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Title: Thyrotoxic and dopaminergic effects of polychlorinated biphenyls

Miscellaneous ·
OSTI ID:6831597

Perturbations in the developing nervous system have been associated with perinatal exposures to polychlorinated biphenyls (PCBs). To determine which PCBs accumulate in brain following perinatal exposure, Sprague-Dawley rats were exposed by gavage to Aroclor 1242 (4 or 16 mg/kg/day) during days 10-16 of gestation. At weaning (day 21), analysis of pup brain (frontal cortex, hippocampus, and caudate putamen) by gas chromatography revealed ten peaks representing 10-14 congeners in PCB-exposed animals. Brain PCB concentrations were greatest in high-dose pups for all congeners except for 2,4,4[prime]-trichlorobiphenyl (PCB 28) which had a higher concentration in the low-dose group. Congeners differed significantly in their degree of bioaccumulation, but no significant differences among brain regions were found. A lack of regionalization of PCB residues in the brain was also demonstrated by autoradiography in weanling rats treated iv with [[sup 14]C]-3,3[prime],4,4[prime]-tetrachlorobiphenyl or [[sup 14]C]-2,2[prime],4,4[prime]-tetrachlorobiphenyl. Time-mated Sprague-Dawley rats were exposed on days 10-16 of gestation to three environmentally-relevant PCBs: 2,4,4[prime]-trichlorobiphenyl (PCB 28), 8 or 32 mg/kg/day; 2,3[prime],4,4[prime],5-pentachlorobiphenyl (PCB 118), 4 or 16 mg/kg/day; or 2,2[prime],4,4[prime],5,5[prime]-hexachlorobiphenyl (PCB 153), 16 or 64 mg/kg/day. At weaning, serum total thyroxin, but not triiodothyronine, was markedly depressed in pups exposed perinatally to PCB 118 or 153; and thyroid glands from PCB 118-treated pups revealed histologic changes suggestive of sustained TSH stimulation. No significant PCB-induced changes were detected in the activity of the rate limiting enzyme in the synthesis of catecholamines, tyrosine hydroxylase, in the caudate putamen at weaning or in adulthood. Likewise no significant changes were detected in dopamine receptor (D1 and D2) concentrations in several regions in the mesocortical and nigrostriatal pathways.

Research Organization:
Illinois Univ., Urbana, IL (United States)
OSTI ID:
6831597
Resource Relation:
Other Information: Thesis (Ph.D.)
Country of Publication:
United States
Language:
English