Study on flies may help offer insight into human metabolic disease
June 1st, 2010 - 1:49 pm ICT by ANIWashington, June 1 (ANI): Commonalities between flies and humans can help offer a valuable new model for galactosemia, a metabolic disease resulting from an inherited defect that prevents the proper metabolism of galactose, a sugar commonly found in dairy products, like milk, say scientists.
The ability to study the disease is limited by a lack of animal models. However, new information suggests that similarities between humans and flies may provide scientists with useful clues.
The inability to breakdown simple sugars in common foods, such as milk, can lead to the accumulation of sugars in the blood, which become toxic and damaging to a variety of organ systems.
People with galactosemia, either classic galactosemia or epimerase deficiency galactosemia, have genetic mutations that decrease their levels of the key enzymes (GALT and GALE) responsible for the metabolism of a common form of dietary sugar.
Without proper levels of these proteins, these people are unable to process the sugar, galactose, which makes up about half of the calories in milk. Both disorders can have severe effects. Patients suffer from liver and brain damage, cataracts, and kidney failure. The disease can be fatal. There is currently no cure and prognosis and treatment remain ill-defined, partly due to the lack of a good animal model that scientists can use to study the disease and to develop potential treatments.
Scientists at Emory University developed flies that carry genetic changes similar to those found in patients with galactosemia.
Like patients with classic galactosemia, flies that are missing GALT survive if they are raised on food that does not contain galactose, but die in development if exposed to high levels of galactose. Flies with impaired GALE function also succumb in greater numbers when exposed to galactose during development, similar to patients with defects in the same area of their metabolic pathway.
The Emory scientists also tested the relationship between the timing of galactose exposure with the fly’s outcome, and designed and characterized flies in which they could remove or control the production of GALT or GALE at variable points in the animal’s development to determine when and where the sugar breakdown was most needed.
These models can help researchers understand how changes in sugar metabolism lead to disease and open the door to novel drug discovery by serving as a testing ground for candidate therapeutics. (ANI)
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Tags: animal model, animal models, brain damage, calories in milk, cataracts, common foods, commonalities, dairy products, dietary sugar, emory university, galactosemia, galt, genetic changes, genetic mutations, kidney failure, metabolic disease, metabolic pathway, organ systems, proper metabolism, simple sugars