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The smoothie for Reduced risk and Treatment of Acquired immunodeficiency syndrome (AIDS)
Yield: 2 serving (about 8 ounce each)
1 cup Tomato
1/2 cup Brazil nut
1 cup green tea drink (Make from 4 grams of green tea, a slice of ginger and a cup of hot water lipped for 5 minute. 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 dream of finding the natural ingredient for prevention and treatment of Acquired immunodeficiency syndrome (AIDS), without adverse effects in replacement of conventional medication has not been abated. Some ingredients have to discard because of not achieving the same potent results in human trials.
Scientist community may have found the smoothie(combined ingredients of garlic, olive and coconut oils) with potential and therapeutic value for reduced risk and treatment of Acquired immunodeficiency syndrome (AIDS)without adverse effects.
Human immunodeficiency virus (HIV) is a lentivirus that causes acquired immunodeficiency syndrome (AIDS) of which can lead to the progression of weakened immune system casues of infectous diseases and cancers. According to the studies, patients with human immunodeficiency virus (HIV) are asscoiated to low levels of vitamin A and selenium(1).
Selenium, a chemical element with symbol Se and antioxidant found in Brazil nut, plays an important role in protection of cell against significant impairments of antioxidative defenses induced human immunodeficiency virus (HIV) (2).
Dr. Delmas-Beauvieux MC and colleagues at the Université Bordeaux II, suggested, selenium supplementation could be of great interest in protecting cells against oxidative stress and glutathione peroxidase (GPX), and glutathione (GSH) are important in expression of natural enzymatic defense system in detoxifying hydrogen peroxide(3).
Vitamin A, a bi-polar molecule formed by bonds between carbon and hydrogen, is a fat soluble vitamin converted from beta-carotene, a powerful antioxidant. Accoridng to the The University of Maryland School of Medicine, deficiency of vitamin A in human immunodeficiency virus (HIV) infection has been associated with more progressive HIV disease(4).
Dr.Mehta S and Dr. Fawzi W. in the study of the effects of vitamins, including vitamin A, on HIV/AIDS patients, said, "periodic vitamin A supplementation of HIV-infected infants and children is beneficial in reducing all-cause mortality and morbidity and is recommended"(5).
According to the Creighton University, green tea, epigallocatechin gallate, theaflavins may be effective in prevention and treatment of sexually transmitted infections caused by HIV (human immunodeficiency virus), HSV (herpes simplex virus) and HPV (human papilloma virus)(6).
Dr. Hamza A and Dr. Zhan CG. said, "(-)-epigallocatechin gallate (EGCG) from green tea is an inhibitor blocking gp120-CD4 binding" by blocking the initial step of HIV-1 entry into the cells"(7).
In support of above blocking, Dr. Williamson MP and colleagues at the University of Sheffield suggested, green tea Epigallocatechin gallate has a potential use as adjunctive therapy in HIV-1 infection(8) through its binding of HIV-1 glycoprotein (gp) 120 to the CD4 molecule on T cells.
The Smoothie of Brazil Nut, Tomato and Green Tea may hold a key for further studies in production of a curable natural remedy for prevention and treatment of Human immunodeficiency virus (HIV) /Acquired immunodeficiency syndrome (AIDS)
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People who are at increased risk of Human immunodeficiency virus (HIV) /Acquired immunodeficiency syndrome (AIDS) due to family history, weaken immunity,....should drink at least one cup or more daily. People with hHuman immunodeficiency virus (HIV) /Acquired immunodeficiency syndrome (AIDS) may drink as much as they can, depending to the digestive toleration.
.
People who are at increased risk of Human immunodeficiency virus (HIV) /Acquired immunodeficiency syndrome (AIDS) due to family history, weaken immunity,....should drink at least one cup or more daily. People with hHuman immunodeficiency virus (HIV) /Acquired immunodeficiency syndrome (AIDS) may drink as much as they can, depending to the digestive toleration.
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References
(1) The enzymatic antioxidant system in blood and glutathione status in human immunodeficiency virus (HIV)-infected patients: effects of supplementation with selenium or beta-carotene by Delmas-Beauvieux MC1, Peuchant E, Couchouron A, Constans J, Sergeant C, Simonoff M, Pellegrin JL, Leng B, Conri C, Clerc M.(PubMed)
(2) Effect of selenium supplementation on CD4+ T-cell recovery, viral suppression and morbidity of HIV-infected patients in Rwanda: a randomized controlled trial by Kamwesiga J1, Mutabazi V, Kayumba J, Tayari JC, Uwimbabazi JC, Batanage G, Uwera G, Baziruwiha M, Ntizimira C, Murebwayire A, Haguma JP,Nyiransabimana J, Nzabandora JB, Nzamwita P, Mukazayire E; Rwanda Selenium Authorship Group.(PubMed)
(3) Plasma Selenium Concentrations Are Sufficient and Associated with Protease Inhibitor Use in Treated HIV-Infected Adults by Hileman CO1, Dirajlal-Fargo S2, Lam SK3, Kumar J3, Lacher C4, Combs GF Jr4, McComsey GA5.(PubMed)
(4) Quantitation of parvalbumin+ neurons and human immunodeficiency virus type 1 (HIV-1) regulatory gene expression in the HIV-1 transgenic rat: effects of vitamin A deficiency and morphine by Sultana S1, Li H, Puche A, Jones O, Bryant JL, Royal W.(PubMed)
(5) Effects of vitamins, including vitamin A, on HIV/AIDS patients by Mehta S1, Fawzi W.(PubMed)
(6) Natural polyphenols: potential in the prevention of sexually transmitted viral infections by Date AA1, Destache CJ2.(PubMed)
(7) How can (-)-epigallocatechin gallate from green tea prevent HIV-1 infection? Mechanistic insights from computational modeling and the implication for rational design of anti-HIV-1 entry inhibitors by Hamza A1, Zhan CG.(PubMed)
(8) Epigallocatechin gallate, the main polyphenol in green tea, binds to the T-cell receptor, CD4: Potential for HIV-1 therapy. by Williamson MP1, McCormick TG, Nance CL, Shearer WT.(PubMed)