

5.  Relative selectivity of some microsomal drug metabolizing enzyme inducers.

Authors:  M A Peters
Journal:  Arch Int Pharmacodyn Ther       Date:  1973-05

6.  [Studies on the formation of the lactone and acid form of the main metabolite of mefruside].

Authors:  K Schlossmann; J Pütter
Journal:  Arzneimittelforschung       Date:  1973-02

7.  The degradation of Mefrusid. The participation of a "lactonase" in drug metabolism.

Authors:  J Pütter; K Schlossmann
Journal:  Biochim Biophys Acta       Date:  1972-11-24

8.  Oxidation and glucuronidation of certain drugs in various subcellular fractions of rat liver: binding of desmethylimipramine and hexobarbital to cytochrome P-450 and oxidation and glucuronidation of desmethylimipramine, aminopyrine, p-nitrophenol and 1-naphthol.

Authors:  C von Bahr; E Hietanen; H Glaumann
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1972

Review 9.  [Pharmacokinetics of acetylsalicylic acid].

Authors:  J Pütter
Journal:  Med Welt       Date:  1976-07-09

10.  Nitroreduction of 5-nitrofuran derivatives by rat liver xanthine oxidase and reduced nicotinamide adenine dinucleotide phosphate-cytochrome c reductase.

Authors:  C Y Wang; B C Behrens; M Ichikawa; G T Bryan
Journal:  Biochem Pharmacol       Date:  1974-12-15       Impact factor: 5.858

  10 in total
  1 in total

1.  Pharmacokinetics of chlorambucil in man after administration of the free drug and its prednisolone ester (prednimustine, Leo 1031).

Authors:  H Ehrsson; I Wallin; S O Nilsson; B Johansson
Journal:  Eur J Clin Pharmacol       Date:  1983       Impact factor: 2.953

  1 in total

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