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. 1986 Feb 1;233(3):755–761. doi: 10.1042/bj2330755

Hydroxyl-radical production and ethanol oxidation by liver microsomes isolated from ethanol-treated rats.

G Ekström, T Cronholm, M Ingelman-Sundberg
PMCID: PMC1153096  PMID: 3085654

Abstract

In order to distinguish between the mechanism of microsomal ethanol oxidation and hydroxyl-radical formation, the rate of cytochrome P-450 (P-450)-dependent oxidation of dimethyl sulphoxide (Me2SO) was determined in the presence and in the absence of iron-chelating compounds, in liver microsomes from control, ethanol- and phenobarbital-treated rats. Ethanol treatment resulted in a specific increase (3-fold) of the microsomal ethanol oxidation and NADPH consumption per nmol of P-450. A form of P-450 was purified to apparent homogeneity from the ethanol-treated rats and characterized with respect of amino acid composition and N-terminal amino acid sequence. Specific ethanol induction of a cytochrome P-450 species having a catalytic-centre activity of 20/min for ethanol and consuming 30 nmol of NADPH/min could account for the results observed with microsomes. Phenobarbital treatment caused 50% decrease in the rate of ethanol oxidation and NADPH oxidation per nmol of P-450. The rate of oxidation of the hydroxyl-radical scavenger Me2SO was increased 3-fold by ethanol or phenobarbital treatment when expressed on a per-mg-of-microsomal-protein basis, but the rate of Me2SO oxidation expressed on a per-nmol-of-P-450 basis was unchanged. Addition of iron-chelating agents to the three different types of microsomal preparations caused an 'uncoupling' of the electron-transport chain accompanied by a 4-fold increase of the rate of Me2SO oxidation. It is concluded that ethanol treatment results in the induction of P-450 forms specifically effective in ethanol oxidation and NADPH oxidation, but not in hydroxyl-radical production, as detected by the oxidation of Me2SO.

