TY - JOUR
T1 - Differential time course of induction of rat liver microsomal cytochrome P-450 isozymes and epoxide hydrolase by Aroclor 1254
AU - Parkinson, Andrew
AU - Thomas, Paul E.
AU - Ryan, Dene E.
AU - Reik, Linda M.
AU - Safe, Stephen H.
AU - Robertson, Larry W.
AU - Levin, Wayne
N1 - Funding Information:
We have determinedb y immunochemical analyses that the time course of induction and magnitude of response are quite different among cytochromesP -450a, P-450b + P-450e, P-45Oc,a nd P-450d and epoxide hydrolase in rats treated with the polychlorinated biphenyl mixture, Aroclor 1254.T hese dissimilar responsest o the inductive effects of Aroclor 1254,a s well as selectedi ndividual polychlorinated biphenyl congeners,p resumably reflect inherent differences in the regulation of these integral membrane proteins. The results of the present study are reminiscent of those reportedb y Berlin and Schimke (66) on the induction of four liver enzymesb y cortisone in adrenalectomizedr ats. This raises the possibility that the relatively small and slow responseo f epoxideh ydrolase and cy-tochromeP -450a (like that of arginase and glutamic-alanine transaminase)c ompared to the large and rapid response of cytochromes P-450b + P-450e, P-45Oc,a nd P-450d( like that of tryptophan pyrrolase and tyrosine-glutamic transaminase) are not a consequenceo f low sensitivity to the effects of the inducer, but a reflection of the slower turnover of these enzymes. This possibility is supported in part by results presentedi n the following paper on the in vivo turnover of cytochromes P-450a, P-450b+ P-450e,P -450ã nd epoxide hydrolase (67). It is now evident that following treatment of rats with certain xenobiotics, the profile of cytochrome P-450 isozymes in
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1983/8
Y1 - 1983/8
N2 - The time course of induction of rat liver microsomal cytochromes P-450a, P-450b + P-450e, P-450c, and P-450d and epoxide hydrolase has been determined in immature male rats administered a single large dose [1500 μmol (500 mg)/kg body wt] of the polychlorinated biphenyl mixture Aroclor 1254. Differential regulation of these xenobiotic-metabolizing enzymes was indicated by their characteristic patterns of induction. The rate of induction of cytochrome P-450a and epoxide hydrolase was relatively slow, and steady-state levels of these enzymes were maintained from approximately Days 9 to 15 after Aroclor 1254 treatment. In contrast, cytochrome P-450c was maximally induced 2 days after Aroclor 1254 treatment and remained at a constant level through Day 15. Steady-state levels of cytochrome P-450d, beginning 1 week after Aroclor 1254 treatment, were preceded by a fairly rapid rate of induction and possibly by a small decline from maximal levels observed around Days 4 to 5. Like those of the other cytochrome P-450 isozymes and epoxide hydrolase, the levels of cytochromes P-450b + P-450e were constant from Day 9 to 15 after Aroclor 1254 treatment. However, an unexpected but reproducible decline (~25%) in total cytochrome P-450 content observed between Days 4 and 9 after Aroclor 1254 treatment principally reflected a dramatic and totally unanticipated decrease (~45%) in the level of cytochromes P-450b + P-450e. This transient decline in the level of cytochromes P-450b + P-450e was not due to an unusual effect of a mixture of polychlorinated biphenyls, since identical results were obtained with two individual congeners, namely 2,3,4,5,4′-penta- and 2,3,4,5,3′,4′-hexachlorobiphenyl, that induced the same isozymes as Aroclor 1254. In contrast, when rats were treated with 2,4,5,2′,4′,5′-hexachlorobiphenyl, which induces cytochromes P-450a and P-450b + P-450e and epoxide hydrolase but not cytochromes P-450c or P-450d, maximal levels of cytochromes P-450b + P-450e were attained on Day 4 and no decrease was observed over the next 11 days. These results suggest that there may be an interaction in the regulation of induction of certain individual cytochrome P-450 isozymes.
AB - The time course of induction of rat liver microsomal cytochromes P-450a, P-450b + P-450e, P-450c, and P-450d and epoxide hydrolase has been determined in immature male rats administered a single large dose [1500 μmol (500 mg)/kg body wt] of the polychlorinated biphenyl mixture Aroclor 1254. Differential regulation of these xenobiotic-metabolizing enzymes was indicated by their characteristic patterns of induction. The rate of induction of cytochrome P-450a and epoxide hydrolase was relatively slow, and steady-state levels of these enzymes were maintained from approximately Days 9 to 15 after Aroclor 1254 treatment. In contrast, cytochrome P-450c was maximally induced 2 days after Aroclor 1254 treatment and remained at a constant level through Day 15. Steady-state levels of cytochrome P-450d, beginning 1 week after Aroclor 1254 treatment, were preceded by a fairly rapid rate of induction and possibly by a small decline from maximal levels observed around Days 4 to 5. Like those of the other cytochrome P-450 isozymes and epoxide hydrolase, the levels of cytochromes P-450b + P-450e were constant from Day 9 to 15 after Aroclor 1254 treatment. However, an unexpected but reproducible decline (~25%) in total cytochrome P-450 content observed between Days 4 and 9 after Aroclor 1254 treatment principally reflected a dramatic and totally unanticipated decrease (~45%) in the level of cytochromes P-450b + P-450e. This transient decline in the level of cytochromes P-450b + P-450e was not due to an unusual effect of a mixture of polychlorinated biphenyls, since identical results were obtained with two individual congeners, namely 2,3,4,5,4′-penta- and 2,3,4,5,3′,4′-hexachlorobiphenyl, that induced the same isozymes as Aroclor 1254. In contrast, when rats were treated with 2,4,5,2′,4′,5′-hexachlorobiphenyl, which induces cytochromes P-450a and P-450b + P-450e and epoxide hydrolase but not cytochromes P-450c or P-450d, maximal levels of cytochromes P-450b + P-450e were attained on Day 4 and no decrease was observed over the next 11 days. These results suggest that there may be an interaction in the regulation of induction of certain individual cytochrome P-450 isozymes.
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U2 - 10.1016/0003-9861(83)90024-3
DO - 10.1016/0003-9861(83)90024-3
M3 - Article
C2 - 6412631
AN - SCOPUS:0020565558
SN - 0003-9861
VL - 225
SP - 203
EP - 215
JO - Archives of Biochemistry and Biophysics
JF - Archives of Biochemistry and Biophysics
IS - 1
ER -