Complementary Nutrients and Supplements
In addition to hormone therapy, a number of nutrients and
supplements have been studied for their ability to enhance cognitive
function. These agents act through a variety of mechanisms, including
boosting antioxidant capabilities, improving blood flow to the brain,
and reducing the rate of neuronal destruction.
Ginkgo (Ginkgo biloba). Ginkgo extracts act as
free-radical scavengers, preventing induced lipid peroxidation in
neural tissue (Koc R et al 1995; Dorman D et al 1992; Huang P et al
2004a; Huang P et al 2004b). Ginkgo has also been shown to relax blood
vessel walls, inhibit platelet-activating factor, enhance
microcirculation, and stimulate neurotransmitters (Yoshikawa T et al
1999).
Several trials show cognitive benefits with the use of ginkgo
(Gebner B et al 1985; Vorberg G 1985). For example, a year-long study
of more than 300 participants with dementia who received 120 mg of an
extract of ginkgo showed stabilized or even improved cognitive
performance during the study (Le Bars PL et al 2000).
Ginseng (Panax ginseng). Ginseng may also be
helpful for cognitive support, especially when taken with ginkgo. In
both animal and clinical research, a combination of ginseng and ginkgo
seems promising. In rats, for example, a ginkgo/ginseng combination was
shown to enhance the learning ability of both older and younger rats
(Petkov VV et al 1993). A recent trial tested more than 250 middle-aged
human participants over a 14-week period. The participants’ cognition
and memory were assessed every four weeks. Overall, there was
significant improvement in participants who received the botanical
combination (120 mg daily of ginkgo and 200 mg daily of ginseng),
including gains in working and long-term memory (Wesnes KA et al 2000).
Huperzine A. Huperzine A, one of the constituents
found in a species of club moss (Huperzia serrata), has been studied in
China for its effects on memory, cognition, and behavior in patients
with Alzheimer’s disease and a variety of other conditions involving
impaired memory and cognition. Preliminary and double-blind research on
huperzine A suggests that it may benefit patients suffering from
dementia (Xu SS et al 1995; Zhang RW et al 1991). This possibility
needs further research and validation, and huperzine is currently in
clinical trials in the United States as a potential treatment for
Alzheimer’s.
Bacopa. Bacopa monniera is an Ayurvedic medicinal
herb that has been used clinically for enhancing memory and
ameliorating epilepsy and insomnia and as a mild sedative. The
antioxidant role of Bacopa may help explain its reported antistress,
immunomodulatory, cognition-facilitating, anti-inflammatory, and
antiaging effects (Russo A et al 2003; Kidd PM 1999).
A study measured bacopa’s ability to enhance memory and reduce
anxiety in 76 adults between 40 and 65 years of age. A significant
effect of Bacopa was shown in the retention of new information
(Roodenrys S et al 2002). Another trial examined the chronic effects of
Bacopa on cognitive function in healthy human participants. The
participants were randomly assigned to receive either 300 mg bacopa or
placebo. The results showed significant improvement in speed of visual
information processing, learning rate, memory consolidation, and
anxiety compared with the placebo group. Maximal effects were evident
after 12 weeks (Stough C et al 2001).
Bacopa may also have the potential to increase T4 levels. The
importance of Bacopa (200 mg/kg) in the regulation of thyroid hormone
concentrations in male mice was investigated. Bacopa had a
thyroid-stimulating effect and increased T4 concentrations by 41
percent (Kar A et al 2002). It did not affect levels of T3. Patients
under the care of a physician for hypothyroidism should not take bacopa
without the consent of their doctor.
Vinpocetine. Vinpocetine, derived from the
periwinkle plant, has been shown to enhance circulation and oxygen
utilization in the brain, increase the brain’s tolerance for diminished
blood flow, and inhibit abnormal platelet aggregation that can
interfere with circulation or cause a stroke (Nosalova V et al 1993).
The effects of vinpocetine on memory function were studied in 50
patients with disturbances of cerebral circulation. Improvement of
cerebral circulation was observed after vinpocetine was administered,
and after one month of vinpocetine treatment, psychological tests
showed an improvement in memory (Hadjiev D et al 1976). In a clinical
trial, vinpocetine produced a significant cognitive improvement in
older patients with chronic cerebral dysfunction (Balestreri R et al
1987).
