Vitamins
Vitamins
Vitamins
min B9 Q9. What's the difference between a milligram (mg), microgram (mcg), and an IU? A9: As metric units of measurement to quantify mass, 1000 micrograms (mcg) equal 1 milligram (mg). An IU (International Unit) is a unit of measurement for vitamins and other specific biologically active substances. The precise definition of one IU differs from substance to substance and is established by international agreement for each substance. There is no equivalence among different substances; for instance, one IU of vitamin E does not contain the same number of milligrams as one IU of vitamin A. For example, vitamin E exists in a number of different forms having different biological activities. Rather than specifying the precise type and mass of vitamin E in a preparation, the Supplement Facts label specifies the number of International Units of vitamin E. The mass equivalents of 1 IU for selected vitamins are: Vitamin A: 1 IU is the biological equivalent of 0.3 g retinol, or of 0.6 g beta-carotene Vitamin D: 1 IU is the biological equivalent of 0.025 g cholecalciferol/ergocalciferol
Vitamin E: 1 IU is the biological equivalent of 2/3 mg (0.667) d-alphatocopherol, or of 1 mg of dl-alpha-tocopherol acetate
11: VITAMIN A
Some foods contain both vitamin A itself, and other substances that can be converted to vitamin A, known as provitamin A, vitamin A precursors or carotenoids . Although it is possible to have a toxic amount of preformed vitamin A, this appears not to be the case with provitamin A, so that it is clearly safer to have more of the latter. Vitamin A is a fat-soluble vitamin, as also are vitamins D, E and K. It is therefore necessary to have some fat in the diet for these vitamins to be adequately absorbed.
One of the most important consequences of vitamin A deficiency is dryness of the eyes eventually leading to blindness. It remains one of the main causes of blindness in the world. Night blindness is also an eye complication of early vitamin A deficiency.
Vitamin A is a vitamin that is needed by the retina of the eye in the form of a specific metabolite, the light-absorbing molecule retinal, that is absolutely necessary for both lowlight (scotopic vision) and color vision. Vitamin A also functions in a very different role, as an irreversibly oxidized form of retinol known as retinoic acid, which is an important hormone-like growth factor for epithelial and other cells. In foods of animal origin, the major form of vitamin A is an ester, primarily retinyl palmitate, which is converted to the retinol (chemically an alcohol) in the small intestine. The retinol form functions as a storage form of the vitamin, and can be converted to and from its visually active aldehyde form, retinal. The associated acid (retinoic acid), a metabolite that can be irreversibly synthesized from vitamin A, has only partial vitamin A activity, and does not function in the retina for the visual cycle. All forms of vitamin A have a beta-ionone ring to which an isoprenoid chain is attached, called a retinyl group. Both structural features are essential for vitamin activity.[1] The orange pigment of carrots beta-carotene can be represented as two connected retinyl groups, which are used in the body to contribute to vitamin A levels. Alpha-carotene and gamma-carotene also have a single retinyl group, which give them some vitamin activity. None of the other carotenes have vitamin activity. The carotenoid beta-cryptoxanthin possesses an ionone group and has vitamin activity in humans. Vitamin A can be found in two principal forms in foods:
Retinol, the form of vitamin A absorbed when eating animal food sources, is a yellow, fat-soluble substance. Since the pure alcohol form is unstable, the vitamin is found in tissues in a form of retinyl ester. It is also commercially produced and administered as esters such as retinyl acetate or palmitate. The carotenes alpha-carotene, beta-carotene, gamma-carotene; and the xanthophyll beta-cryptoxanthin (all of which contain beta-ionone rings), but no other carotenoids, function as vitamin A in herbivores and omnivore animals, which possess the enzyme required to convert these compounds to retinal. In general, carnivores are poor converters of ionine-containing carotenoids, and pure carnivores such as cats and ferrets lack beta-carotene 15,15'-monooxygenase and cannot convert any carotenoids to retinal (resulting in none of the carotenoids being forms of vitamin A for these species).
History
The discovery of vitamin A may have stemmed from research dating back to 1906, indicating that factors other than carbohydrates, proteins, and fats were necessary to keep cattle healthy.[2] By 1917 one of these substances was independently discovered by Elmer McCollum at the University of WisconsinMadison, and Lafayette Mendel and Thomas Burr Osborne at Yale University. Since "water-soluble factor B" (vitamin B) had recently been discovered, the researchers chose the name "fat-soluble factor A" (vitamin A).[2] In 1919, Steenbock (University of Wisconsin) proposed a relationship between yellow plant
pigments (beta-carotene) and vitamin A. Vitamin A was first synthesized in 1947 by two Dutch chemists, David Adriaan van Dorp and Jozef Ferdinand Arens.
Because the conversion of retinol from provitamin carotenoids by the human body is actively regulated by the amount of retinol available to the body, the conversions apply strictly only for vitamin A-deficient humans. The absorption of provitamins depends greatly on the amount of lipids ingested with the provitamin; lipids increase the uptake of the provitamin.[5] The conclusion that can be drawn from the newer research is that fruits and vegetables are not as useful for obtaining vitamin A as was thought; in other words, the IUs that these foods were reported to contain were worth much less than the same number of IUs of fat-dissolved oils and (to some extent) supplements. This is important for vegetarians, as Night blindness is prevalent in countries where little meat or vitamin A-fortified foods are available.
A sample vegan diet for one day that provides sufficient vitamin A has been published by the Food and Nutrition Board (page 120[4]). On the other hand, reference values for retinol or its equivalents, provided by the National Academy of Sciences, have decreased. The RDA (for men) of 1968 was 5000 IU (1500 g retinol). In 1974, the RDA was set to 1000 RE (1000 g retinol), whereas now the Dietary Reference Intake is 900 RAE (900 g or 3000 IU retinol). This is equivalent to 1800 g of -carotene supplement (3000 IU) or 10800 g of -carotene in food (18000 IU).
(Note that the limit refers to synthetic and natural retinol ester forms of vitamin A. Carotene forms from dietary sources are not toxic.[7][8]) According to the Institute of Medicine of the National Academies, "RDAs are set to meet the needs of almost all (97 to 98%) individuals in a group. For healthy breastfed infants, the AI is the mean intake. The AI for other life stage and gender groups is believed to cover the needs of all individuals in the group, but lack of data prevents being able to specify with confidence the percentage of individuals covered by this intake."[9] To reduce the possible risk of bone fracture and osteoporosis in postmenopausal women, an upper limit intake of 1500 g RE/d has been recommended.