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The American Heart Association and other health organizations have concluded that consumers should get their antioxidants from foods rather than supplements. They add that taking supplements may even be harmful. Supplement manufacturers claim that such statements are unfair and that their natural botanical extracts provide numerous health benefits. In fact, some suggest that beneficial effects can only be achieved by taking high-dose supplements. Given that there are currently no DRI defining the kinds of antioxidants or the daily quantities needed, how might you ensure a healthy intake of antioxidants? If you decide to take an antioxidant supplement, how might you research the product to determine its safety and effectiveness?
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Understanding Nutrition (MindTap Course List)
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- Combinations of the proteoglycans glucosamine hydrochloride (GH) and chondroitin sulfate (GS) are available as dietary supplements. These over-the-counter compounds are not subject to most federal regulations - as long as they do not claim any specific health benefits - and may not undergo the same testing and quality assurance methods as regulated drugs. GH and CS supplements are recommended by physicians and medical organizations to assist with joint health, based on a variety of studies and trials of the compounds' effects in model organisms and humans alike. Other studies have concluded that these supplements are safe to use but are no more effective than placebo for the relief of pain and inflammation associated with osteoarthritis. please answer the following questions: a) What is proteoglycan (briefly explain its structure)? b) What is the composition of chondroitin sulfate (GS) (is it acidic, basic, neutral)? c) What is the commercial application of proteoglycan we studied and…arrow_forwardDietary supplement manufacturers can bypass many of the strict regulations that apply to the introduction of new medications into the marketplace. Check all of the regulations with which dietary supplement manufacturers must comply. Check All That Apply Manufacturers must provide the FDA with scientific evidence indicating that their products are foods that provide measurable health benefits. Manufacturers must notify the FDA and provide the agency with information about the safety of any supplement that contains dietary ingredients that were not marketed in dietary supplements prior to 1994, unless the substance had been used in foods. Manufacturers need FDA approval before manufacturing or marketing their products. Manufacturers are required to keep records concerning reports they receive about serious adverse health effects that may have been caused by their products. Manufacturers must obtain approval from a board of practicing physicians before they can market their products for…arrow_forwardMake a literature or internet search, and compare how herbal preparations differ from the manufacture of commercial synthetic drugsarrow_forward
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