In a study to determine how vinpocetine boosts cognition, scientists
measured the electrical firing rate in the neurons of anesthetized
rats. The administration of vinpocetine produced a significant increase
in the firing rate of neurons, and the dose of vinpocetine used to
increase electrical firing corresponded to the dose range that produced
memory-enhancing effects (Gaal L et al 1990).
Additionally, vinpocetine has been shown to protect against
oxidative damage (Pereira C et al 2000). One study suggests that the
antioxidant effect of vinpocetine might contribute to reducing neuronal
damage (Santos MS et al 2000).
Nutraceuticals
Acetyl-L-carnitine. Acetyl-L-carnitine has been
studied extensively relative to the treatment of dementia. It is
believed to be a precursor in the synthesis of acetylcholine and
participates in cellular energy production as well as in the removal of
toxic accumulation of fatty acids. In one study, 30 participants with
mild dementia were treated with 2 g daily of acetyl-L-carnitine, and 30
were treated with placebo. The results after three months showed a
significant improvement in the group receiving the acetyl-L-carnitine
(Passeri M et al 1990). Several other studies also indicate that
acetyl-L-carnitine may be helpful in improving cognitive function in
patients and possibly slowing the progression of Alzheimer’s disease
(Rai G et al 1990; Bonavita E 1986). Animal studies have shown that
acetyl-L-carnitine reverses the age-related decline in the number of
neuron membrane receptors (McDaniel MA et al 2003), and an analysis of
21 clinical trials of acetyl-L-carnitine in the treatment of mild
cognitive impairment and mild Alzheimer’s disease in rats showed it has
demonstrated significant efficacy versus placebo (Ames BN et al 2004).
Acetyl-L-carnitine arginate. Acetyl-L-carnitine
arginate is a patented form of acetyl-L-carnitine that protects brain
cells against the toxic effects of beta-amyloid, the protein implicated
in Alzheimer’s disease (Scorziello A et al 1997). It works by
stimulating the growth of neurites, which are long, branchlike fibers
that connect the brain cells and allow them to communicate, by as much
as 19.5 percent (Taglialatela G et al 1995).
Blueberry extract. Numerous studies have shown that
fruit extracts, which are rich in polyphenols, have the ability to
reverse and slow age-related brain deterioration. Among these,
blueberry extract seems especially effective. One study of rats with
beta-amyloid plaques showed that blueberry extract helped improve their
performance in a maze, leading the authors to state, “Our data indicate
for the first time that it may be possible to overcome genetic
predispositions to Alzheimer disease through diet” (Joseph JA et al
2003). An earlier study by the same research team looked at blueberry
extract’s ability to suppress oxidative stress in the brain, which is
linked to numerous age-related cognitive problems. The study found that
blueberry extracts in particular were powerful neural antioxidants
(Joseph JA et al 2000). These findings have been supported in more
recent studies examining blueberries’ role as antioxidants (Lau FC et
al 2005; Andres-Laceuva C et al 2005).
Ashwagandha. Derived from an Indian herb,
ashwagandha has been studied for its ability to rebuild damaged neural
networks and restore memory in amnesiac mice. Several lab and animal
studies have shown that ashwagandha can increase the growth of
dendrites in the brain (Tohda C et al 2005; Tohda C et al 2000). In
mice, large doses of ashwagandha (50, 100, and 200 mg/kg) were shown to
exert a dose-dependent improvement in memory after administration of
electroconvulsive shock. After one week of therapy with ashwagandha,
the mice exhibited significantly improved memory, leading the authors
to suggest that ashwagandha exhibited a brain enhancing-effect on the
animals (Dhuley JN 2001).
Glyceryl phosphoryl choline. Glyceryl phosphoryl
choline (GPC) is a form of choline that is naturally present in all the
body’s cells. Among aging adults, the rationale for GPC therapy goes
back to the hypothesis, developed more than 30 years ago, that
declining levels of acetylcholine—and a concurrent decrease in the
number of neurons that are its intended target—are responsible for a
range of cognitive deficits (Koistinaho M et al 2005). Acetylcholine is
an essential neurotransmitter involved in muscle control, sleep, and
cognition. Research has shown that GPC is a precursor of acetylcholine
that is safe and well tolerated (Amenta F et al 2005). A review of 13
published studies, involving more than 4000 participants, found that
patients taking GPC exhibited neurological improvement and relief of
clinical symptoms of chronic cerebral deterioration that was clearly
superior to placebo and equal or superior to that obtained with
prescription drugs (Parnetti L et al 2001). The same authors found that
GPC was superior to choline and lecithin and that it deserved wider
study as a therapy for stroke patients seeking to regain full cognitive
function (Parnetti L et al 2001).
