A COMPARATIVE-STUDY OF EFFECTS OF ATRAZINE ON XENOBIOTIC-METABOLIZINGENZYMES IN FISH AND INSECT, AND OF THE IN-VITRO PHASE-II ATRAZINE METABOLISM IN SOME FISH, INSECTS, MAMMALS AND ONE PLANT-SPECIES

Citation
E. Egaas et al., A COMPARATIVE-STUDY OF EFFECTS OF ATRAZINE ON XENOBIOTIC-METABOLIZINGENZYMES IN FISH AND INSECT, AND OF THE IN-VITRO PHASE-II ATRAZINE METABOLISM IN SOME FISH, INSECTS, MAMMALS AND ONE PLANT-SPECIES, Comparative biochemistry and physiology. C. Comparative pharmacologyand toxicology, 106(1), 1993, pp. 141-149
Citations number
38
Categorie Soggetti
Biology,"Pharmacology & Pharmacy",Toxicology
ISSN journal
07428413
Volume
106
Issue
1
Year of publication
1993
Pages
141 - 149
Database
ISI
SICI code
0742-8413(1993)106:1<141:ACOEOA>2.0.ZU;2-8
Abstract
1. Atrazine (3 daily i.p. doses of 0.20 mg/kg or 10 ppb in the water f or 14 days) did not change the xenobiotic metabolizing enzyme activiti es (XME) towards the substrates aldrin epoxidase (AE), NADPH-cytochrom e c reductase (NCCR), 7-ethoxyresorufin O-deethylase (EROD), 1-chloro- 2,4-dinitro-benzene (CDNB) and 1,2-dichloro-4-nitrobenzene (DCNB) in t rout liver (Oncorhynchus mykiss) compared to the controls. 2. Various treatment regimens of atrazine in a semisynthetic diet changed the XME activities towards AE, NCCR, CDNB and DCNB in the cabbage moth (Mames tra brassica L.) soft tissues and midgut compared to the controls. 3. A fife-long cabbage diet induced the XME activity towards CDNB in the cabbage moth soft tissues and midgut, whereas no differences in the ac tivities towards AE, NCCR and DCNB were observed compared to controls on a semi-synthetic diet. 4. The cabbage moth GSTs bound poorly to a g lutathione (GSH)-linked epoxy-activated Sepharose 6-B; however, based on the CDNB activity recovered by a GSH elution, there were no differe nces in the molecular weights of the partly purified subunits (27, 26 and 25 kDa) or the pIs (5.4, 4.8, and 4.1) of the molecules in the sof t tissues or midguts from respectively atrazine treated and control ca bbage moth. 5. The presence of GST isozymes that metabolize atrazine h as been demonstrated in all the 10 species studied (liver of the rainb ow trout, starry flounder (Platichthys stellatus), English sole (Pleur onectes vetulus), rat (Rattus norvegicus, Sprague-Dawley), mouse (Mus musculus, CD-1), leaves of common groundsel (Seneco vulgaris) and midg ut and soft tissues without gut of the cabbage moth and the Hebrew cha racter moth (Orthosia gothica L.). 6. With the exception of common gro undsel, the GST isozyme(s) with atrazine and ethacrynic acid (ETHA) ac tivities are similarly distributed between the species.