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The Good And The Bad Of A Potential Alzheimer's Target

Date:
June 29, 2008
Source:
American Society for Biochemistry and Molecular Biology
Summary:
Research in fruit flies has shown that enhancing the production of a protein called neprilysin can reduce the formation of plaques and neuron death associated with Alzheimer's, at the expense of reducing the flies' lifespan.
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Research in fruit flies has shown that enhancing the production of a protein called neprilysin can reduce the formation of plaques and neuron death associated with Alzheimer's, at the expense of reducing the flies' lifespan.

The buildup of amyloid-beta protein plaques within the brain is a major hallmark of Alzheimer's, and one that is believed to contribute to disease progression. Normally, special enzymes chew up and clear these plaques, and deficiencies in these enzymes are one potential disease cause.

In fact, one major amyloid degrader called neprilysin (NEP) decreases naturally with age and may be the reason the elderly are more at risk for Alzheimer's. Enhancing NEP production might therefore be an attractive therapy, and studies in mice have suggested it has potential. However, no studies have really looked into possible adverse effects of over-activating NEP (after all, nature probably turns it off for a reason).

In this study, research groups led by Koichi Iijima and Kanae Iijima-Ando did just that, using transgenic fruit flies expressing human NEP and/or amlyoid-beta protein. On the positive side, NEP expression did reduce plaque deposits and neuron damage in the flies as expected; on the other hand, NEP also reduced the activity of important neural proteins called CREB proteins and shortened the average lifespan of the flies (normal flies live about 60 days) by about 10 days (although NEP-flies did live longer than those only expressing amyloid protein).

This study illustrates the care that must be taken when considering Alzheimer's treatments, and that it's critical to better understand normal aging when dealing with Alzheimer's or other age-related conditions.


Story Source:

The above story is based on materials provided by American Society for Biochemistry and Molecular Biology. Note: Materials may be edited for content and length.


Journal Reference:

  1. Overexpression of Neprilysin Reduces Alzheimer's Amyloid-² 42 (A²42)-Induced Neuron Loss and Intraneuronal A²42 Deposits, but Causes a Reduction in CREB-Mediated Transcription, Age-Dependent Axon Pathology and Premature Death in DROSOPHILA. JBC, (online June 27, 2008)

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American Society for Biochemistry and Molecular Biology. "The Good And The Bad Of A Potential Alzheimer's Target." ScienceDaily. ScienceDaily, 29 June 2008. <www.sciencedaily.com/releases/2008/06/080627163146.htm>.
American Society for Biochemistry and Molecular Biology. (2008, June 29). The Good And The Bad Of A Potential Alzheimer's Target. ScienceDaily. Retrieved May 26, 2015 from www.sciencedaily.com/releases/2008/06/080627163146.htm
American Society for Biochemistry and Molecular Biology. "The Good And The Bad Of A Potential Alzheimer's Target." ScienceDaily. www.sciencedaily.com/releases/2008/06/080627163146.htm (accessed May 26, 2015).

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