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Common Name: Beta-Cerotene
Synonyms: Provitamin A, trans-beta carotene
Overview:
Beta-carotene belongs to a class of phytochemicals called carotenoids.
It is an orange pigment necessary for photosynthesis. It transmits the
light energy that it absorbs to chlorophyll where it is turned into the
life-energy of the plant. As with all other carotenoids, beta-carotene
is a fat soluble pigment and is responsible for the orange color of
many fruits and vegetables. Beta-carotene is stored in the liver and
can then be converted to Vitamin A as needed. Because of this ability
to be transformed into vitamin A, beta-carotene is what is called a
provitamin. Because the body converts beta-carotene to vitamin A on as
needed basis, it does not have to toxic effects that accompany high
vitamin A intake.
Health Benefits
Beta-carotene is an antioxidant and because of this has been shown to
have many health enhancing properties. This provitamin has
demonstrated:
- The ability to stimulate
the immune system by increasing chemicals needed in monocytes (a white
blood cell responsible for antibody production) to help fight
infections, as well as increase the secretion of tumor necrosis factor
by these same white blood cells.
- That as a precursor
of Vitamin A, beta carotene is an important nutrient for maintaining
healthy eyes. Vitamin A is incorporated into the retina and is
responsible for the ability to see well in dim light. Vitamin A
deficiency is the leading cause of childhood blindness in the
developing world.
- Its ability to inhibit tumor growth in some malignant cell lines including human prostate cancer cells in vitro
(tests conducted in a test tube). The Physician Health Study (a study
of a large number of physicians for a long period of time) showed that
those with a low baseline of beta-carotene experienced a decreased risk
of developing prostate cancer when supplemented with 50mcgs of
beta-carotene. Beta-carotene’s tumor inhibiting properties seem to be
more effective when used in conjunction with vitamins C and E.
- That it may also reduce the risk of heart disease.
- That
high doses of beta-carotene may decrease sensitivity to the sun. It has
proven particularly effective for people with the skin condition caused
by sunlight exposure, such as erythropoietic protoporphyria. This is a
condition that is characterized by the development of hive or eczema
upon exposure to sunlight.
- In preliminary studies
that people with scleroderma (an autoimmune disease characterized by a
hardening of the skin) have a low beta-carotene level and would benefit
from beta-carotene supplementation.
Dietary Sources
Beta-carotene is found in many fruits and vegetable. The more intense
the color, the more beta-carotene it contains. Some of these fruits and
vegetables are:
|
Carrots |
|
Spinach |
|
Lettuce |
|
Tomatoes |
|
Cantaloupe |
|
Sweet Potatoes |
 Winter Squash |
Available forms
Beta-carotene is available in:
Capsules
Gel tablets
Since beta-carotene is fat soluble, it is recommended that it be taken
with meals that contain at least 3 grams of fat to ensure proper
absorption.
Recommended Dosage:
Pediatric
For children younger than 14 years old with erythropoietic
protoporphyria 30 to 150mg a day (250,00 IU) either in a single or
divided dose fro 2 to six weeks is recommended. This needs to be done
under the supervision of the child’s healthcare practitioner.
Adult
For health maintenance, 15-50mg (25,000 to 85,000 IU) per day is recommended.
For adults with erythropoietic protoporphyria, 30-300mg (50,000 to 500,000 IU) per day for 2-6 weeks is recommended.
Contra indications
Studies have shown that beta-carotene supplement in doses greater than
20mg per day may increase of heart disease and cancer in those who
smoke or drink heavily. These people should not use this supplement.
Beta-carotene does not protect against sunburn
Women who are pregnant or breastfeeding should consult a health care provider before using beta-carotene as a supplement.
Some of the side effects of beta-carotene include:
- Skin discoloration. This is a yellow discoloration that will eventually go away if the dosage is reduced.
- Loose stool.
- Bruising
- Joint pain
Drug interactions
People taking the following medications should avoid beta-carotene supplements.
- Cholestyramine taken at the same time as beta-carotene may loer the absorption of this supplement
- Colestipal taken at the same time as beta-carotene may decrease the absorption of the supplement.
- Mineral oil taken at the same time as beta-carotene may decrease its absorption.
- Orlistat may decrease the absorption of beta-carotene
- Lutein intake at the same time as beta-carotene may decrease the uptake of lutien
- Pectin taken with beta carotene may decrease the absorption of beta-carotene.
- The ongoing use of alcohol with beta-carotene supplements may increase the likelihood of liver damage.
- There is no evidence of beta-carotene overdose on record.
Web References
- http://en.wikipedia.org/wiki/Beta_carotene
- http://www.pdrhealth.com/drug_info/nmdrugprofiles/nutsupdrugs/bet_0032.shtml
- http://lpi.oregonstate.edu/infocenter/vitamins/vitaminA/
Printed Reference Material
- Albanes D, Heinonen OP, Taylor PR, et al. Alpha-tocopherol and beta-carotene supplements and lung c
- Albanes D. Beta-carotene and lung cancer: a case study. Am J Clin Nutr. 1999; 69:1345S-1350S.
