Enzymatic alterations and RNA/DNA ratio in intestine of rainbow trout, Oncorhynchus mykiss, induced by chronic exposure to carbamazepine
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- antioxidancia metabolismus MeSH
- časové faktory MeSH
- chemické látky znečišťující vodu aplikace a dávkování toxicita MeSH
- DNA účinky léků metabolismus MeSH
- karbamazepin aplikace a dávkování toxicita MeSH
- Oncorhynchus mykiss MeSH
- RNA účinky léků metabolismus MeSH
- sodíko-draslíková ATPasa antagonisté a inhibitory metabolismus MeSH
- střeva účinky léků enzymologie MeSH
- střevní sliznice metabolismus MeSH
- trávicí systém účinky léků enzymologie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antioxidancia MeSH
- chemické látky znečišťující vodu MeSH
- DNA MeSH
- karbamazepin MeSH
- RNA MeSH
- sodíko-draslíková ATPasa MeSH
We investigated the effect of long-term exposure to carbamazepine (CBZ) on the enzymatic alterations and RNA/DNA ratio in intestine tissue of rainbow trout. Fish were exposed to sublethal concentrations of CBZ (1.0 microg/l, 0.2 or 2.0 mg/l) for 42 days. Digestive enzymes (proteolytic enzymes and amylase) and energy metabolic enzyme (Na(+)-K(+)-ATPase) and antioxidant enzymes (superoxide dismutase [SOD], catalase [CAT], glutathione peroxidase [GPx], and glutathione reductase [GR]) in fish intestine were measured. In addition, intestinal RNA/DNA ratio was determined after 42 days exposure. Carbamazepine exposure at 2.0 mg/l led to significantly inhibited (P < 0.05) activity of Na(+)-K(+)-ATPase. Activities of the antioxidant enzymes SOD, CAT, and GPx in CBZ-treated groups gradually increased at lower concentration of CBZ (1.0 microg/l and 0.2 mg/l), then significantly inhibited (P < 0.05) at 2.0 mg/l. After 42 days, the RNA/DNA ratio in fish intestine was significantly lower (P < 0.05) in groups exposed to CBZ at 2.0 mg/l than in other groups. However, there was no statistical significance (P > 0.05) in the activities of digestive enzymes (proteolytic enzyme and amylase) and GR in all groups. In short, prolonged exposure to CBZ resulted in different responses of various enzymes and significantly lower RNA/DNA ratio in fish intestine. Furthermore, molecular and genetic mechanisms of these physiological responses in fish are not clear, which need to be further studied.
Zobrazit více v PubMed
Mar Environ Res. 2004 Jul;58(1):65-82 PubMed
Comp Biochem Physiol C Toxicol Pharmacol. 2010 Jan;151(1):137-41 PubMed
Nitric Oxide. 1999 Oct;3(5):375-82 PubMed
Comp Biochem Physiol C Toxicol Pharmacol. 2002 Jun;132(2):247-59 PubMed
Water Res. 2002 Jun;36(11):2869-77 PubMed
Environ Toxicol Pharmacol. 2005 Jul;20(1):99-106 PubMed
Environ Toxicol Pharmacol. 2003 Feb;13(2):57-149 PubMed
J Biochem Mol Toxicol. 2002;16(4):182-8 PubMed
Environ Res. 1981 Feb;24(1):15-23 PubMed
Anal Biochem. 1976 May 7;72:248-54 PubMed
J Biol Chem. 1952 Mar;195(1):133-40 PubMed
Aquat Toxicol. 2004 Jun 10;68(2):141-50 PubMed
Bull Environ Contam Toxicol. 1999 Feb;62(2):222-9 PubMed
J Biol Chem. 1975 Jul 25;250(14):5475-80 PubMed
Chem Biol Interact. 2010 Jan 5;183(1):98-104 PubMed
Ecotoxicology. 2007 Mar;16(2):279-87 PubMed
Aquat Toxicol. 2006 Feb 10;76(2):122-59 PubMed
Water Res. 2007 Mar;41(5):1013-21 PubMed
J Biochem Mol Toxicol. 2000;14(1):51-6 PubMed
Comp Biochem Physiol B Biochem Mol Biol. 2007 Jan;146(1):107-14 PubMed
J Appl Toxicol. 2010 Apr;30(3):197-203 PubMed
Chemosphere. 2009 Dec;77(11):1476-81 PubMed
J Gen Physiol. 1947 Mar 20;30(4):291-310 PubMed
Biochem Biophys Res Commun. 1976 Aug 23;71(4):952-8 PubMed
Biochem Pharmacol. 1981 Mar 1;30(5):427-32 PubMed
Eur J Biochem. 1974 Sep 16;47(3):469-74 PubMed
Bull Environ Contam Toxicol. 2002 Aug;69(2):271-7 PubMed
Ecotoxicol Environ Saf. 2003 Oct;56(2):295-301 PubMed
Bull Environ Contam Toxicol. 1979 May;22(1-2):9-16 PubMed