| In Vivo and in Vitro Exposure to PCB 153 Reduces Long-Term Potentiation Rifat J. Hussain,1 Janos Gyori,1,2 Anthony P. DeCaprio,1 and David O. Carpenter1 1Department of Environmental Health and Toxicology, School of Public Health, University at Albany, Rensselaer, New York, USA 2Balaton Limnological Research Institute of the Hungarian Academy of Science, Tihany, Hungary Abstract We examined the effects of gestational and lactational exposure to polychlorinated biphenyl (PCB) 153 (2,4,5,2´,4´,5´-hexaCB) on the magnitude of long-term potentiation (LTP) observed in the CA1 region of hippocampal brain slices prepared from rats at 30 days of age. We compared these actions to those observed when PCB 153 is dissolved in normal Krebs-Ringer solution and perfused on slices from control rats of the same age. In vivo exposure was at three dose levels (1.25, 5, and 20 mg/kg/day) from gestational day 3 through weaning at postnatal day 21. Although responses to low-frequency stimulation of the Schaffer collateral pathway in exposed animals were not different from controls, significantly reduced LTP was induced after tetanic stimulation, even at the lowest dose studied. We observed a comparable depression of LTP when control slices were perfused with Krebs-Ringer that had been equilibrated with PCB 153 in a generator column. Neither in vivo nor in vitro exposure significantly altered the input-output curves obtained before tetanic stimulation, but both suppressed the increase in response observed in controls after tetanic stimulation. Because LTP is thought to be correlated with learning ability, these observations may provide at least a partial mechanism to explain the reduction of intelligence quotient observed in humans exposed to PCBs early in development. Key words: CA1, generator column, gestational/lactational exposure, hippocampus, in vitro exposure, learning. Environ Health Perspect 108:827-831 (2000) . [Online 27 July 2000] http://ehpnet1.niehs.nih.gov/docs/2000/108p827-831hussain/ abstract.html Address correspondence to D.O. Carpenter, School of Public Health, University at Albany, One University Place, B242, Rensselaer, NY 12144. Telephone: (518) 525-2660. Fax: (518) 525-2665. E-mail: carpent@cnsvax.albany.edu Supported by NIEHS P42 ES04913, NIH D43 TW00636, and the U.S.-Hungarian Joint Fund (D. Carpenter) . Received 23 December 1999 ; accepted 17 April 2000. The full version of this article is available for free in HTML or PDF formats. |