Effects of bis(4-chlorophenyl) sulfone on rats following 28-day dietary exposure

Citation
R. Poon et al., Effects of bis(4-chlorophenyl) sulfone on rats following 28-day dietary exposure, J TOX E H A, 57(3), 1999, pp. 185-198
Citations number
32
Categorie Soggetti
Environment/Ecology,"Pharmacology & Toxicology
Journal title
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A
ISSN journal
15287394 → ACNP
Volume
57
Issue
3
Year of publication
1999
Pages
185 - 198
Database
ISI
SICI code
1528-7394(19990611)57:3<185:EOBSOR>2.0.ZU;2-S
Abstract
The short-term oral toxicity of a recently identified environmental polluta nt, bis(4-chloro- phenyl) sulfone (BCPS), was studied. Groups of male Sprag ue-Dawley rats (n = 6) were administered BCPS via the diet at 0 (control), 10, 100 or 1000 ppm for 4 wk. Additional control and 1000 ppm groups were a lso treated for 1, 2, and 3 wk. At termination, high-dose animals showed de pressed growth rate and food consumption, and 1 high dose animal in each of the wk-1, -3, and -4 groups had marked hematuria. Increased liver to body weight ratio was present at 100 ppm and increased kidney to body weight rat io at 1000 ppm. Marked increases in hepatic benzoylresorufin O-dealkylase ( BROD) and pentoxyresorufin O-dealkylase (PROD) activities were detected sta rting at 10 ppm. There was a significant decrease in methoxyresorufin O-dea lkylase (MROD) activity at 1000 ppm. Hepatic UDP-glucuronosyltransferase (U DPGT) and glutathione S-transferase (GST) activities also increased startin g at 100 ppm. A marked increase in urinary excretion of ascorbic acid was a pparent starting at 10 ppm, while there were no changer in urinary N-acetyl glucosaminidase (NAC) activity and protein levels. A threefold increase in serum cholesterol and a 30% increase in platelet counts were observed in th e 1000 ppm group. Levels of thiobarbituric acid-reactive substances (TBARS) were increased by threefold in the liver of the high-dose animals but were not significantly altered in the serum. Tissue BCPS concentrations were do se dependent and followed the order: adipose tissue >> liver > kidneys > br ain, spleen, lungs, in the time-course study involving the control and high -dose groups, most of the treatment effects were clearly present in wk I, a nd the severity of the effects remained at more or less the same levels the reafter. The exceptions were hepatic BROD and PROD activities, which showed a trend toward further increases with time of treatment. Liver and adipose tissue concentrations of BCPS remained unchanged from wk I to wk 4, while kidney concentrations increased with time. The results indicated that BCPS produced hepatic effects at the lowest dose level tested (10 ppm in the die t or 0.8 mg/kg/d).