TY - JOUR
T1 - Dietary exposure of juvenile female mice to polyhalogenated seafood contaminants (HBCD, BDE-47, PCB-153, TCDD): Comparative assessment of effects in potential target tissues
AU - Maranghi, F.
AU - Tassinari, R.
AU - Moracci, G.
AU - Altieri, I.
AU - Rasinger, J. D.
AU - Carroll, T. S.
AU - Hogstrand, C.
AU - Lundebye, A. -K.
AU - Mantovani, A.
PY - 2013/6
Y1 - 2013/6
N2 - Fish represents source of nutrients and major dietary vehicle of lipophilic persistent contaminants. The study compared the effects of two legacy and two emerging fish pollutants (Hexabromocyclododecane HBCD; 2,2',4,4'-Tetrabromodiphenyl ether BDE-47; 2,2',4,4',5,5'-Hexachlorobiphenyl PCB-153; 2,3,7,8-Tetrachlorodibenzo-p-doxin TCDD) in juvenile female mice exposed through a salmon based rodent diet for 28 days (dietary doses: HBCD 199 mg/kg bw/day; BDE-47 450 mu g/kg bw/day; PCB-153 195 mu g/kg bw/day; TCDD 90 ng/kg bw/day). Dose levels were comparable to previously reported developmental Lowest Observed Adverse Effect Levels. None of the treatments elicited signs of overt toxicity, but HBCD increased relative liver weight. All compounds caused changes in liver, thymus and thyroid; spleen was affected by BDE-47 and PCB-153; no effects were seen in uterus and adrenals. Strongest effects in thyroid follicles were elicited by PCB-153, in thymus and liver by BDE-47. HBCD and BDE-47 induced liver fatty changes, but appeared to be less potent in the other tissues. HBCD, BDE-47 and TCDD increased serum testosterone levels and the testosterone/estradiol ratio, suggesting a potential involvement of pathways related to sex steroid biosynthesis and/or metabolism. The results support the role of toxicological studies on juvenile rodents in the hazard characterization of chemicals, due to endocrine and/or immune effects. (C) 2013 Elsevier Ltd. All rights reserved.
AB - Fish represents source of nutrients and major dietary vehicle of lipophilic persistent contaminants. The study compared the effects of two legacy and two emerging fish pollutants (Hexabromocyclododecane HBCD; 2,2',4,4'-Tetrabromodiphenyl ether BDE-47; 2,2',4,4',5,5'-Hexachlorobiphenyl PCB-153; 2,3,7,8-Tetrachlorodibenzo-p-doxin TCDD) in juvenile female mice exposed through a salmon based rodent diet for 28 days (dietary doses: HBCD 199 mg/kg bw/day; BDE-47 450 mu g/kg bw/day; PCB-153 195 mu g/kg bw/day; TCDD 90 ng/kg bw/day). Dose levels were comparable to previously reported developmental Lowest Observed Adverse Effect Levels. None of the treatments elicited signs of overt toxicity, but HBCD increased relative liver weight. All compounds caused changes in liver, thymus and thyroid; spleen was affected by BDE-47 and PCB-153; no effects were seen in uterus and adrenals. Strongest effects in thyroid follicles were elicited by PCB-153, in thymus and liver by BDE-47. HBCD and BDE-47 induced liver fatty changes, but appeared to be less potent in the other tissues. HBCD, BDE-47 and TCDD increased serum testosterone levels and the testosterone/estradiol ratio, suggesting a potential involvement of pathways related to sex steroid biosynthesis and/or metabolism. The results support the role of toxicological studies on juvenile rodents in the hazard characterization of chemicals, due to endocrine and/or immune effects. (C) 2013 Elsevier Ltd. All rights reserved.
KW - Thyroid
KW - Thymus
KW - Feed
KW - Steroid hormones
KW - Liver
KW - SPRAGUE-DAWLEY RATS
KW - POLYBROMINATED DIPHENYL ETHERS
KW - ENHANCED HISTOPATHOLOGY
KW - 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN
KW - HEXABROMOCYCLODODECANE
KW - METABOLISM
KW - EXCRETION
KW - LESIONS
KW - SYSTEM
KW - THYMUS
U2 - 10.1016/j.fct.2013.02.056
DO - 10.1016/j.fct.2013.02.056
M3 - Article
SN - 0278-6915
VL - 56
SP - 443
EP - 449
JO - Food and Chemical Toxicology
JF - Food and Chemical Toxicology
ER -