LAUSR

HighlightsGenetic variation in the aryl hydrocarbon receptor and cytochrome P450 1A2 (CYP1A2) alter sensitivity to developmental PCB exposure.PCB‐treated high‐affinity Ahrb mice had greater deficits in motor function tests associated with nigrostriatal pathways.PCB‐treated Cyp1a2(−/−) knockout mice had greater impairments on tests associated with cerebellar function.Unexpectedly, corn oil‐treated control Cyp1a2(−/−) knockout mice also had deficits on the rotarod test.Our data indicate more than one brain region required for normal motor function are affected by developmental PCB exposure. ABSTRACT Polychlorinated biphenyls (PCBs) are persistent organic pollutants known to cause adverse health effects and linked to neurological deficits in both human and animal studies. Children born to exposed mothers are at highest risk of learning and memory and motor deficits. We developed a mouse model that mimics human variation in the aryl hydrocarbon receptor and cytochrome P450 1A2 (CYP1A2) to determine if genetic variation increases susceptibility to developmental PCB exposure. In our previous studies, we found that high‐affinity AhrbCyp1a2(−/−) and poor‐affinity AhrdCyp1a2(−/−) knockout mice were most susceptible to learning and memory deficits following developmental PCB exposure compared with AhrbCyp1a2(+/+) wild type mice (C57BL/6J strain). Our follow‐up studies focused on motor deficits, because human studies have identified PCBs as a potential risk factor for Parkinson’s disease. Dams were treated with an environmentally relevant PCB mixture at gestational day 10 and postnatal day 5. We used a motor battery that included tests of nigrostriatal function as well as cerebellar function, because PCBs deplete thyroid hormone, which is essential to normal cerebellar development. There was a significant effect of PCB treatment in the rotarod test with impaired performance in all three genotypes, but decreased motor learning as well in the two Cyp1a2(−/−) knockout lines. Interestingly, we found a main effect of genotype with corn oil‐treated control Cyp1a2(−/−) mice performing significantly worse than Cyp1a2(+/+) wild type mice. In contrast, we found that PCB‐treated high‐affinity Ahrb mice were most susceptible to disruption of nigrostriatal function with the greatest deficits in AhrbCyp1a2(−/−) mice. We conclude that differences in AHR affinity combined with the absence of CYP1A2 protein affect susceptibility to motor deficits following developmental PCB exposure.