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Alcohol and Alcoholism Advance Access published online on April 29, 2008

Alcohol and Alcoholism, doi:10.1093/alcalc/agn024
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© The Author 2008. Published by Oxford University Press on behalf of the Medical Council on Alcohol. All rights reserved

Red wine, but not Port wine, protects rat hippocampal dentate gyrus against ethanol-induced neuronal damage—relevance of the sugar content

Ângelo Carneiro1, Marco Assunção1, Victor De Freitas2, Manuel Maria Paula-Barbosa1 and José Paulo Andrade1,*

1 Department of Anatomy, Faculty of Medicine, University of Porto
2 Department of Chemistry, Faculty of Sciences, Center of Investigation in Chemistry, University of Porto, Porto, Portugal

* Corresponding author: Department of Anatomy, Faculty of Medicine, University of Porto, Al. Prof. Hernâni Monteiro, 4200-319 Porto, Portugal. Tel: +351-22-5513616; Fax: +351-22-5513617; E-mail: jandrade{at}med.up.pt

Received 19 September 2007; first review notified 22 November 2007; in revised form 6 December 2007; accepted 5 February 2008


   Abstract

Aims: Chronic ethanol consumption leads to oxidative damage in the central nervous system inducing neuronal degeneration and impairment of brain functions. Nevertheless, it has been reported that grape polyphenols might prevent the alluded ethanol effects. We have reported that prolonged red wine intake improves hippocampal formation oxidative status, a finding not replicated using Port wine. Thus, we thought of interest to compare the effects of chronic ingestion of these wines in the morphology of dentate gyrus (DG) neurons that are particularly vulnerable to alcohol effects. Methods: Six-month-old Wistar rats were fed either with red wine or Port wine (both with 20% ethanol content, v/v), and the results were compared with 20% (v/v) ethanol-treated, ethanol/glucose and pair-fed control groups. After 6 months of treatment, the layer volumes of the DG and the total number of granule and hilar neurons were estimated. The dendritic trees of granule cells were also studied in Golgi-impregnated material. Results: The number of granule cells and the DG layer volumes were similar among all groups. However, the number of hilar neurons was reduced in Port wine, ethanol-treated and ethanol/glucose animals. Furthermore, the granule cells from these groups showed a decrease in the total dendritic length. Conclusions: Although the Port wine and red wine have similar amounts of flavanols with identical ability to protect against oxidative stress, the differences observed are probably related to the very dissimilar processes of wine production, leading in Port wine to a high content of sugars, which are known to have potent pro-oxidant effects.


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