Le. Schweitzer et al., DIFFERENTIAL TOXICITY OF 3 POLYCHLORINATED BIPHENYL CONGENERS IN DEVELOPING SEA-URCHIN EMBRYOS, Environmental toxicology and chemistry, 16(7), 1997, pp. 1510-1514
The relationship between body burden and toxicity of three individual
polychlorinated biphenyl (PCB) congeners in developing sea urchin embr
yos was investigated to evaluate the validity of current predictive mo
dels of PCB toxicity in an invertebrate system. Body burdens of radiol
abeled PCB congeners (IUPAC 47, 77, and 153) accumulated from seawater
were used to determine median effective concentrations (EC50s) for de
velopmental and cytogenetic effects following a 72-h exposure. Congene
r 47, a di-ortho-substituted tetrachlorobiphenyl, was found to be at l
east four times more toxic than congener 77, a non-ortho-substituted (
coplanar) tetrachlorobiphenyl, with EC50s of 47 and >218 mmol/kg, resp
ectively, using an embryo development assay. This result contradicts t
he structure-activity prediction of the mammalian-based toxic equivale
nts (TEQs) approach, demonstrating the need for an ecotoxicologic mode
l. Congener 153, a di-ortho-substituted hexachlorobiphenyl, was virtua
lly nontoxic in terms of developmental effects at the highest dose (10
2 mmol/kg) achievable at its limit of water solubility. Cytogenetic an
alysis was a more sensitive method for assessing toxicity than the emb
ryo development assay. Dose-response relationships were established wi
th mitotic activity being the most sensitive endpoint because the PCBs
appeared to inhibit mitosis. At the highest doses, complete mitotic a
rrest was observed. Congener 77 was found to be at least two times mor
e toxic (EC50 = 30 mmol/kg) than congener 153 (EC50 = 67 mmol/kg) but
not as toxic as congener 47 (EC50 < 16 mmol/kg) using mitotic activity
as the endpoint for toxicity. Thus, the developmental and cytogenetic
endpoints ranked the toxicity of the congeners similarly, but establi
shed different EC50s.