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JCI table of contents: December 14, 2006

EDITORS PICK: Antioxidants decrease disease in a Drosophila model of Alzheimers disease

Alzheimers disease (AD) is one of a number of neurodegenerative disorders in which brain cells damaged by naturally occurring chemicals known as reactive oxygen species (ROS) have been observed. However, whether this oxidative damage causes neurodegeneration or is a consequence of it has not been previously determined. A study appearing online on December 14, in advance of publication in the January print issue of the Journal of Clinical Investigation, indicates that oxidative damage is a factor contributing to neurodegeneration in a Drosophila model of neurodegenerative disorders such as AD.

Mel Feany and colleagues from Brigham and Womens Hospital and Harvard Medical School assessed neuron cell death in Drosophila expressing a neurodegenerative diseaseassociated form of the human protein tau. The number of dying neurons was increased if these insects were also genetically modified to have high levels of ROS. By contrast, if the insects were treated with the antioxidant vitamin E they had decreased numbers of dying neurons. This demonstration that oxidative stress contributes to neurodegeneration in this model of AD suggests that targeting antioxidant pathways might provide a new approach for treating individuals with AD and other related neurodegenerative disorders.

TITLE: Oxidative stress mediates tau-induced neurodegeneration in Drosophila.

AUTHOR CONTACT:
Mel B. Feany
Brigham and Womens Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Phone: (617) 525-4405; Fax: (617) 525-4422; E-mail: mel_feany@hms.harvard.edu.

View the PDF of this article at: https://www.the-jci.org/article.php?id=28769


BONE BIOLOGY: IFN-gamma tips towards bone destruction


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Contact: Karen Honey
press_releases@the-jci.org
212-342-4159
Journal of Clinical Investigation
14-Dec-2006


Page: 1 2 3

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