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Alcohol and Alcoholism Advance Access originally published online on January 9, 2009
Alcohol and Alcoholism 2009 44(2):185-198; doi:10.1093/alcalc/agn109
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© The Author 2009. Published by Oxford University Press on behalf of the Medical Council on Alcohol. All rights reserved

In vitro Neurogenesis from Neural Progenitor Cells Isolated from the Hippocampus Region of the Brain of Adult Rats Exposed to Ethanol during Early Development through Their Alcohol-Drinking Mothers

Ashok K. Singh*, Shveta Gupta, Yin Jiang, Mohammed Younus and Mohammed Ramzan

Department of Veterinary Population Medicine, College of Veterinary Medicine, University of Minnesota, Twin Cities campus, St Paul, MN 55108, USA

* Corresponding author: Department of Veterinary Population Medicine, College of Veterinary Medicine, University of Minnesota, Twin Cities campus, St Paul, MN 55108, USA. E-mail: singh001{at}umn.edu

Received 14 July 2008; first review notified 3 October 2008; in revised form 16 October 2008; accepted 28 November 2008; advance access publication 9 January 2009


   Abstract

Aims: This study was aimed to determine whether ethanol exposure during early development altered neurogenesis in the brain of adult rats. Methods: Pregnant rats were given either ethanol-mixed or mannose-mixed (for control) rodent liquid diet ad libitum. Ethanol drinking continued during pregnancy and nursing. After weaning, the pups (ACo: pups from control mothers, AEo: pups from ethanol exposed mothers) received normal diet and water ad libitum for 11 weeks. Then the rats were anesthetized, their brains were collected and the hippocampal samples were processed for isolation of neural progenitor cells (NPCs). ACo NPCs and AEo NPCs were sequentially grown in media containing different growth factors that induced proliferation and differentiation. Results and Conclusions: Neuronal maturation was significantly delayed in ethanol-exposed rats. ACo NPCs, up to day 7 of culture, exhibited high β-catenin-probe binding, an increase in Ca2+ when exposed to {gamma}-amino butyric acid (GABA) and lack of response to glutamate (Glu) exposure. β-Catenin-probe binding and the stimulatory effects of GABA declined thereafter. ACo NPCs, at culture day 29, exhibited high β-catenin-probe binding, lack of response to GABA and elevated Glu-induced increase in Ca2+i. Cultures of AEo NPCs showed an amplified stimulatory effects of GABA, attenuated stimulatory effects of Glu and attenuated the delayed (culture day 29) increase in the expression of Wnt proteins and β-catenin-probe binding. This suggests a significant alteration in neurogenesis and synapse formation in adult rats exposed to ethanol at early development through their alcohol-drinking mothers.


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