Biochemical markers for differentiation of exposures to nonplanar polychlorinated biphenyls, organochlorine pesticides, or 2,3,7, 8-tetrachlorodibenzo-p-dioxin in trout liver
Language English Country Netherlands Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
9756698
DOI
10.1006/eesa.1998.1675
PII: S014765139891675X
Knihovny.cz E-resources
- MeSH
- Aryl Hydrocarbon Hydroxylases * MeSH
- Biomarkers analysis MeSH
- Cytochrome P-450 CYP1A1 biosynthesis MeSH
- Cytochrome P-450 CYP1A2 biosynthesis MeSH
- Dichlorodiphenyl Dichloroethylene toxicity MeSH
- Enzyme Induction drug effects MeSH
- Glutathione Transferase biosynthesis MeSH
- Injections, Intraperitoneal MeSH
- Insecticides toxicity MeSH
- Isoenzymes biosynthesis MeSH
- Microsomes, Liver drug effects enzymology MeSH
- Ethacrynic Acid metabolism MeSH
- Oncorhynchus mykiss metabolism MeSH
- Polychlorinated Biphenyls toxicity MeSH
- Polychlorinated Dibenzodioxins toxicity MeSH
- Steroid Hydroxylases biosynthesis MeSH
- Substrate Specificity MeSH
- Cytochrome P-450 Enzyme System biosynthesis MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Aryl Hydrocarbon Hydroxylases * MeSH
- Biomarkers MeSH
- Cytochrome P-450 CYP1A1 MeSH
- Cytochrome P-450 CYP1A2 MeSH
- Dichlorodiphenyl Dichloroethylene MeSH
- Glutathione Transferase MeSH
- Insecticides MeSH
- Isoenzymes MeSH
- Ethacrynic Acid MeSH
- Polychlorinated Biphenyls MeSH
- Polychlorinated Dibenzodioxins MeSH
- Steroid Hydroxylases MeSH
- Cytochrome P-450 Enzyme System MeSH
- testosterone 7-alpha-hydroxylase, hamster MeSH Browser
The effects of a single intraperitoneal dose of the prototypical contaminant nonplanar 2,2',4,4',5,5'-hexachlorobiphenyl (PCB 153, 50 mg/kg), p,p'-DDE (50 mg/kg), or 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, 200 ng/kg) on the activities of hepatic detoxification enzymes were examined in the liver of immature rainbow trout (Oncorhynchus mykiss). Different modulations of the tested xenobiotics on microsomal cytochrome P450-dependent testosterone hydroxylase activities were found: PCB 153 specifically induced 16beta-hydroxylase activity, whereas p,p'-DDE decreased cytochrome P4503A-dependent 6beta-hydroxylation as well as 16alpha- and 2alpha-hydroxylation. TCDD did not modulate testosterone hydroxylase activities, but a strong induction of cytochrome P4501A activity was observed after TCDD administration; hence, cytochrome P4501A is not involved in the hydroxylation of testosterone. Trout hepatic microsomal glutathione S-transferase (GST) activity, enhanced by all the xenobiotics tested, was found to be a sensitive nonspecific biochemical marker of oxidative stress; cytosolic glutathione reductase was a less sensitive indicator of oxidative stress and was induced significantly only by treatment with p,p'-DDE. Cytosolic GST activity toward ethacrynic acid (GST-ETHA) was induced by PCB 153 or p,p'-DDE, but not by TCDD. Modulations of hepatic microsomal testosterone hydroxylase activities and induction of GST-ETHA appeared to be suitable biochemical markers of acute exposure to nonplanar PCBs and organochlorines that do not induce cytochrome P4501A enzymes in rainbow trout, whereas microsomal GST and cytosolic glutathione reductase may become early biochemical indicators of oxidative stress.
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