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Organic Solvents as Modifyers of Aldrin Epoxidase in Reconstituted Monooxygenase Systems in Microsomes.

Biochem. Pharmacol. 38, 4217-4223 (1989)
DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
To examine the response of individual cytochrome P-450 species catalysing the epoxidation of aldrin (Wolff T and Guengerich FP, Biochem Pharmacol36: 2581–2588, 1987), monooxygenase systems reconstituted from these species were assayed in the presence of 5% (v/v) = 0.87 M ethanol. The activity of cytochromes P-450pb.b and P-450pb-d, two enzymes inducible by phenobarbital was increased seven-fold. The activity of two other P-450 enzymes purified from these animals was either inhibited by 50%, as observed for cytochrome P-450pb-c or remained unchanged, as noted with cytochrome P-450pcn-e. Two P-450 enzymes purified from untreated rats, cytochromes P-450ut-f and P-450ut-h, showed an inhibition by 50 and 20%, respectively, while the activity of cytochrome P-450ut-a was slightly increased by 50%. Indirect evidence that solvents enhance aldrin epoxidation by interacting with the hemoprotein was obtained by the finding that ethanol stimulated the activity of cytochrome P-450pb-b already, before addition of the lipid component, l-α-1,2-dilauroyl-in-glycero-3-phosphocholine. The Km of cytochrome P-450pb.b for NADPH cytochrome P-450 reductase was not altered by ethanol indicating that the interaction between the two enzymes was not affected by the solvent. Other results indicate that the stimulatory solvent binds to a site, apart from the type I or type II binding site. The potency of various hydrophylic solvents to modify aldrin epoxidase activity was assayed in microsomes of rats pretreated with phenobarbital and of untreated male rats. Ethanol, n-propranol, n-butanol, acetone and tetrahydrofuran enhanced enzyme activity of phenobarbital pretreated rats to a maximal extent of two-fold and, at similar concentrations, inhibited the enzyme activity of untreated rats by 50%. The potency of these solvents correlated with their lipophilicity. Methanol and dimethylsulfoxide only slightly modified the activity of induced and noninduced animals. In the presence of 0.5 M n-propranol as the modifying agent, microsomal epoxidase activity of rats pretreated with pregnenolone-16α-carbonitrile, dexamethasone, 3-methylcholanthrene and of control rats was inhibited by 60–80%, whereas the activity of animals pretreated with phenobarbital, DDT, or the polychlorinated biphenyl mixture, Clophen A 50, was stimulated between two- and three-fold. The results reveal that organic solvents frequently used to dissolve monooxygenase substrates may considerably modify the activity of cytochrome P-450 dependent reactions, in particular when purified enzymes are assayed.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter PB phenobarbital; MC 3-methyl-cholanthrene; PC commercial mixture of polychlorinated biphenyls; DDT 2,2'-bis-(4-chlorophenyl)-1,1,1-trichloro-ethane; PC pregnenolone-16α-carbonitrile; DEX dexamethasone; DLGP l-α-1,2-dilauroyl-sn-glycero-3-phosphocholine Enzymes; NADPH-cytochrome P-450 (cytochrome c) reductase (EC 1.6.2.4); glucose-6-phos-phate dehydrogenase (EC 1.1.1.49)
ISSN (print) / ISBN 0006-2952
e-ISSN 0006-2952
Quellenangaben Band: 38, Heft: 23, Seiten: 4217-4223 Artikelnummer: , Supplement: ,
Verlag Elsevier
Begutachtungsstatus Peer reviewed