Phosphatidylserine. Phosphatidylserine facilitates
the efficient transport of glucose into brain cells and boosts the
production of acetylcholine. It is sold in Europe and Japan as a
prescription drug but is available in the United States as a dietary
supplement.
European studies have shown enhancement in cognitive function when
phosphatidylserine is administered to patients in various stages of
dementia (Corrigan FM et al 1998). Phosphatidylserine has also been
shown to attenuate many neuronal effects of aging and to restore normal
memory in a variety of tasks in animal models (McDaniel MA et al 2003).
In one study, 15 healthy elderly volunteers were given 100 mg of
phosphatidylserine three times daily. They were evaluated at baseline,
after 6 weeks of treatment, and at the end of the 12-week trial. All
but two outcome measures showed significant improvements in cognitive
function (Schreiber S et al 2000).
Coenzyme Q10. Coenzyme Q10 (CoQ10) is a powerful
antioxidant. CoQ10 is incorporated into the mitochondria of cells
throughout the body and facilitates and regulates the oxidation of fats
and sugars into energy. Unfortunately, levels of CoQ10 decrease with
aging. CoQ10 levels in older individuals are only 50 percent of those
present in young adults. A National Academy of Sciences study has
documented that CoQ10 enhances metabolic energy levels of brain cells
(Matthews RT et al 1998).
Vitamins. A typical American diet does not provide
enough essential vitamins. Worse yet, older people are at greater risk
for vitamin deficiency because they tend to eat less, although their
requirements for certain vitamins, such as B6, actually rise with age.
Older people may also have problems with efficient absorption of
nutrients from food. Even healthy older people often exhibit
deficiencies in vitamin B6, vitamin B12, and folate.
Vitamins are involved in biochemical processes throughout the body
and appear to be involved in protecting and enhancing cognitive
function. In particular, the B vitamins play an integral role in the
functioning of the nervous system and help the brain synthesize
chemicals that affect mood. A balanced complex of the B vitamins is
essential for energy and for balancing hormone levels. An article in
the Journal of Psychopharmacology described a study of 76 older men who
were given vitamin B6 or placebo and then tested on memory function.
The authors concluded that vitamin B6 improved storage and information
retrieval (Deijen JB et al 1992). Another study reviewed vitamin B12
deficiency in relation to memory impairment and neuropathy in older
people and concluded that both memory impairment and neuropathy can be
successfully managed with vitamin B12 injections or supplementation
(Carmel R 1996). One study determined that low levels of folate (a B
vitamin) are associated with cognitive deficits and that patients
treated with folic acid for 60 days showed a significant improvement in
both memory and attention efficiency (Fioravanti MFE 1997).
Essential fatty acids. Essential fatty acids are
required for many biological functions, including protection from the
oxidative effects of free radicals. They are also known to be important
for good overall brain health, and a recent study demonstrated in
animal models that supplementation with omega-3 fatty acids actually
switched on brain cell genes that contribute to enhanced functioning
(Fontani G et al 2005; Kitajka K et al 2004). These biochemical details
may help us understand why diets rich in fish oils and other sources of
omega-3 fatty acids are associated with better memory and improved
cognition (Kalmijn S et al 1997).
One of the omega-3 fatty acids in particular, docosahexaenoic acid
(DHA), has attracted significant attention for its ability to boost
brain function. DHA is found in very high concentrations in cell
membranes and is required by developing infant brains. A lack of DHA in
a developing brain results in cognitive and learning deficiencies
(Turner N et al 2003). Studies have shown that DHA helps protect brain
cells by suppressing a neurotoxic substance called amyloid-beta (Likuw
WJ et al 2005), and that supplementation with DHA can reverse the
cognitive effects of DHA deficiencies in childhood (Moriguchi T et al
2003). DHA is so valuable to healthy brain function that some experts
believe infant formula should be supplemented with it (McCann JC et al
2005).
