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The smoothie for reduced risk and Treatment of cystic fibrosis
Yield: 2 serving (about 8 ounce each)
1/8 cup flax seed
1 cup green tea drink (Make from 4 grams of green tea, and a cup of hot water lipped for 5 minutes. Set aside for cooling to room temperature)
1. Place all ingredients in a blender and puree about 1 minute
2. Blend on high speed about 1 minute or until the mixture is thick and the ice is well crushed. Add more green tea drink if needed
3. Serve immediately
The finding the natural ingredients for treatment of cystic fibrosis is considered as a dream of many scientist to replace the long usage adverse effect of conventional medicine to other organs in the body. Unfortunately, many compounds found effective in initial studying failed to confirm the potential in large sample size and multi center.
Cystic fibrosis is a genetic disease passing through the family affecting the body's epithelial cells. The genetic disease cause the building up of mucus of that may block the lungs and ducts and passageway, causing infection and breathing problem.
Recent discoveries from respectable institutions suggested that green tea(1), grape(4) and flax seed(7) exert theirs antioxidant effects through numerous mechanisms in reduced risk and treatment of cystic fibrosis. Epigallocatechin-3-gallate (EGCg), a green tea component exhibited against Stenotrophomonas maltophilia (Sm) isolates from cystic fibrosis (CF) patients, through significantly reduced Sm bacterial counts in an acute infection model(1) back by its anti microbial activities(2).
Green tea has been a precious drink in traditional Chinese culture and used exceptional in socialization for more than 4000 thousand years used in traditional Chinese medicine for treatment of various diseases, including cancers and heart diseases.
According to the Harvard Medical School, Massachusetts General Hospital, fatty acid alterations have been found in the blood and tissues of cystic fibrosis (CF) patients(10).
said, " regular omega-3 supplements may provide some benefits for people with cystic fibrosis with relatively few adverse effects."(8) through restoration of abnormal fatty acid profiles in patients with in cystic fibrosis(9).
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