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Allometric scaling of hepatic biotransformation in rainbow trout.

Authors :
Fitzsimmons PN
Hoffman AD
Fay KA
Nichols JW
Source :
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP [Comp Biochem Physiol C Toxicol Pharmacol] 2018 Dec; Vol. 214, pp. 52-60. Date of Electronic Publication: 2018 Aug 31.
Publication Year :
2018

Abstract

Biotransformation may substantially impact the toxicity and accumulation of xenobiotic chemicals in fish. However, this activity can vary substantially within and among species. In this study, liver S9 fractions from rainbow trout (4-400 g) were used to evaluate relationships between fish body mass and the activities of phase I and phase II metabolic enzymes. An analysis of log-transformed data, expressed per gram of liver (g liver <superscript>-1</superscript> ), showed that total cytochrome P450 (CYP) concentration, UDP-glucuronosyltransferase (UGT) activity, and glutathione S-transferase (GST) activity exhibited small but significant inverse relationships with fish body weight. In contrast, in vitro intrinsic clearance rates (CL <subscript>IN VITRO,INT</subscript> ) for three polycyclic aromatic hydrocarbons (PAHs) increased with increasing body weight. Weight normalized liver mass also decreased inversely with body weight, suggesting a need to express hepatic metabolism data per gram of body weight (g BW <superscript>-1</superscript> ) in order to reflect the metabolic capabilities of the whole animal. When the data were recalculated in this manner, negative allometric relationships for CYP concentration, UGT activity, and GST activity became more pronounced, while CL <subscript>IN VITRO,INT</subscript> rates for the three PAHs showed no significant differences across fish sizes. Ethoxyresorufin O-deethylase (EROD) activity normalized to tissue weight (g liver <superscript>-1</superscript> ) or body weight (g BW <superscript>-1</superscript> ) exhibited a non-monotonic pattern with respect to body weight. The results of this study may have important implications for chemical modeling efforts with fish.<br /> (Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1532-0456
Volume :
214
Database :
MEDLINE
Journal :
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP
Publication Type :
Academic Journal
Accession number :
30172734
Full Text :
https://doi.org/10.1016/j.cbpc.2018.08.004