Lifestyle Changes
Taking steps to improve one’s overall health is highly recommended
to help prevent or minimize age-associated mental impairment. For
example, exercising regularly, not smoking, and monitoring blood
cholesterol levels can reduce the risk of stroke and heart disease and
keep arteries open, supplying the brain with essential oxygen and
nutrients. Abstaining from alcohol can also help preserve mental
function.
Since most people tend to eat less as they age, the consumption of
low-fat, nutrient-rich food is recommended to help prevent nutrient
deficiencies. Eating large quantities of foods rich in antioxidants,
such as blueberries, may provide protection from age-related mental
decline.
Vitamin Depot Online.com Foundation Recommendations
In recent years, inflammation has been implicated in the gradual
loss of mental function that is known as mild cognitive impairment.
Although researchers haven’t yet examined anti-inflammatories such as
ginger and rosemary in the context of mild cognitive impairment, we
believe natural nutrients may play a role in cognitive health. It is
always better to be safe than sorry and to reduce inflammation as much
as possible. There are many positive benefits to reducing inflammation
besides perhaps lowering the risk of cognitive decline. For a complete
description of Vitamin Depot Online.com’s anti-inflammatory program, please see
the chapter titled Inflammation.
The following supplements have also been shown to boost brain function directly:
- Cognitex—This
special formulation was created by the Vitamin Depot Online.com Foundation to
supply a mix of nutrients that support healthy brain function. The
recommended amount is three capsules. Each recommended daily supplement
of Cognitex contains the following:
- Glyceryl phosphoryl choline (GPC)—600 milligrams (mg)
- Phosphatidylserine—100 mg
- Vinpocetine—20 mg
- Phosphatidylcholine-Grape Seed Extract—150 mg
- Sensoril® Ashwagandha (Withania somnifera) Extract—125 mg
- Perluxan™ Hops (Humulus Iupulus) Extract—50 mg
- Ginger (Zingiber officinale) Extract (root)—25 mg
- Rosemary (Rosmarinus officinalis) Extract—50 mg
- Wild blueberry extract—150 mg
- Uridine-5'-monophosphate--50 mg
- Ginkgo biloba—120 mg/day (200 mg/day of Panax ginseng may amplify ginkgo’s effect)
- Acetyl-L-carnitine and acetyl-L-carnitine arginate—1500 to 3000 mg early in the day
- Huperzine A—50 to 100 mcg daily
- Vitamin B6—100 to 750 mg daily (Be sure to take a complete B complex each day when taking daily doses of vitamin B6 in excess of 200 mg.)
- Methylcobalamin (B12)—1000 to 5000 microgram (mcg) daily sublingually
- Folic acid—800 mcg daily orally; should be taken with vitamin B12
- Vitamin C—at least 2000 mg daily
- Mixed vitamin E—400 International units (IU) daily
- CoQ10—30 to 300 mg daily of a highly absorbable form
- Vinpocetine—15 to 30 mg daily
- Bacopa—As directed, depending on extract strength
- EPA/DHA—700 to 2100 mg EPA and 500 to 1500 mg DHA daily with food
In addition, hormone restoration with bioidentical hormones may be
indicated, depending on the levels of vital hormones, including
pregnenolone, estrogen, and testosterone. For more information on
hormone blood testing and hormone restoration, call 1-800-544-4440 or
visit www.lef.org. A reasonable beginning dose of DHEA is 15 to 75 mg,
followed by blood testing in three to six weeks to make sure you have
achieved optimal levels of this hormone. |
Mild Cognitive Impairment Safety Caveats
An aggressive program of dietary supplementation should not be
launched without the supervision of a qualified physician. Several of
the nutrients suggested in this protocol may have adverse effects.
These include:
Acetyl-L-Carnitine
- Acetyl-L-carnitine can cause gastrointestinal symptoms such as nausea and diarrhea.
Coenzyme Q10
- See your doctor and monitor your blood glucose level frequently if
you take CoQ10 and have diabetes. Several clinical reports suggest that
taking CoQ10 may improve glycemic control and the function of beta
cells in people who have type 2 diabetes.
