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Prenatal ethanol exposure enhances NMDAR-dependent long-term potentiation in the adolescent female dentate gyrus

✍ Scribed by Andrea K. Titterness; Brian R. Christie


Book ID
102854008
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
923 KB
Volume
22
Category
Article
ISSN
1050-9631

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✦ Synopsis


Abstract

The dentate gyrus (DG) is a region of the hippocampus intimately involved with learning and memory. Prenatal exposure to either stress or ethanol can reduce long‐term potentiation (LTP) in the male hippocampus but there is little information on how these prenatal events affect LTP in the adolescent female hippocampus. Previous studies suggest that deleterious effects of PNEE can, in part, be mediated by corticosterone, suggesting that prenatal stress might further enhance any alterations to LTP induced PNEE. When animals were exposed to a combination of prenatal stress and PNEE distinct sex differences emerged. Exposure to ethanol throughout gestation significantly reduced DG LTP in adolescent males but enhanced LTP in adolescent females. Combined exposure to stress and ethanol in utero reduced the ethanol‐induced enhancement of LTP in females. On the other hand, exposure to stress and ethanol in utero did not alter the ethanol‐induced reduction of LTP in males. These results indicate that prenatal ethanol and prenatal stress produce sex‐specific alterations in synaptic plasticity in the adolescent hippocampus. © 2010 Wiley Periodicals, Inc., Inc.