- Clark
JH, Russell GJ, Fitzgerald JF, Nagamori KE. Serum beta-carotene,
retinol, and alpha-tocopherol levels during mineral oil therapy for
constipation. Am J Dis Child. 1987;141(11):1210-1212. (abstract)
- DerMarderosian A. Ed. The Review of Natural Products. Tanning Tablets. St. Louis, MO: Facts and Comparisons; 2000. [Date of issue Nov. 1991]
- Elinder
LS, Hadell K, Johansson J, Molgaard J, Holme I, Olsson AG, et al.
Probucol treatment decreases serum concentrations of diet-derived
antioxidants. Arterioscler Thromb Vasc Biol. 1995;15(8):1057-1063. (abstract)
- Facts and Comparisons. Beta Carotene. Loose leaf edition. St. Louis: Mo; Wolters Kluwer Co; Jan 2000 update:7.
- Gabriele
S, Alberto P, Sergio G, Fernanda F, Marco MC. Emerging potentials for
an antioxidant therapy as a new approach to the treatment of systemic
sclerosis. Toxicology. 2000; 155(1-3):1-15.
- Hercberg S, Galan P, Preziosi P. Antioxidant vitamins and cardiovascular disease: Dr Jekyll or Mr Hyde? Am J Public Health. 1999; 89(3):289-291.
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AL, Hollis S, Schofield D, Rieley F, Blann A, Griffin K, Moore T,
Braganza JM, Jayson MI. A double-blind placebo-controlled trial of
antioxidant therapy in limited cutaneous systemic sclerosis. Clin Exp Rheumatol. 2000;18(3):349-356.
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G, Cassano PA. Antioxidant nutrients and pulmonary function: the Third
National Health and Nutrition Examination Survey (NHANES III). Am J Epidemiol. 200015;151(10):975-981.
- Leo MA, Lieber CS. Alcohol, vitamin A, and beta-carotene: Adverse interactions, including hepatotoxicity and carcinogenicity. Am J Clin Nutr. 1999;69(6):1071-1085.
- Liede
KE, Alfthan G, Hietanen JH, Haukka JK, Saxen LM, Heinonen OP.
Beta-carotene concentration in buccal mucosal cells with and without
dysplastic oral leukoplakia after long-term beta-carotene
supplementation in male smokers. Eur J Clin Nutr. 1998;52(12):872-876.
- Martindale: The Complete Drug Reference. 32nd edition. London, UK; Pharmaceutical Press; 1999. Micromedex Inc., on line database.
- Mathews-Roth MM. Photoprotection by carotenoids. Federation Proceedings. 1987;46(5):1890-1893.
- McEvoy Ed. AHFS Drug Information. Bethesda, MD: American Society of Health-System Pharmacists; 2000:3308.
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GS, Goodman G, Thornquist M, Grizzle J, Rosenstock L, Barnhart S, et
al. The beta-carotene and retinol efficacy trial (CARET) for
chemoprevention of lung cancer in high risk populations. Smokers and
asbestos exposed workers. Cancer Res. 1994;54:2038S-2043S.
- Omenn
GS, Goodman GE, Thornquist MD, et al. Risk factors for lung cancer and
for intervention effects in CARET, the Beta-Carotene and Retinol
Efficacy Trial. J Natl Cancer Inst. 1996;88(21):1550-1559. [abstract]
- Physician's Desk Reference. 54th ed. Montvale, NJ: Medical Economics Company, Inc.; 2000:2695.
- Pizzorno JE, Murray MT. Textbook of Natural Medicine, Vol 1. 2nd Edition. Edinburgh, UK: Churchill Livingstone; 1999.
- Pryor WA, Stahl W, Rock CL. Beta carotene: from biochemistry to clinical trials. [Review] Nutr Rev. 2000;58(2 Pt 1):39-53.
- Roodenburg
AJ, Leenen R, van het Hof KH, Weststrate JA, Tijburg LB. Amount of fat
in the diet affects bioavailability of lutein esters but not of
alpha-carotene, beta-carotene, and vitamin E in humans. Am J Clin Nutr. 2000;71(5):1187-1193.
- The
Alpha-tocopherol, Beta-carotene Cancer Prevention Study Group. The
effect of vitamin E and Beta Carotene on incidence of lung cancer and
other cancers in male smokers. N Engl J Med. 1994;330:1029-1035.
- USPDI Vol. II. Beta-Carotene (Systemic). Englewood, CO: Micromedex ® Inc.:Revised 7/9/97.
- Werbach M, Moss J. Textbook of Nutritional Medicine. Tarzana, Calif: Third Line Press; 1999.
- West
KP, Katz J, Khatry SK, LeClerq SC, Pradhan EK, Shrestha SR, et al.
Double blind cluster randomised trial of low-dose supplementation with
vitamin A or beta carotene on mortality related to pregnancy in Nepal.
The NNIPS-2 Study Group. BMJ. 1999;318(7183):570-575. (Available online at: http://www.bmj.com/cgi/content/full/318/7183/570)
- Woutersen
RA, Wolterbeek AP, Appel MJ, van den Berg H, Goldbohm RA, Feron VJ.
Safety evaluation of synthetic beta-carotene. [Review] Crit Rev Toxicol. 1999;29(6):515-542. (abstract)
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