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  1. Ariyoshi T., Takabatake E., Remmer H. Drug metabolism in ethanol-induced fatty liver. Life Sci. 1970 Apr 8;9(7):361–369. doi: 10.1016/0024-3205(70)90238-9. [DOI] [PubMed] [Google Scholar]
  2. Cederbaum A. I., Dicker E., Cohen G. Effect of hydroxyl radical scavengers on microsomal oxidation of alcohols and on associated microsomal reactions. Biochemistry. 1978 Jul 25;17(15):3058–3064. doi: 10.1021/bi00608a018. [DOI] [PubMed] [Google Scholar]
  3. Comai K., Gaylor J. L. Existence and separation of three forms of cytochrome P-450 from rat liver microsomes. J Biol Chem. 1973 Jul 25;248(14):4947–4955. [PubMed] [Google Scholar]
  4. DeCarli L. M., Lieber C. S. Fatty liver in the rat after prolonged intake of ethanol with a nutritionally adequate new liquid diet. J Nutr. 1967 Mar;91(3):331–336. doi: 10.1093/jn/91.3_Suppl.331. [DOI] [PubMed] [Google Scholar]
  5. Haniu M., Ryan D. E., Iida S., Lieber C. S., Levin W., Shively J. E. NH2-terminal sequence analyses of four rat hepatic microsomal cytochromes P-450. Arch Biochem Biophys. 1984 Dec;235(2):304–311. doi: 10.1016/0003-9861(84)90202-9. [DOI] [PubMed] [Google Scholar]
  6. Ingelman-Sundberg M., Hagbjörk A. L. On the significance of the cytochrome P-450-dependent hydroxyl radical-mediated oxygenation mechanism. Xenobiotica. 1982 Nov;12(11):673–686. doi: 10.3109/00498258209038943. [DOI] [PubMed] [Google Scholar]
  7. Ingelman-Sundberg M., Johansson I. Mechanisms of hydroxyl radical formation and ethanol oxidation by ethanol-inducible and other forms of rabbit liver microsomal cytochromes P-450. J Biol Chem. 1984 May 25;259(10):6447–6458. [PubMed] [Google Scholar]
  8. Ingelman-Sundberg M., Johansson I. The mechanism of cytochrome P-450-dependent oxidation of ethanol in reconstituted membrane vesicles. J Biol Chem. 1981 Jun 25;256(12):6321–6326. [PubMed] [Google Scholar]
  9. Ingelman-Sundberg M., Jörnvall H. Induction of the ethanol-inducible form of rabbit liver microsomal cytochrome P-450 by inhibitors of alcohol dehydrogenase. Biochem Biophys Res Commun. 1984 Oct 30;124(2):375–382. doi: 10.1016/0006-291x(84)91563-8. [DOI] [PubMed] [Google Scholar]
  10. Ishii H., Jean-Gil, Lieber J., Lieber C. S. Effect of ethanol on the amount and enzyme activities of hepatic rough and smooth microsomal membranes. Biochim Biophys Acta. 1973 Jan 26;291(2):411–420. doi: 10.1016/0005-2736(73)90493-8. [DOI] [PubMed] [Google Scholar]
  11. Klein S. M., Cohen G., Cederbaum A. I. Production of formaldehyde during metabolism of dimethyl sulfoxide by hydroxyl radical generating systems. Biochemistry. 1981 Oct 13;20(21):6006–6012. doi: 10.1021/bi00524a013. [DOI] [PubMed] [Google Scholar]
  12. Klein S. M., Cohen G., Lieber C. S., Cederbaum A. I. Increased microsomal oxidation of hydroxyl radical scavenging agents and ethanol after chronic consumption of ethanol. Arch Biochem Biophys. 1983 Jun;223(2):425–432. doi: 10.1016/0003-9861(83)90606-9. [DOI] [PubMed] [Google Scholar]
  13. Koop D. R., Coon M. J. Purification of liver microsomal cytochrome P-450 isozymes 3a and 6 from imidazole-treated rabbits. Evidence for the identity of isozyme 3a with the form obtained by ethanol treatment. Mol Pharmacol. 1984 May;25(3):494–501. [PubMed] [Google Scholar]
  14. Koop D. R., Morgan E. T., Tarr G. E., Coon M. J. Purification and characterization of a unique isozyme of cytochrome P-450 from liver microsomes of ethanol-treated rabbits. J Biol Chem. 1982 Jul 25;257(14):8472–8480. [PubMed] [Google Scholar]
  15. Koop D. R., Nordblom G. D., Coon M. J. Immunochemical evidence for a role of cytochrome P-450 in liver microsomal ethanol oxidation. Arch Biochem Biophys. 1984 Nov 15;235(1):228–238. doi: 10.1016/0003-9861(84)90272-8. [DOI] [PubMed] [Google Scholar]
  16. Krikun G., Lieber C. S., Cederbaum A. I. Increased microsomal oxidation of ethanol by cytochrome P-450 and hydroxyl radical-dependent pathways after chronic ethanol consumption. Biochem Pharmacol. 1984 Oct 15;33(20):3306–3309. doi: 10.1016/0006-2952(84)90097-2. [DOI] [PubMed] [Google Scholar]