- Statin drugs (such as lovastatin, simvastatin, and pravastatin) are known to decrease CoQ10 levels.
EPA/DHA
- Consult your doctor before taking EPA/DHA if you take warfarin
(Coumadin). Taking EPA/DHA with warfarin may increase the risk of
bleeding.
- Discontinue using EPA/DHA 2 weeks before any surgical procedure.
Folic Acid
- Consult your doctor before taking folic acid if you have a vitamin B12 deficiency.
- Daily doses of more than 1 milligram of folic acid can
precipitate or exacerbate the neurological damage caused by a vitamin
B12 deficiency.
Ginger
- Do not take ginger if you have a bile duct obstruction or gallstones. Ginger may stimulate bile production.
- High doses of ginger (6 grams or more) can cause damage to the stomach lining and ulcers.
- Ginger can cause anllergic skin reactions.
- Consult your doctor before taking ginger if you take blood
thinners such as warfarin (Coumadin). Ginger can increase the risk of
bleeding.
Ginkgo biloba
- Individuals with a known risk factor for intracranial hemorrhage,
systematic arterial hypertension, diabetes, or seizures should avoid
ginkgo.
- Do not use prior to or after surgery.
- Avoid concomitant use of ginkgo with NSAIDS, blood thinners, diuretics, or SSRI’s.
- Gastrointestinal symptoms (nausea and diarrhea) may occur.
- Allergic skin reactions may occur.
- Elevations in blood pressure may occur.
Huperzine A
- Do not take huperzine A if you have a seizure disorder, cardiac
arrhythmias, asthma, irritable bowel syndrome, inflammatory bowel
disease, or malabsorption syndrome.
- Huperzine A can cause excessive perspiration, blurred
vision, fasciculations (involuntary muscle twitching), dizziness,
bronchospasm, bradycardia, arrhythmias, seizures, urinary incontinence,
increased urination, excessive salivation, and gastrointestinal
symptoms such as nausea, abdominal cramps, diarrhea, and vomiting.
Phosphatidylcholine
- Phosphatidylcholine can cause increased salivation, a metallic
taste, headache, drowsiness, and gastrointestinal symptoms such as
nausea and diarrhea.
Vitamin B6
- Individuals who are being treated with levodopa without taking
carbidopa at the same time should avoid doses of 5 milligrams or
greater daily of vitamin B6.
Vitamin B12 (cyanocobalamin)
- Do not take cyanocobalamin if you have Leber's optic atrophy.
Vitamin C
- Do not take vitamin C if you have a history of kidney stones or of
kidney insufficiency (defined as having a serum creatine level greater
than 2 milligrams per deciliter and/or a creatinine clearance less than
30 milliliters per minute.
- Consult your doctor before taking large amounts of vitamin C
if you have hemochromatosis, thalassemia, sideroblastic anemia, sickle
cell anemia, or erythrocyte glucose-6-phosphate dehydrogenase (G6PD)
deficiency. You can experience iron overload if you have one of these
conditions and use large amounts of vitamin C.
Vitamin E
- Consult your doctor before taking vitamin E if you take warfarin (Coumadin).
- Consult your doctor before taking high doses of vitamin E if you have a vitamin K deficiency or a history of liver failure.
- Consult your doctor before taking vitamin E if you have a
history of any bleeding disorder such as peptic ulcers, hemorrhagic
stroke, or hemophilia.
- Discontinue using vitamin E 1 month before any surgical procedure.
Vinpocetine
- Do not take vinpocetine if you have a history of allergic or hypersensitivity reactions to any vinca alkaloids.
- Consult your doctor before taking vinpocetine if you take
warfarin (Coumadin). Have your international normalized ratio monitored
frequently by your doctor if you take vinpocetine and warfarin.
- Consult your doctor before taking vinpocetine if you have
low blood pressure (including transient low blood pressure or
orthostatic hypotension). Prolonged use of vinpocetine may lead to
slight reductions in systolic and diastolic blood pressures.
- Vinpocetine can cause temporary rapid heartbeat, pressure
headache, facial flushing, dizziness, insomnia, drowsiness, and
gastrointestinal symptoms such as nausea and diarrhea.
For more information see the Safety Appendix |