BACKGROUND: Polybrominated diphenyl ethers (PBDE) are a group of environmental contaminants increasing in North America. Few data are available on neurobehavioral effects at low-dose exposure. OBJECTIVES: Our goal in the present study was to evaluate whether low-dose BDE-47, which is the most abundant PBDE in human samples, affects the neurobehavioral development of rats. METHODS: Dams were exposed to vehicle or low-dose BDE-47 (0.002, 0.02 and 0.2 mg/kg body weight) each 5 days from gestational day 15 to postnatal day (PND) 20 by intravenous injections. Spontaneous locomotor activity of pups was assessed using the open field test on PND 15, 20 and 25. Sensorimotor coordination was assessed using a RotaRod on PND 30. RESULTS: Exposure to BDE-47 increased locomotor activity of pups. Developmental landmarks and sensorimotor coordination were not influenced by exposure to BDE-47. BDE-47 content in adipose tissue of exposed rats was similar to that known for human populations. CONCLUSION: These results indicate neurodevelopmental disruption induced in rats by BDE-47 at levels found in the human population.
BACKGROUND:Polybrominated diphenyl ethers (PBDE) are a group of environmental contaminants increasing in North America. Few data are available on neurobehavioral effects at low-dose exposure. OBJECTIVES: Our goal in the present study was to evaluate whether low-dose BDE-47, which is the most abundant PBDE in human samples, affects the neurobehavioral development of rats. METHODS: Dams were exposed to vehicle or low-dose BDE-47 (0.002, 0.02 and 0.2 mg/kg body weight) each 5 days from gestational day 15 to postnatal day (PND) 20 by intravenous injections. Spontaneous locomotor activity of pups was assessed using the open field test on PND 15, 20 and 25. Sensorimotor coordination was assessed using a RotaRod on PND 30. RESULTS: Exposure to BDE-47 increased locomotor activity of pups. Developmental landmarks and sensorimotor coordination were not influenced by exposure to BDE-47. BDE-47 content in adipose tissue of exposed rats was similar to that known for human populations. CONCLUSION: These results indicate neurodevelopmental disruption induced in rats by BDE-47 at levels found in the human population.
Authors: Margaret A Adgent; Kate Hoffman; Barbara Davis Goldman; Andreas Sjödin; Julie L Daniels Journal: Paediatr Perinat Epidemiol Date: 2013-08-19 Impact factor: 3.980
Authors: Mamta Behl; Julie R Rice; Marjo V Smith; Caroll A Co; Matthew F Bridge; Jui-Hua Hsieh; Jonathan H Freedman; Windy A Boyd Journal: Toxicol Sci Date: 2016-08-26 Impact factor: 4.849
Authors: Joshua M Bradner; Tiffany A Suragh; W Wyatt Wilson; Carlos R Lazo; Kristen A Stout; Hye Mi Kim; Min Z Wang; Douglas I Walker; Kurt D Pennell; Jason R Richardson; Gary W Miller; W Michael Caudle Journal: Exp Neurol Date: 2012-12-31 Impact factor: 5.330