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ToxSci Advance Access published online on June 17, 2009
Toxicological Sciences, doi:10.1093/toxsci/kfp114
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© The Author 2009. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

Effects of Decabrominated Diphenyl Ether (PBDE 209) Exposure at Different Developmental Periods on Synaptic Plasticity in the Dentate Gyrus of Adult Rats in vivo

Tairan Xing, Liang Chen, Yanan Tao, Ming Wang, Jutao Chen and Di-Yun Ruan*

School of Life science, University of Science and Technology of China, Hefei, Anhui, 230027, P.R. China

* Corresponding author Dr. Diyun Ruan, School of Life Science, University of Science and Technology of China, Hefei, Anhui 230027, P.R. China, Tel: +86-551-3606374, Fax: +86-551-3601443, E-mail: ruandy{at}ustc.edu.cn

Received March 27, 2009; revision received May 10, 2009; accepted May 21, 2009


  Abstract

Polybromininated diphenyl ethers (PBDEs) are widely used as flame-retardant additives. Previous studies have demonstrated that PBDEs exposure can lead to neurotoxicity. However, little is known about the effects of PBDE 209 on synaptic plasticity. This study investigated the effect of decabrominated diphenyl ether (PBDE 209), a major PBDEs product, on synaptic plasticity in the dentate gyrus (DG) of rats at different developmental periods. We examined the input/output functions (I/O), paired-pulse reactions (PPR) and the long-term potentiation (LTP) of the field excitatory postsynaptic potential (fEPSP) slope and the population spike (PS) amplitude in vivo. Rats were exposed to PBDE 209 during five different developmental periods: pregnancy, lactation via mother's milk, lactation via intragastric administration, after weaning, and prenatal to life. We found that exposed to PBDE 209 during different developmental periods could impair the synaptic plasticity of adult rats in different degrees. The results also showed that PBDE 209 might cause more serious effects on the postsynaptic cell excitability in synaptic plasticity, and the lactation period was the most sensitive time of development towards PBDE 209.

Key Words: polybromininated diphenyl ethers; dentate gyrus; electrophysiology; long-term potentiation; synaptic plasticity; hippocampus.

kang2000{at}mail.ustc.edu.cn, liangch{at}mail.ustc.edu.cn, taoyanan{at}mail.ustc.edu.cn, wming{at}ustc.edu.cn, jtc{at}ustc.edu.cn


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