Immunochemical analysis of liver microsomal cytochromes P450 of the American alligator, Alligator mississippiensis

Citation
Rp. Ertl et al., Immunochemical analysis of liver microsomal cytochromes P450 of the American alligator, Alligator mississippiensis, TOX APPL PH, 157(3), 1999, pp. 157-165
Citations number
51
Categorie Soggetti
Pharmacology & Toxicology
Journal title
TOXICOLOGY AND APPLIED PHARMACOLOGY
ISSN journal
0041008X → ACNP
Volume
157
Issue
3
Year of publication
1999
Pages
157 - 165
Database
ISI
SICI code
0041-008X(19990615)157:3<157:IAOLMC>2.0.ZU;2-D
Abstract
Ten antibodies raised against various mammalian and fish cytochromes P450 ( CYP) enzymes were used to probe the effects of xenobiotic pretreatment on l iver microsomes of the American alligator, Alligator mississippiensis. Pret reatment with phenobarbital (PB), 3-methyIcholanthrene (3MC), and PB plus 3 MC elicited significant induction of multiple CYP enzymes in alligator, as detected by antibodies to CYP1A, CYP2B, CYP2C, CYP2E, CYP2K, and CYP3A. In contrast to the rat, 3MC treatment induced alligator liver microsomes that were immunoreactive with antibodies to CYP2 family enzymes. Induction of CY P enzymes was not as apparent with the Aroclor 1254 (ARO), and 2,2',4,4' te trachlorobiphenyl (TCB) pretreatment used; fewer CYP enzymes primarily dete cted with antibodies against CYP2C or CYP2E were observed. Clofibrate (CLO; 80 mg/kg Days 1-4), markedly induced CYP4A in rat but this induction was n ot apparent in alligator. A purified PE-induced alligator liver microsomal CYP enzyme cross-reacted with several antibodies raised against CYP2 family enzymes but did not cross-react with antibodies raised against other CYP f amilies. This indicates the PB-inducible CYP in alligator shares some epito pe homology with several CYP2-family enzymes from other animals. These expe riments demonstrate the usefulness and limitations of using antibodies acro ss phylogenetic classes. While indicating the presence of CYP enzymes that have epitope homology with CYP1A, CYP2, CYP3 and CYP4 enzymes in alligator, it remains to be established whether these CYP forms are alligator ortholo gues of mammalian enzymes. In all cases, the relative abundance of alligato r liver microsomal CYP as determined by immunoblot analysis appeared lower than found in rat. The presence and induction of CYP indicated by immunoche mical analysis, corroborated previously reported enzymatic studies of the s ame microsomal preparations (Ertl et al., 1998a). Thus, increases in CYP pr otein by the various inducers employed were paralled by the increases in CY P enzyme-specific or selective activities, e.g., induction of CYP1A protein corresponded with induction of EROD. (C) 1999 Academic Press.