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DMAE - Ginkgo Caps
DMAE is a memory enhancing substance common to a number of drugs that are known to stabilize cell membranes. Cell membrane degradation has been proposed as one of the prime mechanisms of aging. DMAE is a precursor to choline and acetylcholine. However, DMAE has been shown to cross the blood-brain barrier faster than choline. It is the choline inside cells that is converted to phosphatidylcholine, used in the building and repair of cell membranes, especially in the brain. In Europe, the drug Centrophenoxine, which combines DMAE with a synergistic chemical called p-chlorophenoxyacetate, is prescribed to boost cognitive function in the aged. It is likely that all the benefits of Centrophenoxine may be obtained more inexpensively from DMAE. Ginkgo Ginkgo may: DMAE-Ginkgo capsules provide both of these valuable brain nutrients plus additional cofactors, in one capsule. A capsule
contains: Dosage and
use - Four capsules
daily are recommended for those with neural impairment. - This product need not be taken at meals.
DMAE: The
Smart Supplement Another lesser-known compound in fish, dimethylaminoethanol (DMAE), is increasingly favored by medical practitioners for its role in boosting brain power. DMAE has shown positive results in the treatment of a variety of cognitive and disruptive disorders, including attention-deficit hyperactivity disorder (ADHD) and memory lapses. DMAE is even being used in skin care products designed to treat sagging skin and age spots. Help for
Alzheimers Calmer Kids A prescription form of DMAE, called Deaner or Deanol, was already in use in the 1960s and 1970s for the treatment of learning and behavioral problems associated with shortened attention span.4 As early as 1959, treatment with DMAE was demonstrated to result in significantly improved test scores.5 A 1974 report on DMAE focused on two 10-week, double-blind, placebo-controlled trials involving 124 children with ADHD-related diagnoses. In one of these trials, positive results using DMAE were comparable to those using Ritalin®.6 Similar positive results were also seen in a 1975 study, wherein a placebo-controlled trial in 74 children found that DMAE at 500mg daily was as effective as methylphenidate.4 In 1983, the FDA insisted on additional studies to prove the effectiveness of Deaner. Because the clinical trials would have been more expensive than the products sales could support, Deaner was taken off the market. DMAE, however, has continued to be available as a natural nutritional supplement, and is a subject of more recent investigations into so-called smart drugs. Research has shown that DMAEs cholinergic effects help produce brain chemicals such as acetylcholine that are necessary for mental sharpness.8 Some individuals accordingly report that DMAE supplementation causes a noticeable boost in their ability to concentrate. DMAE users also routinely report better memory (especially short-term memory), as well as improved focus, mental clarity, and sleep patterns, all of which may be particularly valuable for those who work in high-pressure or deadline-oriented environments. Many nutritionally aware physicians routinely prescribe DMAE in combination with additional memory enhancers such as phosphatidylcholine, a dietary supplement. DMAEs action as an acetylcholine precursor may help with the memory lapses that commonly occur with normal aging. Healing
Properties Age spots, or liver spots, also may respond effectively to DMAE in cream, gel, or tablet form. Studies have shown that DMAEs membrane-stabilizing properties reduced the accumulation of lipofuscin deposits inside cells.10 Lipofuscin, a brownish cellular pigment consisting of aggregated chunks of molecular waste formed by the inefficient metabolism of fatty acids, tends to occur in the cells of older people and is primarily responsible for age spots. DMAE has been shown to flush excess lipofuscin from affected skin cells.11 DMAE is a potent, site-specific free radical scavenger.12 An in-vitro study found that adding DMAE to myocytes (the hearts pumping cells) protected individuals from cell damage resulting from ischemia, a lack of oxygen and blood flow to the heart, and from metabolic inhibition.13 Taken in the proper dosage, DMAEs antioxidant effects can offer probable benefits of value in the maintenance of overall cellular health. As with all nutritional supplements or medications, check with your regular medical practitioner, caregiver, or pharmacist before incorporating DMAE supplementation in your normal health care regimen. For topical DMAE creams or gels, follow the packages application instructions carefully. Oral tablets or
capsules in doses from 50 to 130 mg are common, while pills containing
up to 600 mg are also available. Regardless of the amount, start slowly
with a low dose and see how you respond before increasing the amount.
DMAE should be taken with meals for best absorption. Capsules can even
be broken open and mixed in fruit juices or smoothies in the morning
for an effective brain kick start to the day. 2. Jope RS, Jenden DJ. Dimethylaminoethanol (deanol) metabolism in rat brain and its effect on acetylcholine synthesis. J Pharmacol Exp Ther. 1979 Dec;211(3):472-9. 3. Millington WR, McCall AL, Wurtman RJ. Deanol acetamidobenzoate inhibits the blood-brain barrier transport of choline. Ann Neurol. 1978 Oct;4(4):302-6. 4. Lewis JA, Young R. Deanol and methylphenidate in minimal brain dysfunction. Clin Pharmacol Ther. 1975 May;17(5):534-40. 5. Pfeiffer CC. Parasympathetic neurohumors. Possible precursors and effect on behavior. Int Rev Neurobiol. 1959;1:195-244. 6. Re O. 2-Dimethylaminoethanol (deanol): a brief review of its clinical efficacy and postulated mechanism of action. Curr Ther Res Clin Exp. 1974 Nov;16(11):1238-42. 7. Ward D. Smart drugs and nutrients: how to improve your memory and increase your intelligence using the latest discoveries in neuroscience. Petaluma, CA: Smart Publications; 1992. 8. Danysz A, Smietanski J, Panek W. The influence of 2-dimethylaminoethanol (DMAE) on the mental and physical efficiency in man. Act Nerv Super (Praha). 1967 Nov;9(4):417. 9. Uhoda I, Faska N, Robert C, Cauwenbergh G, Pierard GE. Split face study on the cutaneous tensile effect of 2-dimethylaminoethanol (deanol) gel. Skin Res Technol. 2002 Aug;8(3):164-7. 10. Dylewski DP, Nandy S, Nandy K. Effects of centrophenoxine on lipofuscin in the retinal pigment epithelium of old mice. Neurobiol Aging. 1983;4(1):89-95. 11. Riga S, Riga D. Effects of centrophenoxine on the lipofuscin pigments in the nervous system of old rats. Brain Res. 1974 Jun 7;72(2):265-75. 12. Zs-Nagy I. Pharmacological interventions against aging through the cell plasma membrane: a review of the experimental results obtained in animals and humans. Ann N Y Acad Sci. 2002 Apr;959:308-20. 13. Post JA, Bijvelt JJ, Verkleij AJ. Phosphatidylethanolamine and sarcolemmal damage during ischemia or metabolic inhibition of heart myocytes. Am J Physiol. 1995 Feb; 268(2 Pt 2): H773-80. 14. Casey DE, Denney D. Dimethylaminoethanol in tardive dyskinesia. N Engl J Med. 1974 Oct 10;291(15):797. 15. Fisman M, Mersky H, Helmes E. Double-blind trial of 2-dimethylaminoethanol in Alzheimers disease. Am J Psychiatry. 1981 Jul;138(7):970-2. 16. Casey DE. Mood
alterations during deanol therapy. Psychopharmacology (Berl). 1979 Apr
11;62(2):187-91.
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These statements have not been evaluated by the FDA. These products are not intended to diagnose, treat, cure, or prevent any disease
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