  17. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  18. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  19. Leo M. A., Iida S., Lieber C. S. Retinoic acid metabolism by a system reconstituted with cytochrome P-450. Arch Biochem Biophys. 1984 Oct;234(1):305–312. doi: 10.1016/0003-9861(84)90353-9. [DOI] [PubMed] [Google Scholar]
  20. Lieber C. S., DeCarli L. M. Hepatic microsomal ethanol-oxidizing system. In vitro characteristics and adaptive properties in vivo. J Biol Chem. 1970 May 25;245(10):2505–2512. [PubMed] [Google Scholar]
  21. Liu S. J., Ramsey R. K., Fallon H. J. Effects of ethanol on hepatic microsomal drug-metabolizing enzymes in the rat. Biochem Pharmacol. 1975 Feb 1;24(3):369–378. doi: 10.1016/0006-2952(75)90220-8. [DOI] [PubMed] [Google Scholar]
  22. Morehouse L. A., Thomas C. E., Aust S. D. Superoxide generation by NADPH-cytochrome P-450 reductase: the effect of iron chelators and the role of superoxide in microsomal lipid peroxidation. Arch Biochem Biophys. 1984 Jul;232(1):366–377. doi: 10.1016/0003-9861(84)90552-6. [DOI] [PubMed] [Google Scholar]
  23. Morgan E. T., Devine M., Skett P. Changes in the rat hepatic mixed function oxidase system associated with chronic ethanol vapor inhalation. Biochem Pharmacol. 1981 Mar 15;30(6):595–600. doi: 10.1016/0006-2952(81)90131-3. [DOI] [PubMed] [Google Scholar]
  24. Morgan E. T., Koop D. R., Coon M. J. Catalytic activity of cytochrome P-450 isozyme 3a isolated from liver microsomes of ethanol-treated rabbits. Oxidation of alcohols. J Biol Chem. 1982 Dec 10;257(23):13951–13957. [PubMed] [Google Scholar]
  25. Mungikar A. M., Hetu C., Joly J. G. Ethanol-inducible liver cytochrome P-450 in the rat: relative specificity for ethanol oxidation activity in vitro. Adv Exp Med Biol. 1980;132:51–56. doi: 10.1007/978-1-4757-1419-7_6. [DOI] [PubMed] [Google Scholar]
  26. NASH T. The colorimetric estimation of formaldehyde by means of the Hantzsch reaction. Biochem J. 1953 Oct;55(3):416–421. doi: 10.1042/bj0550416. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Ohnishi K., Lieber C. S. Reconstitution of the microsomal ethanol-oxidizing system. Qualitative and quantitative changes of cytochrome P-450 after chronic ethanol consumption. J Biol Chem. 1977 Oct 25;252(20):7124–7131. [PubMed] [Google Scholar]
  28. Ohnishi K., Lieber C. S. Respective role of superoxide and hydroxyl radical in the activity of the reconstituted microsomal ethanol-oxidizing system. Arch Biochem Biophys. 1978 Dec;191(2):798–803. doi: 10.1016/0003-9861(78)90422-8. [DOI] [PubMed] [Google Scholar]
  29. Powis G. Effect of a single oral dose of methanol, ethanol and propan-2-ol on the hepatic microsomal metabolism of foreign compounds in the rat. Biochem J. 1975 May;148(2):269–277. doi: 10.1042/bj1480269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Ryan D. E., Iida S., Wood A. W., Thomas P. E., Lieber C. S., Levin W. Characterization of three highly purified cytochromes P-450 from hepatic microsomes of adult male rats. J Biol Chem. 1984 Jan 25;259(2):1239–1250. [PubMed] [Google Scholar]
  31. Teschke R., Moreno F., Petrides A. S. Hepatic microsomal ethanol oxidizing system (MEOS): respective roles of ethanol and carbohydrates for the enhanced activity after chronic alcohol consumption. Biochem Pharmacol. 1981 Jul 1;30(13):1745–1751. doi: 10.1016/0006-2952(81)90004-6. [DOI] [PubMed] [Google Scholar]
  32. Ullrich V., Weber P., Wollenberg P. Tetrahydrofurane - an inhibitor for ethanol-induced liver microsomal cytochrome P450. Biochem Biophys Res Commun. 1975 Jan 2;64(3):808–813. doi: 10.1016/0006-291x(75)90119-9. [DOI] [PubMed] [Google Scholar]
  33. Villeneuve J. P., Mavier P., Joly J. G. Ethanol-induced cytochrome P-450: catalytic activity after partial purification. Biochem Biophys Res Commun. 1976 Jun 7;70(3):723–728. doi: 10.1016/0006-291x(76)90652-5. [DOI] [PubMed] [Google Scholar]

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